Pneumocystis carinii is a common cause of pneumonia in individuals who
are immunosuppressed by HIV infection. Use of molecular biological te
chniques show that P. carinii is a fungus and that infection in man is
not a zoonosis. Invasive tests such as sputum induction or bronchosco
py are used to make the diagnosis of P. carinii pneumonia. Life long p
rimary prophylaxis is given to HIV positive individuals with CD4+ lymp
hocyte counts <0.20 x 10(9)/L or a CD4: total lymphocyte ratio of <1.5
, constitutional symptoms, or with other AIDS defining diseases. Secon
dary prophylaxis is given after a first episode to prevent a recurrenc
e. First choice for primary and secondary prophylaxis is oral co-trimo
xazole 960 mg od or three times week. In patients who are intolerant t
o co-trimoxazole, nebulised pentamidine or dapsone (with or without py
rimethamine) are second and third choices. In a patient with acute PCP
disease, severity should be assessed using clinical, radiographic and
blood gas criteria as those with moderate or severe disease will bene
fit from adjuvant glucocorticoids. Co-trimoxazole (120 mg/kg/day in di
vided doses for 21 days) is first choice therapy for PCP of all degree
s of severity. In patients who fail to respond to co-trimoxazole or wh
o are intolerant to it, second line treatment is iv pentamidine in tho
se with severe disease and oral dapsone with trimethoprim, oral clinda
mycin with primaquine or iv pentamidine in those with mild or moderate
ly severe disease.