Neuromuscular disorders : NMD · 2021
A web-based questionnaire survey on the influence of coronavirus disease-19 on the care of patients with muscular dystrophy.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Matsumura Tsuyoshi, Takada Hiroto, Kobayashi Michio, Nakajima Takashi, Ogata Katsuhisa, Nakamura Akinori, Funato Michinori, Kuru Satoshi, Komai Kiyonobu, Futamura Naonobu, Adachi Yoshiki, Arahata Hajime, Fukudome Takayasu, Ishizaki Masatoshi, Suwazono Shugo, Aoki Masashi, Matsuura Tohru, Takahashi Masanori P, Sunada Yoshihide, Hanayama Kouzou, Hashimoto Hiroya, Nakamura Harumasa
Аннотация
To clarify the influence of coronavirus disease-19 (COVID-19) on the care of muscular dystrophy patients, we performed a questionnaire survey that was posted on the internet on May 11, 2020. By the end of July 2020, 542 responses had been collected. Approximately 30% of patients postponed regular consultations, and one-quarter of patients who received consultation more than once a month used telephone consultations. Two of 84 patients with Duchenne muscular dystrophy had reduced their steroid doses. A shortage of ventilator accessories and infection protection equipment occurred following the onset of COVID-19, and this shortage had a serious impact on medical care and infection prevention measures. Reductions in rehabilitation and other services, and avoidance of outings, led to a decrease in exercise and an increase in caregiver burden. Inpatients were restricted from going out and visiting family members. More than 20% of patients reported physical or mental complaints; however, few required treatment. COVID-19 has seriously affected the activities and quality of life of patients with muscular dystrophy. We will continue this survey and analyze the longitudinal changes.