ArticleBMC pregnancy and childbirth2026
The associations between maternal disability and perinatal outcomes among Black and/or Hispanic women in PRAMS.
Article in BMC pregnancy and childbirth, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
Abstract
backgroundWomen racialized as Black and/or Hispanic have high rates of adverse perinatal outcomes due to systemic racism. It is unknown if rates are higher among Black and/or Hispanic women with disabilities, who may experience additional barriers to perinatal healthcare, including disability-based discrimination (i.e., ableism). Therefore, we examined the associations between maternal disability and preterm birth (< 37 weeks' gestation), low birthweight (< 2500 g), small for gestational age (< 10th percentile), and attendance at a postpartum health visit among Black and/or Hispanic women.
methodsWe conducted a cross-sectional study of Pregnancy Risk Assessment Monitoring System (PRAMS) data from participants who identified as Black and/or Hispanic between 2018 and 2019 across 22 jurisdictions (N = 9,034). Maternal disability was the primary exposure measured using the Washington Group-Short Set of Questions on Functioning, which asks respondents to rate their level of difficulty seeing, hearing, walking or climbing steps, remembering or concentrating, self-care, and communicating. Response options include "no difficulty," "some difficulty," "a lot of difficulty," and "I cannot do this at all." We examined differences in perinatal outcomes by overall disability status, disability severity, and disability type. We adjusted for demographic and clinical factors using multivariable logistic regression.
resultsThe prevalence of disability was 7.7%. There were no significant differences in preterm birth or low birthweight by maternal disability. Participants with any disability were significantly less likely to have a small for gestational age infant (adjusted odds ratio [aOR] = 0.56, 95% confidence interval [CI] = 0.37, 0.86) and to attend the postpartum visit compared to participants without disabilities (aOR = 0.38, 95% CI = 0.25, 0.57). We also found that as the level of self-reported difficulty increased, the odds of attending a postpartum health visit significantly decreased. Participants who reported blindness/low vision, cognition disability, communication disability, or multiple disabilities had significantly lower odds of attending the visit compared to participants without disabilities.
conclusionsMaternal disability was associated with lower odds of attending a postpartum health visit among Black and/or Hispanic participants in PRAMS, while small for gestational age differed by disability status and severity. Future research should identify barriers to postpartum healthcare for Black and/or Hispanic women with disabilities to inform culturally and disability-specific interventions.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.