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诊断因人而异:印度儿童黏多糖贮积症早期诊断的障碍

Diagnosis is in the Eye of the Beholder: Barriers to Early Diagnosis of Mucopolysaccharidosis in Children in India.

作者信息

Grewal Meenu, Muranjan Mamta

机构信息

Department of Pediatrics, Seth Gordhandas Sunderdas Medical College and King Edward Memorial Hospital, Parel, Mumbai, Maharashtra, India.

出版信息

J Pediatr Genet. 2020 Sep 18;10(4):300-304. doi: 10.1055/s-0040-1716707. eCollection 2021 Dec.

Abstract

The present study examined referral pattern and diagnostic practices for mucopolysaccharidosis (MPS) in India in 40 patients with a confirmed diagnosis. Time lag between age of onset of symptoms and consultation with primary physician ranged from 0 to 84 months, between consultation with primary physician and visit to genetic clinic of 0 to 128 months, from visit to genetic clinic and diagnosis of 1 to 111 months, and that between onset of symptoms and diagnosis 1 to 154 months. Major causes for delayed diagnosis were symptoms overlooked by physician (54%), late consultation by care giver (48.6%), late onset of symptoms (43.2%), and resource crunch (32.4%). Diagnosis at referral other than MPS was noted in 45%. Thus, diagnostic delay for MPS is common due to health seeking practices of parents, as well as physicians' clinical practices. Overcoming these barriers would necessitate strengthening awareness and educational activities for physicians and lay public.

摘要

本研究调查了印度40例确诊为黏多糖贮积症(MPS)患者的转诊模式和诊断方法。症状出现年龄与初次咨询医生之间的时间间隔为0至84个月,初次咨询医生与前往基因诊所就诊之间的时间间隔为0至128个月,从前往基因诊所就诊到确诊的时间间隔为1至111个月,症状出现到确诊的时间间隔为1至154个月。诊断延迟的主要原因是医生忽略症状(54%)、照顾者咨询延迟(48.6%)、症状出现较晚(43.2%)和资源短缺(32.4%)。45%的转诊诊断并非MPS。因此,由于家长的就医习惯以及医生的临床诊疗行为,MPS的诊断延迟很常见。克服这些障碍需要加强针对医生和普通公众的宣传和教育活动。

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