Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2004 Jul 19:4:19.
doi: 10.1186/1471-2288-4-19.

Assessing harmful effects in systematic reviews

Affiliations

Assessing harmful effects in systematic reviews

Heather M McIntosh et al. BMC Med Res Methodol. .

Abstract

Background: Balanced decisions about health care interventions require reliable evidence on harms as well as benefits. Most systematic reviews focus on efficacy and randomised trials, for which the methodology is well established. Methods to systematically review harmful effects are less well developed and there are few sources of guidance for researchers. We present our own recent experience of conducting systematic reviews of harmful effects and make suggestions for future practice and further research.

Methods: We described and compared the methods used in three systematic reviews. Our evaluation focused on the review question, study designs and quality assessment.

Results: One review question focused on providing information on specific harmful effects to furnish an economic model, the other two addressed much broader questions. All three reviews included randomised and observational data, although each defined the inclusion criteria differently. Standard methods were used to assess study quality. Various practical problems were encountered in applying the study design inclusion criteria and assessing quality, mainly because of poor study design, inadequate reporting and the limitations of existing tools. All three reviews generated a large volume of work that did not yield much useful information for health care decision makers. The key areas for improvement we identified were focusing the review question and developing methods for quality assessment of studies of harmful effects.

Conclusions: Systematic reviews of harmful effects are more likely to yield information pertinent to clinical decision-making if they address a focused question. This will enable clear decisions to be made about the type of research to include in the review. The methodology for assessing the quality of harmful effects data in systematic reviews requires further development.

PubMed Disclaimer

References

    1. Ernst E. Pittler MH Assessment of therapeutic safety in systematic reviews: literature review. BMJ. 2001;323:546. doi: 10.1136/bmj.323.7312.546. - DOI - PMC - PubMed
    1. Ioannidis JPA. Lau J Completeness of safety reporting in randomized trials: an evaluation of 7 medical areas. JAMA. 2001;285:437–443. - PubMed
    1. Loke YK. Derry S Reporting of adverse drug reactions in randomised controlled trials - a systematic survey. BMC Clin Pharmacol. 2001;1:3. doi: 10.1186/1472-6904-1-3. - DOI - PMC - PubMed
    1. Cuervo GL. Clarke M Balancing benefits and harms in health care. BMJ. 2003;327:65–66. doi: 10.1136/bmj.327.7406.65. - DOI - PMC - PubMed
    1. Aronson JK. Derry S. Loke YK Adverse drug reactions: keeping up to date. Fundam Clin Pharmacol. 2002;16:49–56. doi: 10.1046/j.1472-8206.2002.00066.x. - DOI - PubMed

MeSH terms