Comparison of gynecologic history and laboratory results in HIV-positive women with CD4(+) lymphocyte counts between 200 and 500 cells/mu l and below100 cells/mu l
Dh. Watts et al., Comparison of gynecologic history and laboratory results in HIV-positive women with CD4(+) lymphocyte counts between 200 and 500 cells/mu l and below100 cells/mu l, J ACQ IMM D, 20(5), 1999, pp. 455-462
Objective: To assess rates of sexual activity, contraceptive use, genital i
nfections and dysplasia, and other gynecologic symptoms among well-characte
rized populations of HIV-seropositive women enrolled in two Adult AIDS Clin
ical Trials Group (AACTG) randomized studies.
Methods: Gynecologic data were collected using standardized interview and e
xamination forms from women enrolled in two protocols: ACTG 175, an antiret
roviral trial (CD4(+) lymphocyte counts 200-500 cells/mu l) and ACTG 196, a
Mycobacterium avium complex prophylaxis trial (CD4(+) counts less than or
equal to 100 cells/mu l).
Results: Women enrolled in the two studies were similar in age, race, weigh
t, and history of illicit or injection drug use, but women in ACTG 196 (n =
67) had lower median CD4(+) counts (median, 35 cells/mu l; range, 0-135 ce
lls/mu l versus median, 356 cells/mu l; range, 131-620 cells/mu l; p <.0005
), were less likely to be antiretroviral naive (6% versus 38%; p <.0005), a
nd were more likely to have a Karnofsky score <80 (28% versus 5%; p <.0001)
than women in ACTG 175 (n = 185) at baseline. Recent changes in menstrual
cycle were not different between groups. Women enrolled in ACTG 196 were le
ss likely to be sexually active (40% versus 61%; p <.005), but both groups
reported high levels of contraceptive use. Papanicolaou smear results in AC
TG 196 and ACTG 175 respectively, were: normal, 38% and 50%, atypia, 24% an
d 39%, low-grade squamous intraepithelial lesions (SIL), 27% and 10%, and h
igh-grade Sn, 11% and 0.7% (p <.001).
Conclusions: Gynecologic complications are common among HIV-seropositive wo
men with CD4(+) lymphocyte counts < 500 cells/mu l and are more common and
severe among those with more advanced immunosuppression.