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<div class="noeditbox">Welcome to [[Pathophysiology of Complex Patient Problems|PT 635 Pathophysiology of Complex Patient Problems]] This is a wiki created by and for the students in the School of Physical Therapy at Bellarmine University in Louisville KY. Please do not edit unless you are involved in this project, but please come back in the near future to check out new information!!</div> <div class="editorbox">
'''Original Editors '''-Lori McGarrh [[Pathophysiology of Complex Patient Problems|from Bellarmine University's&nbsp;Pathophysiology of Complex Patient Problems project.]]  
'''Original Editors '''-Lori McGarrh [[Pathophysiology of Complex Patient Problems|from Bellarmine University's&nbsp;Pathophysiology of Complex Patient Problems project.]]  


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== Definition/Description  ==
== Introduction  ==
[[File:Tuberculosis symptoms.png|right|frameless|500x500px]]
Tuberculosis (TB) is an ancient human disease caused by ''Mycobacterium tuberculosis.'' It is an airborne pathogen and is extremely contagious. TB mainly affects the [[Lung Anatomy|lungs]], making pulmonary disease, the most common presentation. However, TB is a multi-systemic disease with a variable presentation. The organ system most commonly affected includes the [[Respiratory System|respiratory system]], the gastrointestinal (GI) system, the lymphoreticular system, the skin, the central nervous system, the musculoskeletal system, the reproductive system, and the liver.<ref name=":0">Adigun R, Bhimji S. [https://www.ncbi.nlm.nih.gov/books/NBK441916/ Tuberculosis]. StatPearls 2017.Available from:https://www.ncbi.nlm.nih.gov/books/NBK441916/ (last accessed 8.3.2020)</ref>
* Tuberculosis is a preventable and treatable infectious disease and is still one of the major contributors of morbidity and mortality in developing countries where we are still struggling to provide adequate access to care.
* TB was one of the top 10 causes of death worldwide in 2018 (being the leading killer of people with [[Human Immunodeficiency Virus (HIV)|HIV]] and a major cause of deaths related to antimicrobial resistance).
* In 2018, there were an estimated 10 million new TB cases worldwide, of which 5.7 million were men, 3.2 million were women and 1.1 million were children. People living with HIV accounted for 9% of the total.
* Eight countries accounted for 66% of the new cases: India, China, Indonesia, the Philippines, Pakistan, Nigeria, Bangladesh, and South Africa.
* In 2018, 1.5 million people died from TB, including 251,000 people with HIV.
* Globally, the TB mortality rate fell by 42% between 2000 and 2018.<ref>WHO [https://www.who.int/tb/publications/factsheet_global.pdf?ua=1 GLOBAL TUBERCULOSIS REPORT 2019] Available from:https://www.who.int/tb/publications/factsheet_global.pdf?ua=1 (last accessed 8.3.2020)</ref>
* Before the 1940s, tuberculosis was the leading cause of death in the United States.<ref name="Pathology" />


Tuberculosis (TB) is an inflammatory, infectious disease that is spread by bacteria called mycobacterium tuberculosis. Pulmonary tuberculosis is a systemic disease that most commonly affects the lungs.<ref name="Pathology">Goodman C, Fuller K. Pathology: Implications for the Physical Therapist. 3rd edition. In: Ikeda, B, Goodman, C. The Respiratory System. St. Louis, MO: Saunders; 2009: 752-758.</ref> Eventually, the TB could spread to other organ systems, which it then becomes extrapulmonary tuberculosis. TB can be placed into the following two categories:&nbsp;&nbsp;[[Image:TUBERCULOSIS.jpg|thumb|Mycobacterium Tuberculosis]]
=== Definition/Description ===
Tuberculosis (TB) is an inflammatory, infectious disease that is spread by bacteria called '''mycobacterium tuberculosis'''. Pulmonary tuberculosis is a systemic disease that most commonly affects the lungs.<ref name="Pathology">Goodman C, Fuller K. Pathology: Implications for the Physical Therapist. 3rd edition. In: Ikeda, B, Goodman, C. The Respiratory System. St. Louis, MO: Saunders; 2009: 752-758.</ref> Eventually, TB could spread to other organ systems, which it then becomes extrapulmonary tuberculosis. TB can be placed into the following two categories:&nbsp;&nbsp;
*Primary Tuberculosis<ref name="Pathology" /> (Dormant or Latent) – Although a person’s body can be infected with mycobacterium tuberculosis, they may not be showing clinical signs and symptoms. Most people have healthy immune systems that will never allow TB to take over their bodies.  
*Secondary Tuberculosis<ref name="Pathology" /> (Active) – This will develop after the immune system of a person is lowered. Reinfection will occur and the person will start to show clinical signs and symptoms.


*Primary Tuberculosis<ref name="Pathology" /> (Dormant or Latent) – Although a person’s body can be infected with mycobacterium tuberculosis, they may not be showing clinical signs and symptoms. Most people have healthy immune systems that will never allow the TB to take over their bodies.  
== Aetiology ==
*Secondary Tuberculosis<ref name="Pathology" /> (Active) – This will develop after the immune system of a person is lowered. Reinfection will occur and the person will start to show clinical signs and symptoms.<br><br>[Photo Courtesy of ''UNSW Embryology'']<ref>The University of New South Wales. Abnormal Development - Bacterial Infection. http://embryology.med.unsw.edu.au/Defect/bacteria.htm</ref>
[[Image:TUBERCULOSIS.jpg|[[Tuberculosis|Mycobacterium Tuberculosis]]|right|frameless]]
*Tuberculosis is spread by airborne particles known as droplet nuclei (spread when infected people sneeze, laugh, speak, sing, or cough).
* In order to contract this disease, a person has to have prolonged exposure with an infected person in an enclosed space.
* It is suspected that there could be a genetic component to susceptibility and resistance, but that has yet to be proven.
* In some countries, it is common for bovine TB to be spread through unpasteurised milk and other dairy products due to cattle with tuberculosis.
The organism has several unique features compared to other bacteria such as the presence of several lipids in the cell wall including mycolic acid, cord factor, and Wax-D. The high lipid content of the cell wall is thought to contribute to the following properties of ''M. tuberculosis'' infection:
* Resistance to several antibiotics
* Difficulty staining with Gram stain and several other stains
* Ability to survive under extreme conditions such as extreme acidity or alkalinity, low oxygen situation and intracellular survival(within the macrophage)<ref name=":0" />
* A reason the bacteria is able to be dormant in someone for years and is able to survive for months in sputum that is not exposed to sunlight and is trapped within the body (primary TB). Once the person’s resistance is lowered, the TB can become active (secondary TB). This could be due to advancing age, [[alcoholism]], cancer, or immunosuppression.[[Tuberculosis|[3]]]


== Prevalence ==
== Epidemiology ==


Before the 1940’s, tuberculosis was the leading cause of death in the United States.<ref name="Pathology" /> With the advancement of drug therapy, scientific and public knowledge, improvement in public health and general living standards, there was a large decline in the incidence of TB. However, immigrants started migrating from third world countries, the number of homeless people started to rise, people having prolonged lifespans, and the increase of the population with HIV resulted in an increase of TB in the mid 1980’s. Between 1985-1992, there was a 20% increase of new cases in the United States.<ref name="Pathology" /> The U.S. is just now beginning to see a decline in TB rates.  
=== Geographic Distribution ===
Tuberculosis is present globally. However; developing countries account for a disproportionate share of tuberculosis disease burden. The bulk of the global burden of new infection and tuberculosis death is borne by developing countries with 6 countries: India, Indonesia, China, Nigeria, Pakistan, and South Africa, accounting for 60% of TB death in 2015, Several countries in Asia, Africa, Eastern Europe, and Latin and Central America continue to have an unacceptably high burden of tuberculosis.


<br>
In more advanced countries, high burden tuberculosis is seen among recent arrivals from tuberculosis-endemic zones, health care workers, and HIV-positive individuals. Use of immunosuppressive agents such as long-term corticosteroid therapy has also been associated with an increased risk.


[[Image:1935 Poster.jpg|Image:1935_Poster.jpg]]&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; [[Image:1940 Poster.jpg|Image:1940_Poster.jpg]]
=== Other Major Risk Factors ===
* '''Socio-economic factors''''':'' Poverty, malnutrition, wars
* '''Immunosuppression''''':'' [[Human Immunodeficiency Virus (HIV)]], chronic immunosuppressive therapy (steroids, monoclonal antibodies against tumor necrotic factor), a poorly developed immune system (children, primary immunodeficiency disorders)
* '''Occupational''''':'' Mining, construction workers, pneumoconiosis (silicosis)<ref name=":0" />
The WHO estimates that 10.4 million individuals became ill with TB and 1.7 million died in 2016. Despite the fall in mortality rate of 3% per year, TB remains the ninth leading cause of death worldwide, counting 1.3 million TB deaths among HIV-negative people and almost 400,000 deaths among HIV-positive people.<ref>Matteelli A, Rendon A, Tiberi S, Al-Abri S, Voniatis C, Carvalho AC, Centis R, D'Ambrosio L, Visca D, Spanevello A, Migliori GB. [https://err.ersjournals.com/content/27/148/180035 Tuberculosis elimination: where are we now?.] European Respiratory Review. 2018 Jun 30;27(148):180035. Available from:https://err.ersjournals.com/content/27/148/180035</ref>


&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Poster made in 1935&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Poster made in the 1940's
=== TB in Prisons ===
* The level of TB in prisons has been reported to be up to 100 times higher than that of the civilian population.
* Cases of TB in prisons may account for up to 25% of a country’s burden of TB.
* Late diagnosis, inadequate treatment, overcrowding, poor ventilation and repeated prison transfers encourage the transmission of TB infection.
* HIV infection and other pathology more common in prisons (e.g. malnutrition, substance abuse) encourage the development of active disease and further transmission of infection.
* Multi-drug resistant tuberculosis (MDR-TB) in prisons High levels of MDR-TB have been reported from some prisons with up to 24% of TB cases suffering from MDR forms of the disease.<ref>WHO [https://www.who.int/tb/areas-of-work/population-groups/prisons-facts/en/ TB in prisons] Available from:https://www.who.int/tb/areas-of-work/population-groups/prisons-facts/en/ (last accessed 8.3.2020)</ref>


&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; [Photo Courtesy of ''NLM'']<ref>National Library of Medicine. Healthy Looks Can Hide Tuberculosis. http://www.nlm.nih.gov/exhibition/visualculture/infectious08.html</ref>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; [Photo Courtesy of ''Archives of Ontario'']<ref>Archives of Ontario. Tuberculosis 18 to 80. http://www.archives.gov.on.ca/english/on-line-exhibits/health-records/big/big_34_tb_18to80.aspx</ref>
== Characteristics/Clinical Presentation ==
[[Image:Symptoms of TB.png|right|frameless|240x240px]]A chronic cough, haemoptysis, weight loss, low-grade fever, and night sweats are some of the most common physical findings in pulmonary tuberculosis.


<br>There were 11,545 tuberculosis cases in the United States that were reported to the Center for Disease Control in 2009. This is estimated to be around 3.8 cases per 100,000 people. This has been the lowest rate reported since 1953, which is when national reporting began. In 2007, the United States reported 544 deaths from Tuberculosis.<ref name="CDC - Trends">Centers for Disease Control and Prevention. Trends in Tuberculosis, 2009. Atlanta, GA. [Web-Page]. 2010. http://www.cdc.gov/tb/publications/factsheets/statistics/TBTrends.htm. Accessed March 18, 2011.</ref>&nbsp;
Secondary tuberculosis differs in clinical presentation from the primary progressive disease. In secondary disease, the tissue reaction and hypersensitivity is more severe, and patients usually form cavities in the upper portion of the lungs.


The TB rate in foreign-born persons in the United States (18.7 cases per 100,000 persons) was approximately 11 times greater than that of U.S.-born persons (1.7 cases per 100,000 persons) in 2009.<ref name="CDC - Trends" /> In 2009, approximately 59% of all TB cases in the United States occurred in foreign-born persons, unchanged from 2008.<ref name="CDC - Trends" />
Pulmonary or systemic dissemination of the tubercles may be seen in active disease. Disseminated tuberculosis may also be seen in the spine, the central nervous system, or the bowel.<ref name=":0" />
 
Although the rates are declining in the United States, TB is still a worldwide epidemic. The highest rates of TB can be found in Southeast Asia, sub-Saharan Africa, and eastern Europe. There are about 200 to 400 cases per 100,000 each year.<ref name="CDC - Trends" />
 
<u>'''Statistics<ref name="CDC - Fact Sheet">Centers for Disease Control and Prevention. Fact Sheet: A Global Perspective on Tuberculosis. Atlanta, GA. [Web-Page]. 2010. http://www.cdc.gov/tb/events/WorldTBDay/resources_global.htm. Accessed March 18, 2011.</ref>:'''</u>
 
*One third of the nation’s population is infected with TB.
*Each year, about 9 million people worldwide are infected with TB
*There are approximately 2 million worldwide deaths each year from TB.
*TB is the most prevalent killer of people who are infected with HIV.
 
<br>
 
<u>'''Rates of TB for different racial and ethnic populations<ref name="CDC - Trends" />'''</u>
 
*American Indians or Alaska Natives: 4.3 cases per 100,000 persons
*Asians: 23.3 cases per 100,000 persons
*African Americans: 7.6 cases per 100,000 persons
*Native Hawaiians and other Pacific Islanders: 16.7 cases per 100,000 persons
*Hispanics or Latinos: 7.0 cases per 100,000 persons
*Whites: 0.9 cases per 100,000 persons<br>
 
== Characteristics/Clinical Presentation  ==


There are usually no symptoms of tuberculosis during the first year of exposure. This is when the disease would be the most curable. Symptoms suggestive of TB include<ref name="Pathology" />:&nbsp;  
There are usually no symptoms of tuberculosis during the first year of exposure. This is when the disease would be the most curable. Symptoms suggestive of TB include<ref name="Pathology" />:&nbsp;  


[[Image:Symptoms of TB.png|frame]]
*Productive cough that lasts longer than 3 weeks  
 
<br>
 
*Productive cough last longer than 3 weeks  
*Weight Loss  
*Weight Loss  
*Fever  
*Fever  
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*Fatigue  
*Fatigue  
*Malaise  
*Malaise  
*Anorexia  
*[[Anorexia Nervosa|Anorexia]]
*Rales could be heard in the lobes of involvement in the lungs&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;  
*Rales could be heard in the lobes of involvement in the lungs&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;  
*Bronchial Breath Sounds&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;  
*Bronchial Breath Sounds&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;  
*Dull chest pain, tightness, or discomfort<ref name="Differential Diagnosis">Goodman C, Snyder T. Differential Diagnosis for Physical Therapists: Screening for Referral. 4th edition. In: Screening for Pulmonary Disease.. St. Louis, MO: Saunders; 2007: 344-345.</ref>&nbsp;&nbsp;  
*Dull chest pain, tightness, or discomfort<ref name="Differential Diagnosis">Goodman C, Snyder T. Differential Diagnosis for Physical Therapists: Screening for Referral. 4th edition. In: Screening for Pulmonary Disease.. St. Louis, MO: Saunders; 2007: 344-345.</ref>&nbsp;&nbsp;  
*Dyspnea<ref name="Differential Diagnosis" /><br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; [Photo Courtesy of ''Connect In'']<ref>Connect In. Tuberculosis. http://connect.in.com/tuberculosis/photos-6-2e3b5d9b17894060.html</ref>
*Dyspnea<ref name="Differential Diagnosis" />  
*Haemoptysis (late-stage symptom)
 
=== Systemic Involvement ===
10%-15% of tuberculosis is extra-pulmonary. It can spread through the blood vessels from organ to organ and/or the lymphatic system. Extra-pulmonary TB can involve the:<ref name="Differential Diagnosis" />&nbsp;
*Kidneys
*Bone Growth Plates
*Lymph Nodes
*Meninges
*Hip Joints - can cause avascular necrosis of the hip
*Elbows
*Vertebrae ([[Pott's Disease]])


== Associated Co-morbidities  ==
== Associated Co-morbidities  ==


*[http://www.physio-pedia.com/index.php5?title=HIV/AIDS HIV/AIDS] - due to comprised immunosuppressive system  
*[http://www.physio-pedia.com/index.php5?title=HIV/AIDS HIV/AIDS] - due to comprised immunosuppressive system  
*Rheumatoid Arthritis<ref name="Differential Diagnosis" /> - due to immunosuppressive treatments  
*[[Rheumatoid Arthritis]]<ref name="Differential Diagnosis" /> - due to immunosuppressive treatments  
*Diabetes Mellitus  
*[[Diabetes|Diabetes Mellitus]]
*End-stage Renal Disease  
*End-stage Renal Disease  
*Gastrointestinal Disease<ref name="Differential Diagnosis" />  
*Gastrointestinal Disease<ref name="Differential Diagnosis" />  
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*Malnutrition
*Malnutrition


<br>
=== Additional Risk Factors<ref name="Differential Diagnosis" /> ===
 
'''<u>Other Risk Factors<ref name="Differential Diagnosis" /></u>'''
 
*Healthcare workers  
*Healthcare workers  
*Older adults  
*Older adults  
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*People who are incarcerated  
*People who are incarcerated  
*Immigrants  
*Immigrants  
*Kids under the age of 5
*Children under the age of 5


== Medications  ==
== Medications  ==


Once tuberculosis is diagnosed, all active cases are treated and many inactive cases are treated. It is unclear if preventive treatment is helpful in people with latent TB. However, it is hoped that the disease will be less likely to become active later in life once the immune system is more likely to be comprimised.<ref name="Pathology" /><br>There are currently 10 drugs that are approved by the FDA to treat TB. The following medications are first-line anti TB agents that form the core medications given<ref name="CDC - Treatment" />:  
Once tuberculosis is diagnosed, all active cases are treated and many inactive cases are treated. It is unclear if preventive treatment is helpful in people with latent TB. However, it is hoped that the disease will be less likely to become active later in life once the immune system is more likely to be compromised.<ref name="Pathology" />  
 
There are currently 10 drugs that are approved by the FDA to treat TB. The following medications are first-line anti-TB agents that form the core medications given<ref name="CDC - Treatment" />:  


*Isoniazid  
*Isoniazid  
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*Ethambutol
*Ethambutol


The recommended time for taking the meds is 6-9 months. Blood work should be performed monthly to check on the liver and make sure it is handling the medicine okay.<ref name="CDC - Treatment">Centers for Disease Control and Prevention. Treatment of Latent Tuberculosis Infection. Atlanta, GA. [Web-Page]. 2010. http://www.cdc.gov/tb/publications/factsheets/treatment/treatmentLTBI.htm. Accessed on March 18, 2011.</ref>  
The recommended time for taking the medication is 6-9 months. Blood work should be performed monthly to check on the liver and make sure it is handling the medicine okay.<ref name="CDC - Treatment">Centers for Disease Control and Prevention. Treatment of Latent Tuberculosis Infection. Atlanta, GA. [Web-Page]. 2010. http://www.cdc.gov/tb/publications/factsheets/treatment/treatmentLTBI.htm. Accessed on March 18, 2011.</ref>
* Many people are not compliant with taking their medicine daily for 9 months. Many people will begin to feel better, so they will decide to stop administering the medicine.
* Compliance is also a problem with homeless people, alcoholics, and drug users.
* If treatment is not completed, multi-drug resistant TB can form which means the person will now be resistant to the medication taken previously.<ref name="Pathology" />
* Multi-drug resistant TB has an even more complicated treatment than before.
* Some people require a pneumonectomy or chemotherapy along with two or more drugs that are used at the same time.<ref name="Differential Diagnosis" />
* Directly Observed Therapy (DOT) should always be used when treating multi-drug resistant TB to ensure the subject is practicing proper compliance.
* Treatments are the same for pulmonary and extra-pulmonary TB.


<br>Unfortunately, many people are not compliant with taking their medicine daily for 9 months. Many people will begin to feel better, so they will decide to stop administering the medicine. Compliance is also a problem with homeless people, alcoholics, and drug users. If treatment is not completed, multidrug-resistant TB can form which means the person will now be resistant to the medication taken previously.<ref name="Pathology" /> Multi-drug resistant TB has an even more complicated treatment than before. Some people require a pneumonectomy or chemotherapy along with two or more drugs that are used at the same time.<ref name="Differential Diagnosis" /> Directly Observed Therapy (DOT) should always be used when treating multi-drug resistant TB to ensure the subject is practicing proper compliance. Treatments are the same for pulmonary and extrapulmonary TB.<br><br><u>'''BCG Vaccine&nbsp;'''</u>  
=== Multidrug-Resistant Tuberculosis (MDR-TB) ===
Tuberculosis (TB) can develop resistance to the antimicrobial drugs used to cure the disease. Multidrug-resistant TB (MDR-TB) is TB that does not respond to at least isoniazid and rifampicin, the 2 most powerful anti-TB drugs. Inappropriate or incorrect use of antimicrobial drugs, or use of ineffective formulations of drugs (such as use of single drugs, poor quality medicines or bad storage conditions), and premature treatment interruption can cause drug resistance, which can then be transmitted, especially in crowded settings such as prisons and hospitals. Treatment options are limited and expensive, recommended medicines are not always available, and patients experience many adverse effects from the drugs. In some cases even more severe drug-resistant TB may develop.<ref name=":1">What is multidrug-resistant tuberculosis (MDR-TB) and how do we control it? [Internet]. WHO. World Health Organization; 2018 [cited 2020 Mar 20]. Available from: <nowiki>https://www.who.int/features/qa/79/en/</nowiki></ref>


The Bacille Calmette-Guerin vaccine was created in 1921.<ref name="BCG">CDC. Role of BCG Vaccine in the Prevention and Control of Tuberculosis in the United States A Joint Statement by the Advisory Council for the Elimination of Tuberculosis and the Advisory Committee on Immunization Practices. Atlanta Georgia. [Web-Page]. 1996. http://www.cdc.gov/mmwr/preview/mmwrhtml/00041047.htm. Accessed on April 19, 2011.</ref>&nbsp; Many more strains have been developed over time. This vaccine is very controversial and its ability to protect individuals from TB has not been validated. It is used widely in foreign countries with high rates of tuberculosis. It is rarely used in the United States, and should only be given to someone after serious discussion with one's MD. This vaccine is not recommended as a way to control TB. The vaccine is problematic because:<ref name="BCG" />
=== Extensively Drug-Resistant Tuberculosis (XDR-TB) ===
XDR-TB, an abbreviation for extensively drug-resistant tuberculosis (TB), is a form of TB which is resistant to at least four of the core anti-TB drugs. XDR-TB involves resistance to the two most powerful anti-TB drugs, isoniazid and rifampicin, also known as multidrug-resistance (MDR-TB), in addition to resistance to any of the fluoroquinolones (such as levofloxacin or moxifloxacin) and to at least one of the three injectable second-line drugs (amikacin, capreomycin or kanamycin).<ref name=":2">Drug-resistant TB: XDR-TB FAQ [Internet]. WHO. World Health Organization; 2018 [cited 2020 Mar 20]. Available from: <nowiki>https://www.who.int/tb/areas-of-work/drug-resistant-tb/xdr-tb-faq/en/</nowiki></ref>


*it has not been tested on people with immunosuppressed systems
MDR-TB and XDR-TB both take substantially longer to treat than ordinary (drug-susceptible) TB, and require the use of second-line anti-TB drugs, which are more expensive and have more side-effects than the first-line drugs used for drug-susceptible TB.<ref name=":1" /><ref name=":2" />
*it has not been shown to protect adults from pulmonary tuberculosis
*it can give a false positive to the skin test, which makes it difficult to tell if someone really has TB
*it should not be used on women who are pregnant
*many of the clinical trials have only been used on children


<br>
== TB Screening ==
Approximately 33% of the world's population has '''latent tuberculosis infection (LTBI'''). For this reason, screening for Mycobacterium tuberculosis infection is essential for public health. People with LTBI are at risk for developing active tuberculosis (TB) and becoming infectious.
* The greatest risk for progression occurs during the first two years of infection.
* The goal of testing for LTBI is to identify individuals who are at high risk of developing active TB.
* The decision to test should presuppose a decision to treat if the result is positive.
* The tuberculin skin test (TST) and the interferon-gamma release assay (IGRA) are the current methods for screening and are based on the measurement of adaptive host immune response.<ref>de Lima Corvino DF, Kosmin AR. [https://www.statpearls.com/kb/viewarticle/30655 Tuberculosis Screening.] InStatPearls [Internet] 2019 Feb 4. StatPearls Publishing.Available from:https://www.statpearls.com/kb/viewarticle/30655 (last accessed 8.3.2020)</ref>


The following statistics have been proven by the Advisory Council for the Elimination of Tuberculosis:<ref name="BCG" />
== BCG Vaccine&nbsp; ==
[[File:TB_Skin_Test.gif|right|frameless]]
The Bacille Calmette-Guérin '''(BCG''') vaccine has existed for 80 years and is one of the most widely used of all current vaccines, reading >80%of neonates and infants in countries where it is part of the national childhood immunization programme.


*Two controlled trials that used the Tice vaccine demonstrated rates of protective efficacy ranging from zero to 75%.
BCG vaccine has a documented protective effect against '''[[meningitis]]''' and disseminated TB in children.  
*Case-control studies using different BCG strains indicated that vaccine efficacies ranged from zero to 80%.
*In young children, the estimated protective efficacy rates of the vaccine have ranged from 52% to 100% for prevention of tuberculous meningitis and miliary TB.
*The estimated protective efficacy rates of the vaccine range from 2% to 80% for prevention of pulmonary TB.


<br>
It does not prevent primary infection and does not prevent reactivation of latent pulmonary infection, the principal source of bacillary spread in the community. The impact of BCG vaccination on transmission of Mtb is therefore limited.


The CDC and the American Academy of Pediatrics recommend that all children adopted from high risk countries who have received the BCG vaccine should act as if they have never received it.<ref name="Differential Diagnosis" /> All children should be given a skin test and treated whether it is dormant or active.<br>
The CDC and the American Academy of Paediatrics recommend that all children adopted from high-risk countries who have received the BCG vaccine should act as if they have never received it.<ref name="Differential Diagnosis" /> All children should be given a skin test and treated whether it is dormant or active.


== Diagnostic Tests/Lab Tests/Lab Values  ==
The Mantoux tuberculin skin test is performed by having 0.1ml of tuberculin purified protein derivative (PPD) injected into the inner layer of the forearm.<ref name="Skin Testing">Centers for Disease Control and Prevention. Tuberculin Skin Testing. Atlanta, GA. [Web-Page]. 2010. http://www.cdc.gov/tb/publications/factsheets/testing/skintesting.htm. Accessed on March 18, 2011.</ref> This will determine if the body’s immune response has been activated by the presence of the bacillus. Upon injection, the skin will elevate around 6-10 mm in diameter. 48 to 72 hours later, the person should have their skin test reaction read. A positive test could reveal a palpable, swollen, hardened, or raised area that should be measured in millimetres. Redness is not measured.<ref name="Skin Testing" /><u></u>
 
== Physical Therapy Management  ==
The Mantoux tuberculin skin test is performed by having 0.1ml of tuberculin purified protein derivitive (PPD) injected into the inner layer of the forearm.<ref name="Skin Testing">Centers for Disease Control and Prevention. Tuberculin Skin Testing. Atlanta, GA. [Web-Page]. 2010. http://www.cdc.gov/tb/publications/factsheets/testing/skintesting.htm. Accessed on March 18, 2011.</ref> This will determine if the body’s immune response has been activated by the presence of the bacillus. Upon injection, the skin will elevate around 6-10 mm in diameter. 48 to 72 hours later, the person should have their skin test reaction read. A positive test could reveal a palpable, swollen, hardened, or raised area that should be measure in millimeters. Redness is not measured.<ref name="Skin Testing" />  
[[File:Chest_xray.gif|right|frameless]]All physical therapists should be aware of the proper personal protective equipment (PPE) that should be worn.&nbsp; There is a specialised mask that is worn that has been sized to specifically fit your face.<ref name="Differential Diagnosis" />
 
# Pulmonary Tuberculosis People with pulmonary TB are typically not treated in physical therapy because medications are vital for curing TB.&nbsp; However, therapists are able to provide [[percussion]] and [[Postural Drainage|postural drainage]] to clear secretions out of the lung.<ref name="Pathology - EP">Goodman C, Fuller K. Pathology: Implications for the Physical Therapist. 3rd edition. In: Infectious Diseases of the Musculoskeletal System. St. Louis, MO: Saunders; 2009: 1198-1199.</ref>
<br>
# Extrapulmonary Tuberculosis Clients with extra-pulmonary TB are usually not seen in the physical therapy setting.&nbsp; However, patients may present in clinic with musculoskeletal problems with unknown causes or [[Arthritis|arthritic pain]].&nbsp; PT's should be prepared to take a thorough history and a proper examination in order to better identify TB.&nbsp; A patient could also be seen in physical therapy if they have had surgery on their back, in which case the normal rehabilitation protocols would be followed.<ref name="Pathology - EP" />
 
It is very important to take a thorough history when TB is suspected.&nbsp; It is important to ask if the person has travelled outside the country recently, their occupation, or if there is any way they have possibly been exposed to someone who could have&nbsp;TB.&nbsp; Recognise your patient's signs and symptoms.&nbsp; Palpation of the lymph nodes could also be informational during an examination.<span style="line-height: 1.5em; font-size: 13.2799997329712px;">&nbsp;</span><ref>Flicr. Bayberry. http://www.flickr.com/photos/zeping/150247200/</ref>  
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; [[Image:TB Skin Test.gif|Image:TB_Skin_Test.gif]]
 
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Mantoux Tuberculin Skin Test<ref>Corporate Health and Productivity. Updating TB Guidelines in for Healthcare Facilities. http://corporatehealthandproductivity.com/category/tbtuberculosis/</ref>
 
<br><u>'''How Are TST Reactions Interpreted?<br>'''</u>Skin test interpretation depends on two factors<ref name="Skin Testing" />:
 
*Measurement in millimeters of the induration
*Person’s risk of being infected with TB and of progression to disease if infected
 
<br>
 
<u>'''Classification of the Tuberculin Skin Test Reaction<ref name="Skin Testing" />'''</u><br>
 
{| style="width: 670px; height: 481px" border="1" cellspacing="1" cellpadding="1" width="670"
|-
| '''An induration of 5 or more millimeters is considered positive in:'''
| '''An induration of 10 or more millimeters is considered positive in:'''
| '''An induration of 15 or more millimeters is considered positive in:'''
|-
| HIV infected persons
| Recent immigrants (&lt; 5 years) from high-prevalence countries
| any person, including persons with no known risk factors for TB. However, targeted skin testing programs should only be conducted among high-risk groups.
|-
| Recent contact of a person with TB disease
| Injection drug users
|
|-
| Persons with fibrotic changes on chest radiograph consistent with prior TB
| Residents and employees of high-risk congregate settings
|
|-
| Patients with organ transplants
| Mycobacteriology laboratory personnel
|
|-
| Persons who are immunosuppressed for other reasons&nbsp;(e.g., taking the equivalent of &gt;15 mg/day of prednisone for 1 month or longer, taking TNF antagonists)
| Persons with clinical&nbsp;conditions that place them at high risk
|
|-
|
| Children &lt; 4 years of age
|
|-
|
| Infants, children, and adolescents exposed to adults in high-risk categories
|
|}
 
<br>
 
A positive reaction to the test is indicative of tuberculosis in the body. However, the test does not reveal if the TB if dormant or active. Other diagnostic tests (e.g. chest x-ray, sputum sample) should be used to identify active tuberculosis.<ref name="Pathology" />
 
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; [[Image:Chest_xray.gif]]
 
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[Photo Courtesy of ''Sao Paulo Medical Journal'']<ref>Sao Paulo Medical Journal. Miliary tuberculosis with positive acid-fast bacilli in a pediatric patient. 2003;121(3). http://www.scielo.br/scielo.php?pid=S1516-31802003000300008&amp;script=sci_arttext. Accessed on April 20, 2011.</ref>
 
== Etiology/Causes  ==
 
Tuberculosis is spread by airborne particles known as droplet nuclei. Droplet nuclei are spread when infected people sneeze, laugh, speak, sing, or cough.<ref name="Pathology" /> In order to contract this disease, a person has to have prolonged exposure with an infected person in an enclosed space. It is suspected that there could be a genetic component to susceptibility and resistance, but that has yet to be proven. In other countries, it is common for bovine TB to be spread through unpasteurized milk and other dairy products due to cattle with tuberculosis.<ref name="Pathology" />
 
<br>The reason the bacteria is able to be dormant in someone for years is it is capable of surviving for months in sputum that is not exposed to sunlight.<ref name="Pathology" /> It becomes trapped within the body (primary TB). Once the person’s resistance is lowered, the TB can become active (secondary TB). This could be due to advancing age, alcoholism, cancer, or immunosupporession.<ref name="Pathology" /><br><br>
 
== Systemic Involvement  ==
 
10%-15% of tuberculosis is extrapulmonary. It can spread through the blood vessels from organ to organ and/or the lymphatic system. Extrapulmonary TB can involve the:<ref name="Differential Diagnosis" />&nbsp;
 
*Kidneys
*Bone Growth Plates
*Lymph Nodes
*Meninges
*Hip Joints - can cause avascular necrosis of the hip
*Elbows
*Vertebrae (Pott's Disease)<br>
 
<u>'''Pott's Disease'''</u>
 
Infection usually begins in the body of the vertebrae. It can then spread to the intervertebral discs and to the adjacent vertebrae. As the infection continues to spread throughout the spine, the following problems can occur:<ref name="Pathology - EP">Goodman C, Fuller K. Pathology: Implications for the Physical Therapist. 3rd edition. In: Infectious Diseases of the Musculoskeletal System. St. Louis, MO: Saunders; 2009: 1198-1199.</ref>
 
*Irritation of the nerve roots
*Pressure from abscess - can produce hip pain if the abscess goes to the psoas muscle
*Collapse of the vertebral body - can cause cord compression and possible paraplegia<br>
 
<u>'''Miliary Tuberculosis<ref name="Differential Diagnosis" />'''</u><u></u><br>This occurs when TB spreads throughout the body. It is more common for this to present in adults over the age of 50 and children with weakened or unstable immune systems.<br>
 
== Medical Management (current best evidence)  ==
 
Treatment does not differ for pulmonary and extrapulmonary tuberculosis.&nbsp; The same medications are used in both cases (see medications).&nbsp; Sometimes decompressive surgery is needed if someone has Pott's Disease.<ref name="Pathology - EP" />
 
== Physical Therapy Management (current best evidence)  ==
 
All physical therapists should be aware of the proper personal protective equipment (PPE) that should be worn.&nbsp; There is a specialized mask that is worn that has been sized to specifically fit your face.<ref name="Differential Diagnosis" />  
 
<br>
 
'''<u>Pulmonary Tuberculosis</u>'''<br>
 
People with pulmonary TB are typically not treated in physical therapy because medications are vital for curing TB.&nbsp; However, therapists are able to provide percussion and postural drainage to clear secretions out of the lung.<ref name="Pathology - EP" />  
 
<br>
 
'''<u>Extrapulmonary Tuberculosis</u>'''
 
Clients with extrapulmonary TB are usually not seen in the physical therapy setting.&nbsp; However, patients may present in clinic with musculoskeletal problems with unknown causes or arthritic pain.&nbsp; PT's should be prepared to take a thorough history and a proper examination in order to better identify TB.&nbsp; A patient could also be seen in physical therapy if they have had surgery on their back, in which case the normal rehabilitation protocals would be followed.<ref name="Pathology - EP" />  
 
<br>
 
It is very important to take a thorough history when TB is suspected.&nbsp; It is important to ask if the person has traveled outside the country recently, their occupation, or if there is any way they have possibly been exposed to someone who could have&nbsp;TB.&nbsp; Recognize your patient's signs and symptoms.&nbsp; Palpation of the lymph nodes could also be informational during an examination.
 
== Alternative/Holistic Management (current best evidence)  ==
 
Holistic managment itself is&nbsp;not recommended due to the severity of Tuberculosis.&nbsp; If not treated with the proper medications, Tuberculosis can lead to death.&nbsp; However, due to the variety of side effects that can occur from the medicine, some people do choose to incorporate certain natural remidies into their lifestyle.&nbsp; The main goal of using herbs and vitamins is to give the immune system a boost.&nbsp; Dietary changes, physical activity, and water are very important for increasing the immune system and for ridding the body of its toxins.&nbsp; Please note that no supporting evidence was found to show if using these remedies&nbsp;are beneficial.&nbsp; The following are the most common remedies used:&nbsp;[[Image:Bayberry.jpg|thumb|Bayberry]]
 
*Garlic<ref>My Natural Cures. Tuberculosis. [Web-Page]. 2010. http://www.my-natural-cures.com/pulmonary-tuberculosis.html. Accessed on March 27, 2011.</ref>  
*Herbal Tea
*Vitamins (A, B's, C, Beta Carotenes)
*Bayberry
*Horsetail
*Sunlight
 
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; <ref>Flicr. Bayberry. http://www.flickr.com/photos/zeping/150247200/</ref>


== Differential Diagnosis  ==
== Differential Diagnosis  ==
Tuberculosis is a great mimic and should be considered in the differential diagnosis of several systemic disorders. The following is a non-exhaustive list of conditions to be strongly considered when evaluating the possibility of pulmonary tuberculosis.
* [[Pneumonia]]
* Malignancy
* Non-tuberculous mycobacterium
* Fungal infection
* Histoplasmosis
* [[Sarcoidosis]]<ref name=":0" />


*Chronic Bronchitis
== Prognosis ==
*Bronchiectasis
Majority of patients with a diagnosis of TB have a good outcome. This is mainly because of effective treatment. Without treatment mortality rate for tuberculosis is more than 50%.
*Atelectasis
*Pneumonia 
*Influenza
*Arthritis (Extrapulmonary)<ref name="Differential Diagnosis" />
 
== Case Reports/ Case Studies ==
 
Jha A, Shojania K, Saint S. [http://proquest.umi.com.libproxy.bellarmine.edu/pqdweb?index=12&did=649987721&SrchMode=2&sid=1&Fmt=4&VInst=PROD&VType=PQD&RQT=309&VName=PQD&TS=1302040037&clientId=1870 Forgotton but not gone]. ''The New England Journal of Medicine.'' June 3, 2004; 350(23):2399 - 2405.
 
Flynn, J.&nbsp;[http://www.tuberculosisjournal.com/article/S1472-9792(03)00092-1/abstract Immunology of tuberculosis and implications in vaccine development.]&nbsp; ''Tuberculosis. ''2004;84(1):93-101.
 
Brudney K, Dobkin J.&nbsp;[http://ukpmc.ac.uk/abstract/MED/1928942/reload=0;jsessionid=CAC3CDA89CCF5DAF7997FEB7B26B99EC.jvm1 Resurgent tuberculosis in New York City. Human immunodeficiency virus, homelessness, and the decline of tuberculosis control programs.]&nbsp; ''The American Review of Respiratory Disease.'' 1991;144(4):745-749.&nbsp;
 
Corbett, EL, Watt, CJ, Walker, N, Maher,&nbsp;D; Williams, BG, Raviglione, MC, Dye, C.&nbsp;[http://archinte.ama-assn.org/cgi/content/abstract/163/9/1009 The Growing Burden of Tuberculosis: <br>Global Trends and Interactions With the HIV Epidemic.] ''Archives of Internal Medicine.'' 2003;163:1009-1021.<br>
 
Colditz, GA, Brewer, TF, Berkey, CS, Wilson, ME, Burdick, E, Fineberg, HV, Mosteller, F.&nbsp;[http://jama.ama-assn.org/content/271/9/698.short Efficacy of BCG Vaccine in the Prevention of Tuberculosis]. ''The Journal of the American Medical Association.''1994;271(9):698-702.
 
== Resources <br> ==
 
Center for Disease Control - Tuberculosis -&nbsp;[http://www.cdc.gov/tb/ http://www.cdc.gov/tb/]
 
Center for Disease Control - Pamphlets, Brochures, Booklets - [http://www.cdc.gov/tb/publications/pamphlets/default.htm www.cdc.gov/tb/publications/pamphlets/default.htm]
 
Charles P. Felton National Tuberculosis Center - [http://www.harlemtbcenter.org/ www.harlemtbcenter.org/]
 
Saratoga County Public Health Tuberculosis Program - [http://saratogacountyny.gov/upload/tbbrochure.pdf saratogacountyny.gov/upload/tbbrochure.pdf]
 
== Recent Related Research (from [http://www.ncbi.nlm.nih.gov/pubmed/ Pubmed]) ==
<div class="researchbox">
<rss>http://eutils.ncbi.nlm.nih.gov/entrez/eutils/erss.cgi?rss_guid=1peHU8KZd8f9OMZF4FMfsU4ukRe1K_KoDoAuxm7JYjGlPwlgf8|charset=UTF-8|short|max=10</rss>
</div>
 
== References  ==


see [[Adding References|adding references tutorial]].  
The following group of patients is more susceptible to worse outcomes or death following TB infection:
* Extremes of age, elderly, infants and young children
* Delay in receiving treatment
* Radiologic evidence of extensive spread.
* Severe respiratory compromise requiring mechanical ventilation
* Immunosuppression
* Multi-drug Resistant (MDR) Tuberculosis<ref name=":0" />


== References ==
<references />  
<references />  


[[Category:Bellarmine_Student_Project]]
[[Category:Bellarmine_Student_Project]]
[[Category:Cardiopulmonary]]
[[Category:Conditions]]
[[Category:Chronic Respiratory Disease - Conditions]]
[[Category:Communicable Diseases]]

Latest revision as of 07:28, 6 January 2022

Introduction[edit | edit source]

Tuberculosis symptoms.png

Tuberculosis (TB) is an ancient human disease caused by Mycobacterium tuberculosis. It is an airborne pathogen and is extremely contagious. TB mainly affects the lungs, making pulmonary disease, the most common presentation. However, TB is a multi-systemic disease with a variable presentation. The organ system most commonly affected includes the respiratory system, the gastrointestinal (GI) system, the lymphoreticular system, the skin, the central nervous system, the musculoskeletal system, the reproductive system, and the liver.[1]

  • Tuberculosis is a preventable and treatable infectious disease and is still one of the major contributors of morbidity and mortality in developing countries where we are still struggling to provide adequate access to care.
  • TB was one of the top 10 causes of death worldwide in 2018 (being the leading killer of people with HIV and a major cause of deaths related to antimicrobial resistance).
  • In 2018, there were an estimated 10 million new TB cases worldwide, of which 5.7 million were men, 3.2 million were women and 1.1 million were children. People living with HIV accounted for 9% of the total.
  • Eight countries accounted for 66% of the new cases: India, China, Indonesia, the Philippines, Pakistan, Nigeria, Bangladesh, and South Africa.
  • In 2018, 1.5 million people died from TB, including 251,000 people with HIV.
  • Globally, the TB mortality rate fell by 42% between 2000 and 2018.[2]
  • Before the 1940s, tuberculosis was the leading cause of death in the United States.[3]

Definition/Description[edit | edit source]

Tuberculosis (TB) is an inflammatory, infectious disease that is spread by bacteria called mycobacterium tuberculosis. Pulmonary tuberculosis is a systemic disease that most commonly affects the lungs.[3] Eventually, TB could spread to other organ systems, which it then becomes extrapulmonary tuberculosis. TB can be placed into the following two categories:  

  • Primary Tuberculosis[3] (Dormant or Latent) – Although a person’s body can be infected with mycobacterium tuberculosis, they may not be showing clinical signs and symptoms. Most people have healthy immune systems that will never allow TB to take over their bodies.
  • Secondary Tuberculosis[3] (Active) – This will develop after the immune system of a person is lowered. Reinfection will occur and the person will start to show clinical signs and symptoms.

Aetiology[edit | edit source]

Mycobacterium Tuberculosis
  • Tuberculosis is spread by airborne particles known as droplet nuclei (spread when infected people sneeze, laugh, speak, sing, or cough).
  • In order to contract this disease, a person has to have prolonged exposure with an infected person in an enclosed space.
  • It is suspected that there could be a genetic component to susceptibility and resistance, but that has yet to be proven.
  • In some countries, it is common for bovine TB to be spread through unpasteurised milk and other dairy products due to cattle with tuberculosis.

The organism has several unique features compared to other bacteria such as the presence of several lipids in the cell wall including mycolic acid, cord factor, and Wax-D. The high lipid content of the cell wall is thought to contribute to the following properties of M. tuberculosis infection:

  • Resistance to several antibiotics
  • Difficulty staining with Gram stain and several other stains
  • Ability to survive under extreme conditions such as extreme acidity or alkalinity, low oxygen situation and intracellular survival(within the macrophage)[1]
  • A reason the bacteria is able to be dormant in someone for years and is able to survive for months in sputum that is not exposed to sunlight and is trapped within the body (primary TB). Once the person’s resistance is lowered, the TB can become active (secondary TB). This could be due to advancing age, alcoholism, cancer, or immunosuppression.[3]

Epidemiology[edit | edit source]

Geographic Distribution[edit | edit source]

Tuberculosis is present globally. However; developing countries account for a disproportionate share of tuberculosis disease burden. The bulk of the global burden of new infection and tuberculosis death is borne by developing countries with 6 countries: India, Indonesia, China, Nigeria, Pakistan, and South Africa, accounting for 60% of TB death in 2015, Several countries in Asia, Africa, Eastern Europe, and Latin and Central America continue to have an unacceptably high burden of tuberculosis.

In more advanced countries, high burden tuberculosis is seen among recent arrivals from tuberculosis-endemic zones, health care workers, and HIV-positive individuals. Use of immunosuppressive agents such as long-term corticosteroid therapy has also been associated with an increased risk.

Other Major Risk Factors[edit | edit source]

  • Socio-economic factors: Poverty, malnutrition, wars
  • Immunosuppression: Human Immunodeficiency Virus (HIV), chronic immunosuppressive therapy (steroids, monoclonal antibodies against tumor necrotic factor), a poorly developed immune system (children, primary immunodeficiency disorders)
  • Occupational: Mining, construction workers, pneumoconiosis (silicosis)[1]

The WHO estimates that 10.4 million individuals became ill with TB and 1.7 million died in 2016. Despite the fall in mortality rate of 3% per year, TB remains the ninth leading cause of death worldwide, counting 1.3 million TB deaths among HIV-negative people and almost 400,000 deaths among HIV-positive people.[4]

TB in Prisons[edit | edit source]

  • The level of TB in prisons has been reported to be up to 100 times higher than that of the civilian population.
  • Cases of TB in prisons may account for up to 25% of a country’s burden of TB.
  • Late diagnosis, inadequate treatment, overcrowding, poor ventilation and repeated prison transfers encourage the transmission of TB infection.
  • HIV infection and other pathology more common in prisons (e.g. malnutrition, substance abuse) encourage the development of active disease and further transmission of infection.
  • Multi-drug resistant tuberculosis (MDR-TB) in prisons High levels of MDR-TB have been reported from some prisons with up to 24% of TB cases suffering from MDR forms of the disease.[5]

Characteristics/Clinical Presentation[edit | edit source]

Symptoms of TB.png

A chronic cough, haemoptysis, weight loss, low-grade fever, and night sweats are some of the most common physical findings in pulmonary tuberculosis.

Secondary tuberculosis differs in clinical presentation from the primary progressive disease. In secondary disease, the tissue reaction and hypersensitivity is more severe, and patients usually form cavities in the upper portion of the lungs.

Pulmonary or systemic dissemination of the tubercles may be seen in active disease. Disseminated tuberculosis may also be seen in the spine, the central nervous system, or the bowel.[1]

There are usually no symptoms of tuberculosis during the first year of exposure. This is when the disease would be the most curable. Symptoms suggestive of TB include[3]

  • Productive cough that lasts longer than 3 weeks
  • Weight Loss
  • Fever
  • Night sweats
  • Fatigue
  • Malaise
  • Anorexia
  • Rales could be heard in the lobes of involvement in the lungs                     
  • Bronchial Breath Sounds                                                                       
  • Dull chest pain, tightness, or discomfort[6]  
  • Dyspnea[6]
  • Haemoptysis (late-stage symptom)

Systemic Involvement[edit | edit source]

10%-15% of tuberculosis is extra-pulmonary. It can spread through the blood vessels from organ to organ and/or the lymphatic system. Extra-pulmonary TB can involve the:[6] 

  • Kidneys
  • Bone Growth Plates
  • Lymph Nodes
  • Meninges
  • Hip Joints - can cause avascular necrosis of the hip
  • Elbows
  • Vertebrae (Pott's Disease)

Associated Co-morbidities[edit | edit source]

Additional Risk Factors[6][edit | edit source]

  • Healthcare workers
  • Older adults
  • Homeless people
  • Overcrowded housing
  • People who are incarcerated
  • Immigrants
  • Children under the age of 5

Medications[edit | edit source]

Once tuberculosis is diagnosed, all active cases are treated and many inactive cases are treated. It is unclear if preventive treatment is helpful in people with latent TB. However, it is hoped that the disease will be less likely to become active later in life once the immune system is more likely to be compromised.[3]

There are currently 10 drugs that are approved by the FDA to treat TB. The following medications are first-line anti-TB agents that form the core medications given[7]:

  • Isoniazid
  • Rifampin
  • Pyrazinamid
  • Ethambutol

The recommended time for taking the medication is 6-9 months. Blood work should be performed monthly to check on the liver and make sure it is handling the medicine okay.[7]

  • Many people are not compliant with taking their medicine daily for 9 months. Many people will begin to feel better, so they will decide to stop administering the medicine.
  • Compliance is also a problem with homeless people, alcoholics, and drug users.
  • If treatment is not completed, multi-drug resistant TB can form which means the person will now be resistant to the medication taken previously.[3]
  • Multi-drug resistant TB has an even more complicated treatment than before.
  • Some people require a pneumonectomy or chemotherapy along with two or more drugs that are used at the same time.[6]
  • Directly Observed Therapy (DOT) should always be used when treating multi-drug resistant TB to ensure the subject is practicing proper compliance.
  • Treatments are the same for pulmonary and extra-pulmonary TB.

Multidrug-Resistant Tuberculosis (MDR-TB)[edit | edit source]

Tuberculosis (TB) can develop resistance to the antimicrobial drugs used to cure the disease. Multidrug-resistant TB (MDR-TB) is TB that does not respond to at least isoniazid and rifampicin, the 2 most powerful anti-TB drugs. Inappropriate or incorrect use of antimicrobial drugs, or use of ineffective formulations of drugs (such as use of single drugs, poor quality medicines or bad storage conditions), and premature treatment interruption can cause drug resistance, which can then be transmitted, especially in crowded settings such as prisons and hospitals. Treatment options are limited and expensive, recommended medicines are not always available, and patients experience many adverse effects from the drugs. In some cases even more severe drug-resistant TB may develop.[8]

Extensively Drug-Resistant Tuberculosis (XDR-TB)[edit | edit source]

XDR-TB, an abbreviation for extensively drug-resistant tuberculosis (TB), is a form of TB which is resistant to at least four of the core anti-TB drugs. XDR-TB involves resistance to the two most powerful anti-TB drugs, isoniazid and rifampicin, also known as multidrug-resistance (MDR-TB), in addition to resistance to any of the fluoroquinolones (such as levofloxacin or moxifloxacin) and to at least one of the three injectable second-line drugs (amikacin, capreomycin or kanamycin).[9]

MDR-TB and XDR-TB both take substantially longer to treat than ordinary (drug-susceptible) TB, and require the use of second-line anti-TB drugs, which are more expensive and have more side-effects than the first-line drugs used for drug-susceptible TB.[8][9]

TB Screening[edit | edit source]

Approximately 33% of the world's population has latent tuberculosis infection (LTBI). For this reason, screening for Mycobacterium tuberculosis infection is essential for public health. People with LTBI are at risk for developing active tuberculosis (TB) and becoming infectious.

  • The greatest risk for progression occurs during the first two years of infection.
  • The goal of testing for LTBI is to identify individuals who are at high risk of developing active TB.
  • The decision to test should presuppose a decision to treat if the result is positive.
  • The tuberculin skin test (TST) and the interferon-gamma release assay (IGRA) are the current methods for screening and are based on the measurement of adaptive host immune response.[10]

BCG Vaccine [edit | edit source]

TB Skin Test.gif

The Bacille Calmette-Guérin (BCG) vaccine has existed for 80 years and is one of the most widely used of all current vaccines, reading >80%of neonates and infants in countries where it is part of the national childhood immunization programme.

BCG vaccine has a documented protective effect against meningitis and disseminated TB in children.

It does not prevent primary infection and does not prevent reactivation of latent pulmonary infection, the principal source of bacillary spread in the community. The impact of BCG vaccination on transmission of Mtb is therefore limited.

The CDC and the American Academy of Paediatrics recommend that all children adopted from high-risk countries who have received the BCG vaccine should act as if they have never received it.[6] All children should be given a skin test and treated whether it is dormant or active.

The Mantoux tuberculin skin test is performed by having 0.1ml of tuberculin purified protein derivative (PPD) injected into the inner layer of the forearm.[11] This will determine if the body’s immune response has been activated by the presence of the bacillus. Upon injection, the skin will elevate around 6-10 mm in diameter. 48 to 72 hours later, the person should have their skin test reaction read. A positive test could reveal a palpable, swollen, hardened, or raised area that should be measured in millimetres. Redness is not measured.[11]

Physical Therapy Management[edit | edit source]

Chest xray.gif

All physical therapists should be aware of the proper personal protective equipment (PPE) that should be worn.  There is a specialised mask that is worn that has been sized to specifically fit your face.[6]

  1. Pulmonary Tuberculosis People with pulmonary TB are typically not treated in physical therapy because medications are vital for curing TB.  However, therapists are able to provide percussion and postural drainage to clear secretions out of the lung.[12]
  2. Extrapulmonary Tuberculosis Clients with extra-pulmonary TB are usually not seen in the physical therapy setting.  However, patients may present in clinic with musculoskeletal problems with unknown causes or arthritic pain.  PT's should be prepared to take a thorough history and a proper examination in order to better identify TB.  A patient could also be seen in physical therapy if they have had surgery on their back, in which case the normal rehabilitation protocols would be followed.[12]

It is very important to take a thorough history when TB is suspected.  It is important to ask if the person has travelled outside the country recently, their occupation, or if there is any way they have possibly been exposed to someone who could have TB.  Recognise your patient's signs and symptoms.  Palpation of the lymph nodes could also be informational during an examination. [13]

Differential Diagnosis[edit | edit source]

Tuberculosis is a great mimic and should be considered in the differential diagnosis of several systemic disorders. The following is a non-exhaustive list of conditions to be strongly considered when evaluating the possibility of pulmonary tuberculosis.

Prognosis[edit | edit source]

Majority of patients with a diagnosis of TB have a good outcome. This is mainly because of effective treatment. Without treatment mortality rate for tuberculosis is more than 50%.

The following group of patients is more susceptible to worse outcomes or death following TB infection:

  • Extremes of age, elderly, infants and young children
  • Delay in receiving treatment
  • Radiologic evidence of extensive spread.
  • Severe respiratory compromise requiring mechanical ventilation
  • Immunosuppression
  • Multi-drug Resistant (MDR) Tuberculosis[1]

References[edit | edit source]

  1. 1.0 1.1 1.2 1.3 1.4 1.5 Adigun R, Bhimji S. Tuberculosis. StatPearls 2017.Available from:https://www.ncbi.nlm.nih.gov/books/NBK441916/ (last accessed 8.3.2020)
  2. WHO GLOBAL TUBERCULOSIS REPORT 2019 Available from:https://www.who.int/tb/publications/factsheet_global.pdf?ua=1 (last accessed 8.3.2020)
  3. 3.0 3.1 3.2 3.3 3.4 3.5 3.6 Goodman C, Fuller K. Pathology: Implications for the Physical Therapist. 3rd edition. In: Ikeda, B, Goodman, C. The Respiratory System. St. Louis, MO: Saunders; 2009: 752-758.
  4. Matteelli A, Rendon A, Tiberi S, Al-Abri S, Voniatis C, Carvalho AC, Centis R, D'Ambrosio L, Visca D, Spanevello A, Migliori GB. Tuberculosis elimination: where are we now?. European Respiratory Review. 2018 Jun 30;27(148):180035. Available from:https://err.ersjournals.com/content/27/148/180035
  5. WHO TB in prisons Available from:https://www.who.int/tb/areas-of-work/population-groups/prisons-facts/en/ (last accessed 8.3.2020)
  6. 6.0 6.1 6.2 6.3 6.4 6.5 6.6 6.7 6.8 Goodman C, Snyder T. Differential Diagnosis for Physical Therapists: Screening for Referral. 4th edition. In: Screening for Pulmonary Disease.. St. Louis, MO: Saunders; 2007: 344-345.
  7. 7.0 7.1 Centers for Disease Control and Prevention. Treatment of Latent Tuberculosis Infection. Atlanta, GA. [Web-Page]. 2010. http://www.cdc.gov/tb/publications/factsheets/treatment/treatmentLTBI.htm. Accessed on March 18, 2011.
  8. 8.0 8.1 What is multidrug-resistant tuberculosis (MDR-TB) and how do we control it? [Internet]. WHO. World Health Organization; 2018 [cited 2020 Mar 20]. Available from: https://www.who.int/features/qa/79/en/
  9. 9.0 9.1 Drug-resistant TB: XDR-TB FAQ [Internet]. WHO. World Health Organization; 2018 [cited 2020 Mar 20]. Available from: https://www.who.int/tb/areas-of-work/drug-resistant-tb/xdr-tb-faq/en/
  10. de Lima Corvino DF, Kosmin AR. Tuberculosis Screening. InStatPearls [Internet] 2019 Feb 4. StatPearls Publishing.Available from:https://www.statpearls.com/kb/viewarticle/30655 (last accessed 8.3.2020)
  11. 11.0 11.1 Centers for Disease Control and Prevention. Tuberculin Skin Testing. Atlanta, GA. [Web-Page]. 2010. http://www.cdc.gov/tb/publications/factsheets/testing/skintesting.htm. Accessed on March 18, 2011.
  12. 12.0 12.1 Goodman C, Fuller K. Pathology: Implications for the Physical Therapist. 3rd edition. In: Infectious Diseases of the Musculoskeletal System. St. Louis, MO: Saunders; 2009: 1198-1199.
  13. Flicr. Bayberry. http://www.flickr.com/photos/zeping/150247200/