Emergence and Evolution of Labor Pain Concern During Pregnancy: A Longitudinal Prospective Cohort Study

ABSTRACT

Background The evolving nature of patient concerns during pregnancy and delivery, including labor pain, plays a key role in guiding antenatal counseling about labor and delivery, but the timing of these concerns has not been well characterized. Understanding when labor pain becomes a prominent concern for pregnant patients can inform the timing of antenatal education about labor analgesia.

Objective This study aimed to determine how labor pain ranks among pregnancy-related concerns identified by nulliparous pregnant patients and how the relative prominence of these concerns changes across gestation.

Method We conducted a prospective, single-center longitudinal cohort study of 53 English-speaking, nulliparous patients. Participants ranked their top seven concerns from a list of 13 pregnancy-related concerns, including labor pain, at 20, 24-, 28-, 32-, and 36-weeks’ gestation. Rankings were scored from 1 (lowest-ranked concern) to 7 (highest-ranked concern), with the six unranked concerns assigned a score of zero. Changes in labor pain concern scores over time were assessed using linear mixed-effects models, adjusting for maternal characteristics and pregnancy- and fetal-related complications.

Results The score for concern about labor pain management increased with advancing gestational age, with mean adjusted rank scores increasing from 1.4 at 20 weeks to 3.8 at 36 weeks (P < 0.001). No demographic or clinical covariates were significantly associated with labor pain score. Peak scores were most commonly reported at 28- and 36-weeks’ gestation.

Discussion While labor pain became a greater salient concern along pregnancy, for some nulliparous patients, concern about labor pain arose as early as 20th week gestation, with significant individual variation in the timing of these concerns.

Competing Interest Statement

Conflicts of Interest/Competing Interest: Dr. Alexander Butwick received honorarium from Edwards Lifesciences for consulting work.

Funding Statement

This study did not receive any funding

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

Ethics committee/IRB of University of California San Francisco gave ethical approval for this work.

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

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I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

Data Availability

All data produced in the present study are available upon reasonable request to the authors

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