Nguyen M T, Weiss P J, Wallace M R
Department of Pharmacy, Naval Medical Center, San Diego, California 92134-5000, USA.
AIDS. 1995 Jun;9(6):573-5. doi: 10.1097/00002030-199506000-00007.
To establish whether an outpatient, 2-day oral desensitization protocol would be both safe and effective in HIV-infected patients with previous trimethoprim-sulfamethoxazole (TMP-SMX) intolerance.
A single center trial of TMP-SMX desensitization in HIV-infected patients with prior TMP-SMX hypersensitivity reactions.
HIV-infected patients with CD4 lymphocyte counts < 250 x 10(6)/l cells or CD4% < 20% with previous non-life-threatening hypersensitivity reactions to TMP-SMX were eligible. The desensitization protocol utilized 40 graduated doses over 36 h; the first 28 doses (7.5 h) of the protocol were given in an outpatient clinic with the remaining doses taken at home.
Twenty-seven (60%) of the 45 subjects completed the protocol and were subsequently maintained on daily TMP-SMX without adverse reactions (mean follow-up, 9 months; range, 4-16 months). Patients with CD4 counts < 100 x 10(6)/l cells were just as likely as patients with higher CD4 counts to tolerate the desensitization. No patient required hospitalization for treatment of an adverse reaction.
Oral desensitization to TMP-SMX in HIV-infected patients is a useful option in the management of patients with advanced HIV disease and prior intolerance to TMP-SMX.
确定一项为期2天的门诊口服脱敏方案对于既往对甲氧苄啶 - 磺胺甲恶唑(TMP - SMX)不耐受的HIV感染患者是否安全有效。
一项针对既往有TMP - SMX过敏反应的HIV感染患者进行TMP - SMX脱敏的单中心试验。
符合条件的为CD4淋巴细胞计数<250×10⁶/l细胞或CD4%<20%且既往对TMP - SMX有非危及生命过敏反应的HIV感染患者。脱敏方案在36小时内使用40个梯度剂量;方案的前28个剂量(7.5小时)在门诊给予,其余剂量在家服用。
45名受试者中有27名(60%)完成了方案,随后每日服用TMP - SMX且无不良反应(平均随访9个月;范围4 - 16个月)。CD4计数<100×10⁶/l细胞的患者与CD4计数较高的患者耐受脱敏的可能性相同。没有患者因不良反应需要住院治疗。
对于晚期HIV疾病且既往对TMP - SMX不耐受的患者,对HIV感染患者进行TMP - SMX口服脱敏是一种有用的治疗选择。