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Saturday, January 7, 2023

Interview with Dr. Ziyad Al-Aly on the COVID pandemic and Long COVID - WSWS

This is the first part of a two-part interview.

Soon after the COVID-19 pandemic began to sicken millions of people, complaints of post-viral syndromes afflicting those who had recovered from the acute bout of infection began to appear on social media, and then in the popular press. At first these reports were anecdotal, but in May 2020, Elisa Perego, an archaeologist at University College London, created the term “Long COVID” as a hashtag on Twitter.

There remains no consensus definition of the disease due to the multi-factorial, and as of yet not fully understood, pathophysiological process that causes the multitude of symptoms associated with Long COVID.

The World Health Organization (WHO) established a clinical case definition for Long COVID in October 2021 based on its understanding at the time, with the caveat that as new evidence emerged on the consequences of COVID-19 infection, there would be changes in the clinical definition to diagnose the condition.

The WHO wrote:

Post COVID-19 condition occurs in individuals with a history of probable or confirmed SARS-CoV-2 infection, usually three months from the onset of COVID-19 with symptoms that last for at least two months and cannot be explained by an alternative diagnosis. Common symptoms include fatigue, shortness of breath, cognitive dysfunction but also others and generally have an impact on everyday functioning. Symptoms may be new onset following initial recovery from an acute COVID-19 episode or persist from the initial illness. Symptoms may also fluctuate or relapse over time.

The British National Institute for Health and Care Excellence (NICE) and the US National Institutes of Health (NIH) and Centers for Disease Control and Prevention (CDC) have provided clinical criteria for post-COVID conditions that qualify as Long COVID. As of September 2022, the CDC estimated that 7.5 percent of US adults (15.6 million) were experiencing ongoing symptoms three or more months after their initial infection.

A recent published study in the Lancet synthesized the global evidence on the prevalence of persistent symptoms in a general post-COVID population and found that on average at least 45 percent of COVID survivors, regardless of the clinical course of their illness, went on to experience one unresolved symptom four months out. More than one-quarter complained of persistent fatigue. Among the hospitalized cohort, imaging and pulmonary studies revealed abnormalities and impaired functioning.

However, evidence of the impact of COVID infections on the health of the population remains sparse and a systematic analysis and study of the long-term impacts of COVID infection and reinfection remain sorely lacking. 

In this regard, the studies being conducted and presented in peer-reviewed publications by Dr. Ziyad Al-Aly and his colleagues have been critical in developiing an insight into Long COVID. Dr. Al-Aly is director of the Clinical Epidemiology Center and chief of research development at the Veterans Affairs St. Louis Health Care System. Their findings underscore the dangers posed by SARS-CoV-2 infection and reinfection, regardless of vaccination status or severity of the disease after recovery from the acute phase of illness, particularly in damage to the heart, lungs and kidneys, and in metabolic diseases, neurological sequalae (after-effects) and mental health outcomes.

Dr. Ziyad Al-Aly [Photo by Dr. Ziyad Al-Aly]

Dr. Al-Aly recounted in a recent talk he gave on Long COVID that when the pandemic first hit the country, “we as a research group in St. Louis started pondering what can we do, what the hell is going on and then how do we as group of researchers and physician scientists do our part to address the challenge with the pandemic.” He added, “As clinical epidemiologists we started deliberating the best way we could contribute to the fight against COVID-19.”

Dr. Al-Aly explained that his group shifted to studying COVID-19. Out of this grew the recognition, brought forward by a coalition of patients afflicted with Long COVID, of the need to study this condition. He was surprised by the breadth of symptoms that affected so many organ systems. “This was a historic moment in the annals of medicine,” he said, “when patients came to the fore and alerted all of us scientists that something here is wrong and needs to be investigated and researched and gave the entity its name.”

But what is Long COVID, what are the true manifestations of the disease and how is it to be researched? The St. Louis group led by Al-Aly set out to address these questions in an unbiased manner, utilizing the Veterans Affairs Health System database. The group published its first report on Long COVID in Nature on April 22, 2021, titled “High-dimensional characterization of post-acute sequelae of COVID-19.” The report laid out the researchers’ extremely concerning finding that “beyond the first 30 days of illness, people with COVID-19 exhibit a higher risk of death and use of health resources.”

This was one of the first investigations into the long-term consequences of COVID infection, underscoring the dangers posed to the population beyond just the initial phase of infection. And the damage inflicted by the infection affected multiple organ systems, regardless of disease severity or age of the person. Perhaps most fundamentally, the report posed concretely the harmful relationship between communicable diseases and their potential consequences for population health despite the oft-repeated and scientifically unproven notion that the exposure of children and young adults to germs is good for them.

Dr. Al-Aly kindly accepted our invitation for an interview to discuss his work and the COVID pandemic.

* * * *

Benjamin Mateus [BM]: Good afternoon, Dr. Al-Aly. I hope you are doing well.

Ziyad Al-Aly [ZA]: Yes, thank you. Delighted to be here.

BM: Thank you for taking the interview, Dr. Al-Aly. Your time is valuable. I have several questions for you but first I’d like to begin by asking you to tell us who you are, what you do, and your interest in Long COVID.

ZA: I’m Ziyad Al-Aly. I'm a clinical epidemiologist at Washington University School of Medicine, and the chief of research and development at the Veterans Affairs (VA) St. Louis Health Care System. And I direct the clinical epidemiology center here at the St. Louis VA.

Very early in the pandemic, we started seeing reports from patients and patient advocacy groups about patients who developed various symptoms after their acute COVID illness had resolved. Clinically, we were also seeing people coming back with lingering symptoms after what we all thought at the time was just an acute infection that if it resolves, it resolves completely in most people and does not really result in any post-acute or chronic sequelae.

But we started receiving those reports and that sort of launched us on a trajectory to understand what's going on with these patients. That led us to the characterization of Long COVID and on a pathway to try to understand the post-acute and long-term consequences of SARS-CoV-2 infection.

BM: Historically, we know that viral infections can lead to post-acute syndromes. Was there any thought at the beginning of the pandemic that this was a possibility, or were people just not aware of these or considering these issues? Maybe you can touch on these points?

ZA: Sure. I think hindsight is always 20-20. Now it’s very clear to us that many viruses in human history have resulted in long-term consequences. But I have to also admit that we as a medical community or the community of medical professionals and people who deal with chronic disease and infectious diseases have generally actually ignored the idea that viruses can result in long-term consequences.

When initially SARS-CoV-2 hit I don't think it was at the forefront of our minds. At least it wasn’t on my mind, although knowing, even dating back to the flu pandemics in the early decades of the 20th century, that flu also resulted in some long-term consequences in some individuals who were infected with the influenza virus. Still, I don’t think that [clinical insight] was sufficiently hardwired in our minds when the pandemic hit. And I think that’s really a lesson learned that we ignored the post-viral condition for the past century. So, when the COVID-19 pandemic hit, we had to relearn all of this [the hard way].

Now, fast forward. Hindsight is 20-20. But what we’re ultimately trying to tell people is that infections with viruses can lead to adverse long-term health consequences—debility and health manifestation in people. This is a major concern, along with mortality.

SARS-CoV-2 is unique and at the same time not unique. It is unique because of its novelty at this moment. It’s really the virus of the moment. But it’s not unique in the sense it’s not the only virus in the world that can lead to long-term sequelae. We have had to almost rediscover this field in the wake of the early days of the pandemic.

And I think an important lesson to take going forward from all this is that we must recognize that pandemics are going to happen. These are one of the certainties of life. Pandemics are going to keep happening and there are going to be pandemics down the road, and we must recognize that pandemics are not only cause acute events, but they could in some instances lead to long-term serious manifestations, which can have enormous consequences not only on health outcomes, but potentially on the economy and societal well-being, given the extent of infections we are witnessing.

All this means, going forward, is that we must think about how to learn from this pandemic and be prepared for the next one. One key step is to evolve our data systems—our data systems need to be able to capture all this information needed to help us assess the toll of post-acute and long-term effects of emerging infectious diseases and build on our collective knowledge. Our medical and health systems need to be able to address the ramifications of mass casualties like we witnessed. And our science needs to be able to anticipate all this and deal with it more proactively. I think that all those are all lessons that we need to learn now, so we don’t really keep repeating those mistakes.

But I think we have also to be honest with ourselves that none of this was… I don't think collectively here in the United States or anywhere in the world that we had that sort of front and center on our minds when the pandemic hit.

BM: Has anybody ever compared the post-viral syndromes between SARS-CoV-1 and SARS-CoV-2?

ZA: No, not to my knowledge. I think that this is really to your point, Benjamin, is that we haven’t really invested in or thought sufficiently about the post-viral condition to fully characterize different viruses and their long-term consequences, nor do comparative analyses to try to understand similarities and differences in the long-term adverse health consequences of different viruses—the disease processes at play.

So, what are the consequences of SARS-CoV-1, SARS-CoV-2, and MERS? What about Ebola and post-polio? And post flu? And we draw quite a bit of comparison to COVID versus flu, but I also have to admit, what are the five-year outcomes of COVID versus flu? Does anybody know the answer? It’s not known. Look, the flu has been around a very long time, meaning we should know these things, but we don’t. It’s been around for more than a hundred years, but we’ve also ignored it for more than a hundred years.

Dr. Al-Aly at his desk [Photo by Dr. Ziyad Al-Aly]

And as a result, when you ignore something, you don’t have a lot of knowledge about it. So going back to your question of SARS-CoV-1 and SARS-CoV2, there isn’t a whole lot of data out there that can give us a full view for a comparative analysis or the long-term consequences of one versus the other.

BM: Regarding ME/CFS—myalgic encephalomyelitis/chronic fatigue syndrome—is there a better understanding now that this may be a post-viral syndrome that has manifested in a blanket name for this disease, whose pathophysiological mechanisms are poorly understood?

ZA: There are many hypotheses on ME/CFS, which has been talked about for more than 30 years. But it has been substantially underfunded and therefore not sufficiently studied. One of the hypotheses of the pathobiology of ME/CFS is that it’s initially triggered… or the initiating event is a viral infection.

So, what is the virus that initiates ME/CFS still needs to be clarified. But many of those patients, when they are eventually diagnosed with the condition, when they track back the origins of their symptomatology, in a lot of these patients the triggering event is an upper respiratory tract infection or some sort of an infection with fever that only lasted a few days or just symptoms of a cough, some shortness of breath and sore throat for a few days… what we generally classify broadly under the umbrella of an upper respiratory tract infection or the symptomatology that overlaps substantially or what we commonly refer to as upper respiratory tract infection. It's at least clear from those data that that maybe the triggering event is a viral infection.

But I also caveat that by saying that the science on that is not definitive. The identity of that virus has not been pinned down. Still, all of this speaks to the notion that we are talking about, that these entities may have a viral origin and they could be broadly classified under the post-viral illness category, or more appropriately called an infection-associated chronic illness. That’s the term that most people prefer to use. There are different terminologies, and the field is still nascent and evolving but presently the most accepted term is infection-associated chronic illnesses.

However, those baskets of conditions, including ME/CFS, have not been sufficiently studied for us to sit and have a conversation without the data being available to review. The short answer is that we don’t really know conclusively if ME/CFS is initiated by a virus and then which virus. But plausibly, there are hypotheses suggesting that may be the case.

BM: Which raises the topic that has captured the attention of the mainstream press and social media, that is, the pseudo-scientific construct of immunity debt. Additionally, many people, whether they’re politically reactionary or they just don’t know, think that getting infected is somehow good for building your immunity. Within the confines of long COVID and these post viral acute syndromes, what would you tell someone who raises those issues?

ZA: Sure. I hear that a lot and I hear people saying that “a cold never really killed anyone!” And it is true that getting a cold doesn’t really kill anyone [immediately]. But I would like to ask the question, “Does a person who gets, between the ages of 20 and 50, if they get five colds and another person with the same characteristics gets 20 colds, do they have the same risk of cardiovascular outcomes or neurologic outcomes?”

And the answer to that is that we don’t really know. People trivialize infections because they don’t really see immediately the [long-term] consequences of infections. That’s not only true for SARS-CoV-2, but also for a lot of other infections. Even going back to the mildest infection that people generally try to trivialize—the common cold —but we don’t really know what repeat infection means for the life of a person, though we should. Are those people who have more colds at higher risk of long-term disease?

BM: These are important questions and in the context of the pandemic not inconsequential.

ZA: And I would posit, based on some of the evidence we have obtained from our studies, I would hypothesize that the person who gets more infections actually has a higher risk of long-term outcomes, even with a cold.

People trivialize these things without really knowing that there are phases of infection, and it may be true that in the acute phase, if you’re only observing for a few days after an upper respiratory tract infection with a common cold and they quickly bounce back and seemingly on the surface there is no real damage, we can’t be certain on the long-term impact it will have on their health.

We really don’t know, but this is really what we need: more understanding of repeat infections.

Now, with SARS-CoV-2, we know because we’ve done some work to characterize these risks between one, two or three infections. And it is abundantly clear that the people who got hit twice or three times with COVID have it worse compared to those with only one prior infection, both in the acute phase and the long-term phase or post-acute viral phase.

So I think that this idea that infections provide you with immunity and that’s going to shield you and it’s going to totally offset the long-term cost of an infection is bizarre to me. It’s too simplistic and wishful thinking. I wish this was true—to be a kid in a candy store trying to imagine life like that. It would be nice to get one infection that would immunize us from subsequent infections and carry no further risk—it would be wonderful, but that’s simply not the case at all, at least for SARS-CoV-2.

BM: Just one more question along this line before circling back to something you mentioned earlier. What is the latest hypothesis around the mechanism behind post-COVID syndrome? Is it the persistence of the virus? Is it immune dysregulation? Is it a vasculitis and micro-thrombi?

ZA: Brilliant question, Benjamin. But the short answer is we still don’t definitely know with absolute certainty. There are multiple hypotheses and many interesting experimental works that are being done by researchers throughout the world on this question.

One central hypothesis suggests the idea of viral persistence in “immune-privileged sites.” And when we say viral persistent, it doesn’t mean the whole virus but fragments of the viral RNA or proteins that reside in immune-privileged sites that provoke chronic inflammation. That hypothesis is plausible, but it still remains in the realm of a hypothesis, meaning it would still need to be supported with evidence or refuted with evidence. That’s what hypotheses are—a line of thinking that would need to be tested experimentally and clinically to validate whether it's true or false. In other words, we would conclude that a certain hypothesis is not valid based on A, B, C, D, and E evidence.

At this point, I still classify viral persistence under the umbrella of a hypothesis. And there are a lot of other hypotheses that have been presented. One of them, as you pointed out, is immune dysregulation. Another revolves around the idea of a microbiome dysbiosis. This idea that within us, within the human body, there are more bacteria than human cells. And with viral infections, these microbiomes are disturbed, causing “microbiome dysbiosis,” which then provokes a state of ill health or disease. Again, all of those are hypotheses.

I also have to say that they’re not necessarily mutually exclusive. The idea there could be immune dysfunction does not really exclude the possibility that viral persistence or microbiome dysbiosis is causing chronic inflammation or a state of disease.

When we speak about Long COVID, and we both have studied it and thought about it deeply, to know it’s not really one thing. At the end of the day, it’s unlikely to be one thing. We can certainly classify it under the broad umbrella of post-acute illness or post-viral illness. That would be correct. But I think we have to be reluctant to oversimplify a complex condition like that and make it one thing. It’s unlikely to be just one thing.

When I speak to the “lay press” I give the example of our conception of cancer a hundred years ago, when we lumped all cancers under one category—this is tumor outgrowth or this is cancer—but we now know that there are more than 800 types of malignancies and all have different genomic signatures and different responses to treatment, and so on.

In that sense, the field of Long-COVID [and post-acute viral syndromes] is really that nascent or that embryonic in the sense that maybe ultimately, over time, we’ll recognize Long COVID type A, type B, and type C with different manifestations, different responses to treatment, and also different pathophysiology on different mechanisms, meaning, that some of it, maybe Type A, is driven by viral persistence, but type B is driven by microbiome dysbiosis.

The field is nascent or embryonic, which means we have to have an open-minded approach to it and learn from the evidence and adjust our thinking accordingly.

To be continued.

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Interview with Dr. Ziyad Al-Aly on the COVID pandemic and Long COVID - WSWS
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Most people who ended up with long COVID started with a mild case, new study shows - CBS News

Sarah Wulf Hanson is the lead research scientist of Global Health Metrics at the University of Washington and Theo Vos is a professor of health metric sciences with the University of Washington.


The big idea

Even mild COVID-19 cases can have major and long-lasting effects on people's health. That is one of the key findings from our recent multicountry study on long COVID-19 – or long COVID – recently published in the Journal of the American Medical Association.

Long COVID is defined as the continuation or development of symptoms three months after the initial infection from SARS-CoV-2, the virus that causes COVID-19. These symptoms last for at least two months after onset with no other explanation.

We found that a staggering 90% of people living with long COVID initially experienced only mild illness with COVID-19. After developing long COVID, however, the typical person experienced symptoms including fatigue, shortness of breath and cognitive problems such as brain fog – or a combination of these – that affected daily functioning. These symptoms had an impact on health as severe as the long-term effects of traumatic brain injury. Our study also found that women have twice the risk of men and four times the risk of children for developing long COVID.

We analyzed data from 54 studies reporting on over 1 million people from 22 countries who had experienced symptoms of COVID-19. We counted how many people with COVID-19 developed clusters of new long-COVID symptoms and determined how their risk of developing the disease varied based on their age, sex and whether they were hospitalized for COVID-19.

We found that patients who were hospitalized for COVID-19 had a greater risk of developing long COVID – and of having longer-lasting symptoms – compared with people who had not been hospitalized. However, because the vast majority of COVID-19 cases do not require hospitalization, many more cases of long COVID have arisen from these milder cases despite their lower risk. Among all people with long COVID, our study found that nearly one out of every seven were still experiencing these symptoms a year later, and researchers don't yet know how many of these cases may become chronic.

Why it matters

Compared with COVID-19, relatively little is known about long COVID.

Our systematic, multicountry analysis of this condition delivered findings that illuminate the potentially steep human and economic costs of long COVID around the world. Many people who are living with the condition are working-age adults. Being unable to work for many months could cause people to lose their income, their livelihoods and their housing. For parents or caregivers living with long COVID, the condition may make them unable to care for their loved ones.

We think, based on the pervasiveness and severity of long COVID, that it is keeping people from working and therefore contributing to labor shortages. Long COVID could also be a factor in how people losing their jobs has disproportionately affected women.

We believe that finding effective and affordable treatments for people living with long COVID should be a priority for researchers and research funders. Long COVID clinics have opened to provide specialized care, but the treatments they offer are limited, inconsistent and may be costly.

What's next

Long COVID is a complex and dynamic condition – some symptoms disappear, then return, and new symptoms appear. But researchers don't yet know why.

While our study focused on the three most common symptoms associated with long COVID that affect daily functioning, the condition can also include symptoms like loss of smell and taste, insomnia, gastrointestinal problems and headaches, among others. But in most cases these additional symptoms occur together with the main symptoms we made estimates for.

There are many unanswered questions about what predisposes people to long COVID. For example, how do different risk factors, including smoking and high body-mass index, influence people's likelihood of developing the condition? Does getting reinfected with SARS-CoV-2 change the risk for long COVID? Also, it is unclear how protection against long COVID changes over time after a person has been vaccinated or boosted against COVID-19.

COVID-19 variants also present new puzzles. Researchers know that the Omicron variant is less deadly than previous strains. Initial evidence shows lower risk of long COVID from Omicron compared with earlier strains, but far more data is needed.

Most of the people we studied were infected with the deadlier variants that were circulating before omicron became dominant. We will continue to build on our research on long COVID as part of the Global Burden of Disease study – which makes estimates of deaths and disability due to all diseases and injuries in every country in the world – in order to to get a clearer picture of how COVID-19's long-term toll shifted once omicron arrived.

The Conversation

This article is republished from The Conversation under a Creative Commons license.

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Most people who ended up with long COVID started with a mild case, new study shows - CBS News
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Associations between punitive policies and legal barriers to consensual same-sex sexual acts and HIV among gay men and other men who have sex with men in sub-Saharan Africa: a multicountry, respondent-driven sampling survey - The Lancet

Background

Few assessments of associations between structural-level factors and HIV among gay men and other men who have sex with men (MSM) have been conducted, especially in sub-Saharan Africa. Our objective was to examine HIV testing history, HIV status, and stigmas among MSM living in ten countries with heterogeneous legal environments.

Methods

This study used pooled data from ten country-specific, cross-sectional studies done in 25 sites in Burkina Faso, Cameroon, CĂŽte d'Ivoire, The Gambia, Guinea-Bissau, Nigeria, Senegal, Eswatini, Rwanda, and Togo. MSM were recruited by respondent-driven sampling and were eligible if they met country-specific requirements for age, area of residence, and self reported being assigned male sex at birth and having anal sex with a man in the past 12 months. Policy related to same-sex sexual behaviour for each country was categorised as not criminalised or criminalised. Countries were also categorised on the basis of recent reports of prosecutions related to same-sex sexual acts. Legal barriers were defined as those that legally prevented registration or operation of sexual orientation related civil society organisations (CSOs). Individual data on HIV testing history, HIV status, and stigma were collected via interviewer-administered sociobehavioural questionnaires and HIV testing. Multilevel logistic regression with random intercepts was used to assess the association between policies, recent prosecutions, legal barriers to CSOs, and HIV-related factors with adjusted odds ratios (aORs) and 95% CIs.

Findings

Between Aug 3, 2011, and May 27, 2020, we recruited 8047 MSM with a median age of 23 years (IQR 21–27). 4886 (60·7%) lived in countries that criminalise same-sex sexual acts. HIV prevalence among MSM was higher in criminalised settings than non-criminalised settings (aOR 5·15, 95% CI 1·12–23·57); higher in settings with recent prosecutions than in settings without prosecutions (12·06, 7·19–20·25); and higher in settings with barriers to CSOs than without barriers to CSOs (9·83, 2·00–48·30). HIV testing or status awareness was not associated with punitive policies or practices. Stigma was associated with HIV status but did not consistently vary across legal environments. Disparities in HIV prevalence between MSM and other adult men were highest in punitive settings.

Interpretation

Structural risks including discriminatory country-level policies, prosecutions, and legal barriers might contribute to higher HIV prevalence among MSM. Taken together, these data highlight the importance of decriminalisation and decreasing enforcement, alongside stigma reduction, as central to effective control for HIV.

Funding

National Institutes of Health.

Translation

For the French translation of the abstract see Supplementary Materials section.

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Associations between punitive policies and legal barriers to consensual same-sex sexual acts and HIV among gay men and other men who have sex with men in sub-Saharan Africa: a multicountry, respondent-driven sampling survey - The Lancet
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Friday, January 6, 2023

A doctor's plea for a safe consumption site for Kenora as it deals with spike in HIV/AIDS - CBC.ca

More cases of HIV/AIDS have been reported in Kenora, Ont., in the last 12 months than in the last eight years, and a doctor practising in the community says a safe consumption site is needed to help address the issue.

In 2022, the Northwestern Health Unit (NWHU) reported nine confirmed cases of HIV/AIDS in the northwestern Ontario city. In the previous eight years, there were only eight confirmed cases, according to NWHU data. 

Dr. Jonny Grek says that number may be much higher — he's seen 15 new cases reported in the past nine months, and said the health unit's data lags behind what he's seeing at the ground level. 

"Our numbers are from the street point-of-care testing, which are then followed up with a lab confirmed test — and so far, there have been no false positives on the point-of-care testing," Grek told CBC News in an interview. 

The NWHU's medical officer of health, Dr. Young Hoon, doesn't dispute Grek's numbers, but said the NWHU must follow provincial standards for reporting cases and cannot rely on preliminary testing or other clinical information to confirm them.

Grek practises family medicine at Kenora's Paterson Medical Centre, and provides outreach and street medicine through the Sunset Country Family Health Team. He's seen a lot of struggle on Kenora's streets since he came to the area 4½ years ago.

The attitude and the feel on the streets here is one of, I would say, despair on top of despair. - Dr. Jonny Grek

"The attitude and the feel on the streets here is one of, I would say, despair on top of despair," he said.

He works closely with people who may be more vulnerable to viruses, including those who use drugs, are homeless or underhoused, or work in the sex trade.

Being a street doctor means Grek literally meets people where they're at. Sometimes, they may feel more comfortable doing a consultation at the homeless shelter or the Kenora Fellowship Centre.

HIV (human immunodeficiency virus) attacks the immune system, or its ability to fight off disease. Left untreated, HIV can lead to AIDS (acquired immunodeficiency syndrome), which can be controlled through various treatments. 

In Ontario in 2020, it's estimated over 22,000 people were living with HIV, according to the Ontario HIV Epidemiology and Surveillance Initiative.

The virus is primarily spread through bodily fluids including blood and semen. Young Hoon said unprotected sex, and sharing needles or drug preparation equipment are the most common ways people contract HIV/AIDS.

Officials in Kenora recently held an emergency council meeting where members of the public shared their concerns regarding public safety in the downtown area. 

Grek, who was at the meeting, said there was a collective agreement that conversations about these issues need to be had — but there was also a lot of anger and resentment about the situation.

He said he would like to see more empathy toward people who use drugs, rather than judgment and fear of them.

Safe consumption sites

As part of addressing the opioid crisis, there have been calls for safe consumption sites — where people are legally allowed to bring drugs for use in a clean, safe environment, and may also receive addiction support from health-care workers.

In Ontario, there are 26 safe consumption sites. But the closest one to Kenora is Path 525, at 525 Simpson St. in Thunder Bay, Ont.

In the latter half of 2022, the NWHU worked with LBCG Consulting for Impact Inc. to conduct a supervised consumption services feasibility study. The study looked at whether supervised consumption services are needed in Kenora, Dryden, Fort Frances and Sioux Lookout, and what form they might take.

"The main goal is to prevent [opioid] overdoses, but it does have the ability to increase access to the clean needles and drug preparation equipment, and that of course would reduce the spread of HIV," said Young Hoon.

The NWHU is currently reviewing drafts of the report, with hopes of finalizing and publishing the results in February.

Drug paraphernalia is shown at Vancouver safe consumption site
Drug paraphernalia is shown at the Molson Overdose Prevention Site in the downtown Eastside of Vancouver on Sept. 10, 2019. In Kenora, there's no safe consumption site, but the rise in HIV/AID in the Ontario city is prompting a call for one. (Ben Nelms/CBC)

In Grek's view, a safe consumption site "would mean everything" for Kenora.

"We're past the point here where we can stop people from using drugs. We are way past the point of being able to control or stabilize even the unsafe … the toxic supply of drugs that are in the market at the moment," he said. "But what we're not past the point of is showing that people who use drugs are human beings." 

And when — not if — Kenora recognizes this is the right approach, he said, it must be more than "just a drop-in space where you go and use drugs and then you leave."

He encourages people to challenge their perspectives by having open conversations, like the one held at last week's Kenora council meeting.

"We all get healthier when we learn more, especially if it means that we're just a bit more open minded to people," he said.

Ramping up testing, prevention programs

Anyone who believes they're at risk of getting HIV/AIDS can receive a blood test by reaching out to their primary health-care provider, or going to a community health centre, primary care or outreach clinic. Some NWHU offices also offer testing, said Young Hoon.

A headshot of Dr. Kit Young Hoon, the medical officer of health for the Northwestern Health Unit.
Dr. Kit Young Hoon, the NWHU's medical officer of health, says, 'Early detection and treatment of HIV means that people with HIV can live with it for a very, very long time and live with it in a healthy way.' (Submitted by Lindsay Koch)

Young Hoon emphasized that conversations with health-care practitioners are confidential.

"Many years ago, when less was known and there [were] less treatment options for HIV, the diagnosis of it did feel like it could be a death sentence, but it's not that way anymore," she said. "Early detection and treatment of HIV means that people with HIV can live with it for a very, very long time and live with it in a healthy way."

But treatment must start as soon as possible.

Testing helps prevent spread of HIV, as does access to clean needles and barrier protection like condoms during sex. A list of needle distribution sites can be found on the NWHU's website. Many clinics also give out condoms for free.

Making these services accessible to vulnerable populations — people who are underhoused or affected by poverty — is critical, Young Hoon said.

The health unit is closely monitoring HIV/AIDS case numbers to see what additional actions may be needed.

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A doctor's plea for a safe consumption site for Kenora as it deals with spike in HIV/AIDS - CBC.ca
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Thursday, January 5, 2023

Kids prescribed antibiotics but not fed breast milk at triple risk of asthma: study - Prince Rupert Northern View - The Northern View

A Canadian study suggests children who were not breastfed while receiving antibiotics in the first year of life had triple the risk of developing asthma because they lacked specific protective sugars found in human milk.

Dr. Stuart Turvey, a lead researcher, said antibiotics such as amoxicillin are commonly prescribed to treat a wide range of infections in young children, but the medications have also been linked with disrupting the development of a healthy gut microbiome.

“What we’ve known for some time was that babies that got antibiotics early in life were at higher risk of having asthma at school age and beyond but no one knew why,” said Turvey, a pediatrician at BC Children’s Hospital.

The study, published Wednesday in the journal Med, found that sugars in breast milk, which make up about 20 per cent of its indigestible carbohydrates, promote the growth of the B. infantis bacteria to help make other bacteria in order to train the immune system and prevent the development of asthma and allergies.

Researchers also said they identified the breast milk sugars that offer this protection, which could potentially be used to supplement formula for infants that need antibiotics but for whom breastfeeding is not an option.

“Children are born with pretty much no bacteria,” Turvey said. “Then these communities (of bacteria) start to build, with pioneer species that help the other ones colonize. So the timing matters,” he said of when people are prescribed antibiotics, which “confuse” kids’ immune systems in the first few months of their lives.

The research involved a total of 2,521 children in Vancouver, Edmonton, Winnipeg and Toronto. It showed 17 per cent of the kids received antibiotics in the first year of life.

Three groups of kids were compared — those who received no antibiotics, those who were given them while being breastfed and those who got them without being breastfed.

When a subset of 1,338 children were three months old, researchers collected a dirty diaper to test the stool. A year later, another diaper was collected for a stool sample from the same kids, said Turvey, adding the expense of the relatively new technology prohibited all of the children’s samples from being tested.

“We got the poop samples and then we did metagenomics, a type of genetic sequencing, to identify all the bacteria by the DNA that’s there. This (B. infantis) came up as a really strong signal,” he said.

At age five, all the children were assessed for asthma. Those who did notreceive breast milk but had been prescribed antibiotics were at three times the risk of having the condition.

“The children who received the antibiotics while breastfeeding weren’t at any higher risk than the children whodid not have antibiotics,” Turvey said.

“One important thing was that any breastfeeding was protective. So it wasn’t just exclusive breastfeeding, with no other form of nutrition.”

Asthma is a top reason for kids visiting for emergency rooms and doctors’ offices, often while missing school, he said, adding that despite the findings, amoxicillin is a potentially life-saving drug for very young kids.

The study findings could spur clinical trials to determine if the natural sugars in breast milk can be used to supplement formula for the benefit of people who can’t breastfeed their children, Turvey said. Chemists could make synthetic versions of the sugars, similar to some that are already in formula, he added.

“More knowledge about the protective ones could inform that process.”

Ailbhe Smyth, a volunteer with a Vancouver chapter of La Leche League, which supports breastfeeding mothers, said those who are struggling with what is often a challenging experience, as it was for her, should not take the findings as another reason to feel guilty about being “a perfect parent.”

Fewer public health clinics were offering support through lactation specialists even before the pandemic and some women are opting for private consultants to avoid long wait lists, Smyth said.

“But that’s still a barrier. Some people just don’t have the extra money to do that,” she said, adding: “I think support doesn’t only need to come from the health-care system because it has to come from society in general.”

—Camille Bains, The Canadian Press

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B.C. expanding PharmaCare coverage to include diabetes, heart failure and blood clot drugs | Globalnews.ca - Global News

Thousands of British Columbians will soon benefit from the B.C. government’s expansion of the B.C. PharmaCare program.

Starting Thursday, drug coverage is expanded to include medications used to treat Type 2 diabetes, heart failure and blood clots.

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“This is a very significant step in our province,”  said Adrian Dix, B.C.’s minister of health.

“The medication in question affects 245,000 people. These are much-needed medications in our province.”

Drug coverage for two medications will be expanded from limited coverage to regular benefits — those are dapagliflozin (Forxiga) and apixaban (generics).

Two other medications, empagliflozin (Jardiance) and semaglutide (Ozempic), that are covered by PharmaCare under specific medical circumstances will have their limited criteria expanded, according to the B.C. Ministry of Health.

“The changes will ensure that coverage is aligned with clinical evidence and will improve patient access to appropriate medications,” ministry staff said in a release.

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Dapagliflozin (Forxiga) is approved by Health Canada to treat several conditions such as heart failure, Type 2 diabetes and chronic kidney disease.

It was first listed as a limited coverage benefit through PharmaCare for patients with heart failure with “reduced ejection fraction” on Jan. 11, 2022, a condition where the muscle of the left ventricle is not pumping normally.

Currently, approximately 2,000 patients in British Columbia benefit from dapagliflozin under limited coverage, according to the ministry. The expansion to a regular benefit is expected to benefit 5,000 more patients in the first year.

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Apixaban (generics) is a blood thinner medication used to prevent or treat blood clots.

Currently, 45,000 patients in British Columbia benefit from apixaban under limited coverage, according to the B.C. government. The expansion to a regular benefit is projected to benefit approximately 24,000 more patients, officials say.

The expansion of limited coverage criteria for empagliflozin (Jardiance) and semaglutide (Ozempic) will make it easier for patients to apply for coverage of these two medications that work to lower blood sugar levels in adults with Type 2 diabetes, according to the government.

PharmaCare has changed the coverage from third-line to second-line.

Patients now will only have to try one drug, metformin, before their physician can request coverage of empagliflozin or semaglutide, according to the ministry.

PharmaCare is a publicly funded program that helps B.C. residents pay for some prescription drugs, medical supplies and pharmacy services.

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Breastfeeding babies can offset the risk of asthma from antibiotics - UBC Faculty of Medicine

Breastfeeding can protect infants from the risk of asthma due to antibiotic exposure, according to a new study led by Dr. Stuart Turvey, a UBC professor in the department of pediatrics and investigator at BC Children’s Hospital.

Dr. Stuart Turvey

Dr. Stuart Turvey

The study, published recently in the journal Med, found that children who were not breastfed while taking antibiotics had three times the risk of developing asthma compared to those who were breastfed while taking antibiotics.

Asthma affects around one in seven children around the world and is the leading cause of pediatric emergency room visits and missed school days. It can also lead to lifelong poor lung health.

The community of gut microbes, or microbiota, early in life supports immune development to help prevent asthma, however, antibiotic exposure seems to disrupt this delicate microbial balance.

“Increasingly, we have come to understand the enormous influence infant gut health has on overall health,” says Dr. Turvey. “While strides have been made to reduce unnecessary antibiotic prescriptions, we realize they are still an important treatment for babies when warranted. According to our findings, breastfeeding may be one of the most influential factors in protecting these babies when they require antibiotics.”

Darlene Dai

Darlene Dai

Dr. Turvey and his team used data collected from children who participated in the Canadian Healthy Infant Longitudinal Development (CHILD) study to examine whether breastfeeding could promote a healthy gut and potentially reduce the risk of asthma due to antibiotic exposure.

The CHILD study is the largest multidisciplinary, longitudinal, population-based birth cohort study in Canada, where investigators have tracked the health, growth and environments of kids from birth into school age, and made important discoveries about how asthma and allergies develop.

“Working with the CHILD study, we had access to the microbiota composition within stool samples from infants as well as the makeup of their mother’s milk,” says Darlene Dai, a PhD candidate in UBC’s Experimental Medicine program and co-author of the study. “We were able to identify which beneficial microbes contributed to protection and pinpoint the components in the milk that nurture these beneficial microbes.”

Dr. Charisse Petersen

Dr. Charisse Petersen

These components are called human milk oligosaccharides, which make up around 20 per cent of carbohydrates in human breast milk and are mostly indigestible by infants. Instead, their main purpose is to support the colonization of beneficial infant bacteria.

“We realize that breastfeeding is not always an option for infants who have been exposed to antibiotics,” says Dr. Charisse Petersen, research associate in UBC’s department of pediatrics and another co-author of the study. “We are hopeful that supplementation of the beneficial microbes and the necessary prebiotics identified in the study may be able to provide protection. Our findings could greatly improve how we treat and care for infants who need antibiotics and further reduce the burden of asthma both for these children and society.”

A version of this story was originally published by the BC Children’s Hospital Research Institute.

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