Establishment of a thalassaemia major quality improvement collaborative in Pakistan.


Journal

Archives of disease in childhood
ISSN: 1468-2044
Titre abrégé: Arch Dis Child
Pays: England
ID NLM: 0372434

Informations de publication

Date de publication:
05 2020
Historique:
received: 22 06 2018
revised: 04 12 2018
accepted: 23 12 2018
pubmed: 10 2 2019
medline: 31 7 2020
entrez: 10 2 2019
Statut: ppublish

Résumé

The aim of this study was to establish multidisciplinary care for patients with transfusion-dependent thalassaemia (TDT) by creating a TDT quality improvement (QI) collaborative in a resource-constrained setting. This study presents our initial experience of creating this collaborative, the baseline characteristics of the participants, the proposed QI interventions and the outcome metrics of the collaborative. TDT QI collaborative is a database comprising patients with TDT from four centres in Karachi, Pakistan. Study variables included symptoms of cardiac or endocrine dysfunction, physical examination including anthropometry and Tanner staging, chelation therapy, results of echocardiography, T2* cardiac MRI (CMR) and serum ferritin. The main outcome of this collaborative was improvement in TDT-related morbidity and mortality. Interventions addressing the key drivers of outcome were designed and implemented. At the time of reporting, the total number of patients in this database was 295. Most patients reported cardiac symptoms corresponding to New York Heart Association class 2. Approximately half (52%, n=153) of the patients demonstrated severe myocardial iron overload (T2* <10 ms). Majority of the patients (58%, n=175) were not on adequate chelation therapy. There was no difference in echocardiographic measures of systolic and diastolic left ventricle among the different spectrums of iron overloaded myocardium. Using T2* CMR and endocrine testing, we have identified significant burden of iron siderosis in our patients with TDT. Lack of adequate iron load assessment and standardised management was observed. Interventions designed to target these key drivers of outcome are the unique part of this QI-based TDT registry.

Identifiants

pubmed: 30737261
pii: archdischild-2018-315743
doi: 10.1136/archdischild-2018-315743
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

487-493

Informations de copyright

© Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Zahra Hoodbhoy (Z)

Department of Paediatrics and Child Health, Aga Khan University, Karachi, Pakistan.

Lubaina Ehsan (L)

Medical College, Aga Khan University, Karachi, Pakistan.

Najveen Alvi (N)

Department of Paediatrics and Child Health, Aga Khan University, Karachi, Pakistan.

Fatimah Sajjad (F)

Medical College, Aga Khan University, Karachi, Pakistan.

Aleezay Asghar (A)

Medical College, Aga Khan University, Karachi, Pakistan.

Omair Nadeem (O)

Medical College, Aga Khan University, Karachi, Pakistan.

Asim Qidwai (A)

Afzaal Memorial Thalassemia Foundation, Karachi, Pakistan.

Shabneez Hussain (S)

Laboratory and Clinical Department, Fatimid Foundation, Karachi, Pakistan.

Erum Hasan (E)

Kashif Iqbal Thalassemia Care Center, Karachi, Pakistan.

Sadaf Altaf (S)

Department of Paediatrics and Child Health, Aga Khan University, Karachi, Pakistan.

Salman Kirmani (S)

Department of Paediatrics and Child Health, Aga Khan University, Karachi, Pakistan.

Babar S Hasan (BS)

Department of Paediatrics and Child Health, Aga Khan University, Karachi, Pakistan.

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