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Michael Doumit

Explore the profile of Michael Doumit including associated specialties, affiliations and a list of published articles. Areas
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Articles 17
Citations 110
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Recent Articles
1.
Doumit M, Pacey V, Jaffe A, Gray K
Respir Med . 2024 Nov; 234():107847. PMID: 39490937
Background: Cystic fibrosis (CF) outpatient care has evolved into a hybrid model, incorporating telehealth and face-to-face reviews. This study explores the acceptability of the hybrid model of care from the...
2.
Southern K, Addy C, Bell S, Bevan A, Borawska U, Brown C, et al.
J Cyst Fibros . 2023 Dec; 23(1):12-28. PMID: 38129255
This is the second in a series of four papers updating the European Cystic Fibrosis Society (ECFS) standards for the care of people with CF. This paper focuses on establishing...
3.
Doumit M, Strachan R, Lazarus R, Middleton P, Dentice R, Marouvo J, et al.
Health Serv Insights . 2023 Oct; 16:11786329231205145. PMID: 37854074
Background: Standard of care recommend that patients with cystic fibrosis (CF) require screening investigations to assess for complications. Changing models of care due to the COVID19 pandemic may have impacted...
4.
McKay I, van Dorst J, Katz T, Doumit M, Prentice B, Owens L, et al.
Gut Microbes . 2022 Dec; 15(1):2156254. PMID: 36573804
Cystic fibrosis (CF) is a multisystem, autosomal, recessive disease primarily affecting the lungs, pancreas, gastrointestinal tract, and liver. Whilst there is increasing evidence of a microbial 'gut-lung axis' in chronic...
5.
Doumit M, Chuang S, Middleton P, Selvadurai H, Sivam S, Ruseckaite R, et al.
J Cyst Fibros . 2022 Sep; 22(3):581-586. PMID: 36163166
Background: The onset of the COVID-19 pandemic was associated with restricted community movement and limited access to healthcare facilities, resulting in changed clinical service delivery to people with cystic fibrosis...
6.
Doumit M, Ledwos R, Plush L, Chuang S, Gray M, Jaffe A, et al.
Arch Dis Child . 2022 Mar; 107(8):752-754. PMID: 35277380
Objective: To investigate the validity and home use of a personal ultrasonic spirometer. Methods: Supervised spirometry was performed using laboratory equipment and a personal ultrasonic spirometer. In addition, the ability...
7.
Doumit M, Cox A, Butler J, Luxton N, Jaffe A, Chuang S
Pediatrics . 2021 Nov; 148(6). PMID: 34814163
No abstract available.
8.
Coffey M, McKay I, Doumit M, Chuang S, Adams S, Stelzer-Braid S, et al.
BMJ Open . 2020 Apr; 10(4):e033916. PMID: 32295774
Introduction: Chronic gastrointestinal and respiratory conditions of childhood can have long-lasting physical, psychosocial and economic effects on children and their families. Alterations in diet and intestinal and respiratory microbiomes may...
9.
Prentice B, Wales S, Doumit M, Owens L, Widger J
Pediatr Pulmonol . 2019 Sep; 54(12):1921-1926. PMID: 31475469
Background: Children with cystic fibrosis (CF) are routinely managed in a multidisciplinary clinic at tertiary pediatric centers. However, children with bronchiectasis may not be managed in the same way. We...
10.
Fitzgerald D, Doumit M, Abel F
Paediatr Respir Rev . 2018 Nov; 28:11-17. PMID: 30414815
Spinal muscular atrophy [SMA] is the most common genetic cause of childhood mortality, primarily from the most severe form SMA type 1. It is a severe, progressive motor neurone disease,...