May 27, 2021 at 05:30PM https://ift.tt/2SxnZeS Cindy Loose / Kaiser Health News
The day Dr. Elizabeth Dawson was diagnosed with COVID-19, she awoke feeling as if she had a bad hangover. Four months later, in February 2021, she tested negative for the virus, but her symptoms have only worsened.
Dawson is among what “waves and waves” of “long-haul” COVID patients who remain sick long after testing negative for the virus. A significant percentage are suffering from syndromes that few doctors understand or treat. the ranks of patients were swelled by pandemic newcomers. For some, the consequences are life altering.
Before last fall, Dawson, 44, a dermatologist from Portland, Oregon, routinely saw 25 to 30 patients a day, cared for her 3-year-old daughter and ran long distances. Today, her heart races when she tries to stand. She has severe headaches, constant nausea, and brain fog so extreme that, she says, it “feels like I have dementia.” Her fatigue is severe: “It’s as if all the energy has been sucked from my soul and my bones.” She can’t stand for more than 10 minutes without feeling dizzy.
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Through her own research, Dawson recognized she had typical symptoms of postural orthostatic tachycardia syndrome, or POTS, a disorder of the autonomic nervous system, which controls involuntary functions such as heart rate, blood pressure and vein contractions that assist blood flow. It’s a serious condition that sometimes overlaps with autoimmune problems, which involve the immune system attacking healthy cells. Before COVID-19, an estimated 3 million Americans had POTS.
Many of those patients report it took them years to find a diagnosis. With her own suspected diagnosis in hand, Dawson soon discovered there were no specialists in autonomic disorders in Portland—in fact, there are only 75 board-certified autonomic disorder doctors in the U.S. The nonprofit organization Dysautonomia International provides a list of a handful of clinics and about 150 U.S. doctors who have been recommended by patients and agreed to be on the list.
For people without such connections and knowledge of the medical industry, particularly the low-income people and Black women long-COVID disproportionately affects, appointments typically must be made months in advance.
Dr. Peter S. Rowe of Johns Hopkins University in Baltimore, a prominent researcher who has treated POTS and CFS patients for 25 years, says every doctor with expertise in POTS is seeing long-haul COVID patients with POTS, and every long-COVID patient he has seen with CFS also had POTS. He expects the lack of available treatment for these conditions to create a worsening public health scenario. “Decades of neglect of POTS and CFS have set us up to fail miserably,” says Rowe, who also recently authored a paper on how COVID-19 can trigger CFS.
A “significant infusion of health care resources and a significant additional research investment” will be needed to address the growing caseload, the American Autonomic Society said in a recent statement.
Lauren Stiles, who founded Dysautonomia International in 2012 after being diagnosed with POTS, says patients who have suffered for decades worry about the growing number of people “who need testing and treating but the lack of growth in doctors skilled in autonomic nervous system disorders.” On the other hand, she hopes increasing awareness among physicians will at least get patients with dysautonomia diagnosed more quickly than in the past.
Congress has allocated $1.5 billion to the National Institutes of Health over the next four years to study post-COVID-19 conditions, and requests for proposals have already been issued. The National Institutes of Health’s Goldstein says that the miserable experience of the pandemic opens up a unique opportunity for advances in treatment: researchers can study a large sample of people who got the same virus at roughly the same time, yet some recovered and some did not.
Long-term symptoms are common among those who were infected with SARS-CoV-2. A published in February in the Journal of the American Medical Association’s Network Open found that 27% of COVID-19 survivors ages 18-39 had persistent symptoms three to nine months after testing negative for the viral disease. The percentage was slightly higher for middle-aged patients, and 43% for patients 65 and over. The most common complaint: persistent fatigue. A Mayo Clinic study published this month found that 80% of long-haulers complained of fatigue and nearly half of “brain fog.” Less common symptoms are inflamed heart muscles, lung function abnormalities and acute kidney problems.
Larger studies still need to be conducted to determine the true scale of the issue. However, “even if only a tiny percentage of the millions who contracted COVID suffer long-term consequences,” says Rowe, “we’re talking a huge influx of patients, and we don’t have the clinical capacity to take care of them.”
Yet even with these new cases, some physicians discount conditions like POTS and CFS, both much more common in women than men. With no biomarkers, some have argued that the syndromes are sometimes psychological.
The experience of POTS patient—and current patient advisory board member of Dysautonomia International—Jaclyn Cinnamon is typical. She became ill in college 13 years ago, and saw dozens of doctors seeking an explanation for her racing heart, severe fatigue, frequent vomiting, fever and other symptoms. For years, without results, she saw specialists in infectious disease, cardiology, allergies, rheumatoid arthritis, endocrinology and alternative medicine—and a psychiatrist, “because some doctors clearly thought I was simply a hysterical woman,” she says.
It took three years for her to be diagnosed with POTS. The test is simple: Patients lie down for five minutes and have their blood pressure and heart rate taken. They then either stand or are tilted to 70-80 degrees and their vital signs are retaken. The heart rate of those with POTS will increase by at least 30 beats per minute, and often as much as 120 beats per minute within 10 minutes. POTS and CFS symptoms range from mild to debilitating.
The doctor who diagnosed Cinnamon told her he didn’t have the expertise to treat POTS. Nine years after the onset of the illness, she finally received treatment that alleviated her symptoms. Although there are no federally approved drugs for POTS or CFS, experienced physicians use a variety of medicines including fludrocortisone, commonly prescribed for Addison’s disease, that can improve symptoms. Some patients are also helped by specialized physical therapy that first involves a therapist assisting with exercises while the patient is lying down, then later the use of machines that don’t require standing, such as rowing machines and recumbent exercise bicycles. Some recover over time; some do not.
Dawson says she can’t imagine the “darkness” experienced by patients who lack her access to a network of health care professionals. A retired endocrinologist urged her to have her adrenal function checked. Dawson discovered that her glands were barely producing cortisol, a hormone critical to vital body functions. Medical progress, she says, is everyone’s best hope.
Stiles, whose organization funds research and provides physician and patient resources, is optimistic. “Never in history has every major medical center in the world been studying the same disease at the same time with such urgency and collaboration,” she says. “I’m hoping we’ll understand COVID and post-COVID syndrome in record time.”
KHN (Kaiser Health News) is a national newsroom that produces in-depth journalism about health issues. Together with Policy Analysis and Polling, KHN is one of the three major operating programs at KFF (Kaiser Family Foundation). KFF is an endowed nonprofit organization providing information on health issues to the nation.
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