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The Diagnosis of Opportunistic Infections

 

This area is under development.  Please excuse the incomplete areas.

 

Direct links
OI Diagnosis Treatment
Pneumocystis carinii pneumonia (PCP) Dx Tx
Toxoplasma gondii encephalitis Dx Tx
Cryptococcus neoformans Dx Tx
cytomegalovirus infection Dx Tx
histoplasmosis Dx Tx
aspergillosis Dx Tx
cryptosporidiosis Dx Tx
nocardiosis Dx Tx
coccidioidomycosis Dx Tx
acyclovir-resistant herpes simplex Dx Tx
severe refractory human papilloma virus (HPV) Dx Tx
progressive multifocal leukoencephalopathy (PML) Dx Tx
late stage Pseudomonas aeruginosa pneumonia Dx Tx

 

Blue links are under development and are not working.

 

Pneumocystis carinii pneumonia (PCP)
Clinical presentation: in many cases the clinical scenario is diagnostic

Known HIV infection or known/suspected risk factors for HIV

CD4 < 200, usually < 100

Any combination of the following:

Insidious onset of symptoms

Cough, usually nonproductive or minimally productive, especially associated with inspiration

Fever
Sweats or nightsweats

Progressive dyspnea or dyspnea on exertion

Weight loss and anorexia

Oral candidiasis

Previous history of PCP

Nonadherent to prophylaxis for PCP

Elevated HIV viral load

LDH usually elevated

Chest x-ray Bilateral diffuse alveolar and interstitial infiltrates or any variety of patterns: normal, patchy alveolar, rarely cavitary
Pulse oximeter Technique: perform pulse oximetry at rest and with exercise (rapid walking)

Reduced O2 saturation on room air or decreasing O2 saturation on room air with exercise

Arterial blood gas Increased alveolar-arterial oxygen gradient
Induced sputum for Pneumocystis carinii smear Technique: performed after good oral hygiene obtained and optimally induced by trained respiratory technician with normal saline aerosol

Comment: This technique is fairly sensitive (as sensitive as bronchoalveolar lavage?) and very specific for PCP

Fiberoptic bronchoscopy with bronchoalveolar lavage Technique: Fluid sent for Pneumocystis carinii examination as well as microbiologic studies for acid fast bacilli (AFB), fungi, and virus (especially CMV)

Studies for cytopathology should also be considered.

Comment: This is the optimal examination due to the possibility of concomitant pathogens in persons with severe disease

 

 

 

Toxoplasma gondii encephalitis
Clinical presentation
Known HIV infection or suspected/known risk factors for HIV

CD4 count < 100
Any combination of the following:

Fever
Headache

Altered mental status

Focal neurologic deficits

Toxoplasma gondii IgG antibodies
Computerized tomography (CT) of brain with and without intravenous contrast
Magnetic resonance imaging (MRI) of brain with and without intravenous contrast
Cerebrospinal fluid (CSF) analysis
Positron emission tomography
Brain biopsy

 

 

 

Cryptococcus neoformans infections (cryptococcosis)
Clinical presentation
Known HIV infection or suspected/known risk factors for HIV

CD4 count < 100
Any combination of the following:

Cough, usually nonproductive

Dyspnea or dyspnea on exertion
Headache

Altered mentation
Nuchal rigidity

Seizures

Focal neurologic deficits including decreased visual acuity, hearing loss

Chest x-ray
Computerized tomography (CT) of brain with and without intravenous contrast
Magnetic resonance imaging (MRI) of brain with and without intravenous contrast
Cerebrospinal fluid (CSF) analysis including India ink and fungal cultures
Cryptococcal antigen detection from blood and CSF
Fungal smears and cultures of blood, sputum

 

 

 

cytomegalovirus (CMV) infections
Clinical presentation
Known HIV infection or suspected/known risk factors for HIV

CD4 count < 100, usually < 50

Any combination of the following:

Fever

Cough, usually nonproductive

Dyspnea or dyspnea on exertion

Loss of visual acuity, unilateral or bilateral

Abnormal retinal exam

Floaters in visual field

Headache

Focal neurologic deficits
Diarrhea

Chest x-ray
Shell vial cultures of bronchoalveolar lavage, urine
CMV antigen (blood) assay
Tissue cytopathology - bronchoalveolar lavage, lung biopsy, GI tract biopsy, liver biopsy, etc.

 

 

 

histoplasmosis (Histoplasma capsulatum infection)
Clinical presentation
Known HIV infection or suspected/known risk factors for HIV

CD4 count < 100, usually < 50

Any combination of the following:

Fever

Cough, usually nonproductive

Dyspnea, or dyspnea on exertion

Mucosal ulcerations (usually painless): mouth, rectum, genital tract

Papular skin rash

Diarrhea

Splenomegaly

Direct buffy coat smear for fungi
Blood cultures for fungi
Urine histoplasma antigen
Bone marrow examination with fungal smears, fungal cultures, histopathology including special tissue stains for fungi
Smear and culture of mucosal ulcers
Biopsy of skin lesions with smears and cultures for fungi and histopathology including special tissue stains for fungi
Fiberoptic bronchoscopy with bronchoalveolar lavage

 

 

aspergillosis
Clinical presentation
Known or suspected advanced HIV infection
History of IVDU or history of environmental exposure (hay, etc.)
CD4 count < 100
Pulmonary nodules or cavitary lesion
Intracranial perivascular infection or abscess
Aspergillus urine antigen
Biopsy material for fungal smears and cultures is the gold standard for sensitivity and specificity.

 

 

 

cryptosporidiosis
Clinical presentation

Known HIV infection or suspected/known risk factors for HIV

CD4 count < 100, usually < 50

Diarrhea, usually voluminous and watery

Any combination of the following:

Abdominal cramps

Nausea and vomiting

Weight loss, possibly rapid

Right upper quadrant abdominal pain and tenderness

Modified acid fast stain of the stool
Endoscopic aspiration of duodenum and/or biliary tree for cryptosporidiosis

 

 

 

acyclovir-resistant herpes simplex
Clinical presentation
Known or suspected advanced HIV infection
CD4 usually < 200 and uncontrolled HIV viral load
History of recurrent herpes simplex infection
History of long term suppressive therapy with acyclovir
Nonhealing ulcerative disease in area of previously acyclovir responsive herpes simplex
Viral culture for herpes simplex
Assay for thymidine kinase in isolated HSV
Lack of response to high dose acyclovir (800 mg po 5 times per day) is a low technology but effective approach to diagnosis

 

 

 

progressive multifocal leukoencephalopathy (PML)
Clinical presentation
Known or suspected advanced HIV infection
CD4 usually < 100 and uncontrolled HIV viral load
Focal neurologic deficits without other explanation
Magnetic resonance imaging (MRI) of brain with and without intravenous contrast
CSF analysis including JC virus PCR
Brain biopsy with cytopathology

 

 

 

Pseudomonas aeruginosa pneumonia (late stage AIDS)
Clinical presentation
Known or suspected advanced HIV infection
CD4 <50
Multiple hospitalizations and extensive antibiotic exposure
Malnutrition
Cough productive of purulent sputum
High fevers and rigors
CXR with bilateral lobular infiltrates
Sputum gram stain (large numbers of gram negative bacilli and WBCs) and culture (growing the organism obviously)
Blood cultures are often diagnostic also
CBC which reveals relative or absolute leukocytosis with a shift to immature forms
Antibiotic resistance may develop while on therapy

 

 

Updated 12.18.2005

 

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