SAFETY OF DAPSONE AS PNEUMOCYSTIS-CARINII PNEUMONIA PROPHYLAXIS IN HUMAN IMMUNODEFICIENCY VIRUS-INFECTED PATIENTS WITH ALLERGY TO TRIMETHOPRIM SULFAMETHOXAZOLE/
Mg. Beumont et al., SAFETY OF DAPSONE AS PNEUMOCYSTIS-CARINII PNEUMONIA PROPHYLAXIS IN HUMAN IMMUNODEFICIENCY VIRUS-INFECTED PATIENTS WITH ALLERGY TO TRIMETHOPRIM SULFAMETHOXAZOLE/, The American journal of medicine, 100(6), 1996, pp. 611-616
OBJECTIVE: TO assess the safety of dapsone prophylaxis of Pneumocystis
carinii pneumonia (PCP) in patients with prior intolerance td trimeth
oprim/sulfamethoxazole (TMP/SMX). METHODS: We conducted a retrospectiv
e study in the categorical human immunodeficiency virus out-patient pr
ogram of a university hospital. Patients who had filled prescriptions
for dapsone at our pharmacy between January 1991 and April 1994 were e
valuated and 75 patients were found eligible for analysis. RESULTS: Th
e overall incidence of adverse events (AE) in our study cohort was 39%
. The most common AEs were anemia (23%) and rash (16%). However, after
critical evaluation of each case, only 3 cases of anemia (4%) and 2 c
ases of rash (3%) were judged to be ''likely related'' to dapsone. Onl
y 5/75 patients (7%) developed the same intolerance to dapsone as prev
iously experienced on TMP/SMX, and none of these cases was viewed as '
'likely related'' to dapsone. A dapsone regimen of 100 mg qd and a pri
or episode of PCP were associated with a higher incidence of AEs. Eigh
t cases of PCP occurred in spite of dapsone prophylaxis for an inciden
ce of 7 cases per 1,000 patient-months. Seven of the cases of PCP occu
rred in patients who were receiving secondary prophylaxis. CONCLUSIONS
: Given the low incidence of AEs judged to be ''likely related'' to da
psone, this drug is a reasonable choice for PCP prophylaxis in patient
s with prior AEs to TMP/SMX.