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Might Rare Factors Account for Most of the Mortality of Preterm Babies?

Basso, Olgaa,b,c; Wilcox, Allen J.a

doi: 10.1097/EDE.0b013e31821266c5
Reproduction: Original Article

Background: Preterm delivery has a variety of causes, with each of these presumably carrying its own mortality risk. To the extent that they add to the risk of mortality, the various pathologic factors triggering preterm delivery will confound the causal contribution of gestational age to mortality, inflating the observed rates of gestational-age-specific mortality. We have previously estimated that about half of the mortality of US preterm singletons may be due to unmeasured pathologies that increase mortality risk and also cause preterm birth. In this paper, we examine the impact that rare factors may have, at least in theory, on preterm mortality.

Methods: We constructed a simple model of gestational-age-specific mortality, in which we arbitrarily selected a function to represent the mortality due to immaturity alone (“baseline” risk). We then added “unmeasured” confounding factors that cause mortality and also cause preterm birth. This construct allowed us to calculate, in simple scenarios, the proportion of preterm mortality that could be caused by unmeasured confounding.

Results: We found that rare pathologies with moderate-to-strong effects can substantially contribute to preterm mortality. The presence of such rare factors can also produce an intersection of gestational-age-specific mortality curves when stratifying by known risk factors.

Conclusions: It is possible that a few relatively rare factors may account for a large fraction of preterm mortality. The search for such factors should be a primary focus of future research on preterm delivery.

Author Information

From the aEpidemiology Branch, NIEHS, Durham, NC; bDepartment of Obstetrics and Gynecology, Royal Victoria Hospital, McGill University, Montreal, Quebec, Canada; and cDepartment of Epidemiology, Biostatistics, and Occupational Health, McGill University, Montreal, Quebec, Canada.

Submitted 7 July 2010; accepted 9 November 2010; posted 3 March 2011.

Supported in part by the Intramural program of the NIH, National Institute of Environmental Health Sciences (Z01 ES044003).

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Correspondence: Olga Basso, Department of Obstetrics and Gynecology, Royal Victoria Hospital, McGill University, 687 Pine Ave West, Room F9.05, Montreal, Quebec, H3A 1A1, Canada. E-mail:

© 2011 Lippincott Williams & Wilkins, Inc.