Relevant Dermatoses Among U.S. Military Service Members: An ...



3vd disease :: Article Creator

13 Signs And Symptoms Of Lyme Disease

We include products we think are useful for our readers. If you buy through links on this page, we may earn a small commission Here's our process.

Healthline only shows you brands and products that we stand behind.

Our team thoroughly researches and evaluates the recommendations we make on our site. To establish that the product manufacturers addressed safety and efficacy standards, we:
  • Evaluate ingredients and composition: Do they have the potential to cause harm?
  • Fact-check all health claims: Do they align with the current body of scientific evidence?
  • Assess the brand: Does it operate with integrity and adhere to industry best practices?
  • We do the research so you can find trusted products for your health and wellness.

    Was this helpful?

    Lyme disease can cause many symptoms in addition to the typical oval or bulls-eye rash. These can range from mild flu-like symptoms like fatigue to neurological issues and mood changes.

    Lyme disease is an underreported, under-researched, and often debilitating disease transmitted by spirochete bacteria. The spiral-shaped bacteria, Borrelia burgdorferi, are transmitted by blacklegged deer ticks. Lyme's wide range of symptoms mimic those of many other ailments, making it difficult to diagnose (1, 2).

    The blacklegged ticks can also transmit other disease-causing bacteria, viruses, and parasites. These are known as coinfections (1). These ticks that transmit Lyme are increasing their geographical spread. As of 2016, they were found in about half the counties in 43 of 50 states in the United States (3).

    Lyme is the fifth most reported of notifiable diseases in the United States, with an estimated 329,000 new cases found annually (4). But in some states, estimates suggest that Lyme disease is profoundly underreported (4). Some studies estimate that there are as many as 1 million cases of Lyme in the United States every year (5).

    Most people with Lyme who are treated right away with three weeks of antibiotics have a good prognosis.

    But if you're not treated for weeks, months, or even years after infection, Lyme becomes more difficult to treat. Within days of the bite, the bacteria can move to your central nervous system, muscles and joints, eyes, and heart (6, 7).

    Lyme is sometimes divided into three categories: acute, early disseminated, and late disseminated. But the progression of the disease can vary by individual, and not all people go through each stage (8).

    Every individual reacts to the Lyme bacteria differently. You may have some or all of these symptoms. Your symptoms may also vary in severity. Lyme is a multi-system disease.

    Here is a list of 13 common signs and symptoms of Lyme disease.

    The signature rash of a Lyme tick bite looks like a solid red oval or a bull's-eye. It can appear anywhere on your body. The bull's-eye has a central red spot, surrounded by a clear circle with a wide red circle on the outside.

    The rash is flat and usually doesn't itch. The rash is a sign that the infection is spreading within your skin tissues. The rash expands and then resolves over time, even if you're not treated.

    Thirty percent or more of people with Lyme disease don't remember having the rash (9).

    Even fewer people remember a tick attachment. Estimates range from 20 to 50 percent (10). The ticks in the nymph stage are the size of poppy seeds, and their bites are easy to miss.

    The initial red rash usually appears at the site of the bite within 3 to 30 days (11). Similar but smaller rashes can appear three to five weeks later, as the bacteria spread through tissues (12). Sometimes the rash is just a red blotch (1, 13). The rash can also take other forms, including a raised rash or blisters (14).

    If you do have a rash, it's important to photograph it and see your doctor to get treated promptly.

    Summary:

    If you see a flat rash shaped like an oval or bull's-eye anywhere on your body, it could be Lyme. See your doctor.

    Whether or not you see the tick bite or the classic Lyme rash, your early symptoms are likely to be flu-like. Symptoms are often cyclical, waxing and waning every few weeks (12).

    Tiredness, exhaustion, and lack of energy are the most frequent symptoms. The Lyme fatigue can seem different from regular tiredness, where you can point to activity as a cause. This fatigue seems to take over your body and can be severe.

    You may find yourself needing a nap during the day, or needing to sleep one or more hours longer than usual.

    In one study, about 84 percent of children with Lyme reported fatigue (8). In a 2013 study of adults with Lyme, 76 percent reported fatigue (15).

    Sometimes Lyme-related fatigue is misdiagnosed as chronic fatigue syndrome, fibromyalgia, or depression (8).

    In some Lyme cases, fatigue can be disabling (16).

    Summary:

    Extreme fatigue is a frequent symptom of Lyme.

    Joint pain and stiffness, often intermittent, are early Lyme symptoms. Your joints may be inflamed, warm to the touch, painful, and swollen. You may have stiffness and limited range of motion in some joints (1).

    Pain may move around. Sometimes your knees may hurt, whereas other times it's your neck or your heels. You may also have bursitis (16). Bursae are the thin cushions between bone and surrounding tissue.

    The pain may be severe, and it may be transitory. More than one joint may be affected. Most often the large joints are involved (12).

    People often attribute joint problems to age, genetics, or sports. Lyme should be added to that list, as these statistics indicate:

  • One study estimates that 80 percent of people with untreated Lyme have muscle and joint symptoms (17).
  • Fifty percent of people with untreated Lyme have intermittent episodes of arthritis (17).
  • Two-thirds of people have their first episode of joint pain within six months of the infection (18).
  • Use of anti-inflammatory drugs may mask the actual number of people with joint swelling (19).
  • Summary:

    Joint pain that comes and goes, or moves from joint to joint, could be a sign of Lyme.

    Other common flu-like symptoms are headaches, dizziness, fever, muscle pain, and malaise.

    About 50 percent of people with Lyme disease have flu-like symptoms within a week of their infection (18).

    Your symptoms may be low-level, and you may not think of Lyme as a cause. For example, when fever occurs, it's usually low-grade (18).

    In fact, it can be difficult to distinguish Lyme flu symptoms from a common flu or viral infection. But, unlike a viral flu, for some people the Lyme flu-like symptoms come and go.

    Here are a few statistics from different studies of Lyme patients:

  • Seventy-eight percent of children in one study reported headaches (8).
  • Forty-eight percent of adults with Lyme in one study reported headaches (20).
  • Fifty-one percent of children with Lyme reported dizziness (8).
  • In a 2013 study of adults with Lyme, 30 percent experienced dizziness (15).
  • Thirty-nine percent of children with Lyme reported fevers or sweats (8).
  • Among adults with Lyme, 60 percent reported fever in a 2013 study (15).
  • Forty-three percent of children with Lyme reported neck pain (8).
  • A smaller number of children with Lyme reported sore throats (8).
  • Summary:

    Low-level flu symptoms that periodically return could be a sign of Lyme.

    Sleep disturbances in Lyme are common.

    Joint pain may wake you up at night. Your body temperature may fluctuate, and night sweats or chills can wake you.

    Your face and head may feel flushed.

    Here are some of the statistics from studies:

  • In a 2013 study, 60 percent of adults with early Lyme reported sweats and chills (15).
  • The same study reported that 41 percent experienced sleep disturbances (15).
  • Twenty-five percent of children with Lyme reported disturbed sleep (8).
  • Summary:

    Sleep disturbances are common with Lyme, including night sweats and chills.

    There are many kinds and degrees of cognitive disturbances, and they can be scary.

    You may notice that you have difficulty concentrating in school or at work.

    Your memory may have lapses that weren't there before. You may have to reach to remember a familiar name.

    You may feel as though you're processing information more slowly.

    Sometimes when driving or taking public transportation to a familiar place, you may forget how to get there. Or you may be confused about where you are or why you're there.

    You might get to a store to shop, but entirely forget what it was that you were supposed to look for.

    You might at first attribute this to stress or age, but the decline in capabilities may worry you.

    Here are some statistics:

  • Seventy-four percent of children with untreated Lyme reported cognitive problems (8).
  • Twenty-four percent of adults with early Lyme reported difficulty concentrating (15).
  • In later Lyme, 81 percent of adults reported memory loss (21).
  • Summary:

    Lyme bacteria can affect your brain and mental processes.

    Bright indoor light may feel uncomfortable or even blinding.

    Light sensitivity is bad enough for some people to need sunglasses indoors, in addition to wearing sunglasses outdoors in normal light.

    Light sensitivity was found in 16 percent of adults with early Lyme (15).

    In the same study, 13 percent reported blurry vision.

    Summary:

    Light sensitivity, including to indoor light, is a symptom of Lyme.

    Neurological symptoms can be subtle and sometimes specific.

    In general, you may feel unsure of your balance or less coordinated in your movements.

    Walking down a slight incline on your driveway might take an effort that it never did before.

    You might trip and fall more than once, although this never happened to you before.

    Some Lyme effects are very specific.

    For example, the Lyme bacteria may affect one or more of your cranial nerves. These are the 12 pairs of nerves that come from your brain to your head and neck area.

    If the bacteria invade the facial nerve (the seventh cranial nerve), you can develop muscle weakness or paralysis on one or both sides of your face. This palsy is sometimes mistakenly called Bell's palsy. Lyme disease is one of the few illnesses that cause palsies on both sides of the face. Or you may have numbness and tingling on your face.

    Other affected cranial nerves can cause loss of taste and smell.

    A Centers for Disease Control and Prevention (CDC) study of 248,074 reported Lyme disease cases nationwide from 1992 to 2006 found that 12 percent of Lyme patients had cranial nerve symptoms (9).

    As the Lyme bacteria spread through the nervous system, they can inflame the tissues where the brain and spinal cord meet (the meninges).

    Some of the common symptoms of Lyme meningitis are neck pain or stiffness, headache, and light sensitivity. Encephalopathy, which alters your mental state, is less common.

    These neurological symptoms occur in about 10 percent of adult individuals with untreated Lyme disease (18).

    Summary:

    Neurological problems, ranging from balance issues, to stiff neck, to facial palsy, could be symptoms of Lyme.

    Skin symptoms appear early in Lyme (21).

    You may have unexplained skin rashes or large bruises without usual cause.

    Skin outbreaks may be itchy or unsightly. They could also be more serious, such as B cell lymphoma (21).

    Other skin ailments associated with Lyme are:

  • morphea, or discolored patches of skin (21)
  • lichen sclerosus, or white patches of thin skin (21)
  • parapsoriasis, a precursor to skin lymphoma
  • In Europe, some of the skin diseases that result from Lyme transmitted by a different Borrelia species are:

  • borrelial lymphocytoma, which is common in Europe as an early Lyme marker (22)
  • acrodermatitis chronica atrophicans (21)
  • Summary:

    In addition to the classic Lyme rash, other unexplained rashes can be Lyme symptoms.

    Lyme bacteria can invade your heart tissue, a condition called Lyme carditis.

    Carditis can range from mild to severe.

    The bacterial interference in your heart can cause chest pains, light-headedness, shortness of breath, or heart palpitations (23).

    The inflammation caused by the infection blocks the transmission of electrical signals from one chamber of the heart to the other, so the heart beats irregularly. This is known as heart block.

    Lyme can also affect the heart muscle itself.

    How common is Lyme carditis? Here are some statistics:

  • The CDC reports that only 1 percent of reported Lyme cases involve carditis (23).
  • Other studies report that 4 to 10 percent of Lyme patients (or more) have carditis (24, 25). However, these figures may include a broader definition of carditis.
  • Children can also have Lyme carditis (24).
  • With treatment, most people will recover from an episode of Lyme carditis. However, it has caused occasional deaths. The CDC reported three sudden Lyme carditis deaths from 2012–2013 (26).

    Summary:

    Lyme bacteria can affect your heart, producing a range of symptoms.

    Lyme can affect your moods.

    You may be more irritable, anxious, or depressed.

    Twenty-one percent of early Lyme patients reported irritability as a symptom. Ten percent of Lyme patients in the same study reported anxiety (15).

    Summary:

    Mood swings can be a symptom of Lyme.

    Some people with Lyme may have sharp rib and chest pains that send them to the emergency room, suspecting a heart problem (27).

    When no problem is found, after the usual testing, the ER diagnosis is noted as an unidentified "musculoskeletal" cause.

    You can also have strange sensations like skin tingling or crawling, or numbness or itchiness (27).

    Other symptoms have to do with cranial nerves.

  • Ear-ringing (tinnitus). Tinnitus can be a nuisance, especially at bedtime when it seems to get louder as you're trying to fall asleep. About 10 percent of people with Lyme experience this (15).
  • Hearing loss. One study reported that 15 percent of Lyme patients experienced loss of hearing (28).
  • Jaw pain or toothaches that are not related to actual tooth decay or infection.
  • Summary:

    Lyme can be the cause of unexplained sensations or pain.

    Children are the largest population of Lyme patients.

    The CDC study of reported Lyme cases from 1992–2006 found that the incidence of new cases was highest among 5- to 14-year-olds (9). About one quarter of reported Lyme cases in the United States involve children under 14 years old (29).

    Children can have all the signs and symptoms of Lyme that adults have, but they may have trouble telling you exactly what they feel or where it hurts.

    You may notice a decline in school performance, or your child's mood swings may become problematic.

    Your child's social and speech skills or motor coordination may regress. Or your child may lose their appetite.

    Children are more likely than adults to have arthritis as an initial symptom (25).

    In a 2012 Nova Scotian study of children with Lyme, 65 percent developed Lyme arthritis (30). The knee was the most commonly affected joint.

    Summary:

    Children have the same Lyme symptoms as adults, but are more likely to have arthritis.

    If you have some of the signs and symptoms of Lyme, see a doctor — preferably one familiar with treating Lyme disease.

    The International Lyme and Associated Diseases Society (ILADS) can provide a list of Lyme-aware doctors in your area (31).

    Summary:

    Find a doctor familiar with treating Lyme disease.

    What about tests?

    The commonly used ELISA test is not a reliable indicator for many Lyme patients (32).

    The Western blot test tends to be more sensitive, but it still misses 20 percent or more of Lyme cases (32).

    At-home testing is also available. You can buy a test kit online from LetsGetChecked here.

    If you don't have the initial Lyme rash, diagnosis is usually based on your symptoms and your potential exposure to blacklegged ticks. The doctor will rule out other possible diseases that may cause the same symptoms.

    Summary:

    Lyme diagnosis is usually based on your symptoms.

    What to do if you have a blacklegged tick bite

    Remove the tick by pulling it directly out with fine-tipped tweezers. Lift upward with slow and even pressure. Don't twist when removing it. Don't crush it or put soap or other substances on it. Don't apply heat to it.

    Place the tick in a resealable container. See if you can identify what kind of a tick it is.

    Immediately after removing the tick, wash your skin well with soap and water or with rubbing alcohol.

    Not all ticks carry Lyme. The Lyme bacteria is transmitted only by blacklegged ticks in their nymph or adult stage.

    Save the tick to show your doctor. The doctor will want to determine if it's a blacklegged tick and if there's evidence of feeding. Ticks enlarge as they feed. Your risk of getting Lyme from an infected tick increases with the length of time that the tick fed on your blood.

    Summary:

    Pull the tick out with tweezers and save it in a resealable container for identification.

    Antibiotics work

    If you have the classic Lyme rash or other symptoms of early Lyme, you'll need at least three weeks of oral antibiotics. Shorter courses of treatment have resulted in a 40 percent relapse rate (33).

    Even with three weeks of antibiotics, you may need one or more courses of antibiotics if your symptoms return.

    Lyme is tricky and affects different people in different ways. The longer you've had symptoms, the more difficult it is to treat.

    Summary:

    At least three weeks of oral antibiotics are recommended when you have symptoms of early Lyme.

    Lyme is a serious tick-borne disease with a wide range of symptoms.

    If you get treated as soon as possible with an adequate course of antibiotics, you'll have a better outcome.

    Finding a Lyme-aware doctor is important.


    What Is Prion Disease?

    Prion diseases are rare, fatal neurodegenerative disorders caused by misfolded prion proteins (PrP) in the brain. This can lead to memory loss, behavior changes, and movement problems.

    Prion diseases are a group of rare neurodegenerative disorders that can affect both humans and animals.

    They're caused by abnormally folded proteins in the brain, particularly the misfolding of PrPs.

    This leads to a progressive decline in brain function.

    Around 300 new cases of prion disease are reported each year in the United States.

    They can be:

  • Acquired through contaminated food or medical equipment
  • Inherited via mutations in the gene that codes for PrP
  • Sporadic, where the misfolded PrP develops without any known cause
  • In people with prion disease, the misfolded PrP can bind to healthy PrP, which causes the healthy protein to also fold abnormally.

    Misfolded PrP begins to accumulate and form clumps within the brain, damaging and killing nerve cells.

    This damage causes tiny holes to form in brain tissue, making it appear sponge-like under a microscope. (That's why you may see prion diseases referred to as "spongiform encephalopathies.")

    Researchers are still working to understand more about prion diseases and find an effective treatment. But they do know some things.

    Read on to find out about the different types of prion disease, if there are any ways to prevent them, and more.

    Prion disease can occur in both humans and animals. Below are some different types of prion diseases. More information about each disease follows the table.

    Human prion diseases
  • Creutzfeldt-Jakob disease (CJD). First described in 1920, CJD can be acquired, inherited, or sporadic. Most cases of CJD are sporadic.
  • Variant Creutzfeldt-Jakob disease (vCJD). This form of CJD can be acquired through eating the contaminated meat of a cow.
  • Fatal Familial insomnia (FFI). FFI affects the thalamus, which is the part of your brain that manages sleeping and waking cycles. One of the main symptoms of this condition is worsening insomnia. The mutation is inherited in a dominant manner, meaning an affected person has a 50 percent chance of transmitting it to their children.
  • Gerstmann-Straussler-Scheinker syndrome (GSS). GSS is also inherited. Like FFI, it's transmitted in a dominant manner. It affects the cerebellum, which is the part of the brain that manages balance, coordination, and equilibrium.
  • Kuru. Kuru was identified in a group of people from New Guinea. The disease was transmitted via a form of ritual cannibalism in which the remains of deceased relatives were consumed.
  • Risk factors for these diseases include:

  • Genetics. If someone in your family has an inherited prion disease, you're at an increased risk of having the mutation, too.
  • Age. Sporadic prion diseases tend to develop in older adults.
  • Animal products. Consuming animal products that are contaminated with a prion can transmit a prion disease to you.
  • Medical procedures. Prion diseases can be transmitted through contaminated medical equipment and nervous tissue. Cases where this has happened include transmission through contaminated cornea transplants or dura mater grafts.
  • Animal prion diseases
  • Bovine spongiform encephalopathy (BSE). Commonly called "mad cow disease," this type of prion disease affects cows. Humans who consume meat from cows with BSE can be at risk for vCJD.
  • Chronic wasting disease (CWD). CWD affects animals like deer, moose, and elk. It gets its name from the drastic weight loss observed in sick animals.
  • Scrapie. Scrapie is the oldest form of prion disease, having been described as far back as the 1700s. It affects animals like sheep and goats.
  • Feline spongiform encephalopathy (FSE). FSE affects domestic cats and wild cats in captivity. Many of the cases of FSE have occurred in the United Kingdom, with some also seen in other parts of Europe and Australia.
  • Transmissible mink encephalopathy (TME). This very rare form of prion disease affects mink. A mink is a small mammal that's often raised for fur production.
  • Ungulate spongiform encephalopathy. This prion disease is also very rare and affects exotic animals that are related to cows.
  • Diseases caused by prions

    The prion diseases highlighted above aren't the only diseases linked to prions.

    Other neurodegenerative diseases, like Alzheimer's and Parkinson's, are also associated with misfolded proteins in the central nervous system. And research has found that some of these misfolded proteins may be prions.

    But some scientists believe that these proteins only act in a prion-like way. They argue that they can't be prions as the diseases they cause, like Alzheimer's, aren't thought to be infectious.

    Prion diseases have very long incubation periods, often on the order of many years. When symptoms develop, they progressively worsen, sometimes rapidly.

    Common symptoms of prion disease include:

    There's currently no cure for prion disease. But treatment focuses on providing supportive care.

    Examples of this type of care include:

  • Medications. Some medications can be prescribed to help treat symptoms. Examples include:– reducing psychological symptoms with antidepressants or sedatives– providing pain relief using opiate medication– easing muscle spasms with drugs like sodium valproate and clonazepam
  • Assistance. As the disease advances, many people need help taking care of themselves and performing daily activities.
  • Providing hydration and nutrients. In advanced stages of the disease, IV fluids or a feeding tube may be required.
  • Scientists continue to work to find an effective treatment for prion diseases.

    Some of the potential therapies being investigated include the use of anti-prion antibodies and "anti-prions" that inhibit the replication of abnormal PrP.

    Since prion diseases can present similar symptoms to other neurodegenerative disorders, they can be difficult to diagnose.

    The only way to confirm a diagnosis of prion disease is through a brain biopsy performed after death.

    But a healthcare professional can use your symptoms, medical history, and several tests to help diagnose prion disease.

    The tests they may use include:

  • MRI. An MRI can create a detailed image of your brain. This can help healthcare professional visualize changes in brain structure that are associated with prion disease.
  • Cerebrospinal fluid (CSF) testing. CSF can be collected and tested for markers associated with neurodegeneration. In 2015, a test was developed to specifically detect markers of human prion disease.
  • Electroencephalography (EEG). An EEG records electrical activity in your brain. Abnormal patterns can occur with prion disease, particularly with CJD, where short periods of increased activity may be seen.
  • Several measures have been taken to prevent the transmission of acquired prion diseases. Because of these proactive steps, acquiring a prion disease from food or a medical setting is now extremely rare.

    Some of the preventive steps taken include:

  • setting tight regulations on importing cattle from countries where BSE occurs
  • prohibiting parts of the cow like the brain and spinal cord from being used in food for humans or animals
  • preventing those with a history of or risk for exposure to prion disease from donating blood or other tissues
  • using robust sterilization measures on medical instruments that have come into contact with the nervous tissue of someone with suspected prion disease
  • destroying disposable medical instruments
  • There's currently no way to prevent inherited or sporadic forms of prion disease.

    If someone in your family has an inherited prion disease, you may consider consulting with a genetic counselor to discuss your risk of developing the disease.

    Prion diseases are a rare group of neurodegenerative disorders caused by abnormally folded proteins in your brain.

    The misfolded protein forms clumps that damage nerve cells, leading to a progressive decline in brain function.

    Some prion diseases are genetically transmitted, while others can be acquired through contaminated food or medical equipment. Other prion diseases develop without any known cause.

    There's currently no cure for prion diseases. Instead, treatment focuses on providing supportive care and easing symptoms.

    Researchers continue to work to discover more about these diseases and to develop potential treatments.


    Huntington's Disease News

    Establishing a Novel Strategy to Tackle Huntington's Disease

    Sep. 2, 2022 — A new platform takes on Huntington's disease via an innovative ...

    New Mouse Model to Shed Light on the Mystery Surrounding Huntington's Disease Onset and Improve the Targeting of Potential Therapies

    Feb. 2, 2022 — Researchers have developed a new mouse model of Huntington's disease that recapitulates more Huntington's disease-like characteristics than earlier models, providing new clues to the ...

    New Study Puts Focus on Early Symptoms of Huntington's Disease

    Sep. 7, 2021 — Psychiatric and cognitive symptoms emerge at an early stage in Huntington's disease. However, research so far has mainly focused on movement impairment, a symptom associated with the more ...

    Glial Cells Help Mitigate Neurological Damage in Huntington's Disease

    June 24, 2021 — Glia affected by Huntington's disease respond by tuning down synapse genes, which has a protective ...

    Huntington's Disease Driven by Slowed Protein-Building Machinery in Cells

    Mar. 5, 2021 — The gene for Huntington's disease was found nearly 40 years ago, yet there are no approved treatments. A new study shows the problem may lie with slowed protein ...

    Researchers Link Cases of ALS and FTD to a Huntington's Disease-Associated Mutation

    Dec. 4, 2020 — A study has made a surprising connection between frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS), two disorders of the nervous system, and the genetic mutation normally ...

    Novel Pathology Could Improve Diagnosis and Treatment of Huntington's and Other Diseases

    June 30, 2020 — Scientists have discovered a novel pathology that occurs in several human neurodegenerative diseases, including Huntington's disease. The article describes how SAFB1 expression occurs in both ...

    Antihistamines and Similar Drugs Could Slow Down Huntington's Disease

    June 9, 2020 — Scientists have described a potential new therapeutic strategy for slowing down early-stage Huntington's ...

    New Method to Map Cholesterol Metabolism in Brain

    May 29, 2020 — Researchers have developed new technology to monitor cholesterol in brain tissue which could uncover its relation to neurodegenerative disease and pave the way for the development of new ...

    Optimal Time to Treat Huntington's Disease Identified

    May 26, 2020 — The earliest brain changes due to Huntington's disease can be detected 24 years before clinical symptoms show, according to a new ...

    Immune Molecule's Complex Role in Huntington's Disease

    May 26, 2020 — Knocking out the immune cytokine IL-6 exacerbates symptoms in HD model mice and affects neural connection genes, a new study ...






    Comments

    Popular posts from this blog

    Orchestra BioMed™ Announces FDA Breakthrough Device Designation for Virtue® Sirolimus-Eluting Balloon for Treatment of Below-the-Knee Peripheral Artery Disease - Vascular Disease Management