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DOI 10.1186/1471-2288-8-62

Медицинская библиотека · BMC medical research methodology · 2008

The HCV Synthesis Project: scope, methodology, and preliminary results.

Stern Rebecca K, Hagan Holly, Lelutiu-Weinberger Corina, Des Jarlais Don, Scheinmann Roberta, Strauss Shiela, Pouget Enrique R, Flom Peter

СтатьяМетаанализПоддержка NIH: внешняя программаОбзорПеревод в очереди

Аннотация

BACKGROUND

The hepatitis C virus (HCV) is hyper-endemic in injecting drug users. There is also excess HCV among non-injection drug users who smoke, snort, or sniff heroin, cocaine, crack, or methamphetamine.

METHODS

To summarize the research literature on HCV in drug users and identify gaps in knowledge, we conducted a synthesis of the relevant research carried out between 1989 and 2006. Using rigorous search methods, we identified and extracted data from published and unpublished reports of HCV among drug users. We designed a quality assurance system to ensure accuracy and consistency in all phases of the project. We also created a set of items to assess study design quality in each of the reports we included.

RESULTS

We identified 629 reports containing HCV prevalence rates, incidence rates and/or genotype distribution among injecting or non-injecting drug user populations published between January 1989 and December 2006. The majority of reports were from Western Europe (41%), North America (26%), Asia (11%) and Australia/New Zealand (10%). We also identified reports from Eastern Europe, South America, the Middle East, and the Caribbean. The number of publications reporting HCV rates in drug users increased dramatically between 1989 and 2006 to 27-52 reports per year after 1998.

CONCLUSION

The data collection and quality assurance phases of the HCV Synthesis Project have been completed. Recommendations for future research on HCV in drug users have come out of our data collection phase. Future research reports can enhance their contributions to our understanding of HCV etiology by clearly defining their drug user participants with respect to type of drug and route of administration. Further, the use of standard reporting methods for risk factors would enable data to be combined across a larger set of studies; this is especially important for HCV seroconversion studies which suffer from small sample sizes and low power to examine risk factors.

Для цитирования: Stern Rebecca K, Hagan Holly, Lelutiu-Weinberger Corina, Des Jarlais Don, Scheinmann Roberta, Strauss Shiela, Pouget Enrique R, Flom Peter. The HCV Synthesis Project: scope, methodology, and preliminary results.. BMC medical research methodology. 2008. DOI: 10.1186/1471-2288-8-62.

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Обработка статьи · этапы, ошибки и управление
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