Referral Rates and Diagnostic Evaluation for Primary Ciliary Dyskinesia in Patients With Laterality Defects Who Meet Primary Ciliary Dyskinesia Evaluation Criteria.

IF 2.7 3区 医学 Q1 PEDIATRICS
Alyssa K Salinas, Gerard Smits, Stephen B Spurgin, Tanya M Martínez-Fernandez, Yadira M Rivera-Sánchez
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引用次数: 0

Abstract

Objective: To determine if pediatric patients with laterality defects and meet the diagnostic criteria for primary ciliary dyskinesia (PCD) evaluation are being referred to and evaluated by pediatric pulmonologists. There are organ laterality defects in 50% of patients with PCD. Thus, patients with laterality defects are more likely to raise suspicion for PCD than those without laterality defects. We hypothesize that even in patients with laterality defects who meet PCD evaluation criteria, referral rates are low, leading to underdiagnosis (2).

Subjects and methods: A retrospective chart review of patients with laterality defects who met two or more of the PCD evaluation criteria was conducted at Dallas Children's Health using the electronic medical record. The four PCD evaluation criteria were laterality defect, chronic daily cough, nasal congestion starting in infancy, and NRDS of unclear etiology requiring oxygen or positive pressure for 24 h or longer. Referral rates to pediatric pulmonary medicine and genetics were determined. Completion of an evaluation by these services was analyzed.

Results: The electronic medical record search for laterality defects identified 433 patients. Of the 369 patients who met the inclusion and exclusion criteria for analysis, 189 (51%) met only one inclusion criterion for PCD evaluation (laterality defect), and 49% met 2 or more of the criteria. Of the 79 patients who met the bare minimum of two criteria for PCD evaluation, 41% were referred to pulmonary, 18% to genetics, and only 16% were evaluated for PCD. Of the 27 patients who met all 4 PCD criteria for evaluation, 96% were referred to pulmonary, 85% to genetics, and 93% were evaluated for PCD. Among the 369 patients studied, there were no significant differences in the referral rate associated with patient demographics, including sex, race, ethnicity, and insurance type. The frequency of referrals increased with the number of PCD criteria.

Conclusions: A substantial number of pediatric patients meeting two PCD referral criteria are not referred to pediatric pulmonologists, and a larger number are not being evaluated for PCD. As expected, patients with three or four PCD referral criteria have a higher rate of referral to pulmonary than those meeting the minimum two criteria. Many patients who meet all four criteria still need to be evaluated for PCD, even when referred to pulmonary or genetics. Most of the patients with laterality defects had congenital heart disease (CHD), and this was identified as the main etiology for respiratory symptoms for most of the patients who were not referred or evaluated. This highlights the importance of PCD education and awareness efforts for Pediatric specialists and subspecialists, including pediatric pulmonologists. It supports PCD being an underdiagnosed chronic condition and thus underscores the importance of acute clinical awareness and lower threshold to refer and evaluate patients for PCD, especially when other diagnoses, such as CHD are present.

符合原发性纤毛运动障碍评估标准的侧侧缺陷患者原发性纤毛运动障碍的转诊率和诊断评价。
目的:了解小儿肺科医师是否会诊并评估具有侧翼缺损且符合原发性纤毛运动障碍(PCD)诊断标准的患儿。50%的PCD患者存在器官侧侧缺损。因此,有侧侧缺损的患者比没有侧侧缺损的患者更容易引起对PCD的怀疑。我们假设,即使在侧侧缺陷符合PCD评估标准的患者中,转诊率也很低,导致诊断不足(2)。研究对象和方法:在达拉斯儿童健康中心使用电子病历对满足两个或两个以上PCD评估标准的侧侧缺陷患者进行回顾性图表回顾。PCD的4个评价标准为侧侧缺损、慢性每日咳嗽、婴儿期开始的鼻塞、病因不明需要吸氧或正压24小时及以上的NRDS。对儿童肺部医学和遗传学的转诊率进行了测定。分析了这些服务的评估完成情况。结果:通过电子病历检索发现侧位缺陷患者433例。在符合纳入和排除标准的369例患者中,189例(51%)仅符合PCD评估的一项纳入标准(侧性缺损),49%符合2项或以上标准。在79名符合PCD评估最低两项标准的患者中,41%被转介到肺部,18%被转介到遗传学,只有16%被评估为PCD。在27例符合所有4项PCD评估标准的患者中,96%转至肺部,85%转至遗传学,93%转至PCD评估。在研究的369名患者中,转诊率与患者人口统计数据(包括性别、种族、民族和保险类型)没有显著差异。转介的频率随着PCD标准的数量而增加。结论:大量符合两项PCD转诊标准的儿科患者没有转诊给儿科肺科医生,更多的患者没有接受PCD评估。正如预期的那样,具有三个或四个PCD转诊标准的患者转诊到肺部的比例高于满足最低两个标准的患者。许多符合所有四项标准的患者仍然需要对PCD进行评估,即使涉及肺部或遗传学。大多数侧侧缺损患者患有先天性心脏病(CHD),这被确定为大多数未转诊或评估的患者呼吸道症状的主要病因。这突出了PCD教育和意识努力对儿科专家和亚专家,包括儿科肺科医生的重要性。它支持PCD是一种未被诊断的慢性疾病,因此强调了急性临床意识和较低的转诊和评估PCD患者的重要性,特别是当其他诊断(如冠心病)存在时。
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来源期刊
Pediatric Pulmonology
Pediatric Pulmonology 医学-呼吸系统
CiteScore
6.00
自引率
12.90%
发文量
468
审稿时长
3-8 weeks
期刊介绍: Pediatric Pulmonology (PPUL) is the foremost global journal studying the respiratory system in disease and in health as it develops from intrauterine life though adolescence to adulthood. Combining explicit and informative analysis of clinical as well as basic scientific research, PPUL provides a look at the many facets of respiratory system disorders in infants and children, ranging from pathological anatomy, developmental issues, and pathophysiology to infectious disease, asthma, cystic fibrosis, and airborne toxins. Focused attention is given to the reporting of diagnostic and therapeutic methods for neonates, preschool children, and adolescents, the enduring effects of childhood respiratory diseases, and newly described infectious diseases. PPUL concentrates on subject matters of crucial interest to specialists preparing for the Pediatric Subspecialty Examinations in the United States and other countries. With its attentive coverage and extensive clinical data, this journal is a principle source for pediatricians in practice and in training and a must have for all pediatric pulmonologists.
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