Nonserious Adverse Events in Randomized Trials with Opioid-Dependent Pregnant Women: Direct versus Indirect Measurement

Hendrée E. Jones, Karol Kaltenbach, Sarah H. Heil, Susan M. Stine, Mara G. Coyle, Amelia M. Arria, Kevin E. O'Grady, Peter Selby, Peter R. Martin

Research output: Contribution to journalArticle

Abstract

Background and Objectives: How best to measure the occurrence of adverse events during a randomized clinical trial is an issue that has not been adequately examined in the research literature. Focus of this study was on the examination of the relative frequency of occurrence of adverse events directly recorded during the conduct of the trial compared to an indirect determination of adverse events derived from data collected as part of the trial. Methods: A secondary analysis of nonserious adverse events that occurred in the Maternal Opioid Treatment: Human Experimental Research (MOTHER) Study was undertaken. MOTHER was a randomized clinical trial of methadone versus buprenorphine in 175 opioid-dependent pregnant women. Results: The two methods of recording adverse events failed to agree on where differences in the frequency of occurrence of adverse events between the medication conditions might exist. Moreover, indirect assessment indicated all participants had experienced at least one adverse event, yet indirect coverage of adverse events was incomplete. Conclusions: Findings suggest indirect examination of occurrence of adverse events should be cautiously undertaken, because indirect assessment of adverse events makes no distinction between what might be simply typical variation in behavior rather than systematic changes in behavior attributable to study condition, and lacks coverage of the full spectrum of adverse events. Scientific Significance: Contemporaneous direct measurement of adverse events likely yield reasonably valid estimates of the rate of occurrence of the adverse events, while indirect measu-rement of adverse events may not be sufficiently reliable. (Am J Addict 2012;21:S1-S4)

Original languageEnglish (US)
Pages (from-to)S1-S4
JournalAmerican Journal on Addictions
Volume21
DOIs
StatePublished - Nov 1 2012

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Opioid Analgesics
Pregnant Women
Randomized Controlled Trials
Research
Mothers
Buprenorphine
Methadone
Therapeutics

ASJC Scopus subject areas

  • Medicine (miscellaneous)
  • Psychiatry and Mental health
  • Clinical Psychology
  • Medicine(all)

Cite this

Nonserious Adverse Events in Randomized Trials with Opioid-Dependent Pregnant Women : Direct versus Indirect Measurement. / Jones, Hendrée E.; Kaltenbach, Karol; Heil, Sarah H.; Stine, Susan M.; Coyle, Mara G.; Arria, Amelia M.; O'Grady, Kevin E.; Selby, Peter; Martin, Peter R.

In: American Journal on Addictions, Vol. 21, 01.11.2012, p. S1-S4.

Research output: Contribution to journalArticle

Jones, HE, Kaltenbach, K, Heil, SH, Stine, SM, Coyle, MG, Arria, AM, O'Grady, KE, Selby, P & Martin, PR 2012, 'Nonserious Adverse Events in Randomized Trials with Opioid-Dependent Pregnant Women: Direct versus Indirect Measurement', American Journal on Addictions, vol. 21, pp. S1-S4. https://doi.org/10.1111/j.1521-0391.2012.00289.x
Jones, Hendrée E. ; Kaltenbach, Karol ; Heil, Sarah H. ; Stine, Susan M. ; Coyle, Mara G. ; Arria, Amelia M. ; O'Grady, Kevin E. ; Selby, Peter ; Martin, Peter R. / Nonserious Adverse Events in Randomized Trials with Opioid-Dependent Pregnant Women : Direct versus Indirect Measurement. In: American Journal on Addictions. 2012 ; Vol. 21. pp. S1-S4.
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