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[儿童溃疡性结肠炎。治疗期间柳氮磺胺吡啶和磺胺吡啶的水平]

[Ulcerative colitis in children. Levels of salicylazosulfapyridine and sulfapyridine during treatment].

作者信息

Guastavino E, Litwin N H, Heffes Nahmod L, Licastro R

机构信息

Hospital Nacional Prof. Alejandro Posadas, Servicio de Pediatría, Buenos Aires, Argentina.

出版信息

Acta Gastroenterol Latinoam. 1988;18(2):107-13.

PMID:2908013
Abstract

Salicylazosulfapyridine (SASP) is a drug used in the treatment of ulcerative colitis (UC) owing to the therapeutic action of the 5-aminosalicylic acid produced by the splitting of the molecule in the cecum, which also yields the absorbable compound Sulphapyridine (SP). The aim of our work was to assess the levels of the drug in blood (SASP and SP), to correlate them with undesirable effects in any, to verify their fluctuations in the dosing interval and to investigate the extent of the excretion of the drug in the children who were studied. 10 children (6 to 16 years) with UC, who were treated with SASP (dOsage schedule 0.5-2.0 g/day in a 12 hours interval), were studied. Blood levels of SASP and SP were assessed at 6 and 12 hours after doses, and total fecal excretion of SASP was determines in 24 hs specimens. All the determinations were performed according to Hansson and Sandberg. SP plasma levels were 17.7 +/- 9.0 ug/ml (range 6.8-36.3 ug/ml) at 6 hours after doses. and 14.1 +/- 7.2 ug/ml (range 5.7-25.0 ug/ml) at 12 hours after doses. SASP plasma levels were 15.5 +/- 15.4 ug/ml (range 2.1-53.4 ug/ml) at 6 hours after doses, and 14.0 +/- 20.4 ug/ml (range 3.9-70.7 ug/ml) at 12 hours after doses. The 24 hours fecal excretion was 17.4 to 236 mg. These values were correlated with the given doses (r = 0.88) calculated as SASP g/m2 body surface 24 hs. There was no statistical correlation between doses and SP or SASP levels in this group, and the respective levels of SASP and SP at 6 and 12 hours after doses showed no significative differences.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

柳氮磺胺吡啶(SASP)是一种用于治疗溃疡性结肠炎(UC)的药物,这是因为该分子在盲肠中分解产生的5-氨基水杨酸具有治疗作用,同时还会产生可吸收的化合物磺胺吡啶(SP)。我们研究的目的是评估血液中该药物(SASP和SP)的水平,将其与不良反应进行关联,验证其在给药间隔内的波动情况,并研究该药物在受试儿童中的排泄程度。对10名患有UC的儿童(6至16岁)进行了研究,他们接受SASP治疗(给药方案为0.5 - 2.0克/天,每12小时一次)。在给药后6小时和12小时评估SASP和SP的血液水平,并在24小时的粪便样本中测定SASP的总粪便排泄量。所有测定均按照汉森和桑德伯格的方法进行。给药后6小时,SP血浆水平为17.7±9.0微克/毫升(范围为6.8 - 36.3微克/毫升),给药后12小时为14.1±7.2微克/毫升(范围为5.7 - 25.0微克/毫升)。给药后6小时,SASP血浆水平为15.5±15.4微克/毫升(范围为2.1 - 53.4微克/毫升),给药后12小时为14.0±20.4微克/毫升(范围为3.9 - 70.7微克/毫升)。24小时粪便排泄量为17.4至236毫克。这些值与以SASP克/平方米体表面积24小时计算的给定剂量相关(r = 0.88)。该组中剂量与SP或SASP水平之间无统计学相关性,给药后6小时和12小时SASP和SP的各自水平也无显著差异。(摘要截断于250字)

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