Literature DB >> 23536257

The views of Pakistani doctors regarding genetic counseling services - is there a future?

Myla Ashfaq1, Farhana Amanullah, Ayesha Ashfaq, Kelly E Ormond.   

Abstract

Pakistan is a densely populated country in South Asia with a high burden of genetic disease. A dearth of medical genetic services exists and master's level trained genetic counselors (GCs) are currently not a part of the healthcare system. This study is the first to determine the views of Pakistani medical doctors (MDs) towards genetic counseling services in Pakistan, including what manner a master's level genetic counselor might be incorporated into the healthcare system. Fifty-one MDs practicing in the city of Karachi completed a self-administered survey of twenty questions. Of the 49 respondents who answered a specific question, 100 % (49/49) felt that they would refer at least some, if not all, of their relevant patients to a genetic's clinic if one existed in Karachi. Overall, the respondents showed a positive attitude towards the provision of genetic counseling services as a part of the healthcare system of Pakistan. Some of the proposed roles identified specifically for GCs included: explaining how Down syndrome occurs (66.1 %), discussing genes associated with breast cancer (77.4 %), and explaining the inheritance pattern of β-thalassemia (65.5 %). In contrast, the review of medical and family history and discussion of medical procedures such as ultrasound and amniocentesis were typically seen as the role of a physician. A majority of the respondents (98 %) were in favor of premarital carrier screening for thalassemia and would refer patients to a GC to describe the importance of carrier screening (84.3 %) and to help explain carrier screening results (94.1 %). Many respondents selected GCs as the ideal provider of education and support for people with inherited conditions (43.8 %), followed by specialist MDs (26 %) and general physicians (22.9 %). Considering the high burden of genetic disease in the country, we encourage the development of genetic counseling services in Pakistan.

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Year:  2013        PMID: 23536257     DOI: 10.1007/s10897-013-9578-2

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  16 in total

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Journal:  J Genet Couns       Date:  2009-10-09       Impact factor: 2.537

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Journal:  Prenat Diagn       Date:  2006-10       Impact factor: 3.050

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Authors:  Faiza Ahmed; Sadia Mahmud; Juanita Hatcher; Shaista M Khan
Journal:  BMC Nurs       Date:  2006-09-19
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3.  Novel C8orf37 mutations cause retinitis pigmentosa in consanguineous families of Pakistani origin.

Authors:  Zeinab Ravesh; Mohammed E El Asrag; Nicole Weisschuh; Martin McKibbin; Peggy Reuter; Christopher M Watson; Britta Baumann; James A Poulter; Sundus Sajid; Evangelia S Panagiotou; James O'Sullivan; Zakia Abdelhamed; Michael Bonin; Mehdi Soltanifar; Graeme C M Black; Muhammad Amin-ud Din; Carmel Toomes; Muhammad Ansar; Chris F Inglehearn; Bernd Wissinger; Manir Ali
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