Skip to main content
. 1998 Jun;42(6):1309–1314. doi: 10.1128/aac.42.6.1309

TABLE 1.

Treatment of P. cariniia

Agent(s) (route)b Dose Options or commentsb
First line: TMP-SMX (i.v. or p.o.) 15–20 mg of TMP/kg/day and 75–100 mg of SMX/kg/day Treat through rash with reduced dose; desensitize
Second line
 Dapsone (p.o.) with TMP (p.o. or i.v.) 100 mg of dapsone/day and 15–20 mg of TMP/kg/day Side effects include methemoglobinemia and glucose-6-phosphate dehydrogenase deficiency; may be tolerated in patients with sulfa drug allergy
 Atovaquone (p.o.) 750 mg of liquid p.o. t.i.d. Variable absorbance; absorbance is improved with fatty food; few side effects
 Pentamidine isethionate (i.v.) 4 mg/kg/day; 300 mg/day maximum Lower dose (2–3 mg/kg may be used); intramuscular administration not advised
Third line
 Trimetrexate (i.v.) with folinic acid 30–45 mg of trimetrexate/m2/day with 80–100 mg of folinic acid/m2day Efficacy equal to that of pentamidine; anemia, marrow toxicity; early relapse
 Clindamycin (i.v. or p.o.) and primaquine 450–600 mg of clindamycin every 6 h and 15–30 mg of primaquine base once a day Side effects include methemoglobinemia and diarrhea (may substitute pyrimethamine for primaquine)
Others
 Pyrimethamine (p.o.) with sulfadiazine (p.o.) Load of 50 mg of pyrimethamine b.i.d. for 2 days and then 25–50 mg q.d., load of 75 mg/kg of sulfadiazine and then 100 mg/kg/day Not studied fully; maximum of 4 g of sulfadiazine in two doses (up to 8 g total)
 Pyrimethamine-sulfadoxine Not standardized Long half-life; should not be used in patients with sulfa drug allergy
 Piritrexim-folinic acid Under study Like trimetrexate
 8-Aminoqunoline Under study
 Macrolides and sulfonamides Under study Synergy; macrolides alone are inactive
a

Adjunctive therapies (see text) include corticosteroids (high dose with rapid taper), possibly gamma interferon, and GM-CSF. Abbreviations: i.v., intravenous; p.o., oral; t.i.d., three times a day; q.d., once a day; b.i.d., twice a day. 

b

Based on the clinical judgment of the physician; some agents are not approved by the U.S. Food and Drug Administration for this indication (ranking of therapies is based on the author’s experience) (see also references 26 and 48).