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儿童特发性肺含铁血黄素沉着症复发的临床特征及危险因素。

Clinical features and risk factors for recurrence of idiopathic pulmonary hemosiderosis in children.

机构信息

Division of Pediatric Pulmonology and Immunology, West China Second University Hospital, Sichuan University, Chengdu, 610041, China.

Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education, Chengdu, 610041, China.

出版信息

BMC Pulm Med. 2024 Sep 19;24(1):461. doi: 10.1186/s12890-024-03267-4.

Abstract

BACKGROUND

This study aims to review the clinical characteristics, therapeutic response and outcome of idiopathic pulmonary hemosiderosis (IPH), and discover the risk factors for recurrence in children with IPH, which will be helpful for the early diagnosis and reasonable treatment of this disease.

METHODS

Children with a diagnosis of IPH were enrolled in the study. Clinical data of the children were collected and analysed.

RESULTS

A total of 32 patients with regular follow-up after diagnosis were included in this study. Anaemia, cough and haemoptysis constituted the most common initial symptoms of the disease, and the incidences were 90.6%, 75% and 56.2%, respectively. The mean gap between the onset of symptoms and diagnosis was 5 (0.25-36) months. Most of the children experienced remission (complete and partial remission) over the course of 6 months of treatment, but 19 of the children experienced relapse. The causes of disease recurrence included respiratory tract infection (37.5%), corticosteroid (CS) reduction (18.8%), and irregular medication (6.3%). Interestingly, we found that children with history of allergy (HR 4.255, 1.107-16.356) tended to experience disease recurrence (p = 0.01).

CONCLUSIONS

Cough and anaemia are the most common symptoms in children with IPH. The recurrence rate of this disease is high, and respiratory tract infection is the most common cause of its recurrence. High-dose CS impluse therapy cannot reduce the recurrence rate of the disease. Allergic history was an import factor associated with disease recurrence.

TRIAL REGISTRATION

This study is a retrospective and observational study, which does not involve human specimens or clinical intervention. Therefore, clinical trial registration is not required, and there is no clinical trial number. However, the study was approved by the Institutional Review Board/Ethics Committee affiliated with West China Second University Hospital, Sichuan University (Ethics review number 2022074).

摘要

背景

本研究旨在回顾特发性肺含铁血黄素沉着症(IPH)的临床特征、治疗反应和转归,并发现 IPH 患儿复发的危险因素,这将有助于该疾病的早期诊断和合理治疗。

方法

纳入诊断为 IPH 的患儿,收集并分析患儿的临床资料。

结果

本研究共纳入 32 例定期随访的患儿。贫血、咳嗽和咯血是疾病最常见的首发症状,发生率分别为 90.6%、75%和 56.2%。症状出现至确诊的平均间隔时间为 5(0.25-36)个月。大多数患儿在 6 个月的治疗过程中经历了缓解(完全和部分缓解),但有 19 例患儿复发。疾病复发的原因包括呼吸道感染(37.5%)、皮质类固醇(CS)减量(18.8%)和不规则用药(6.3%)。有趣的是,我们发现有过敏史的患儿(HR 4.255,1.107-16.356)更容易发生疾病复发(p=0.01)。

结论

咳嗽和贫血是 IPH 患儿最常见的症状。该病复发率高,呼吸道感染是其最常见的复发原因。大剂量 CS 冲击治疗不能降低疾病的复发率。过敏史是与疾病复发相关的重要因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfc4/11411803/f506e9a94f8e/12890_2024_3267_Fig1_HTML.jpg

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