Health intervenes in neighborhoods; says cholera under control
The healthcare system has epidemics and disease outbreaks. It does not, however, address the chronic diseases that affect and kill thousands.
Public Health teams are still in the neighborhoods in action to prevent the spread of cholera.
However, the Ministry of Health is still awaiting the results of three tests on an equal number of patients with suspected signs of the disease. Teams of health workers and epidemiologists are in the affected areas, carrying educational messages about the need for the population to educate themselves and have access to safe drinking water.
“There are no new details of the situation, but all our teams are in the neighborhoods where cases have been reported,” Carlos Suero, Director of Communications of the Ministry of Health, told Hoy.
The situation
Dr. Gina Estrella, director of Risk Management and Disaster Attention of the Ministry of Health, emphasized that tests from the Doctor Defilló Laboratory have registered only 17 proven cases. Therefore, three more trials are expected.
The specialists
Both the Dominican Society of Infectious Diseases and the Society of Gastroenterology have insisted on the need for the authorities to make more comprehensive interventions in the affected areas. Dr. Clevy Perez has been adamant that Public Health should convince the Government of the need to supply water permanently to the inhabitants of the neighborhoods. The Society of Gastroenterology has said the same. Furthermore, they believe education and hygienic measures should be taken to the utmost.
Doctors
In another order, but in the same field of Health, the doctors met with the National Council of Social Security after the union, which groups the professionals continued with the strikes and disaffiliation to the ARS.
This time the strike and disaffiliation affected the affiliates of the Administradora de Riesgos de Salud Humano. Unfortunately, no agreements were reached at yesterday’s meeting, but the parties were summoned for next week.
Neither the Minister of Health, Dr. Daniel Rivera, nor the National Social Security Council president, Luis Miguel De Camps, participated in the last meeting. This time there has been one of the system’s most complex and extended crises. Doctors are demanding their demands and want changes.
2 years 3 months ago
Health, Local
Public Health monitors two with suspected cholera
Santo Domingo, DR
A low incidence of viruses that weeks ago created pressures on the health system, among them influenza, Covid-19, and dengue, while the authorities put more emphasis on the control of cholera, produced by bacteria, to prevent its further spread.
Santo Domingo, DR
A low incidence of viruses that weeks ago created pressures on the health system, among them influenza, Covid-19, and dengue, while the authorities put more emphasis on the control of cholera, produced by bacteria, to prevent its further spread.
Yesterday, the Ministry of Public Health kept under surveillance two hospitalized patients suspected of cholera, but with stable evolution, and assured that the case of a patient coming from Boca Chica with a diarrhea condition is not cholera, but that in any case, for preventive purposes, they proceeded to intervene in the community where he resides.
The details were given to Listín Diario by Dr. Gina Estrella, in charge of Emergencies and Disasters of the Ministry of Public Health, who assured that the country maintains up to now the figure of 17 confirmed cases of cholera and that in Zurza, where an outbreak was registered, control of the cases was achieved and that the dredging of the Isabela river was started to guarantee its fluidity.
He recalled that in addition to Zurza, cases were initially detected in Capotillo and two imported cases in San Carlos. However, prevention interventions are extended to all health areas of Greater Santo Domingo, as well as active surveillance at the national level. He said that out of 90 random cholera tests taken over the weekend in La Zurza and Capotillo, only four were positive, of which two were asymptomatic persons.
Regarding the cases of the influenza virus, Covid-19, and dengue, which maintained high levels of circulation during the last months of last year, the director of Emergencies and Disasters pointed out that they currently maintain a low incidence at the national level.
2 years 3 months ago
Health, Local
Jamaica among beneficiaries of multimillion-dollar vaccine initiative
JAMAICA is among 12 countries set to benefit from a multimillion-dollar vaccine initiative which is expected to strengthen COVID-19 vaccination delivery and lessen hesitancy in taking the jab.
Under the project, which is called Canada's Global Initiative for Vaccine Equity (CanGIVE), CAD$45 million was donated to Pan American Health Organization (PAHO) and CAD$70 million donated to United Nations Children's Fund (UNICEF).
Canada's Minister of International Development Harjit Sajjan said the project is his country's commitment to equitable access to COVID-19 vaccines so as to strengthen health systems.
"COVID has dominated much of our lives in the last three years [but] the pandemic has slipped a bit from the headlines over the last few months. It's good to see that our lives are getting back to normal but we need to remember that COVID is still here," said Sajjan, who was speaking at the event launch held at the International Seabed Authority in Kingston on Friday.
"Although we wish that we could turn a page on COVID altogether, we know that is not a simple thing to do. There is still work to do to control the spread of this virus, moving to recovery, and to build stronger health systems," he added.
Of the funds donated to UNICEF, CAD$5.5 million will assist with boosting Jamaica's vaccine efforts such as reinforcing childhood vaccination, establishing two new oxygen plants in two hospitals, providing technical assistance to optimise the oxygen supply chain in the country, upgrading cold chain equipment, and training public health staff in cold chain management and monitoring.
And CAD$4.7 million of the funds donated to PAHO will be allocated to initiatives such as increasing access to COVID-19 vaccination by strengthening health systems, and developing and supporting the implementation of information systems and digital platforms for COVID-19 vaccine surveillance. The funds will also assist with generating demand for COVID-19 vaccines through outreach, risk communication and community engagement.
Minister of Health and Wellness Dr Christopher Tufton said the funds under CanGIVE are timely.
"It provides a well-needed boost to our initiatives, new energy to increase awareness, and [will] hopefully to let Jamaicans and those in the regions recognise the importance of these efforts," he said.
"What is appealing about this initiative is that at a time when we recognise that our overall vaccination programmes are losing momentum, the five components of the initiative speak to the strengthening of health systems, not just for COVID but of vaccinations generally," he added
Tufton said in coming weeks the health ministry will launch an initiative that will seek to re-emphasise and focus the attention of Jamaicans around the value of immunisation, and hopefully provide a greater incentive and motivation for all concerned parents and others to participate in the programme.
The other countries to benefit from CanGIVE are Bangladesh, Ghana, Haiti, Congo, South Africa, Tanzania, Mozambique, Senegal, Nigeria, Côte d'Ivoire and Colombia.
2 years 3 months ago
PAHO/WHO | Pan American Health Organization
OPS y Canadá intensifican esfuerzos para llevar vacunas contra COVID-19 a poblaciones en situación de vulnerabilidad en América Latina y el Caribe
PAHO and Canada step up efforts to bring COVID-19 vaccines to populations in situations of vulnerability in Latin America and the Caribbean
Oscar Reyes
13 Jan 2023
PAHO and Canada step up efforts to bring COVID-19 vaccines to populations in situations of vulnerability in Latin America and the Caribbean
Oscar Reyes
13 Jan 2023
2 years 3 months ago
We don’t need to pay doctors more, but we need more doctors to pay
The underlying causes of the overcrowding in our hospital emergency departments is obvious enough, and there have been many expert medical views expressed on possible solutions to the problem. One I can recommend is our own Chris Luke who has put forward his views here.…
The post We don’t need to pay doctors more, but we need more doctors to pay appeared first on Irish Medical Times.
2 years 3 months ago
Editorial, Opinion, comment, overcrowding, Terence Cosgrave
Specialists look positively at complex, dynamic landscape of wet AMD
With emerging treatment options and technological advances that make detection and monitoring more precise, timely and easier, wet age-related macular degeneration continues to be a vibrant area of research and innovation.The path is not always smooth: The risk for severe inflammatory events cooled down the early enthusiasm for Beovu (brolucizumab, Novartis), and concerns about septum dislodgem
ent and potential adverse events led Genentech to voluntarily recall Susvimo (ranibizumab injection).However, progress and innovation never come without challenges, and the landscape for wet AMD today
2 years 3 months ago
Authorities clean, but unsanitary conditions are part of La Zurza
Even though authorities continue to carry out cleaning tasks in La Zurza to contain the spread of cholera in the national territory, unsanitary actions are still part of a large number of residents who refuse to apply disease-fighting security measures.
Since the presence of the Vibrio cholera bacterium was discovered in the country again, the neighborhood above has led to several infections of the condition. It has caused the appearance of others in neighboring sectors such as Villa Agricolas, for which the ministries of Health Public, Public Works, Environment, and the National District Mayor’s Office are stepping up sanitation efforts.
In addition to cleaning the wells, the community is constructing four containers to collect garbage that falls from the houses in the upper part of the community so that it does not contaminate the waters. When speaking with this outlet, Juan Luis Vásquez, a member of the team doing the work, stated that they are also encouraging people not to throw their waste in the area to avoid disease outbreaks. “We’re trying to make them aware because we’re doing this for their benefit,” he explained.
Another government measure to halt the spread of the disease is the dredging of a large portion of the Isabela River, which borders La Zurza and, according to authorities, contains the bacteria that transmits cholera. According to official information, a dividing mesh will be placed around the stream once the sanitation is completed to prevent it from becoming clogged with solid waste again.
2 years 3 months ago
Health, Local
Deficiencies trigger emotional disorders in the Dominican Republic
The economic and health disturbances faced by the Dominican population, especially due to the loss of jobs and the constant threats of outbreaks and epidemics, have become two important stressors that are contributing to an increase in the cases of young people and adults who have mental health problems.
This is stated by psychologist María de Los Santos, president of the Association of Health Psychologists (ASOPSALUD), noting that it is common to receive patients with emotional conditions in hospital consultations, manifested mainly in panic attacks, post-traumatic stress, social isolation, sleep disorder, depression, use and abuse of psychoactive substances, deep sadness, and suicide attempts.
She said that although cases of this nature have always attended the psychological services of health centers, currently or in the post-pandemic there has been a greater increase in emotional disorders since during the pandemic many people lost their jobs, and loved ones and they felt afraid of getting sick and not being able to seek financial support. “Now we are receiving more people with grief, grief in the Dominican population, people have little tolerance, they get irritated easily.”
The president of the Association of Health Psychologists said that in hospital consultation, especially in hospitalized patients who are going through a medical breakdown, there are frequent cases of mothers who become ill and are emotionally affected because they cannot afford the treatment and fear die and leave their young children alone. Many people believe that getting sick will affect the family economy or that they will not be able to enter the professional and productive world, which also leads them to depression.
2 years 3 months ago
Health, Local
Medical News, Health News Latest, Medical News Today - Medical Dialogues |
AbbVie raises sales outlook of Skyrizi, Rinvoq to USD 17.5 billion in 2025
New Delhi: AbbVie Inc on Tuesday raised its 2025 sales forecast of its newer immunology drugs Skyrizi and Rinvoq to more than $17.5 billion as it hopes to replace the loss of revenue from its blockbuster rheumatoid arthritis drug Humira.
Also Read: AbbVie, Teva finalize USD 6.6 billion US opioid settlements
The company's previous sales outlook for Skyrizi and Rinvoq in 2025 was more than $15 billion.
AbbVie also expects peak sales of the drugs to exceed $21 billion in 2027. The two drugs are part of the company's long-term growth strategy to offset Humira's loss of exclusivity.
The drug maker has been in contract negotiations with insurers and pharmacy benefit managers for Humira for this year, and said in October that pricing of its rivals would determine the drug's sales this year.
2 years 3 months ago
State News,News,Delhi,Industry,Pharma News,Latest Industry News
Medical News, Health News Latest, Medical News Today - Medical Dialogues |
FDA approves first rescue treatment of asthma for adults
The US Food and Drug Administration (FDA) has approved albuterol/budesonide (Airsupra) for prevention and treatment of bronchoconstriction and to reduce the risk of exacerbations in people with asthma aged 18 years and older.
Airsupra is a first-in-class, pressurised metered-dose inhaler (pMDI), fixed-dose combination rescue medication containing albuterol, a short-acting beta2-agonist (SABA), and budesonide, an anti-inflammatory inhaled corticosteroid (ICS).
The US approval was based on positive results from a global Phase III clinical trial programme for Airsupra comprising four studies involving more than 4,000 patients (including the MANDALA and DENALI trials1,2), which was conducted successfully by Avillion under an exclusive clinical co-development agreement with AstraZeneca.
Under its 2018 agreement, Avillion had regulatory responsibility including filing the New Drug Application (NDA) through to FDA approval in the US. Following this approval, AstraZeneca has the option, upon making certain financial payments to Avillion, to commercialise Airsupra in the US.
This milestone continues Avillion's 100% successful rate in clinical co-development partnerships for the global pharmaceutical and biotech industry.
In MANDALA, Airsupra significantly reduced the risk of severe exacerbations compared to albuterol in patients with moderate to severe asthma when used as an as-needed rescue medication in response to symptoms.1 The results from the MANDALA trial were published in the New England Journal of Medicine in May 2022.1 In DENALI, Airsupra significantly improved lung function compared to the individual components, albuterol and budesonide, in patients with mild to moderate asthma.2 The safety and tolerability of Airsupra in both trials were consistent with the known profiles of the components with the most common adverse events including headache, oral candidiasis, cough and dysphonia.
The co-development partnership between AstraZeneca and Avillion has recently expanded to include the BATURA study, a randomised Phase IIIb decentralised trial to further assess the role of Airsupra in reducing the risk of asthma exacerbations.
The Airsupra clinical co-development programme was funded by Blackstone Life Sciences, Royalty Pharma and Abingworth.
Bradley E. Chipps, Past President of the American College of Allergy, Asthma & Immunology and Medical Director of Capital Allergy & Respiratory Disease Center in Sacramento, US, said: "People with asthma are at risk of severe exacerbations regardless of their disease severity or level of control. Current albuterol rescue inhalers alleviate acute symptoms, but do not treat the underlying inflammation in asthma. The approval of Airsupra means that, for the first time, adults with asthma in the US have a rescue treatment to manage both their symptoms and the inflammatory nature of their disease."
Allison Jeynes, MD, Chief Executive Officer of Avillion, said: "We're delighted that our clinical co-development programme with AstraZeneca has been successful and that Airsupra has been approved in the US as a new treatment option for asthma patients. The Airsupra approval continues our 100% success rate facilitating clinical co-development programmes with pharma companies, demonstrating the strong value our innovative model can provide to partners and the excellence and dedication of our international team. We've had an excellent working relationship with AstraZeneca and are excited to continue our partnership with the BATURA Phase IIIb study, which is looking to continue building the evidence base of Airsupra to reduce the risk of asthma exacerbations."
Asthma
Asthma is a chronic, inflammatory respiratory disease with variable symptoms that affects as many as 262 million people worldwide,4 including over 25 million in the US.5
Patients with asthma experience recurrent breathlessness and wheezing, which varies over time, and in severity and frequency.6 These patients are at risk of severe exacerbations regardless of their disease severity, adherence to treatment or level of control.
There are an estimated 136 million asthma exacerbations globally per year,9 including 10 million in the US;5 these are physically threatening and emotionally significant for many patients11 and can be fatal.
Inflammation is central to both asthma symptoms7 and exacerbations.12 Many patients experiencing asthma symptoms use a SABA (e.g. albuterol) as a rescue medicine;13-15 however, taking a SABA alone does not address inflammation, leaving patients at risk of severe exacerbations,16 which can result in impaired quality of life,17 hospitalisation18 and frequent oral corticosteroid (OCS) use.18 Treatment of exacerbations with as few as 1-2 short courses of OCS are associated with an increased risk of adverse health conditions including type 2 diabetes, depression/anxiety, renal impairment, cataracts, cardiovascular disease, pneumonia and fracture.19 International recommendations from the Global Initiative for Asthma no longer recommend SABA alone as the preferred rescue therapy.
MANDALA, DENALI and the CREST (Combination REliever STudies) programme
The CREST clinical trial programme studied the efficacy and safety of PT027 and included the MANDALA,1,20,21 DENALI2,22,23 and TYREE25 Phase III trials.
MANDALA1,20,21 was a Phase III, randomised, double-blind, multicentre, parallel-group, event-driven trial evaluating the efficacy and safety of Airsupra compared to albuterol on the time to first severe asthma exacerbation in 3,132 adults, adolescents, and children (aged 4–11 years) with moderate to severe asthma taking ICS alone or in combination with a range of asthma maintenance therapies, including long-acting beta2-agonists (LABA), leukotriene receptor antagonists (LTRA), long-acting muscarinic antagonists (LAMA) or theophylline. The trial comprised a two-to-four-week screening period, at least a 24-week treatment period and a two-week post-treatment follow-up period.
Patients were randomly assigned to one of the following three treatment groups in a 1:1:1 ratio: Airsupra 180/160mcg (excluding children aged 4–11 years), albuterol/budesonide 180/80mcg or albuterol 180mcg, taken as an as-needed rescue medicine. Airsupra and the albuterol comparator were delivered in a pMDI using AstraZeneca's Aerosphere delivery technology. The primary efficacy endpoint was the time to first severe asthma exacerbation during the treatment period. Secondary endpoints included severe exacerbation rate (annualised), total systemic corticosteroid exposure (annualised), asthma control and health-related quality of life.
Results from the positive MANDALA Phase III trial showed that Airsupra demonstrated a statistically significant reduction in the risk of a severe exacerbation versus albuterol rescue in patients with moderate to severe asthma1,21. Compared with albuterol rescue, Airsupra at the 180mcg albuterol/160mcg budesonide dose reduced the risk of a severe exacerbation by 27% (p<0.001) in adults and adolescents
Primary and secondary endpoint results in adults and adolescents
(pre-planned on-treatment efficacy analysis)
Deterioration of asthma requiring use of SCS for ≥3 days, or inpatient hospitalisation, or emergency room visit, that required SCS. bBefore discontinuation of randomised treatment or change in maintenance therapy.
CI, confidence interval; SCS, systemic corticosteroid; SD, standard deviation
Primary endpoint results in adults, adolescents, and children
(pre-planned on-treatment efficacy analysis)
Deterioration of asthma requiring use of SCS for ≥3 days, or inpatient hospitalisation, or emergency room visit, that required SCS. bBefore discontinuation of randomised treatment or change in maintenance therapy.
CI, confidence interval
Adverse events (AEs) were similar across the treatment groups in the trial and consistent with the known safety profiles of the individual components, with the most common AEs including nasopharyngitis and headache.
DENALI2,23,24 was a Phase III, randomised, double-blind, placebo-controlled, multicentre, parallel-group trial evaluating the efficacy and safety of Airsupra compared to its components albuterol and budesonide on improvement in lung function in 1,001 adults, adolescents, and children aged 4–11 years with mild to moderate asthma previously treated either with SABA as-needed alone or in addition to regular low-dose ICS maintenance therapy. The trial comprised a two-to-four-week screening period, a 12-week treatment period and a two-week post-treatment follow-up period.
Patients were randomly assigned to one of the following five treatment groups in a 1:1:1:1:1 ratio: Airsupra 180/160mcg four times daily (excluding children aged 4–11 years), albuterol/budesonide 180/80mcg four times daily, albuterol 180mcg four times daily, budesonide 160mcg four times daily (excluding children aged 4–11 years) and placebo four times daily. Airsupra, the albuterol and budesonide comparators and placebo were delivered in a pMDI using AstraZeneca's Aerosphere delivery technology. The dual primary efficacy endpoints were change from baseline in FEV1 area under the curve 0-6 hours over 12 weeks of Airsupra compared to budesonide to assess the effect of albuterol and change from baseline in trough FEV1 at Week 12 of Airsupra compared to albuterol to assess the effect of budesonide. Secondary endpoints included the time to onset and duration of response on day one, number of patients who achieved a clinically meaningful improvement in asthma control from baseline at Week 12 and trough FEV1 at Week 1.
In the trial, Airsupra demonstrated a statistically significant improvement in lung function measured by forced expiratory volume in one second (FEV1), compared to the individual components albuterol and budesonide, and compared to placebo in patients with mild to moderate asthma aged 12 years or older. Onset of action and duration of effect were similar for Airsupra and albuterol. The safety and tolerability of Airsupra in DENALI was consistent with the known profiles of the components.
2 years 3 months ago
Medicine,Pulmonology,Medicine News,Pulmonology News,Top Medical News
News Archives - Healthy Caribbean Coalition
Noncommunicable Diseases and Mental Health in Small Island Developing States – A Discussion Paper by Civil Society
Photo credit: NCD Alliance/Still from Turning the Tide video series
The Healthy Caribbean Coalition (HCC) has led the development of this discussion paper in collaboration with a group of like-minded civil society representatives from other Small Island Developing States (SIDS) regions, and with the support of the NCD Alliance (NCDA), a global network of CSOs also dedicated to NCD prevention and control worldwide.
This discussion paper was developed as a contribution to the High-Level Technical Meeting and Ministerial Conference on NCDs and Mental Health in SIDS, which will be convened by the World Health Organization (WHO) in Barbados, in January and June 2023 respectively.
This discussion paper outlines the unique characteristics of SIDS and the challenges they face, particularly related to their size, geography, and small populations; constraints for achieving economies of scale due to their small domestic markets, limited resources, and undiversified economies; and threats from the climate crisis and food and nutrition insecurity. These challenges, among others, have been aggravated by the 2019 coronavirus (COVID-19) pandemic, which has put at further risk SIDS’ efforts to mount efficient and effective responses to their disproportionate burden of NCDs, using approaches that are equity- and rights-based, multisector, and multistakeholder.
Civil society is a critical stakeholder, along with government and the private sector free from conflicts of interest, in the response to the major NCDs—heart disease and stroke, diabetes, cancer, chronic respiratory diseases, and mental, neurological, and substance abuse disorders (MNSDs). CSOs advocate for and contribute to interventions that address NCDs and their risk factors—particularly poor diets, tobacco use, alcohol use, physical inactivity, and air pollution—as well as the determinants of health—social, economic, environmental, commercial, political, legal, and other non-medical factors that strongly influence health outcomes. In producing this discussion paper, HCC, NCDA, and SIDS civil society representatives analysed the NCD situation in SIDS across various regions, built on global and regional frameworks for the reduction of NCDs and their underlying causes, and identified priorities, recommendations, and key asks for inclusion in the report of the January 2023 High-Level Technical Meeting and the outcome document of the June 2023 Ministerial Conference on NCDs and Mental Health in SIDS.
Read or download the discussion paper.
Authors welcome comments on this discussion paper at hcc@healthycaribbean.org until 28 February 2023.
The post Noncommunicable Diseases and Mental Health in Small Island Developing States – A Discussion Paper by Civil Society appeared first on Healthy Caribbean Coalition.
2 years 3 months ago
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PAHO/WHO | Pan American Health Organization
PAHO platform brings health monitoring of chronic diseases to remote populations
PAHO platform brings health monitoring of chronic diseases to remote populations
Cristina Mitchell
12 Jan 2023
PAHO platform brings health monitoring of chronic diseases to remote populations
Cristina Mitchell
12 Jan 2023
2 years 3 months ago
GOP House Opens With Abortion Agenda
The Host
Julie Rovner
KHN
Julie Rovner is Chief Washington Correspondent and host of KHN’s weekly health policy news podcast, “What the Health?” A noted expert on health policy issues, Julie is the author of the critically praised reference book “Health Care Politics and Policy A-Z,” now in its third edition.
Having spent its entire first week choosing a speaker, the Republican-led U.S. House finally got down to legislative business, including passing two bills backed by anti-abortion groups. Neither is likely to become law, because they won’t pass the Senate nor be signed by President Joe Biden. But the move highlights how abortion is sure to remain a high-visibility issue in the nation’s capital.
Meanwhile, as open enrollment for the Affordable Care Act nears its Jan. 15 close, a record number of people have signed up, taking advantage of renewed subsidies and other help with medical costs.
This week’s panelists are Julie Rovner of KHN, Margot Sanger-Katz of The New York Times, Alice Miranda Ollstein of Politico, and Sarah Karlin-Smith of the Pink Sheet.
Panelists
Sarah Karlin-Smith
Pink Sheet
Alice Miranda Ollstein
Politico
Margot Sanger-Katz
The New York Times
https://www.nytimes.com/by/margot-sanger-katz
Among the takeaways from this week’s episode:
- The House now has a speaker after 15 rounds of full-chamber roll call votes. That paved the way for members to be sworn in, committee assignments to be made, and new committee chairs to be named. Cathy McMorris Rodgers (R-Wash.) and Jason Smith (R-Mo.) will be taking the helm of major health committees.
- McMorris Rodgers will lead the House Energy and Commerce Committee; Smith will be the chairman of Ways and Means. Unlike McMorris Rodgers, Smith has little background in health issues and has mostly focused on tax issues in his public talking points. But Medicare is likely to be on the agenda, which will require the input of the chairs of both committees.
- One thing is certain: The new GOP-controlled House will do a lot of investigations. Republicans have already reconstituted a committee to investigate covid-19, although, unlike the Democrats’ panel, this one is likely to spend time trying to find the origin of the virus and track where federal dollars may have been misspent.
- The House this week began considering a series of abortion-related bills — “statement” or “messaging” bills — that are unlikely to see the light of day in the Senate. However, some in the caucus question the wisdom of holding votes on issues like these that could make their more moderate members more vulnerable. So far, bills have had mostly unanimous support from the GOP. Divisions are more likely to emerge on topics like a national abortion ban. Meanwhile, the Title X program, which pays for things like contraception and testing for sexually transmitted infections, is becoming a hot topic at the state level and in some lawsuits. A case in Texas would restrict contraception availability for minors through this program.
- It’s increasingly clear that abortion pills are going to become an even bigger part of the abortion debate. On one hand, the FDA has relaxed some of the risk evaluation and mitigation strategies (REMS) from the prescribing rules surrounding abortion pills. The FDA puts these extra restrictions or safeguards in place for certain drugs to add additional protection. Some advocates say these pills simply do not bring that level or risk.
- Anti-abortion groups are planning protests in early February at large pharmacies such as CVS and Walgreens to try to get them to walk back plans to distribute abortion pills in states where they are legal.
- A growing number of states are pressuring the Department of Health and Human Services to allow them to import cheaper prescription drugs from Canada — or, more accurately, importing Canada’s price controls. While this has long been a bipartisan issue, it has also long been controversial. Officials at the FDA remain concerned about breaking the closed supply chain between drugs being manufactured and delivered to approved U.S. buyers. The policy is popular, however, because it promises lower prices on at least some drugs.
- Also in the news from the FDA: The agency granted accelerated approval for Leqembi for the treatment of Alzheimer’s disease. Leqembi is another expensive drug that appears to work, but also carries big risks. However, it is generally viewed as an improvement over the even more controversial Alzheimer’s drug Aduhelm. Still to be determined is whether Medicare — which provides insurance to most people with Alzheimer’s — will cover the drug.
- As the Affordable Care Act enrolls a record number of Americans, it is notable that repealing the law has not been mentioned as a priority for the new GOP majority in the House. Rather, the top health issue is likely to be how to reduce the price of Medicare and other health “entitlement” programs.
Plus, for extra credit, the panelists recommend their favorite health policy stories of the week that they think you should read, too:
Julie Rovner: The Washington Post’s “Social Security Denies Disability Benefits Based on List With Jobs From 1977,” by Lisa Rein
Margot Sanger-Katz: Roll Call’s “Providers Say Medicare Advantage Hinders New Methadone Benefit,” by Jessie Hellmann
Alice Miranda Ollstein: The New York Times’ “Grant Wahl Was a Loving Husband. I Will Always Protect His Legacy.” By Céline Gounder
Sarah Karlin-Smith: KHN’s “Hospitals’ Use of Volunteer Staff Runs Risk of Skirting Labor Laws, Experts Say,” by Lauren Sausser
Also mentioned in this week’s podcast:
- KHN’s “States Challenge Biden to Lower Drug Prices by Allowing Imports From Canada,” by Phil Galewitz
- Politico’s “Next Frontier in the Abortion Wars: Your Local CVS,” by Alice Miranda Ollstein and Lauren Gardner
- KFF’s “Millions of Uninsured People Can Get Free ACA Plans,” by Jared Ortaliza, Justin Lo, Gary Claxton, Krutika Amin, and Cynthia Cox
TRANSCRIPT
Click here for a transcript of the episode.
KHN’s ‘What the Health?’Episode Title: GOP House Opens With Abortion AgendaEpisode Number: 279Published: Dec. 12, 2023
Tamar Haspel: A lot of us want to eat better for the planet, but we’re not always sure how to do it. I’m Tamar Haspel.
Michael Grunwald: And I’m Michael Grunwald. And this is “Climavores,” a show about eating on a changing planet.
Haspel: We’re here to answer all kinds of questions. Questions like: Is fake meat really a good alternative to beef? Does local food actually matter?
Grunwald: You can follow us or subscribe on Stitcher, Apple Podcasts, Spotify, or wherever you listen.
Julie Rovner: Hello and welcome back to KHN’s “What the Health?” I’m Julie Rovner, chief Washington correspondent at Kaiser Health News. And I’m joined by some of the best and smartest health reporters in Washington. We’re taping this week on Thursday, Jan. 12, at 10 a.m. As always, news happens fast, and things might have changed by the time you hear this. So here we go. Today we are joined via video conference by Alice Miranda Ollstein of Politico.
Alice Miranda Ollstein: Good morning.
Rovner: Margot Sanger-Katz of The New York Times.
Margot Sanger-Katz: Hello.
Rovner: And Sarah Karlin-Smith of the Pink Sheet.
Sarah Karlin-Smith: Hi, everybody.
Rovner: So no interview this week, but lots of news, so we will get right to it. We’re going to start with the new Congress, where the House finally has a speaker after 15 rounds of full-chamber roll calls. Settling the speaker meant that the rest of the House could be sworn in and things like committee chairs elected. Two key health committees, Energy and Commerce and Ways and Means, will both have new chairs, not just new because they’re Republican, but new because they have not chaired the committee previously. Energy and Commerce will be headed by a woman for the first time, Cathy McMorris Rodgers of Washington state, who’s had a longtime interest in health policy and was also in the Republican leadership. Over at Ways and Means, the new chairman is Jason Smith of Missouri, who I confess I had never heard of before this. Does anyone know anything about him? And does he have any interest in health care?
Ollstein: Most of what he said about chairing the committee has been about things other than health care. It’s been a lot on taxes, for instance. The new House majority is very “exorcised” about the IRS funding that the previous Congress approved and trying to get rid of that. But he has shown some interest in some telehealth provisions. And so I think also I’m sure we’re going to discuss some interest in, shall we say, revisiting Medicare’s benefits and funding …
Rovner: Yeah, we’re going to get to that next.
Ollstein: So there could be some things, but it doesn’t seem that he’s been a big health care guy or will be a big health care guy going forward.
Rovner: In the olden days, when I started covering this, the chairman of the Ways and Means Committee frequently did not have either an interest or an expertise in health care. But the chairman of the Ways and Means health subcommittee did. That’s where pretty much everything came from. Do we know yet who is going to chair the Ways and Means health subcommittee …? We do not. So we’ll wait to see that. But yes …. even though I read Chairman Smith’s little introduction about what he’s interested in — and I know he mentioned rural health — but he did not anywhere mention Medicare. And of course, the Ways and Means Committee has jurisdiction over most of Medicare in the House. It is going to come up, as far as we can tell, right?
Sanger-Katz: One imagines so because some of the promises that leadership has made to its members to think about how to balance the budget in the long term, to consider entitlement reform, whatever that may mean. And, you know, Medicare is where the money is. So you would think that the Ways and Means Committee would want to be looking seriously at how to reform the program, if that’s the interest of leadership on this policy area.
Rovner: And they’ve already said that they want to tie any debt ceiling vote, which [is] one of those things that Congress absolutely has to do to reforms, quote-unquote, of the Medicare and Social Security programs. Because, again, as Margot said, that’s where the money goes. So we expect to see Medicare as an issue, regardless of what the Ways and Means Committee does, right?
Ollstein: That’s right. There were a lot of calls for Democrats to address the debt ceiling issue during their final months in power. They did not do so. That means that it’s going to be a big, messy fight this year. One of the biggest things to watch. This is an instance where the Republican House majority will be able to flex its muscles even though they don’t have the Senate and White House, because they can trigger a budget standoff that puts the faith and credit of the country in jeopardy and demand concessions, including cuts to Medicare. So we’ll see how that goes.
Rovner: Although I will say, Sen. Brian Schatz of Hawaii was on Twitter, and he didn’t ask me anything much to the horror of his communications staff. But one of the questions that somebody asked him was, “Why didn’t you do the debt ceiling?” And he just said: We didn’t have the votes. So that at least answers the question of why didn’t they take care of this before the Republicans took the majority back? Well, one thing we do know is going to happen is that the new Republican-controlled House is going to do a lot of investigations. Indeed, one of the first orders of business in the new Congress was the re-establishment of a committee on the covid pandemic with a new focus on investigating the origins of the virus and the government’s response to it. What are we expecting out of that?
Karlin-Smith: As you said, Julie, I think two of the things is, one, they’re going to do more investigation into the origin of the virus. Republicans have pushed the potential theory that this was borne out of a lab in China, not necessarily something more naturally occurring. And I think a lot of scientists have said this theory has been fairly close to disproven and find that the focus on it distracts from really dealing with the current pandemic. But I think we should expect a lot of that. And that will include, I think, a lot of relitigation of Anthony Fauci and his particular role in the NIH [National Institutes of Health] and funding different types of research on viruses, both in the U.S. and abroad. The second thing I think they’re going to look very closely at is how the U.S. has spent the covid funding that Congress has doled out and appropriated. That’s certainly a lot of money. And I think, again, oversight is always probably … it’s a good thing to see if Congress gives money, are we spending it? … Does it actually get to where it needs to go? Does it go to where it’s supposed to go? I think that … in general, I think most people think that’s a good thing. Sometimes what ends up happening is it gets taken a little bit to … this disingenuous step forward in Washington, where everything gets questioned or they pick on jurisdictions for not spending the money fast enough when it’s just not realistic. So you have to read between the lines really carefully when you’re looking at some of the findings from that type of work. Because sometimes, again, when you give a state $1,000,000 to do something, they’re not often able to make that change in two months.
Rovner: And then if they do, they get criticized for spending it on the wrong thing, so …
Karlin-Smith: Right.
Sanger-Katz: But I will say, speaking as a journalist, not as a congressional investigator, I do think that the covid funding is really ripe for a lot of investigation. There’s already been very good reporting that a lot of the small-business programs were broadly defrauded. I think there was a real emphasis by Congress and — in a bipartisan way, Republicans obviously voted for these bills as well. But I think there was a real emphasis on just getting money out the door. People were so scared of a catastrophic economic collapse that, unlike a lot of programs that Congress designs that fund various things, there weren’t a lot of initial safeguards, there wasn’t a lot of process or administrative burden associated with getting money. And so that means it really is valuable to look and see where did it go, who may have defrauded the program, what are ways that in the next crisis it might be possible to do these kinds of programs in a way that is more efficient. You know, it occurs to me that in addition to the small-business money, hospitals got a whole lot of money as part of these programs. And again, there’s been some journalism about this, but I do think I’m all for more oversight, trying to learn some real lessons. I agree with Sarah that there is probably some of this that’s going to veer into the disingenuous and kind of “gotcha.” But there may be some useful and interesting findings as a result of this process as well.
Rovner: And as we saw with the Jan. 6 committee, Congress has powers that journalists don’t. As we know, the Justice Department has powers that Congress doesn’t. But Congress has pretty good investigatory powers. They can subpoena things when they need to. So, yes, I imagine we’re going to learn something about the fate of all of those dollars that went out the door.
Ollstein: Just to be fair, Republicans have sort of claimed that the Democrat-led effort to investigate covid didn’t have any financial accountability aspect. That’s not true. It did. They really scrutinized a lot of government contracts — like no-bid government contracts that funneled lots and lots of money to things that did not pan out or help anybody. There has been some of that already. But I agree that there’s definitely more to look at.
Rovner: And there … obviously, there was a Republican and a Democratic administration handling the covid pandemic. So one presumes there are things to investigate on both sides. Well, even while the House committees are gearing up, Republicans are bringing “statement” bills to the floor, bills that we know the Senate won’t take up and the president won’t sign. And despite the fact that abortion rights drove a lot of the midterm elections in the other direction, two of the first bills brought to the floor by the new Republican majority seek to do the bidding of anti-abortion groups. This, apparently, making Republican moderates, particularly those in swing districts, not so happy. Alice, are we looking at pretty much the same split in the Republicans in the House as in a lot of states — the people who think that the Republicans didn’t do well because they should have done more and people who think the Republicans didn’t do well because they should have done less?
Ollstein: Yeah, absolutely. And there’s a split on how to talk about it or whether to talk about it as well. It’s not just the actions, it’s the messaging in addition. And so, yes, there are some in the House who are, like, why are we doing this? Why are we taking these votes that have no chance of becoming law? It just puts our members from swing districts in a more vulnerable position. The things they voted on so far this week have pretty unanimous support on the Republican side, I would say. I think where you could start to see some bigger divides are when they get into votes on an actual national abortion restriction that would put a gestational limit on the procedure, or something like that, which absolutely some members want to do and want to take a vote on. I think that’s where you could start to see some Republicans being, like, wait, wait, wait, wait, why are we doing this? But the things so far are, like you said, they’re “messaging” bills, but they’re ones that have pretty broad support on the conservative side.
Rovner: And we should mention, I mean, one of them was just a sense of Congress that, you know, that bombing pregnancy crisis centers is bad. Or that violence against pregnancy centers …
Sanger-Katz: I’m not going to give credit for this correctly, but I saw a tweet on this topic last week when the list of demands and the list of these bills that we’re going to get a vote on was released where someone asked, Oh, did D-Triple-C [the Democratic Congressional Campaign Committee] co-author this list? Where I do think there is an interesting tension, as Alice said, where the particular message bills that the most conservative members of the House Republican caucus want to vote on are those issues where we see in public opinion polling, where we see in the last election that the majority of Americans are not really with those most conservative Republicans. And I think a lot of moderate Republicans would just prefer not to vote on those issues, particularly because they know that they can’t make them policy. And we were talking about changes to Medicare and Social Security, and I think that also falls very much in that category where there might be a situation in which if Republicans really thought that they could reform these programs, maybe they would want to take the political risk, because I do think it’s an important long-term goal of many Republicans. But I think there’s also a frustration, you know, why would we take all these votes on something that is generally unpopular? Everyone knows that both Social Security and Medicare are really, really popular programs and people are very wary of changes to them. There is a political risk in taking a bunch of votes saying that you want to pull money out of those programs or change them structurally when you can’t even achieve it.
Rovner: Yeah. Well, speaking of that, during Wednesday’s abortion debate on the House floor, Republican moderate Nancy Mace of South Carolina kept saying to any cable outlet that would put a microphone in front of her that Congress should be making birth control more widely available instead of voting on abortion. But we are also seeing the first shots fired in an effort to restrict birth control. Well, last month, a Trump-appointed judge ruled that the Title X family planning program is illegally providing contraception to minors. Now, this is a fight that dates back to even before I started covering it. It was called “the Squeal Rule” in the early 1980s, an effort by the Reagan administration to require parental involvement before teens could use Title X family planning services. It was eventually struck down in federal court, but now it’s back. Is this where we’re headed?
Ollstein: I think it’s really important to watch things in law and policy that are just directed at minors because inevitably it does not stop there. Like, that’s sort of the testing ground. It’s where people are more comfortable with more restrictions and more hoops to jump through. But as we’ve seen with gender-affirming care, it doesn’t stop there. What’s tested out as a policy for minors is inevitably proposed for adults as well, and so …
Sanger-Katz: What’s the adult version of this, Alice? Like who? Like spousal consent?
Rovner: Yes, there had been — I was just going to say — not so much in contraception, although originally it was, but also on abortion that, yeah, if there’s a partner that the partner would have to consent.
Ollstein: But there’s also been spousal consent stuff for more permanent … getting your tubes tied, those kinds of things. That’s been a debate as well. And, I mean, in the abortion space we’ve seen this for, in terms of like traveling across state lines for an abortion. That’s been a restriction for minors that’s also been proposed for adults. So it’s just this phase we should absolutely watch — as well as Title X program continues to be a space for proposed restrictions. It’s a lever that they’re able to hold because it does have federal funding and it does have constraints that other pots of money don’t have.
Rovner: My favorite piece of trivia is that the Title X program has not been reauthorized since 1984 because Congress has never been able to find the votes. You know, when the Democrats were in charge and wanted to do it, the Republicans would have all of these amendments that the Democrats probably couldn’t fight off. The Republicans wanted to do it and put all these stringent rules that the Democrats wouldn’t have. So, literally, this program has been … it gets funded every year, but it’s been marching along for now several decades without Congress having formally reauthorized it.
Ollstein: Yeah, that’s why you keep seeing different presidential administrations trying to put their stamp on it through rulemaking, which, of course, can be rolled back by the subsequent president, as we’ve seen with [Donald] Trump and [Joe] Biden. And so it just keeps going back and forth. And these clinics that are out there getting this funding, which, again, can’t be used for abortion, for contraception, STD testing, fertility stuff, all kinds of stuff, but not abortion. But they keep having to comply with these wildly different rules. It’s really difficult.
Rovner: Yeah, it is. All right. Well, last week we talked about the Biden administration’s effort to make abortion pills more available through both pharmacies and the mail. On the one hand, some abortion rights advocates say that the FDA is still overregulating the abortion pill by requiring extra hoops for both pharmacies and doctors to jump through in order to offer or write prescriptions for a medication that’s proved safe and effective over two decades. On the other hand, we now have the specter of abortion opponents protesting at CVSes or Walgreens near you. And Alice, they’re already planning to do that, right?
Ollstein: Yeah, that’s right. They would have done it sooner, but they didn’t want to step on the March for Life, which is coming up in a couple of weeks. And so they’re planning these protests at CVS and Walgreens around the country for early February, trying to pressure the company to walk back its announcement that they will participate in the distribution of abortion pills in states where they remain legal, which is, by our count, currently 18 can’t do this either because abortion is banned entirely or because there are laws specifically restricting how people get the pills.
Rovner: Sarah, I want you to talk about some of these extra hoops that have to be jumped through because a lot of people think it’s just for this pill and it’s not. This is something that the FDA has for any drug that’s potentially abusable, right?
Karlin-Smith: Yeah, I wouldn’t say abusable is the right word, but basically people call this a REMS. It stands for risk evaluation and mitigation strategy. And it’s actually an authority Congress gave the FDA to — we use this term “safe and effective,” but we know all drugs, even when we say that “safe” term, will come with risks. And the idea here is that when the benefit-risk balance would be … so that it would be … FDA might say, OK, this is actually too risky to approve. However, we think we could make it kind of safe enough if we put in a little extra safeguards instead of just letting it go out there. Here’s a drug, doctors, you can prescribe it, follow the normal pathway, which is that the federal government, or at least the FDA, doesn’t really have a lot of say in exactly how the practice of medicine works. That’s left up to states. And, you know, doctors individually. They implement other practices to help ensure that safety balance is there. So one famous example is Accutane, which is an acne drug. It’s incredibly harmful to a developing fetus and birth defects. So women of pregnancy, bearing age are usually required to take regular pregnancy tests and so forth and monitor the status of that. And you’re not supposed to use the drug while pregnant because of the incredible harm you do to a baby. So there’s everything from things like that to just simply more written literature might be provided for certain drugs. Sometimes in the cases of the abortion pill, you know, who could actually dispense it and when was restricted. Sometimes there are particular sorts of trainings doctors have to take to get that extra authority to prescribe the drug. And again, the idea is that just to provide a little extra safeguard. Again, the controversy over the years with this pill is that people feel like it doesn’t meet that standard to have a REMS, that it can be safe and effective through our normal prescribing systems. Actually, Stat this week had an interesting interview with Jane Henney, who was the FDA commissioner when they first approved this drug. And she …
Rovner: Yeah, in the year 2000.
Karlin-Smith: Right. Which is actually …
Rovner: Right at the end of the Clinton administration.
Karlin-Smith: Actually predates this formal REMS authority. But there were others, different authorities that then evolved into REMS. But she said she thought that a lot of these restrictions would be gone by now and that what, at the time, what they were waiting for was more U.S.-specific experience with the drug, because what they were basing the original approval on was a lot of use of the drug in France, which had such a different health system than the U.S., they were a little bit uncomfortable, I guess, opening the floodgates in a way. So I thought that was an interesting historical point that came out this week.
Rovner: But clearly, Alice, I mean, this is going to be the next big fight in abortion, right, is trying to restrict the abortion pill?
Ollstein: Absolutely. I’ve been writing about this since before Roe v. Wade was overturned. The pills were already becoming one of the most popular and now are the most popular way to terminate a pregnancy in the U.S., which makes sense. You can take them in the comfort of your home with the people that you want to be with you, not in a scary medical environment. It’s also a lot cheaper than having a surgical procedure. So but then, of course, with the pandemic, people started using them even more because it was more dangerous to go to a clinical setting. And so this has been a big focus of both sides of this fight for a long time: either how to increase access to the pills or restrict them. Also, now that Roe v. Wade has been overturned, the pills and the ability to order them online from overseas in this legal gray area, that’s been a major way people have been getting around state bans, and the anti-abortion groups know that. And so they want to look at any way they can to crack down on this. And so with the Biden administration opening up a new potential pathway with these local retail pharmacies, they’re of course going to try to crack down on that as well.
Karlin-Smith: I mean, we talked about this before in the podcast, but I think this issue of federal preemption, if it gets teed up, is going to be a big thing that’s beyond just abortion, in terms of when does FDA’s approval of a drug trump state regulations around how it’s going to be used? And, you know, I feel like some people have not been satisfied on the … who want more access to abortion drugs in terms of how FDA has handled the rollback of the REMS. But you also have to wonder if they’re operating in this setting where, again, if you push things too far and you get a legal challenge, given how our courts are, right? And how politically it can backfire. And so it’s a complicated balance there.
Rovner: Well, speaking of drugs that are in gray areas that people order online, my KHN colleague Phil Galewitz reports that four states — Florida, Colorado, New Hampshire, and New Mexico — are now pressuring the Biden administration to allow them to import prescription drugs from Canada in an effort to reduce the cost of drugs for their residents. Now, despite the fact that this has been and remains a very bipartisan ask, the FDA, under both Republican and Democratic commissioners, has strongly objected to it over the years. Somebody remind us why this is so controversial.
Karlin-Smith: I think the big thing FDA has objected to is that when you allow importation in the way states have often asked for it, you basically often give up the supply chain oversight that we have in the U.S. that ensures people are not getting drugs that are counterfeit and have somehow been tampered with as they’ve gotten through the supply chain. And so, actually, I was refreshing my memory, and I can’t believe how long ago it is. When the Trump administration first became the first administration to say, Oh, actually, OK, we are going to agree that we think this could be come safely. Then they put out regulations that tried to … basically like made it so that to do importation, you would almost have to mimic the same supply-chain safety measures we already have for the FDA. So it became this double-edged sword of, sure, you can do the importation, but you’re going to have to jump to this level of hurdles that then makes it unusable. And so I think that’s the key barrier here, is that can a state actually propose a program that would get sign-off? And I think it’s not really surprising to me that the Trump team tried to thread the needle in that way of giving people the win of saying, Oh, we’ll allow it without actually making it feasible.
Sanger-Katz: I think it also highlights what a weird ask this is in some ways because what the states are looking to do is they are not looking to import drugs from other countries because they think that other countries have better manufacturing, have better safety protocols, have different drugs. They just want to import the lower prices that other countries pay for the same drugs. And so this is, in some ways, a very cludgy workaround that the states are basically asking for price regulation of drugs. But that obviously is a very difficult political act. So instead they’re saying, well, can we just import the prices that some other country has negotiated. And then it raises all these other issues about, Well, you know, there is like a reason why, in general, the United States has regulatory control over the drug supply.
Rovner: Also, Canada doesn’t have enough drugs to serve all of these states. I mean, that’s the thing that I’ve never managed to get over. And, in fact, Canada has said that they’re not anxious to do this because they don’t have enough drugs to serve both Canada and the United States. I mean, it also seems just literally impractical.
Sanger-Katz: I mean, we are seeing, of course, like in the Inflation Reduction Act, there were new measures that would allow Medicare, in particular, to start negotiating for lower prices for certain drugs. Obviously, that policy has a fair number of limitations, including that it’s only for Medicare, it’s only for certain drugs, and it’s not going to be instant. But while we did get some new timeline from the Biden administration this week, and it looks like that policy is going to start rolling out. So I think states are asking for this now because they want to import prices from other countries. But also, for the first time, Medicare, or the federal government is starting to take on drug prices directly. And we’re going to see how that looks relatively soon.
Rovner: Yes, this ship turns very slowly, but it does seem to be turning a little bit. Well, as we previewed last week, the FDA has approved another controversial Alzheimer’s disease drug, Leqembi. I think that’s how you say it, which has a Q without a U. Sarah, you’ve been following this. Are we headed down potentially the same road we traveled with Aduhelm? It feels kind of familiar. It’s a drug that we think works, but we don’t really know, and it has some big risks and will be expensive.
Karlin-Smith: Yeah, I mean, similar, but slightly different. And perhaps the analogy that things slowly make their way in a different direction is also right here. This drug, I think most people see it as an improvement on Aduhelm because it has, in one major clinical trial, shown some benefit on people’s cognitive decline slowing a bit. However, the big debate there is that … how meaningful the change that was seen in the trial is. Is it really going to be meaningful in people’s lives and is that worth the price? The company is … actually a similar company is involved here, but they priced it quite a bit lower than the original Aduhelm price, even lower than the price of Aduhelm now. It’s still seen as on the very high end of what a lot of cost-effective watchdogs say is a fair price. And as of right now, CMS [the Centers for Medicare & Medicaid Services] or Medicare is not going to be covering it at all because right now the drug only has what’s known as an accelerated approval. So we’re going to, over the next probably less than a year, in about nine months or so, FDA will have to weigh in on whether it gives the drug a full formal approval. And at that point, we’ll see if Medicare also gives the sign-off that they think this drug might actually be effective for people and are willing to pay for it. I think my bottom line on this drug is, you know, it provides some hope and some improvement for people, but it looks like to be a small clinical benefit for a big trade-off in risks. So I think as more data comes out over time, we’ll see again if that benefit-risk trade-off for most people falls on the right side of the coin.
Rovner: And we’ll watch this whole process go forward again. All right. Finally this week, but not least, there’s also news on the health insurance coverage front. With the end of open enrollment for the Affordable Care Act coverage rapidly approaching in most states, by Jan. 15, officials at the Department of Health and Human Services this week reported that enrollment is already up 13% from last year to almost 16 million people, including about 3.1 million people who are new enrollees. In the meantime, though, my colleagues over the firewall at KFF report that some 5 million more uninsured Americans are actually eligible for free health care coverage under the ACA. It feels ironic because this is not the first year of expanded subsidies and there’s been relatively little media coverage of open enrollment. Is it just that it takes time for knowledge of these offers to trickle down to people? Or that the Biden administration put a lot more effort into outreach this year?
Sanger-Katz: I think it’s all of the above. I think for the first few years of the Obamacare program, there were a lot of complaints that this insurance really wasn’t affordable enough for people. And, obviously, that’s why Congress, first in part of the pandemic stimulus bill and now again in the Inflation Reduction Act, really jacked up the subsidies and made the plans cheaper and, in many cases, have more wraparound benefits so that low-income people could get insurance that was either free or relatively low-premium and also didn’t ask them to pay a lot out-of-pocket for their own care. And we can see also that the Biden administration did a lot of outreach. I mean, it’s definitely the case that they both, through Congress, made the plans cheaper and also, through various administrative actions, made the plans more widely publicized. And I just want to highlight, I think last year was the record year for Obamacare enrollment. And now we’re seeing this huge increase on top of a record year. So these things seem to matter. I think the affordability of plans, the availability of free plans for a lot of uninsured Americans is very appealing. And yet the people who are uninsured and poor, I think, are difficult to reach. There is a lot of long-standing opposition to Obamacare. There are a lot of places where there are a lot of uninsured Americans, where there’s not particularly effective and robust outreach. People don’t know how to find these things, how to sign up. And it is really administratively complex to sign up for these plans. I mean, I don’t know how many of our listeners have tried to do it. It’s not impossible. It is on the internet. You know, anyone can do it. And you don’t have to have someone holding your hand. But I think in many cases you probably do want someone holding your hand if it’s your first time doing it. There are, in many markets, lots of choices. It’s confusing. It’s hard to know what the best option is, sometimes it’s a little bit hard to figure out what it’s going to cost you until you enter in a lot of information about your income. And you might also be scared that if you’re not sure or you put something in wrong, you could get in trouble. So I think this is just an ongoing challenge of getting all these people who are now eligible for these really low-cost plans to actually interact with the system and get insurance.
Rovner: One thing I guess bears mentioning is that with the Republicans just, you know, plan to do all of these things like try to repeal the Inflation Reduction Act because they don’t like the drug price provisions … [but] they are not talking about repealing the Affordable Care Act anymore, right? Have we finally come to the end of that particular fight?
Sanger-Katz: It sure looks that way.
Ollstein: Yeah. The right the writing has been on the wall in terms of the lack of that talk on the campaign trail for a few years now. I was joking with some colleagues that, you know, the “repeal Obamacare” is tired; the “repeal the drug price negotiation provisions” is wired. That’s the new talking point, although that’s not going to happen either, obviously, because of the control of the Senate and because of how insanely expensive it would be to repeal that. But the Republicans definitely have moved on to other targets.
Sanger-Katz: Although I will say, you know, once again, the fact that House leadership has committed to proposing cuts to health entitlement programs, the fact that they have committed to proposing a budget that balances in 10 years means that, I think, it will be extremely difficult for them to avoid talking about particular cuts or changes to Affordable Care Act programs. You know, again, it’s just like this is where the dollars are. They can take a lot of dollars out of Medicare, that is very politically unpopular. They can take some dollars out of Medicaid, you know, the largest expansion of which is part of ACA. They can take money out of these subsidies, which, you know, have been supercharged in recent years beyond even what Congress initially passed in 2010. And I do think, as Alice said, you know, this is not a popular talking point. I don’t think Republicans, by and large, want to be talking about repealing Obamacare anymore. And yet I think they are backed into this corner where they’re going to have to make and propose specific modifications and cuts to these programs in order to achieve these high-level philosophical goals that they’ve signed up for. And so I think it will be interesting to see what does it look like, maybe they’re not going to call it Obamacare repeal anymore, but they might still be sucking $1,000,000,000,000 out of Medicaid, like some of the Trump administration budgets did.
Rovner: Yeah. And it’s important to mention, again, I mean, the Republicans talk about all these things they’re going to do and people are thinking, Oh, my God, if they vote for this balanced budget, in 10 years it’s going to happen. They can’t do most of these things without the Senate and/or the president unless they have two-thirds to override, which they don’t. The one place that we do think they could exercise some leverage, obviously, is this debt ceiling vote where the Congress has to vote to raise the debt ceiling or the U.S. will default on things that it has already bought but not paid for — basically paying the credit card bill. And that, certainly, they’re going to try to make some entitlement changes. But all of these other things that they say they’re, quote-unquote, “going to do,” they’re mostly just quote-unquote, “making political statements,” right?
Sanger-Katz: But they’re going to have to talk about them. They’re going to have to write things down. They’re going to have to have specific dollars attached to this. I do think that it will be politically salient and that it will create some visibility into, like, well, how do you balance the budget in 10 years? What does entitlement reform look like? And they’re not saying Obamacare repeal anymore and they don’t want to, they understand that they don’t want to. And yet I think they’re going to be in this position where they’re going to effectively have to lay out something that looks like Obamacare repeal, something that looks like Social Security reform, something that looks like big changes to Medicare. And we will have a political debate about that because Democrats are just salivating to have those conversations. I think they feel like that is very strong political ground on them. They think that voters trust them to protect those very popular programs if they’re under assault. And, you know, which is very similar to the political dynamic we saw when Republicans were really trying in earnest, when they had full control of government and wanted to repeal Obamacare.
Rovner: Yes. And I would say, as we absolutely saw in 2017, when they failed to repeal it, Republicans very much agree on their goals, but they very much disagree on how to get there. There is no unified Republican plan for either reforming, you know, the Affordable Care Act or Medicare or Medicaid, I mean, except for basically cutting money out of it. So I will be interested, as Margot says, to see what they actually put down on paper.
Sanger-Katz: And, sorry, just one more thing on this point, which is, again, I think that the kinds of show votes that the Republican House leadership is going to have to put on these issues are probably not going to be particularly politically productive and may be politically damaging to them. But I do think, setting that aside for the moment, I do think we are entering in an environment of much higher interest rates, of really more accelerating federal debt. You know, there are a lot of conditions right now that are potentially ripe for thinking about government spending and particularly thinking about these big categories of government spending that are our federal health care programs. I think the last few years there’s been this sense that, you know, debt is free and the deficit doesn’t matter. And I think inflation is high, interest rates are rising. I do think that we’re in a moment where there may be a greater sense of a need to confront this problem. And I’m interested in what that conversation looks like, which may be a little bit different than the kind of highly ideological conversation that we’re going to see in the very near term.
Rovner: I was going to say that that would require actually having substantive talks about what might work, which we don’t know is going to happen, but we can cross our fingers and hope. All right. That is the news for this week. Now it is time for our extra-credit segment where we each recommend a story we read this week we think you should read, too. Don’t worry if you miss it; we will post the links on the podcast page at khn.org and in our show notes on your phone or other mobile device. Sarah, why don’t you go first this week?
Karlin-Smith: Sure. I took a look at a story by Kaiser Health News’ Lauren Sausser: “Hospitals’ Use of Volunteer Staff Runs Risk of Skirting Labor Laws, Experts Say.” I thought this was a fascinating story about hospitals’ reliance on volunteers, not for the types of activities I usually associate hospital volunteers with, which would be …
Rovner: Like candy stripers.
Karlin-Smith: Right. Like light … I don’t know, “light” is not the right word, but, you know, visiting people, comforting them in some way, providing added benefit of sorts. And this is really people that are being asked to do medical care and the basics, some of the basic care you need when you are in a hospital. And I think her story cites about $5 billion maybe in the U.S. of free labor through these types of volunteers. And the question becomes, you know, is this violating labor laws? And should these people be getting paid for the work, or should they … are they basically, because they’re using volunteers, taking money and job opportunities away from other people? And I thought it was a fascinating story just because I had no idea of all of this, you know, volunteer labor was being used and the impacts on these hospitals during the pandemic, when they couldn’t have volunteers. And just, I think, important to think about, too, how this impacts the quality of care as well people receive.
Rovner: Hospitals are very clever. Margot.
Sanger-Katz: I wanted to recommend an article from Jessie Hellman at Roll Call called “Providers Say Medicare Advantage Hinders New Methadone Benefit.” And I’ve been doing a lot of reporting on the Medicare Advantage program lately. And so I was a little bit jealous of this story. Congress just recently required Medicare to pay for methadone. You know, a very evidence-based treatment for opioid addiction that it hadn’t been covering before. And what this article found is that these Medicare Advantage plans, or private competitors to the government Medicare program, have been enacting a lot of roadblocks that make it hard for people to get this treatment. So they technically cover it, but they require often what’s called prior authorization, where you have to … doctors and others have to jump through a lot of hoops to prove that the person really needs it. And when I saw this article, I put out a bat signal on my Twitter and I said, Can anyone think of the medical reason why you would want to have … restrict access to methadone treatment? And, you know, this is just a Twitter poll, but no one could come up with the reason. They could think of lots of reasons why the insurance company might not want to cover it, because it’s expensive, because patients who have opioid addiction probably are pretty expensive in general. And so, you know, this could be a way to avoid paying for a complex treatment or a way to discourage patients who have complex health care needs from choosing a Medicare Advantage plan. Anyway, so just a good story and just, you know, another illustration of, you know, even after Congress does something like add a new benefit, there’s always value in doing oversight to see how is that actually working in the real world and is it giving patients the care that was intended?
Rovner: Yes. And we will be talking, I think, much more about Medicare Advantage this year. Alice.
Ollstein: So I have a very sad piece to recommend. It is an op-ed by Céline Gounder, who is a public health expert that we all know well, as well as the widow of Grant Wahl, the soccer journalist who died covering the World Cup. And she wrote about how her husband’s death has been co-opted by anti-vax conspiracy theorists who are trying to draw some connection to what happened to him and being vaccinated for covid. But she really smartly walks through the misinformation playbook because it is a very sort of predictable playbook with very predictable points and, you know, dismantles them one by one. And I think it’s really helpful for the inevitable next time we see this come up to be prepared in advance and be able to refute those points. Very tragic but very helpful thing to know.
Rovner: Yeah. Céline is our colleague now at KHN, in addition to everything else that she does, and I can just say to these trolls: Don’t mess with Céline. It really was a very good piece. Well, my extra credit this week is from The Washington Post, and it’s a great story that ran in the dead week between Christmas and New Year’s. So I … gave it an extra week. It’s called “Social Security Denies Disability Benefits Based on List With Jobs From 1977,” by Lisa Rein. And while I’ve known for a long time that the Social Security disability program has a multiyear backlog, one thing I didn’t know until I read this story is that a lot of otherwise likely eligible people get their benefits denied because they could theoretically do jobs that largely no longer exist. Among the jobs the government says people who are disabled might be able to do are nuts sorter, dowel inspector, or egg processor. That’s because the last time the labor market data used to determine if a disabled person might be able to do a job was last updated 45 years ago. The agency has been working since 2012 to update its listing of jobs that could be done by sedentary individuals. But somehow the new directory of jobs has not made it into use yet. Meanwhile, thousands of people deserving of disability benefits are being steered to jobs that are now largely automated, offshored, or otherwise obsolete, something that clearly needs to be fixed.
OK, that is our show for this week. As always, if you enjoy the podcast, you could subscribe wherever you get your podcasts. We’d appreciate it if you’ve left us a review — that helps other people find us, too. Special thanks, as always, to our ever-patient producer, Francis Ying. As always, you can email us your comments or questions. We’re at whatthehealth — all one word — @kff.org. Or you can tweet me. I’m still at Twitter for now: @jrovner. Sarah?
Karlin-Smith: I’m @SarahKarlin
Rovner: Margot?
Sanger-Katz: @sangerkatz
Rovner: Alice.
Ollstein: @AliceOllstein
Rovner: We will be back in your feed next week. In the meantime, be healthy.
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2 years 3 months ago
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Health Archives - Barbados Today
#SpeakingOut – We must do better
I spent about eight hours in the Accident and Emergency Department at the hospital with a relative recently. Before me, my brother spent about 14 hours with the same relative and then another brother spent about five. Together, waiting with the relative, we spent almost 30 hours before she was seen by a doctor. I have heard of others who spent days waiting to be seen.
There was a young woman there with a child. The boy she carried was unwell, and he vomited on the floor. It was a large amount. That vomit stayed there in full view and smell of those nearby and passers-by for over an hour before a worker came to clean it and I believe that this only occurred because I spoke to the Patient Advocate about the smell and this forced him to make a second call to the housekeeping department.
This is the hospital that taxpayers pay for and the treatment there is abominable. If the problem is staffing, then every effort must be made to get to the bottom of this crisis. It is totally unacceptable, shameful, insensitive and uncaring for people to go through this nonsense when they have to visit there. Despite whatever administration is in, this foolishness continues. People sat quietly waiting their turn whilst one lady vented her frustration. Some people die before getting treated.
This is WRONG by any standard. We do not need nice sounding rhetoric about how to fix the problem. We want it fixed NOW. A modern hospital cannot operate at this rate for decades, whilst highly paid bureaucrats get paid for running an inefficient operation mandated to deal with the health of the majority of Black people in this country. Our social systems were set up to serve the people and this must be made to happen. Others can attest to the absolute poor attitude of some civil servants, who, at the end of the day, are inefficient but continue to underperform in their positions indefinitely. This needs to change NOW.
On another note, no pun intended, the banks are drunk and crazy. I went to a bank to do a transaction and wanted to use the drop box. When I realised that there were no envelopes to put the money in, I inquired about one and was told by a worker there that I had to bring my own envelope to expedite the transaction. Was her head good? To pay them their money? And the thing about it, is that there were boxes full of envelopes at various stations sitting idly by. I moved from one station to the next and was told the same garbage before one guy gave me one. It seems like the more we change, the more we remain the same. But we seem to like it so.
Ian Marshall
The post #SpeakingOut – We must do better appeared first on Barbados Today.
2 years 3 months ago
Health, Health Care, Speaking Out
Ministry of Health lays down safety measures to combat Flu season
Prime Minister of St Kitts and Nevis, Dr Terrance Drew, who is also responsible for the Ministry of health, has taken to his social media account to caution the people of St Kitts and Nevis regarding the precautions during the influenza season.
The Caribbean region is in the middle of the influenza season, typically from November to March.
The Ministry of Health in St Kitts has detailed ways for the people to address the issues around respiratory diseases. The Minister of Health, Dr Terrance Drew, has taken to his social media account to share ways in which people can limit the transmission of these infections.
The Ministry of Health in St Kitts and Nevis has shared the information available to them regarding the infections. The Ministry has stated that Influenza (flu) is an acute and very contagious respiratory tract infection that can be caused by influenza type A (H3N2) and type B viruses.
Currently, the country is facing growing concerns over emerging Influenza, Respiratory Syncytial Virus (RSV), and the new strain of COVID-19.
The Ministry of Health update details that they are monitoring the new omicron subvariant of Covid-19 that is emerging in some areas of the North-Eastern USA. The sources reveal that this is the most transmittable variant of the disease. However, the infection is much less severe in the variant. Meanwhile, the Respiratory Syncytial Virus (RSV) is a respiratory virus which causes cold and cough-like symptoms.
The Ministry of Health further stated that RSV Infection is not severe and individuals can recover from it within a week; however, children younger than four and older are still vulnerable.
The Ministry of Health has laid out some guidelines to combat the situation. The first is using masks for isolated individuals who have tested positive for the Covid-19 virus, RSV or Influenza. If the individuals are tested positive, they are required to remain in isolation.
Covers are also mandatory if visiting the hospital or healthcare centres. The Ministry of Health advises people to see the doctor regularly in case they develop flu-like symptoms or suffer from a persistent cold.
2 years 3 months ago
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Medical News, Health News Latest, Medical News Today - Medical Dialogues |
Smartwatch can detect short-time hypoxemia compared to a medical-grade pulse oximeter
Czech Republic: A recent study in Digital Health has found that the Apple Watch Series 6 can accurately detect reduced levels of blood oxygen saturation (SpO2) below 90% compared to a medical-grade pulse oximeter.
Czech Republic: A recent study in Digital Health has found that the Apple Watch Series 6 can accurately detect reduced levels of blood oxygen saturation (SpO2) below 90% compared to a medical-grade pulse oximeter.
"The technology used in this smartwatch is adequately advanced for the indicative SpO2 measurement outside the clinic and can detect states of reduced blood oxygen saturation," the researchers wrote in their study.
Pulse oximetry as an indirect peripheral SpO2 measurement method is a relatively new metric in smartwatches. Still, it is becoming routinely available in new models, allowing convenient SpO2 monitoring at home or, with some restrictions due to movement obviating the need for a dedicated pulse oximeter. Additionally, the SpO2 sensor of the smartwatch does not need an attachment to a finger to complicate daily activities. This might help mountaineers in high altitudes or athletes in training, and patients with lung diseases such as COPD (chronic obstructive pulmonary disease), cardiovascular disease, or dealing with concerns or consequences of COVID-19. The ability of smartwatches, in particular, to measure SpO2 without conscious use intervention might help detect intermittent hypoxemia associated with sleep apnea.
Against the above background, Jakub Rafl, Czech Technical University in Prague, Kladno, Czech Republic, and colleagues explored how a commercially available smartwatch that measures peripheral blood oxygen saturation (SpO2) can detect hypoxemia compared to a medical-grade pulse oximeter.
For this purpose, 24 healthy participants were recruited. Each participant wore an Apple Watch Series 6 (smartwatch) on the left wrist and Masimo Radical-7 pulse oximeter sensor on the left middle finger. The people breathed via a breathing circuit with a three-way non-rebreathing valve in three phases. The people inhaled the ambient air in the first 2-minute initial stabilization phase. Then the participants breathed the oxygen-reduced gas mixture (12% O2) in the 5-minute desaturation phase, temporarily reducing their blood oxygen saturation. In the final stabilization phase, people inhaled the ambient air until SpO2 returned to normal. SpO2 measurements were simultaneously taken from the pulse oximeter and the smartwatch in 30-s intervals.
The study revealed the following findings:
- There were 642 individual pairs of SpO2 measurements. The bias in SpO2 between the smartwatch and the oximeter was 0.0% for all the data points.
- The bias for SpO2 less than 90% was 1.2%.
- The differences in individual measurements between the smartwatch and oximeter within 6% SpO2 can be expected for SpO2 readings 90%–100% and up to 8% for SpO2 readings less than 90%.
"As a representative of wearables, Apple Watch Series 6 provides reliable values of SpO2 compared to a medical-grade pulse oximeter, at both normal and optimal levels and induced desaturation with SpO2 below 90%," the researchers wrote.
"In this smartwatch, the SpO2 monitoring technology used is sufficiently advanced for the indicative measurement of SpO2 outside the clinic and can detect states of reduced blood oxygen saturation", they concluded.
Reference:
Rafl J, Bachman TE, Rafl-Huttova V, Walzel S, Rozanek M. Commercial smartwatch with pulse oximeter detects short-time hypoxemia as well as standard medical-grade device: Validation study. DIGITAL HEALTH. 2022;8. doi:10.1177/20552076221132127
2 years 3 months ago
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WHO warns of high global cholera outbreaks and vaccine shortages
The world is experiencing an unprecedented number of cholera outbreaks in countries affected by natural disasters and other crises, while vaccines to prevent this disease have become extremely scarce, according to the World Health Organization (WHO), which issued a warning on Wednesday.
“31 countries have reported outbreaks, more widespread and lethal than normal, and the figure is 50% higher than in previous years,” Tedros Adhanom Ghebreyesus, WHO director-general, warned at a press conference in 2022.
Tedros emphasized that Haiti, Syria, and Malawi are among the most affected countries and that the simultaneous outbreaks have resulted in a vaccine shortage, prompting the international immunization coordination mechanism to reduce the doses administered to each patient.
“Despite this unprecedented measure, stocks remain very low and production is at its maximum capacity,” Tedros lamented, urging countries that have recently experienced outbreaks to step up prevention of potential new infections.
2 years 3 months ago
Health, World
Health Archives - Barbados Today
#BTColumn – We need action, not (empty) resolutions!
Disclaimer: The views and opinions expressed by the author(s) do not represent the official position of Barbados TODAY.
Disclaimer: The views and opinions expressed by the author(s) do not represent the official position of Barbados TODAY.
As we move into any New Year, one tradition is to make a New Year’s resolution. Some social marketing research shows that a majority of these resolutions focus on improving personal health, such as losing some weight, doing more exercise, and paying more attention to eating and drinking habits. Gym registrations traditionally spike in January, but quickly taper off. Coming after a long season of gorging on food and drinks, a health resolution is a good idea, but for many it’s too little too late. A better idea would perhaps be to set health resolutions at the start of the festive season; after all, an ounce of prevention is better than a pound of cure.
In Barbados, the festive season seems to start around the middle of November, as our advertisers seem to merge Black Friday sales shopping, adopted from high-income countries, into Independence Day into Christmas and then New Year’s Day, to be shortly followed by Errol Barrow Day on January 21st. Through sales and other gimmicks, we are encouraged to ‘shop till you (or at least your money, including end-of-year bonuses) drop’ and generally fete, eat, drink and be merry. For too many people, this translates to about six to eight weeks of unbridled activity (while stocks and funds last).
The food festivities start with Independence, with persons invited to sample as many conkies as possible to determine whose conkies, made with or without raisins, are the best. After ‘conkie season’, the Christmas season officially or unofficially starts: ham, stuffed turkey, jug-jug, black cake (often alcohol-infused) are washed down with sorrel, juices and a wide variety of alcoholic beverages. Mouth-watering desserts, including chocolates, sweets, biscuits and ice-creams, complete the feasts. The volumes of food and drink consumed are designed to keep our obesity figures as high as they are, in the top 20 of the world, and obese persons fuel our chronic non-communicable disease (CNDC) pandemic.
Therefore, we must reset our efforts at prevention and treatment of these CNDCs. Sure, many people behave like ‘one-day Christians’, who do many wrong things for six days a week, and on the seventh day suddenly remember the path to ‘health righteousness’. We have no shortage of speeches on the effect of the CNDCs on deaths, sickness and even the economy, in between a tsunami of advertisements that promote inappropriate health habits.
In the background, COVID-19 lurks. The pandemic may or may not be over, but the virus is still here. At a recent press conference, the Deputy Chief Medical Officer offered statistics to support a rising rate of documented COVID-19 infections on the island, even while admitting that fewer persons were coming forward for testing. Nonetheless, the Chief Medical Officer (CMO) noted that there was a cessation of many of the official (‘mandatory’) COVID-19 protection measures from midnight the same day. This coincided with the day where the media were reporting and showing crowds of persons, mainly without masks, jamming into stores to take advantage of VAT-free
shopping. The media has also been showing crowds of un-masked persons enjoying various events, many of them indoors, apparently dismissive of the threat posed by COVID-19. It must be remembered that some people here remain unvaccinated, or have refused to get the booster shots. Vulnerable individuals, and this group includes the elderly and those harbouring CNDCs, are at increased risk of severe illness and death from COVID-19.
Worldwide, in spite of best efforts, which include mitigation measures, vaccinations, specific medications like antiviral medications and monoclonal antibody treatments [neither of which we could easily afford here], COVID-19 still kills about one in one hundred persons who contract the disease, with a higher rate in vulnerable persons.
The ‘mantra’ of our Ministry of Health (MOH) over the last three decades has been “Your health is your responsibility”. Philosophy: great. Is it working with the CNDC pandemic? There is no statistical evidence to support this (so the CMO has stopped releasing annual statistics). Will it work with the COVID-19 pandemic? The MOH has cut back on releasing the COVID-19 dashboard (daily statistics), which allowed anyone interested to keep track of the pandemic here. Official statistics to follow what is happening here are harder to come by, but a rising COVID-19 rate is likely.
The resumption of Q in the Community, a monthly physical activity event aimed at getting the elderly to become more physically active, is a good thing. It unfortunately had to be stopped at the height of the COVID-19 pandemic. What is not so good now is that a high proportion of our elderly have one or more CNDCs, and are thus vulnerable to a serious health outcome. It is perhaps unfortunate that the crowds of elderly persons coming out to this function have generally declined to wear face masks.
Internationally, we see COVID-19 is on the rise again, with the emergence of new variants of the Omicron strain, specifically the XBB.1.5 which is surging in China, far away, and in the USA, much closer to us. But this virus has shown that geographic distance is no barrier to its spread. Vaccination, the three Ws – not Weekes, Worrell and Walcott but Wash your hands, Wear your mask and Watch your (social) distance – offer some protection. While the CMO has relaxed many restrictions, it should still be the case that ‘your health is your responsibility’. Act now.
At one stage in life, we were fearful that a masked person may cause you harm, and many still do, when our crime situation is being looked at. But now, no thanks to COVID-19, we are also fearful that unmasked persons may cause you harm as well.
So our health focus needs to last longer than the first week of a New Year, as many New Year Resolutions do. The CNDCs have caused, and continue to cause, significant suffering and death, and have overwhelmed our health care services. And that was before the COVID-19 pandemic. As a disease, COVID-19 creates many health problems, but among other issues it makes the CNDCs worse, and actually accelerates the demise of many CNDC patients. And right now, another ‘virus’ has crippled our main hospital, making life and death even harder for anyone who becomes ill.
We must embrace healthy eating, get adequate amounts of both sleep and exercise, and make sure we keep our weight under control. In conjunction with your personal physician, we must ensure that your blood sugar, blood pressure, and blood cholesterol are kept within your target range. “Thou shalt not smoke”, and if you must drink, practice moderation. Ensure that your COVID-19 vaccinations are up to date, and practise all COVID-19 prevention measures. Our resolution is to be healthy all year round.
Dr. Colin V. Alert, MB BS, DM. is a family physician and associate UWI family medicine lecturer.
The post #BTColumn – We need action, not (empty) resolutions! appeared first on Barbados Today.
2 years 3 months ago
Column, Health, lifestyle
FAO activates protocols for Avian Influenza outbreaks in the region
Given the recent confirmation of the presence of Highly Pathogenic Avian Influenza (HPAI) cases in Chile, Colombia, Ecuador, Mexico, Peru, and Venezuela, the Food and Agriculture Organization of the United Nations Agriculture (FAO) regional office for Latin America and the Caribbean reported that it is in contact with both the official veterinary services as well as the ministries of Agricultur
e, Livestock, and the Environment of the affected countries. “We want to appeal to the public to calm down. We have been actively warning about this situation since March of this year, particularly last September due to the start of bird migrations from North America to South America,” said Andrés González, FAO Livestock, Animal Health, and Biodiversity Officer.
“We have active coordination with international organizations, and we are managing ways to assist recently affected countries,” he added. He also stated that there is no scientific evidence that HPAI is transmitted to humans through the consumption of birds or properly prepared eggs. González explained that the countries’ prevention, early detection, and response plans are being supported in the regional emergency of Highly Pathogenic Avian Influenza with the assistance of national representations, through an incident command group led by the FAO’s Animal Health division, and in close coordination with the regional steering committee of the Global Framework for the Progressive Control of Transboundary Diseases of Animals (GF-TADs).
Latin America and the Caribbean produce 20.4% of the world’s poultry meat and 10% of the world’s eggs, making this a vital sector for the livelihoods of millions of small and medium-sized agricultural producers. As a result, it is critical to activate the region’s emergency protocols as soon as possible.
2 years 3 months ago
Health, World
Health Archives - Barbados Today
Education key to curbing substance abuse – Minister Abrahams
By Michron Robinson
Education on substance abuse at all levels of society is critical. That’s according to Minister of Home Affairs and Information Wilfred Abrahams who was speaking to Barbados TODAY after a special church service on Sunday marking the start of Drug Awareness Month at the Church of the Nazarene at Collymore Rock.
He noted that because people don’t understand the effects of substance abuse, its troubling nature is downplayed. “Unless people are educated on what to look for, they may dismiss it as something else. We need to advise and educate ourselves. We need to spot substance abuse in our families, in our communities and even teachers need to spot it in schools… and from as young an age as possible. A lot of Bajans think it is cool to smoke weed, to sneak a drink, to smoke cigarettes, but our children need to be given the information [so they] understand the dangers of it,” he urged.
While recalling that the majority of persons impacted by substance abuse are males, the Minister of Home Affairs said the NCSA will be working towards spreading the word.
“This is the month that the NCSA is focusing on getting the message out, across to the people. Nine out of ten people who have substance abuse problems are males. That’s a reality we cannot escape. During this month – look out we will put a lot of information out there,” he promised.
The Minister added that the Christian church has an important role to play in wrestling Barbados’ crime problem to the ground. “One of the greatest social organisations is the church, historically and in Barbadian culture, most of us have come up in the church, we get our grounding in the church, we learn our ethics and our values from our grandparents and the church. I believe the church has a significant role to play in the fight against substance abuse,” he said.
Pastor of the Church of the Nazarene Reverend David Holder promised his church would do more to help those with drug abuse. “Our gospel is about changing lives. The church now has to get more involved in the community. We need to get out and that is one of the things we intend to do at Collymore Rock – help them through the gospel,” Holder said. (MR)
The post Education key to curbing substance abuse – Minister Abrahams appeared first on Barbados Today.
2 years 3 months ago
Feature, Health