4.4 Review

How Many Cancer Patients Use Complementary and Alternative Medicine: A Systematic Review and Metaanalysis

Journal

INTEGRATIVE CANCER THERAPIES
Volume 11, Issue 3, Pages 187-203

Publisher

SAGE PUBLICATIONS INC
DOI: 10.1177/1534735411423920

Keywords

complementary therapies; complementary and alternative medicine; systematic review; prevalence; alternative medicine; CAM use; cancer

Funding

  1. FP5 project Concerted Action for Complementary and Alternative Medicine Assessment in the Cancer Field (CAM-Cancer)
  2. Quality of Life and Management of Living Resources programme, European Commission [QLRT-2001-00786]
  3. AG Biologische Krebstherapie, Deutsche Krebshilfe [70-301]

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Background. No comprehensive systematic review has been published since 1998 about the frequency with which cancer patients use complementary and alternative medicine (CAM). Methods. MEDLINE, AMED, and Embase databases were searched for surveys published until January 2009. Surveys conducted in Australia, Canada, Europe, New Zealand, and the United States with at least 100 adult cancer patients were included. Detailed information on methods and results was independently extracted by 2 reviewers. Methodological quality was assessed using a criteria list developed according to the STROBE guideline. Exploratory random effects metaanalysis and metaregression were applied. Results. Studies from 18 countries (152; >65 000 cancer patients) were included. Heterogeneity of CAM use was high and to some extent explained by differences in survey methods. The combined prevalence for current use of CAM across all studies was 40%. The highest was in the United States and the lowest in Italy and the Netherlands. Metaanalysis suggested an increase in CAM use from an estimated 25% in the 1970s and 1980s to more than 32% in the 1990s and to 49% after 2000. Conclusions. The overall prevalence of CAM use found was lower than often claimed. However, there was some evidence that the use has increased considerably over the past years. Therefore, the health care systems ought to implement clear strategies of how to deal with this. To improve the validity and reporting of future surveys, the authors suggest criteria for methodological quality that should be fulfilled and reporting standards that should be required.

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