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骨髓移植后肠壁囊样积气和腹腔积气的保守治疗

Conservative management of pneumatosis intestinalis and pneumoperitoneum following bone-marrow transplantation.

作者信息

Ade-Ajayi N, Veys P, Stanton M, Drake D P, Pierro A

机构信息

Surgery and Host Defence Directorates, The Great Ormond Street Hospital for Children, London WC1N 3JH, UK.

出版信息

Pediatr Surg Int. 2002 Dec;18(8):692-5. doi: 10.1007/s00383-002-0762-y. Epub 2002 Nov 20.

Abstract

Pneumatosis intestinalis (PI), with or without pneumoperitoneum (PP), may complicate allogenic bone-marrow transplantation (BMT). The aim of our study was to establish the incidence and outcome of this complication following BMT in children. A departmental database was used to identify children who underwent BMT in the 4-year period up to December 1999. The medical records of children who developed PI with or without PP were obtained for further study. All patients were managed without recourse to surgery. Conservative management included 7 days of intravenous antibiotics and 10 days of intestinal rest supported by parenteral nutrition. In the study period, 138 BMTs were carried out. Six children (4%) with a total of 7 episodes of PI/PP were identified, 1 boy and 5 girls with a median age of 8.5 years (range 0.8-11). Neutropenia was noted in 3 children at the time of presentation. Other risk factors identified included alternative BMT donors (5/6), steroid therapy (6/7), and graft-versus-host disease (5/6). Organisms were isolated from stool cultures sent at the time of diagnosis in 3 out of 7 instances. Diarrhoea was the predominant presenting symptom. All patients recovered from the acute episode, but 5 died at a mean of 12 months from the development of PI/PP (range 6-17 months). This mortality of 83% compares with a mortality of 33% (43 of 132) for the remainder of children who underwent BMT during the study period. Thus, while initial recovery can be anticipated, the medium-term mortality in this group of children is high.

摘要

肠壁积气(PI)伴或不伴气腹(PP)可能是异基因骨髓移植(BMT)的并发症。我们研究的目的是确定儿童BMT后这种并发症的发生率和结局。利用科室数据库识别在截至1999年12月的4年期间接受BMT的儿童。获取发生PI伴或不伴PP的儿童的病历以进行进一步研究。所有患者均未进行手术治疗。保守治疗包括静脉使用抗生素7天和肠道休息10天,并给予肠外营养支持。在研究期间,共进行了138例BMT。确定有6名儿童(4%)共发生7次PI/PP,其中1名男孩和5名女孩,中位年龄为8.5岁(范围0.8 - 11岁)。3名儿童在发病时出现中性粒细胞减少。确定的其他危险因素包括替代BMT供者(5/6)、类固醇治疗(6/7)和移植物抗宿主病(5/6)。7例中有3例在诊断时从粪便培养物中分离出微生物。腹泻是主要的首发症状。所有患者均从急性发作中康复,但5例在PI/PP发生后平均12个月(范围6 - 17个月)死亡。这83%的死亡率与研究期间接受BMT的其余儿童33%(132例中的43例)的死亡率相比。因此,虽然可以预期初期康复,但这组儿童的中期死亡率很高。

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