» Articles » PMID: 34876494

Improving Access and Guideline Adherence in Pulmonary Care in Patients With Duchenne Muscular Dystrophy

Overview
Journal Respir Care
Publisher Mary Ann Liebert
Specialty Pulmonary Medicine
Date 2021 Dec 8
PMID 34876494
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Duchenne muscular dystrophy (DMD) is a devastating, progressive neuromuscular disease that results in cardiopulmonary failure and death. In 2018, the DMD Care Considerations guidelines were updated to improve the multidisciplinary approach to care and promote early respiratory management. We sought to evaluate the impact of a multidisciplinary clinic on access to pulmonary care and adherence to respiratory care guidelines.

Methods: Utilizing retrospective data, we assessed for pulmonary care between 2016-2019 and congruence with guidelines from March 2018-February 2019. Using a standardized visit protocol, subjects were monitored for adherence to pulmonary function testing (PFT) and polysomnography (PSG) recommendations.

Results: Of the 84 subjects with DMD, only 51.2% had prior pulmonary involvement, and approximately one-third were seen in the year prior to clinic onset. Only 23% of subjects with a pulmonary referral completed this visit. After clinic initiation, the average age of a subject's first pulmonary contact decreased from 11.8 y to 7.9 y ( < .001), and 45% of the 77 unique clinic subjects had no previous pulmonary encounter. Adherence to PFT guidelines increased in both ambulatory (8.7% to 86.1%) and non-ambulatory subjects (25.9% to 90.1%). Approximately 79% of subjects seen in clinic either completed or had an order for PSG in the last 12 months.

Conclusions: Development of a multispecialty clinic expanded access to pulmonary care and evaluation in subjects with DMD. Continued care in this clinic will allow a better understanding of barriers to access and the opportunity to monitor long-term pulmonary health.

Citing Articles

Unveiling the Respiratory Muscle Strength in Duchenne Muscular Dystrophy: The Impact of Nutrition and Thoracic Deformities, Beyond Spirometry.

Yuksel Kalyoncu M, Gokdemir Y, Yilmaz Yegit C, Yanaz M, Gulieva A, Selcuk M Children (Basel). 2024; 11(8).

PMID: 39201929 PMC: 11352812. DOI: 10.3390/children11080994.


COVID-19 Mimics Pulmonary Dysfunction in Muscular Dystrophy as a Post-Acute Syndrome in Patients.

Tyagi S, Pushpakumar S, Sen U, Mokshagundam S, Kalra D, Saad M Int J Mol Sci. 2023; 24(1).

PMID: 36613731 PMC: 9820572. DOI: 10.3390/ijms24010287.


The mobile sleep medicine model in neurologic practice: Rationale and application.

Boulos M, Chi L, Chernyshev O Front Neurol. 2022; 13:1032463.

PMID: 36388176 PMC: 9650181. DOI: 10.3389/fneur.2022.1032463.

References
1.
Tzeng A, Bach J . Prevention of pulmonary morbidity for patients with neuromuscular disease. Chest. 2000; 118(5):1390-6. DOI: 10.1378/chest.118.5.1390. View

2.
LoMauro A, DAngelo M, Aliverti A . Assessment and management of respiratory function in patients with Duchenne muscular dystrophy: current and emerging options. Ther Clin Risk Manag. 2015; 11:1475-88. PMC: 4592047. DOI: 10.2147/TCRM.S55889. View

3.
Andrews J, Soim A, Pandya S, Westfield C, Ciafaloni E, Fox D . Respiratory Care Received by Individuals With Duchenne Muscular Dystrophy From 2000 to 2011. Respir Care. 2016; 61(10):1349-59. DOI: 10.4187/respcare.04676. View

4.
EMERY A . Population frequencies of inherited neuromuscular diseases--a world survey. Neuromuscul Disord. 1991; 1(1):19-29. DOI: 10.1016/0960-8966(91)90039-u. View

5.
Katz S, McKim D, Hoey L, Barrowman N, Kherani T, Kovesi T . Respiratory management strategies for Duchenne muscular dystrophy: practice variation amongst Canadian sub-specialists. Pediatr Pulmonol. 2012; 48(1):59-66. DOI: 10.1002/ppul.22548. View