Lyme Disease is a bacterial infection caused by Borrelia burgdorferi. This disease is transmitted to humans by ticks. Lyme arthritis was recognized as a clinical manifestation in 1976. Researchers at Yale University investigated a cluster of arthritis in children from the three contiguous communities of Old Lyme, Lyme, and East Haddam, Connecticut. If left untreated it can spread to other organs and cause permanent damage to joints, heart and nervous system. Lyme disease is diagnosed based on symptoms, physical findings, and the possibility of exposure to infected ticks. Laboratory testing is required to confirm the presence of Borrelia burgdorferi in the system of the host. Most cases of Lyme disease can be treated successfully with a few weeks of antibiotics. Steps to prevent Lyme disease include using insect repellent, removing ticks promptly, landscaping, and integrated pest management.
Microbiology:
Borrelia burgdorferi is a Gram negative bacteria belonging to the group of spirochete. It is a highly specialized, motile, two-membrane, spiral-shaped bacteria which lives primarily as an extracellular pathogen. It can survive inside the host for months even years. It has an unusual genome which consists of linear chromosomes and many linear and circular plasmids. 21 different plasmids were found, which represents the largest known complement of plasmids of all bacteria and constitutes one third of the spirochete's DNA.
Laboratory testing has confirmed that most of the virulence of the bacteria is linked to plasmids. After growing bacteria in cultures, results have shown that Borrelia loses some it’s plasmids and was unable to contract the disease in the laboratory animals. Borrelias plasmids encode for certain genes that play major role in its virulence. Borrelia burgdorferi has show susceptibility to antibiotics in vitro, but has shown more resistance to antibiotics used in vivo. The subdivision of this group of closely related organisms into the four distinct species B. burgdorferi sensu stricto. B. garinii, B. afzelii, and B. japonica. are found in Europe. In North America, all isolates of B. burgdorferi belong to the same species B. burgdorferi sensu stricto.
Diagnosis:
Lyme disease is diagnosed based on certain symptoms which can be determined by physical findings and a history of possible exposure to infected ticks. Laboratory tests are helpful in confirming the infection by Borrelia burgdorferi but is not recommended if the patient has erythema migrans. Erithema migrans is a localized manifestation of Lyme disease in it’s earlier form. It is localized on the same spot where the tick bite has occurred in form of a red rash resembling a bulls eye.
Physicians should be careful when determining Lyme disease infection because the symptoms can be similar to other bacterial infections. Not all patients with Lyme disease will develop the characteristic bulls-eye rash, and many may not remember having a tick bite. Laboratory testing is not recommended for persons who do not have symptoms of Lyme disease.
Picture 2: Infectious Cycle of Borrelia burgdorferi
Laboratory testing:
Serologic tests are insensitive during the first 1 or 2 weeks of infection because B. burgdorferi has a very slow reproduction rate. Confirming the infection depends mostly on detection of a positive IgM response, which may still represent a false-positive response.
There are several test that can be used in determining Lyme disease but thy are not all validated yet. The tests that are proven to be most effective are the blood tests which determine the presence of antibodies made during contact with the bacteria. There are two test recommended by the Center for Disease Control and Prevention in the form of the Elisa and
ELISA test:
The first test is the ELISA, This is a rapid test where antibody or antigen is linked to an enzyme as a means of detecting a match between the antibody and antigen. An antigen is a substance that induces the production of antibodies because it is recognized by the body as a threat. Antigens can be chemicals, bacteria, viruses, or pollen. The test is widely used in the medical laboratory for determining Lyme disease. It allows testing of your blood with an antigen to see if your immune system recognizes it, or tests your blood with an antibody to see if a particular substance or antigen is present in your system. This test is very sensitive and is positive for everyone with Lyme disease and some people that don’t as well. IgM antibodies become detectable 3–4 weeks after the infection and reaches it’s peak after 6–8 weeks and decline over the next 4 months. IgG antibodies appear 6–8 weeks after the infection and remain detectable for many years. If the test proves positive another test is required to confirm the findings.
Western blot test:
A western blot or immunoblot is a method to detect protein in a given sample of tissue. It uses gel electrophoresis to separate denatured proteins by mass. The proteins are then transferred out of the gel and onto a membrane typically nitrocellulose, where they are "probed" using antibodies specific to the protein. As a result, the amount of protein can be examined in a given sample and compare levels between several groups. Samples are taken from either tissue or from cell culture. The samples are cooled or frozen rapidly. They are homogenized using sonication or mechanical force. Samples are boiled from one to five minutes in a buffer solution. The proteins of the sample are separated according to molecular weight using gel electrophoresis. In order to make the proteins accessible to antibody detection, they are moved from within the gel onto a membrane made of nitrocellulose. Dr. Nelson has stressed the importance of formation of tiny black blotches, which indicate the presence of B. burgdorferi.
Symptoms:
Lyme disease has many signs and symptoms, but skin signs, arthritis and/or various neurological symptoms are often present. Like syphilis, the symptoms frequently seem to resolve, yet the disease progresses. Conventional therapy is with antibiotics. People who suspect they have been exposed to Lyme disease should consult a doctor with knowledge of the disease immediately.
Early symptoms are expressed in the form of: Erythema migrans, fever, fatigue , headache and muscle and joint soreness.
The late symptoms manifest in the form of: Neuropathy, Bell’s palsy, rheumatoid arthritis and other autoimmune reactions.
Treatment:
The first 24–72 hours of tick attachment is necessary for transmission of the spirochete. Removal of the tick within 24 hours of attachment is enough for prevention of Lyme disease. If an engorged tick is found, a single, 200-mg dose of Doxycycline usually is enough to prevent the development of Lyme disease. There is a high chance of reinfection if the patient was treated with antibiotics in the first weeks. Flu-like illness during summer is a more difficult issue. Most patients may have same symptoms as Lyme disease but are not caused by B. burgdorferi infection. Nevertheless, if we receive a patient with febrile illness followed by headaches and joint or muscle pain, without respiratory or gastrointestinal symptoms, antibiotic treatment is recommended. Early neurological symptoms should be treated with Ceftriaxone, 2 g/day intravenously for 2–4 weeks(4). Lyme arthritis should be treated for 30–60 days with Doxycycline 200 mg/day orally or with Ceftriaxone 2 g/day intravenously for 2–4 weeks. During my interview, Dr. Nelson has specified that there is a possibility of Lyme arthritis to persist even after therapy which indicates autoimmune reaction. In this case treatment needs to incorporate anti-inflammatory drugs.
Lyme Disease, Everything You Need to Know
Med Tech blog
This little blog is being created to satisfy some questions that new medical techs that are just starting out in the field can refer to. I know how hard it can be when you are starting out in the medical field. They teach us in school many things but what they don't teach us is how to deal with all kinds of doctors today without being treated like total idiots. We all know how confusing it can be when we are given something to do without any clarification and expected to make no mistakes......Soooo, I will be posting complete explanations of all procedures that one medical technician is expected to know how to complete. If anyone needs further explanations please feel free to post questions as I will be glad to elaborate....
Labels: med tech , medical technician
Hypovolemic Shock
When low blood flow or perfusion is first detected, a number of systems are activated in order to restore perfusion. The result is that the heart beats faster, the blood vessels constrict and become smaller in diameter, and kidneys are working and trying to retain fluid in the circulatory system. This helps to increase blood flow to the most important organs in the body, like the brain and heart.
The cardiovascular system responds to hypovolemic shock by increasing the heart rate, increasing myocardial contractility, and constricting peripheral blood vessels. The cardiovascular system also responds by redistributing blood to the brain, heart, and kidneys and away from skin, muscle, and GI tract. As mentioned before, the body is trying to redirect the blood flow to the heart and brain. If it doesn’t, it can cause permanent damage.
Treatment: The purpose of the treatment is to quickly restore the blood that was lost and prevent further
blood loss as well. There are three thing that we need to include in the therapy. As mentioned before, blood volume needs to be restored by transfusion and oxygen levels need to be controlled. The blood needs to be supplied with the adequate amount of oxygen, and also prevent further blood loss.
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Labels: Human Physiology
Trichomonas Vaginalis, a flagellated protozoan, causes Trichomoniasis, an exogenous sexually transmitted disease. It manifests in male and female genitourinary tracts. In most men infection is asymptomatic, they are generally considered to be the carriers of this bacterium. In women a wide range of clinical picture ranging from acute to chronic or asymptomatic is observed. Recent data have shown that the annual incidence of Trichomoniasis is more than 170 million cases worldwide.
History of Disease: T. vaginalis is a primitive eukaryotic organism. Although it is similar in many respects to other eukaryotes, it differs in its energy metabolism and shows remarkable similarity to primitive anaerobic bacteria. Trichomonas vaginalis is a pear-shaped trophozoite (7 to 23 µm long) with four anterior flagella and a fifth forming the outer edge of a short undulating membrane. It was first described by Donne in 1836. The study of T. Vaginalis has been in progress throughout the last 60 years and has gone from developing cultures and defining nutritional requirements to finding an effective treatment. In the 1960s and 1970s, research focused on biochemical tests and microscopic examination to understand the growth characteristics and behavior of the organism. It was not until the 1980s that immunologic methods and molecular biological techniques became available for study. Research involving these techniques has provided information on identification and characterization of many virulence factors of T. vaginalis. However, the research to better understand this organism is still in progress. Trichomonas vaginalis is emerging as one of the most important cofactors in increasing HIV transmission, particularly in African-American communities of the United States.
Forms of the Organism: Humans are the only natural host for T. vaginalis. This parasite is a distinctive flagellate trophozoite. The organisms typically are transferred during sexual intercorse. T. vaginalis is observed more frequently in females attending STD clinics and also in prostitutes than in postmenopausal women and virgins. The flagellates die outside the human body unless they are protected from drying. In the United States, black women have higher rates of trichomoniasis than white women, and socioeconomic factors such as a lower level of education are associated with a higher prevalence rate of trichomoniasis.
Source of the Organism: The only carriers of T. vaginalis are humans, and can be found in the human urogenital tract. It is sexually transmitted to the other person. However, there have been cases reported where it was transmitted through toilet seats in public bathrooms.
Life Cycle: The trophozoite is the only form of this organism and appears to lack a cystic stage. The trophozoite lives in close association with the epithelium of the urogenital tract and reproduces by binary fission. T. vaginalis is anaerobic and contains no mitochondria in its cytoplasm. Instead, specialized granules called hydrogenosomes are found throughout the cytoplasm. T. vaginalis derives its carbon from reduction of glycogen and glucose into succinate, acetate, malate and hydrogen. It produces some carbon dioxide, but not via the Krebs cycle pathway. Transfer of the relatively delicate trophozoite is usually directly from person to person.
Clinical Symptoms: The incubation period for women ranges between 5 and 28 days. The classic symptoms associated with the clinical diagnosis of T. vaginalis include a yellowish-green discharge, dysuria, and also hemorrhagic lesions found on the cervix. In women it can also produce vulvovaginal soreness and also abdominal discomfort. Unfortunately these symptoms are also characteristics of other STD’s, so the best way to find the organism is isolation and microscopic examination. Even though the organism can be found in the endocervix, endocervical disease is not caused by T. vaginalis. Infected women can show inflammation of the exocervix, which is closely tied with this organism. Trichomonads an also be fond in the urethra and paraurethral glands in more then 95% of women, which shows the relation between the organism and urinary infections. Some cases showed the spread of T. vaginalis to the fallopian tubes, but is extremely rare. In Extreme cases complications can manifest in form of vaginitis emphysematosa, which shows manifestation of gas bubbles in the vaginal wall.
Treatment: Most strains of T. Vaginalis are susceptible to Metronidazole and related drugs. Metronidazole is administered in an inactive form and must be modified in the hydrogenosome to become cytotoxic. Recommended regimes are: Metronidazole 2g orally in a single dose or, Metranidazole 400- 500mg twice daily for 7 days. Patients should be advised not to take alcohol with this treatment, nor some 48 hours after, because of the possibility of allergic reactions, nausea and vomiting.
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Labels: Microbiology