Zacà Valerio, Metra Marco, Danesi Rossella, Lombardi Carlo, Verzura Giulia, Dei Cas Livio
Section on Cardiovascular Diseases, Department of Experimental and Applied Medicine, University of Brescia, Italy.
Ther Adv Respir Dis. 2009 Feb;3(1):11-4. doi: 10.1177/1753465808101549.
Pulmonary arterial hypertension [PAH] is a rare but well-known cardiovascular condition potentially associated with human immunodeficiency virus [HIV] infection and is currently recognized to be one of the most ominous noninfectious HIV complications. Although there is no clear evidence supporting the use of any medication for the treatment of HIV-related PAH, many of the currently available agents have been shown to exert some clinical benefits HIV-PAH patients. To date, no data are available regarding the potential effects of sitaxsentan, a selective endothelin type-A receptor antagonist, in this peculiar patient population. We report the case of a successful switch to sitaxsentan in a HIV-infected patient with PAH initially receiving bosentan who developed a late treatment-related side-effect.
肺动脉高压(PAH)是一种罕见但广为人知的心血管疾病,可能与人类免疫缺陷病毒(HIV)感染有关,目前被认为是最凶险的非感染性HIV并发症之一。尽管尚无明确证据支持使用任何药物治疗HIV相关的PAH,但目前许多可用药物已显示对HIV-PAH患者有一定临床益处。迄今为止,关于选择性内皮素A受体拮抗剂西他生坦在这一特殊患者群体中的潜在作用尚无数据。我们报告了1例HIV感染合并PAH的患者,该患者最初接受波生坦治疗,出现了晚期治疗相关副作用,成功换用西他生坦的病例。