Dd. Sin et Sd. Shafran, DAPSONE-INDUCED AND PRIMAQUINE-INDUCED METHEMOGLOBINEMIA IN HIV-INFECTED INDIVIDUALS, Journal of acquired immune deficiency syndromes and human retrovirology, 12(5), 1996, pp. 477-481
Clinically significant methemoglobinemia can develop as a result of me
dications. Although dapsone and primaquine are known to produce methem
oglobinemia in susceptible individuals, methemoglobinemia has been rep
orted only rarely in the human immunodeficiency virus (HIV) population
. We describe five cases of methemoglobinemia caused by either primaqu
ine or dapsone alone or in combination. The initial methemoglobin leve
l ranged from 15.3% in the patient whose methemoglobinemia was caused
by primaquine alone to 33.1%. Five patients developed symptomatic meth
emoglobinemia requiring hospitalization for 1 to 12 days. Two cases re
sulted from intentional overdoses of dapsone, and three developed with
in several days of commencing primaquine while dapsone remained presen
t in the bloodstream. The four severe cases required intravenous methy
lene blue, supplemental oxygen, plus erythrocyte transfusions, whereas
the mild case responded to oxygen therapy plus discontinuation of the
precipitating drugs. Blood gases and pulse oximetry do not aid in the
diagnosis, which requires cooximetry. Our study indicates that dapson
e and primaquine alone or in combination can produce clinically signif
icant methemoglobinemia in HIV-infected individuals, either in the set
ting of an overdose or when primaquine is instituted before dapsone ha
s been cleared from the bloodstream.