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Establishment of a thalassaemia major quality improvement collaborative in Pakistan
Zahra Hoodbhoy1, Lubaina Ehsan2, Najveen Alvi1
1Department of Paediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
Insights
This study established a quality improvement collaborative for transfusion-dependent thalassaemia (TDT) patients in Pakistan. It revealed significant iron overload and inadequate chelation therapy, highlighting the need for standardized care to improve TDT patient outcomes.
Area of Science:
- Hematology
- Cardiology
- Endocrinology
- Quality Improvement Science
Background:
- Transfusion-dependent thalassaemia (TDT) requires lifelong transfusions, leading to iron overload.
- Multidisciplinary care is crucial for managing TDT complications.
- Resource-constrained settings face unique challenges in providing optimal TDT care.
Purpose of the Study:
- To establish a multidisciplinary quality improvement (QI) collaborative for TDT patients in a resource-limited setting.
- To characterize baseline patient data and identify key areas for intervention.
- To implement and evaluate QI interventions aimed at reducing TDT-related morbidity and mortality.
Main Methods:
- A TDT QI collaborative database was created, enrolling 295 patients from four centers in Karachi, Pakistan.
- Data collected included cardiac and endocrine symptoms, anthropometry, chelation therapy status, echocardiography, T2* cardiac MRI (CMR), and serum ferritin.
- Interventions were designed to address identified drivers of poor outcomes.
Main Results:
- 52% of patients had severe myocardial iron overload (T2* <10 ms).
- 58% were not receiving adequate chelation therapy.
- Cardiac symptoms were common (NYHA class 2), with no significant differences in echocardiographic measures across iron overload spectrums.
Conclusions:
- Significant iron siderosis burden exists in TDT patients in this setting.
- Inadequate iron load assessment and standardized management were identified as critical issues.
- The QI-based TDT registry and its targeted interventions offer a unique approach to improving patient care.
Objectives:
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.
Design And Setting:
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.
Results:
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.
Conclusion:
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.
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