International Registry of Cardiovascular diseases in Women (IROCW): Assessing the feasibility of large data registry in absence of funding and electronic database; initial data from Iraq

Abstract Funding Acknowledgements Type of funding sources: None. Background There is unmet need of sex focused registries to be the first step towards sex focused trials and guidelines. In Iraq due to absent electronic database and research funding, it is challenging to initiate long term cardiovasc...

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Veröffentlicht in:European journal of preventive cardiology 2023-05, Vol.30 (Supplement_1)
Hauptverfasser: Farhan, H A S A N, Abdulkhaleq, I P E K A, Dilshad Mohammed Saeed, N A Z N A Z, Talal Yaseen, H U D A, Sabah Naji Al-Hwayzee, N O O R, Skuk, M R, Mosa Mohammad, A M E E N, Dakhil, Z A
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Sprache:eng
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Zusammenfassung:Abstract Funding Acknowledgements Type of funding sources: None. Background There is unmet need of sex focused registries to be the first step towards sex focused trials and guidelines. In Iraq due to absent electronic database and research funding, it is challenging to initiate long term cardiovascular registries. Also, for women patients follow up, it is challenging to contact them by male doctors due to cultural causes. Purpose IROCW aims to portrait the demographics focusing on sex-specific risk factors, presentation, in-hospital and 1-month outcomes of women admitted to cardiac centers or cardiology wards in general hospitals. Patients with any of the following diagnoses were included in the registry: IHD (ACS admitted to CCU or chronic coronary syndromes admitted for elective catheterization), arrhythmia, heart failure and valvular heart disease. Methods Under the Umbrella of Iraqi Scientific Council of Cardiology, a female interventional cardiologist was among leaders of the study, so, she enhanced the recruitment of female trainees besides male doctors to participate in data collection and patients follow up to bridge the cultural barriers. IROCW is a prospective, multicentre, cross-sectional study. Data collection using paper forms was done by investigators then data entry started and stopped after seven weeks to assess feasibility and reliability of data entry into google form that was designed for the registry. If the registry is feasible using paper forms and google form, then the next phase will be international and assessing 12-month cardiovascular outcomes (target number=10,000 patients; total number in all four arms of registry). Results n=150, mean age=60 years, 89.3% of patients reside in urban areas. Women were mostly married (67.8%) or widowed (25.5%). They were illiterate (47.3%) or having primary education (34.7%). 60% of women's family total income
ISSN:2047-4873
2047-4881
DOI:10.1093/eurjpc/zwad125.124