Ehrlichiosis natural history, complications and prognosis
|
Ehrlichiosis Microchapters |
|
Diagnosis |
|---|
|
Treatment |
|
Case Studies |
|
Ehrlichiosis natural history, complications and prognosis On the Web |
|
American Roentgen Ray Society Images of Ehrlichiosis natural history, complications and prognosis |
|
FDA on Ehrlichiosis natural history, complications and prognosis |
|
CDC on Ehrlichiosis natural history, complications and prognosis |
|
Ehrlichiosis natural history, complications and prognosis in the news |
|
Blogs on Ehrlichiosis natural history, complications and prognosis |
|
Risk calculators and risk factors for Ehrlichiosis natural history, complications and prognosis |
Overview
The prognosis is usually good for human granulocytotropic anaplasmosis (HGA). Individuals suffering from HGA should fully recover without treatment in 2 months. However, proper treatment of HGA will expedite the recovery process. Symptoms that are commonly associated with HGA include sudden onset of fever and intense pains. Progression of the disease may lead to serious complications including neurological disorders and ARDS. Co-infection remains the greatest threat associated with death as a result of HGA. Thus individuals with compromised immune systems or the elderly should be closely monitored in order to reduce the likelihood of an opportunistic infection. Human monocytotropic ehrlichiosis (HME) presents a very different scenario than that of HGA. HME is far more dangerous as well as deadly. An incubation period of 7-10 days will often follow an infected tick bite. Initial symptoms include fever, headache, and malaise. Further complications will follow the onset of infection, these complications may prove to be extremely dangerous and should be closely monitored for the patients safety.
Natural History
Infection varies according to the Ehrlichiae agent responsible for the infection. Listed below are the progressive pathways of each infection:
Human granulocytotropic anaplasmosis
Early Stage
- Sudden onset of fever with rigors
- Severe Myalgia
- Early Symptoms such as pain, nausea, vomiting, weight loss, cough, and confusion
Late Stage
- Toxic-like Syndrome
- ARDS
- Neurological disorders
- Liver complications
If left untreated
- Usually achieve a full recovery in 2 months
- Immuno-compromised individuals may suffer severe infections or even death as a result of an opportunistic co-infection.
Human monocytotropic ehrlichiosis
Early Stage
- Incubation of 7-10 days
- Initial presenting symptoms include fever, headache, and malaise.
- More severe infections will include myalgia, diaphoresis, weight loss, maculopapular rash, and confusion.
Late Stage
- Progression of symptoms requires hospitalization
- Majority of infected patients require intensive care
- Even with medical therapy 2.7% of infected patients die
If left untreated
- HME remains a life-threatening disease
- Without proper treatment patients may suffer from hypotension, respiratory failure, acute renal failure, and hemorrhagic manifestations
- Death
Complications
- Respiratory distress syndrome
- Hepatitis
- Kidney damage
- Lung damage
- Other organ damage
- Seizure
- Candidiasis
- Opportunistic nosocomial infections[1]
- Death
Prognosis
Human granulocytotropic anaplasmosis
- The prognosis for HGE is usually good.
- With proper treatment, patients should fully clear infection
- About Half of infected individuals will require 6 days of hospitalization
- Even in the absence of treatment, infected patients should clear infection within 2 months
- Death associated with opportunistic co-infection.
Human monocytotropic ehrlichiosis
- HME is a severe illness with many complications
- Even in the presence of proper medical therapy, nearly 2.7% of infected patients will die
- Infection must be closely monitored in order to reduce the amount of possible complications
References
- ↑ Thomas, Rachael J (1 August 2009). "Current management of human granulocytic anaplasmosis, human monocytic ehrlichiosis and ehrlichiosis". Expert Review of Anti-infective Therapy. 7 (6): 709–722. doi:10.1586/eri.09.44. PMC 2739015. PMID 19681699. Unknown parameter
|month=ignored (help); Unknown parameter|coauthors=ignored (help)