Mittelviefhaus H
Universitäts-Augenklinik Freiburg.
Klin Monbl Augenheilkd. 1992 Feb;200(2):123-7. doi: 10.1055/s-2008-1045724.
It is generally accepted that toxoplasmic retinochorioiditis should be treated when central visual function is threatened. Although controlled trials of treatment led to contradictory results, a combination of pyrimethamin, sulphadiazine and folinic acid is regarded to be the most effective treatment strategy. Nevertheless, hematological complications necessitate a discontinuation of these drugs in up to 1/4 of the patients. Clindamycin, a semisynthetic antibiotic, also has an antitoxoplasmal effect on animals and is less toxic to the bone marrow. A theoretical advantage is that Clindamycin can penetrate and act on the encysted form of the parasite and that it will accumulate in the uveal tissue of the eye. Between 1983 and 1991 we performed 102 courses of treatment in 90 patients with presumed toxoplasmic retinochorioiditis. 900-1800 mg Clindamycin were given in combination with 60-80 mg Fluorcortolon which was gradually decreased during a 4 to 6 week period. In general Clindamycin was given for 6 weeks. Duration varied from 4 to 12 weeks. 15 patients experienced side effects of treatment. 6 of them complained of diarrhea and gastrointestinal bleeding and 7 patients developed allergic exanthem and acne. Mild lymphopenia and hepatotoxicity were further complications. In 8 patients the drugs had to be discontinued; 4 times for gastrointestinal discomfort, 3 times for allergic exanthem and in one patient for mild hepatotoxicity. We did not observe any serious complications during therapy. Only 9 complications were attributable to clindamycin, they disappeared immediately after discontinuing treatment.
一般认为,当中心视觉功能受到威胁时,应治疗弓形虫性视网膜脉络膜炎。尽管治疗的对照试验得出了相互矛盾的结果,但乙胺嘧啶、磺胺嘧啶和亚叶酸联合使用被认为是最有效的治疗策略。然而,血液学并发症使得多达四分之一的患者不得不停用这些药物。克林霉素是一种半合成抗生素,对动物也有抗弓形虫作用,且对骨髓毒性较小。理论上的优势在于,克林霉素可以穿透并作用于寄生虫的包囊形式,并且会在眼部的葡萄膜组织中蓄积。1983年至1991年间,我们对90例疑似弓形虫性视网膜脉络膜炎患者进行了102个疗程的治疗。给予900 - 1800毫克克林霉素,并联合60 - 80毫克氟氢可的松,氟氢可的松在4至6周内逐渐减量。一般来说,克林霉素给药6周。疗程从4周至12周不等。15例患者出现治疗副作用。其中6例抱怨腹泻和胃肠道出血,7例出现过敏性皮疹和痤疮。轻度淋巴细胞减少和肝毒性是进一步的并发症。8例患者不得不停药;4例因胃肠道不适停药,3例因过敏性皮疹停药,1例因轻度肝毒性停药。我们在治疗期间未观察到任何严重并发症。只有9例并发症可归因于克林霉素,停药后立即消失。