Rhodococcus hoagii: Difference between revisions
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Rhodococcus hoagii
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*Most commonly infects people with cell-mediated immunodeficiency, particularly [[HIV]], with or without a notable infectious exposure |
*Most commonly infects people with cell-mediated immunodeficiency, particularly [[HIV]], with or without a notable infectious exposure |
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===Risk Factors=== |
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*HIV accounts for 65% of cases |
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*Solid organ and hematopoietic stem cell transplantation |
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*Diabetes |
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*Alcohol abuse |
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*Chronic renal failure |
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*Leukemia, lymphoma, lung cancer |
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*Sarcoidosis |
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*Preterm infants |
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==Clinical Manifestations== |
==Clinical Manifestations== |
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==Management== |
==Management== |
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*Recommend using at least two agents given increasing rates of resistance |
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**First-line: combination of [[macrolide]] or [[fluoroquinolone]] plus [[rifampin]] |
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**First-line: combination of [[macrolide]] or [[fluoroquinolone]] plus two of: [[vancomycin]], [[imipenem]], [[linezolid]], or an [[aminoglycoside]] |
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**Doses are: |
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***[[Azithromycin]] 500 mg PO/IV once followed by 250 mg PO/IV daily |
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***Fluoroquinolones: [[moxifloxacin]] 400 mg PO daily (preferred), [[levofloxacin]] 500 mg PO daily, or [[ciprofloxacin]] 750 mg PO BID |
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***[[Rifampin]] 600 mg PO once daily |
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**Increasing resistance to [[doxycycline]], [[rifampin]], and [[TMP-SMX]] |
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*Treatment usually 6 months or longer |
*Treatment usually 6 months or longer |
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{{DISPLAYTITLE:''Rhodococcus equi''}} |
{{DISPLAYTITLE:''Rhodococcus equi''}} |
Revision as of 14:11, 15 March 2021
Background
Microbiology
- Facultative intracellular, non-spore-forming, Gram-positive, weakly acid-fast coccobacillus
- Within the family Nocardiaceae and order Actinomycetes
- Obligate aerobic and facultatively intracellular
- Found in dry and dusty soil
- Makes red pigment, hence the name
Epidemiology
- Infects domesticated animals: Horses (and in foals it causes pneumonia), Goats, Pigs, Sheep, and Cattle
- Most commonly infects people with cell-mediated immunodeficiency, particularly HIV, with or without a notable infectious exposure
Risk Factors
- HIV accounts for 65% of cases
- Solid organ and hematopoietic stem cell transplantation
- Diabetes
- Alcohol abuse
- Chronic renal failure
- Leukemia, lymphoma, lung cancer
- Sarcoidosis
- Preterm infants
Clinical Manifestations
- Necrotizing pneumonia is usual presentation, as well as nodules, cavitation, pleural effusion, and lung abscess
- Typically subacute onset with fever, cough, and fatigue, as well as pleuritic chest pain
- Specifically in immunocompromised patients, it can cause a cavitary lung disease and is on the differential with mycobacteria and nocardiosis
- Extrapulmonary disease can occur with or without pulmonary involvement
- In conjunction with other infections, can have abscesses in liver, spleen, thyroid, kidney, psoas, bone, prostate, intraabdominal cavity, and paraspinous tissue
- Extrapulmonary disease without pulmonary involvement has three main presentations:
- Localized infection following traumatic inoculation, causing wound infection, traumatic septic arthritis, or endophthalmitis
- Isolated bacteremia with fever, typically recently after chemotherapy causing neutropenia
- Gastrointestional inoculation followed by lymphatic dissemination, causing peritonitis, pelvic masses, and mesenteric adenitis
- Others include otitis media with mastoiditis, colonic polyp infection, and osteomyelitis
Management
- Recommend using at least two agents given increasing rates of resistance
- First-line: combination of macrolide or fluoroquinolone plus rifampin
- First-line: combination of macrolide or fluoroquinolone plus two of: vancomycin, imipenem, linezolid, or an aminoglycoside
- Doses are:
- Azithromycin 500 mg PO/IV once followed by 250 mg PO/IV daily
- Fluoroquinolones: moxifloxacin 400 mg PO daily (preferred), levofloxacin 500 mg PO daily, or ciprofloxacin 750 mg PO BID
- Rifampin 600 mg PO once daily
- Increasing resistance to doxycycline, rifampin, and TMP-SMX
- Treatment usually 6 months or longer