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Global prevalence of preterm birth among Pacific Islanders: A systematic review and meta-analysis

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The epidemiology of preterm birth among Pacific Islanders is minimally understood. The purpose of this study was to estimate pooled prevalence of preterm birth among Pacific Islanders and to estimate their risk of preterm birth compared to White/European women. We searched MEDLINE, EMBASE, Web of Science Core Collection, Cochrane Library, CINAHL, Global Health, and two regional journals in March 2023. Observational studies were included if they reported preterm birth-related outcomes among Pacific Islanders. Random-effects models were used to estimate the pooled prevalence of preterm birth with 95% confidence interval (CI). Bayes meta-analysis was conducted to estimate pooled odds ratios (OR) with 95% highest posterior density intervals (HPDI). The Joanna Briggs Institute checklists were used for risk of bias assessment. We estimated preterm birth prevalence among Pacific Islanders in the United States (US, 11.8%, sample size [SS] = 209,930, 95% CI 10.8%-12.8%), the US-Affiliated Pacific Islands (USAPI, SS = 29,036, 6.7%, 95% CI 4.9%-9.0%), New Zealand (SS = 252,162, 7.7%, 95% CI 7.1%-8.3%), Australia (SS = 20,225, 6.1%, 95% CI 4.2%-8.7%), and Papua New Guinea (SS = 2,647, 7.0%, 95% CI 5.6%-8.8%). Pacific Islanders resident in the US were more likely to experience preterm birth compared to White women (OR = 1.45, 95% HPDI 1.32–1.58), but in New Zealand their risk was similar (OR = 1.00, 95% HPDI 0.83–1.16) to European women. Existing literature indicates that Pacific Islanders in the US had a higher prevalence of preterm birth and experienced health inequities. Learning from New Zealand’s culturally-sensitive approach to health care provision may provide a starting point for addressing disparities. The limited number of studies identified may contribute to higher risk of bias and the heterogeneity in our estimates; more data is needed to understand the true burden of preterm birth in the Pacific region.
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RESEARCH ARTICLE
Global prevalence of preterm birth among
Pacific Islanders: A systematic review and
meta-analysis
Bohao WuID
1
, Veronika ShabanovaID
2,3
, Kendall ArslanianID
4
, Kate Nyhan
5,6
,
Elizabeth IzampuyeID
1
, Sarah Taylor
2
, Bethel Muasau-Howard
7
, Alec Ekeroma
8
, Nicola
L. HawleyID
1
*
1Department of Chronic Disease Epidemiology, Yale School of Public Health, New Haven, CT, United
States of America, 2Department of Pediatrics, Yale School of Medicine, New Haven, CT, United States of
America, 3Department of Biostatistics, Yale School of Medicine, New Haven, CT, United States of America,
4Department of Social and Behavioral Sciences, Yale School of Public Health, New Haven, CT, United
States of America, 5Harvey Cushing/John Hay Whitney Medical Library, Yale University, New Haven, CT,
United States of America, 6Department of Environmental Health Sciences, Yale School of Public Health,
Yale University, New Haven, CT, United States of America, 7Department of Obstetrics and Gynecology,
Lyndon B Johnson Tropical Medical Center, Pago Pago, American Samoa, 8National University of Samoa,
Apia, Samoa
*nicola.hawley@yale.edu
Abstract
The epidemiology of preterm birth among Pacific Islanders is minimally understood. The pur-
pose of this study was to estimate pooled prevalence of preterm birth among Pacific Island-
ers and to estimate their risk of preterm birth compared to White/European women. We
searched MEDLINE, EMBASE, Web of Science Core Collection, Cochrane Library, CINAHL,
Global Health, and two regional journals in March 2023. Observational studies were included
if they reported preterm birth-related outcomes among Pacific Islanders. Random-effects
models were used to estimate the pooled prevalence of preterm birth with 95% confidence
interval (CI). Bayes meta-analysis was conducted to estimate pooled odds ratios (OR) with
95% highest posterior density intervals (HPDI). The Joanna Briggs Institute checklists were
used for risk of bias assessment. We estimated preterm birth prevalence among Pacific
Islanders in the United States (US, 11.8%, sample size [SS] = 209,930, 95% CI 10.8%-
12.8%), the US-Affiliated Pacific Islands (USAPI, SS = 29,036, 6.7%, 95% CI 4.9%-9.0%),
New Zealand (SS = 252,162, 7.7%, 95% CI 7.1%-8.3%), Australia (SS = 20,225, 6.1%, 95%
CI 4.2%-8.7%), and Papua New Guinea (SS = 2,647, 7.0%, 95% CI 5.6%-8.8%). Pacific
Islanders resident in the US were more likely to experience preterm birth compared to White
women (OR = 1.45, 95% HPDI 1.32–1.58), but in New Zealand their risk was similar (OR =
1.00, 95% HPDI 0.83–1.16) to European women. Existing literature indicates that Pacific
Islanders in the US had a higher prevalence of preterm birth and experienced health inequi-
ties. Learning from New Zealand’s culturally-sensitive approach to health care provision may
provide a starting point for addressing disparities. The limited number of studies identified
may contribute to higher risk of bias and the heterogeneity in our estimates; more data is
needed to understand the true burden of preterm birth in the Pacific region.
PLOS GLOBAL PUBLIC HEALTH
PLOS Global Public Health | https://doi.org/10.1371/journal.pgph.0001000 June 14, 2023 1 / 19
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OPEN ACCESS
Citation: Wu B, Shabanova V, Arslanian K, Nyhan
K, Izampuye E, Taylor S, et al. (2023) Global
prevalence of preterm birth among Pacific
Islanders: A systematic review and meta-analysis.
PLOS Glob Public Health 3(6): e0001000. https://
doi.org/10.1371/journal.pgph.0001000
Editor: Hermano Alexandre Lima Rocha, Federal
University of Ceara, UNITED STATES
Received: August 8, 2022
Accepted: May 4, 2023
Published: June 14, 2023
Copyright: ©2023 Wu et al. This is an open access
article distributed under the terms of the Creative
Commons Attribution License, which permits
unrestricted use, distribution, and reproduction in
any medium, provided the original author and
source are credited.
Data Availability Statement: All data can be found
in the manuscript and supporting information files.
Funding: This works was supported by the US
National Institute of Health (PI: Hawley, NLH, grant
number R03HD093993). The funders had no role
in the design, analysis or compiling this
manuscript.
Competing interests: The authors have declared
that no competing interests exist.
Introduction
In light of persistent disparities in perinatal health between minority and majority populations
globally, greater attention is being paid to understanding unique risks that explain minority
populations increased risk of preterm birth (live birth before 37 weeks gestation [1]). Despite
efforts over the past several decades to intervene, preterm birth remains the leading cause of
both neonatal and under five year death [2,3]. In 2014, which is the most recent estimate from
the World Health Organization, the global prevalence of preterm birth was 10.6% (uncertainty
interval 9.0%-12.0%) [4].
Pacific Islanders are particularly underrepresented in perinatal health research, and little is
known about the prevalence of preterm birth among this group. Data from the Pacific Islands
themselves is sparse, both as a result of geographic isolation (~1000 islands across 300,000
square miles [5]) and nascent research infrastructure. Pacific Islander migrants are, however,
among the fastest growing minority groups in the United States (US), New Zealand, and Aus-
tralia. In the US, 1.2 million people identified as Native Hawaiian or Other Pacific Islanders
(NHOPI) in 2010 [6]. In the 2018 census 24.6% of New Zealanders identified as Māori or
Pacific Islander [7], and in Australia (2016), ~250,000 people reported Pacific Islander ethnic-
ity [8]. While data from these settings should allow for ethnicity-specific examination of health
outcomes, Pacific Islanders continue to be aggregated with other minority groups; in the US
with Asian or Native Americans (or Pacific Islanders are omitted from analyses because of
small sample size), and in Australia with Indigenous Australian groups.
Health challenges common among Pacific Islanders, such as, disproportionately high prev-
alence of obesity and obesity-related complications [5], may put them at a higher risk of pre-
term birth [5,9]. Obesity is a significant risk factor for pre-eclampsia and pre-pregnancy
diabetes [10,11], which have been associated with indicated preterm births [12]. Endemic
tropical illnesses may also increase risk [12,13]: Papua New Guinea, for example, still has a
high rate of malaria [14]. Furthermore, Pacific Islander migrants in developed countries may
have limited access to social services [1518] and reportedly experience discrimination [19],
which may worsen their perinatal health outcomes.
To better understand the epidemiology of preterm birth among Pacific Islanders and the
need for perinatal health intervention, this systematic review and meta-analysis aims to: (a)
estimate the pooled prevalence of preterm birth among Pacific Islanders globally; and (b) iden-
tify whether Pacific Islanders were more likely to experience preterm birth compared to non-
Hispanic White/European women.
Materials and methods
Protocol and registration
This review (PROSPERO ID: CRD42021283377, protocol [20]) followed Preferred Reporting
Items for Systematic Reviews and Meta Analyses (PRISMA) [21] and Meta-analysis of Obser-
vational Studies in Epidemiology (MOOSE) reporting guidelines [22] and received Institu-
tional Review Board exemption.
Study population
Studies reporting outcomes of Pacific Islanders, including Native Hawaiians, residents in
Micronesia, Melanesia, and Polynesia were eligible for inclusion. Countries/territories were
selected based on the Pacific Island Countries [23] and previous studies [5,15], including US-
affiliated Pacific Islands (USAPI: American Samoa, Guam, Commonwealth of the Northern
Mariana Islands [CNMI], Federated States of Micronesia, Republic of the Marshall Islands
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Preterm birth prevalence among Pacific Islanders: A meta-analysis
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[RMI], and Palau), Kiribati, Nauru, Papua New Guinea, Solomon Islands, Fiji, New Caledonia,
Vanuatu, Tonga, Tuvalu, Tokelau, Niue, French Polynesia, New Zealand (Māori, the indige-
nous Polynesian people of New Zealand), Samoa, and the Cook Islands. Studies from the US
(Hawai’i and the contiguous US) and Australia (individuals from Ni-Vanuatu, Tahiti, and the
Pitcairn islands; Aboriginal and Torre Strait Islanders were not included) were included, since
there are large migrant populations in both countries.
Information sources
We searched MEDLINE ALL (Ovid), EMBASE (Ovid), Web of Science Core Collection (as
licensed at Yale [20]), Cochrane Library, CINAHL (EBSCOhost), and Global Health. The
Pacific Journal of Reproductive Health and Pacific Health Dialog were searched manually
since they are not well indexed in major bibliographic databases. Backwards and forwards cita-
tion chaining was searched by hand via Google Scholar. Reports from international, national,
state-level, and territorial government agencies were searched manually.
Search strategy
The search strategy was developed by the first author in consultation with all co-authors,
including a medical librarian (KN). The search used two concepts: (1) Pacific Islanders and (2)
preterm birth outcomes. Appropriate controlled vocabulary terms and keyword search terms
were used (MEDLINE ALL example, S1 Table) and archived [24].
Study selection
Peer-reviewed observational studies and agency reports published before March 17
th
2023
were included. Case reports and case-control studies were excluded due to inability to estimate
prevalence. While doctoral theses were included, conference abstracts and master’s theses
were not since final study outcomes may not have been available/reported.
Using Covidence data management software, each article was screened by two authors
independently at the title-abstract and full-text screening stages. Authors met to reach consen-
sus on inclusion and reasons for exclusion. Screening questions are presented in S2 Table.
Studies using the same datasets with the same study period were examined for potential sample
overlap. Where overlap was identified, only the study with the largest sample size was retained
in analyses.
Data extraction
Data extraction was completed by the first author and checked by the senior author. Extracted
information included preterm birth-related outcomes (prevalence among Pacific Islander
women and non-Hispanic White/European women), data source, publication date, data col-
lection period, study country/setting, study design, gestational age (GA) measurement
method, Pacific Islander ethnicity, and sample size.
For the prevalence estimate, if a study reported prevalence but not the absolute number of
events, this number was calculated with N(Preterm Births) = P*N(total Pacific Islanders) and
rounded to the next whole number, where N represented sample size and P represented preva-
lence of preterm birth. To compare risk among Pacific Islander and White/European women,
the prevalence among the two groups and the modelling outcomes (odds radio [OR], model-
ling method, and adjusted confounders) were recorded. For studies reporting prevalence, OR
were calculated with OR = ad/bc.
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Preterm birth prevalence among Pacific Islanders: A meta-analysis
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Risk of bias assessment
The Joanna Briggs Institute (JBI) [25] checklist for prevalence studies [26] was used for the
assessment in prevalence meta-analyses; the checklist for cross-sectional studies [27] was used
for meta-analyses comparing risk. Two authors (BW and EI) completed appraisals and dis-
agreements were discussed to reach consensus. Total scores represented the proportion of
“checks” with 100% the maximum possible score. Egger’s test [28] (for prevalence meta-analy-
ses) and weight-function models [29] (for Bayesian risk comparison meta-analyses) were used
to assess publication bias.
Synthesis of results
Stratified by study country/territory, we conducted prevalence meta-analyses of preterm birth
among Pacific Islander women and comparison of preterm birth risk meta-analyses between
Pacific Islander women and non-Hispanic White women in the US and New Zealand. As ran-
dom-effects models (DerSimonian and Laird method) [30] consider the included studies to be
a representative sample of possible articles on the research question of interest, these models
were used for the pooled prevalence with 95% confidence intervals (CI). I
2
is usually high in
prevalence meta-analysis but may not indicate the data is inconsistent [31,32], and it can be
biased in small meta-analyses [33], so we reported tau with both the inverse variance (IV)
method (weighting more to studies with a larger sample size) and the generalized linear mixed
models (GLMM) method (weighting more to studies with smaller sample size) for the hetero-
geneity assessment. We compared the estimated tau
2
[IV] to the within-study variances, with
tau
2
[IV] larger than within-study variance indicating the weights of any two studies are
approximately equal [34]. A large proportion of equal weights in a meta-analysis indicates the
heterogeneity exists. Prediction intervals were presented in which future studies effects may
fall based on present evidence. Subgroup analyses by Pacific Islander ethnicity were conducted
to understand the between-study heterogeneity.
For the pooled risk comparison estimate, we used a Bayesian meta-analysis method [35] due to
the relatively small number of studies identified by our search. Pooled ORs with 95% highest pos-
terior density intervals (HPDI) were reported. We assumed no association, so we restricted the
effect ln(OR) to normal prior centered at ln(OR)
p
= 0 (no effect), and the prior standard deviation
was restricted to σ
p
= 4; the priori expected heterogeneity was restricted to tau 0.98 with 95%
probability as half-normal priori with scale 0.5. Tau with 95% HPDI were used for the heterogene-
ity assessment. Prediction intervals and subgroup analyses by ethnicity were also provided.
All analyses were performed using RStudio (RStudio, Inc., Boston, MA, USA). The R pack-
age meta [36] was used to conduct prevalence meta-analyses and to generate Forest plots and
package dmetar [37] was used to perform Egger’s test for the corresponding publication bias
assessment; package bayesmeta [38] was used to conduct Bayes meta-analyses, and package
RoBMA [39] was used to perform the corresponding publication bias assessment (Bayes factor
[BF]<3 indicating weak evidence[40]). R code is provided in S1 Appendix.
Results
Study selection
We identified 10,077 articles from six databases and 15 articles from gray literature on Decem-
ber 3
rd
2021, and updated our search (2nd search) in these six databases on March 17
th
2023
(Fig 1). After removing duplicates, title-abstract and full-text screening, and adding articles
through citation chaining, we found 118 articles reporting preterm birth-related outcomes
among Pacific Islanders among which 55 articles reported results related to our objectives.
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Preterm birth prevalence among Pacific Islanders: A meta-analysis
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After removing studies with overlapping data (S3 Table), we included 33 articles that reported
preterm birth prevalence, and 15 articles that compared risk between Pacific Islander and
White/European women.
Study characteristics
Of the 33 studies that reported prevalence of preterm birth among Pacific Islander women, 13
(39.4%) studies [4153] were conducted in the US, 5 (15.2%) studies were conducted in the
Fig 1. PRISMA flow diagram of study selection.
https://doi.org/10.1371/journal.pgph.0001000.g001
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Preterm birth prevalence among Pacific Islanders: A meta-analysis
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USAPI [5458] (CNMI [57,58], Palau [56], and RMI [54,55]), 7 (21.2%) studies were from
New Zealand [5965], 2 (6.1%) studies were from Australia [66,67], 4 (12.1%) studies [6871]
reported preterm birth prevalence in Papua New Guinea, 1 study was from Solomon Island
[72], and 1 study was from Vanuatu [73] (Table 1). Of the 15 studies used for the risk compari-
son meta-analysis, 12 (80.0%) [4148,50,53,74,75] were conducted in the US, and 3 (20.0%)
were from New Zealand [7678].
Almost half of the 41 total included studies [41,44,47,49,5155,6163,6567,70,72,73,
77,79,80] (43.9%) did not report the method used to estimate GA. Seven (17.1%) studies used
last menstrual period (LMP) only [45,47,48,56,60,78,79] and seven (17.1%) used clinical/
obstetric estimates [43,46,50,57,59,74,81]. In two (4.9%) studies [58,64], GA was deter-
mined by the obstetric care provider at birth; two (4.9%) studies used ultrasound [68,76] and
one used Dubowitz assessment [69] (2.4%). The remaining three studies [42,71,75] (7.3%)
used a combination of ultrasound, LMP, and/or clinical estimate. Most included studies
defined preterm birth as occurring before 37 weeks, four (9.8%) [41,54,63,73] did not report
their GA threshold, two [58,62] (4.9%) used <36 weeks, and one [68] (2.4%) used <38 weeks.
Risk of bias
For the prevalence meta-analysis, risk of bias scores ranged from 55.6% to 100.0%, with higher
scores indicating lower risk of bias (S4 and S5 Tables). For the meta-analysis comparing risk,
risk of bias scores ranged from 37.5% to 100.0%; confounders included in models and model-
ling methods were summarized for each study in S6 Table.
Synthesis of results
Prevalence of preterm birth. In the US, the random-effects pooled prevalence of preterm
birth among Pacific Islanders was 11.8% (95% CI 10.8%-12.8%; tau [IV] = 0.17, 95% CI 0.16–
0.41; tau [GLMM] = 0.27), and the prediction interval ranged from 8.3% to 16.4% (Fig 2A). In
subgroup analysis, the random-effects pooled prevalence of preterm birth among Marshallese
(20.5%, 95% CI 17.7%-23.7%, tau[IV] = 0.12, tau[GLMM] = 0.06) was twice the pooled preva-
lence among the general Pacific Islander population in the US, and almost the same for other
ethnicities (S1 Fig). The pooled prevalence was lower in the USAPI (6.7%, 95% CI 4.9%-9.0%,
tau[IV] = 0.36, 95% CI 0.22–1.10; tau[GLMM] = 0.34), but the prevalence interval ranged
from 2.0% to 20.4% (Fig 2B).
The random-effects pooled prevalence of preterm birth among Pacific Islanders overlapped
in New Zealand, Australia, and Papua New Guinea (Fig 2C–2E). In New Zealand, the pooled
prevalence was 7.7% (95% CI 7.1%-8.3%, tau[IV] = 0.09, 95% CI 0.06–0.36; tau[GLMM] =
0.08) and the prediction interval ranged from 6.0% to 9.7%. In subgroup analysis (S2 Fig), we
found no obvious difference between the prevalence among Māori (8.4%, 95% CI 7.1%-9.8%)
and other Pacific Islanders (7.5%, 95% CI 6.8%-8.3%). In Australia, the pooled prevalence was
6.1% (95% CI 4.2%-8.7%, tau[IV] = 0.27; tau[GLMM] = 0.19). The pooled prevalence of pre-
term birth in Papua New Guinea was 7.0% (95% CI 5.6%-8.8%, tau[IV] = 0.17, 95% CI 0–1.05;
tau[GLMM] = 0.12), and the prediction interval ranged from 2.9% to 15.9%.
Comparison of preterm birth risk between Pacific Islander and White/
European women
Based on 12 studies from the US, we estimated the pooled odds of preterm birth among Pacific
Islander women to be 46% higher than among non-Hispanic White women (OR = 1.45, 95%
HPDI 1.32–1.58, tau = 0.16, 95% HPDI 0.11–0.24 (Fig 3A). In subgroup analysis, Hawaiian
(OR = 1.34, 95% HPDI 1.21–1.44, tau = 0.04, 95% HPDI 0.00–0.17), Marshallese (OR = 1.72,
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Preterm birth prevalence among Pacific Islanders: A meta-analysis
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Table 1. Characteristics of included studies for preterm birth among Pacific Islanders.
Study Data
collection
Study design State/Setting, Dataset Pacific Islanders GA measurement
method
PTB
definition
US (N = 18:13 were used for prevalence estimate; 12 were used for risk comparison)
Crowell et al., 2007 [47]
a, b, c, d
1968–1994 Retrospective
cohort study
e
Hawaii State,
birth record files
Hawaiian (n = 69,350)
Samoan (n = 7,054)
White (n = 108,981)
LMP GA <37
weeks
Andrasfay et al., 2021
[48]
a, b
(G2 cohort)
1978–1995 Retrospective
cohort study
e
California,
California birth records
Hawaiian/Pacific Islander
(n = 1,577); White
(n = 185,949)
LMP GA <37
weeks
Korinek et al., 2021 [44]
a, b
1989–2015 Retrospective
cohort study
e
State of Utah,
Utah Population Database
NHOPI (n = 10,438)
White (n = 1,177,278)
Not reported GA <37
weeks
Nembhard et al., 2019
[42]
a, b, c, d
1997–2013 Cross-sectional
study
Arkansas,
Vital record files
Marshallese (n = 2,488,
missing value 270)
Non-Hispanic White
(n = 65,800)
Ultrasound (74%) GA <37
weeks
Mathews et al., 2003 [79]
c
2001 Cross-sectional
study
e
US continent,
National Vital Statistics Reports
Hawaiian (n = 6,411)
White (n = 3,177,698)
LMP GA <37
weeks
Hirai et al., 2013 [45]
a, b,
c, d
2002–2009 Cross-sectional
study
e
Hawaii,
Linked Infant Death Cohort Files
Native Hawaiian (n = 40,917)
White (n = 33,683)
LMP GA <37
weeks
Centers for Disease
Control and Prevention
et al., 2011 [52]
a
2003–2008 Descriptive
study
e
Washington State, King County,
US government census
Hawaiians/Pacific Islanders
(n = 2,200)
Not reported GA <37
weeks
Wong et al., 2008 [80]
c
2003 Retrospective
cohort study
US continent,
National Natality Files
Samoan (n = 1,835)
Guamanian (n = 30,353)
Hawaiian (n = 1,302)
Not reported GA <37
weeks
Schempf et al., 2010 [75]
b, c, d
2003–2005 Cross-sectional
study
e
California and Hawaii,
birth certificates
Native Hawaiian (n = 16,805)
Guamanian (n = 1,406)
Marshallese (n = 938)
Samoan (n = 4,820)
Tongan (n = 1,594)
White (n = 10,144)
CA: LMP;
HA: clinical estimate
GA <37
weeks
Altman et al., 2019 [49]
a,
c
2007–2012 Retrospective
cohort study
California,
birth records
Hawaiian (n = 756)
Guamanian (n = 844)
Samoan (n = 2,852)
Other Pacific Islander
(n = 5,422)
More than one (n = 596)
Not reported GA <37
weeks
Ratnasiri et al., 2018 [74]
b
2007–2016 Retrospective
cohort study
California,
Birth Statistical Master Files
N for races was not reported Obstetric estimate GA <37
weeks
Wartko et al., 2017 [41]
a,
b
2008–2012 Retrospective
cohort study
Washington State, King County,
birth records
NHOPI (n = 1,853)
White (n = 62,950)
Not reported Not reported
Hawaii State Department
of Health et al., 2019 [50]
a, b, d
2012–2015 Descriptive
study
e
Hawaii,
Pregnancy Risk Assessment
Monitoring System
Native Hawaiian (n = 5,050)
Samoan (n = 300)
Other Pacific Islander
(n = 950)
White (n = 4,400)
Clinical estimate GA <37
weeks
Public Health
Department, Seattle &
King County et al., 2015
[51]
a
2013 Descriptive
study
e
Washington State, King County,
birth certificate data
Pacific Islander (n not
reported)
White (n = 13,061)
Not reported GA <37
weeks
Quan et al., 2021 [81]
c
2015–2017 Cross-sectional
study
e
National Natality File NHOPI (n = 9,476) Obstetric estimate GA <37
weeks
Martin et al., 2019 [43]
a,
b
2016–2018 Descriptive
study
e
US continent,
Natality Data Files
NHOPI (n = 28,244)
White (n = 6,005,206)
Obstetric estimate GA <37
weeks
Hamilton et al., 2021
[46]
a, b
2019–2020 Descriptive
study
e
US continent,
Natality Data Files
NHOPI (n = 19,382)
White (n = 3,755,477)
Obstetric estimate GA <37
weeks
(Continued)
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Table 1. (Continued )
Study Data
collection
Study design State/Setting, Dataset Pacific Islanders GA measurement
method
PTB
definition
Hamilton et al., 2022
[53]
a, b
2021 Descriptive
study
e
US continent,
Natality Data Files
NHOPI (n = 9,517)
White (n = 1,884,554)
Obstetric estimate GA <37
weeks
USAPI (N = 5)
Fox et al., 2005 [58]
a
1986–1996 Retrospective
cohort study
e
Commonwealth of the Northern
Mariana Islands,
hospital records
Women from
Commonwealth of the
Northern Mariana Islands
(n = 10,756)
Determined by the
birth attendant
GA <36
weeks
Dela Cruz et al., 2018
[57]
a
2007–2014 Retrospective
cohort study
Commonwealth of the Northern
Mariana Islands,
hospital records
Chamorro/Carolinian
(n = 2,799)
Other Pacific Islander
(n = 785)
Obstetric estimate GA <37
weeks
Berger et al., 2016 [56]
a
2007–2013 Retrospective
cohort study
Palau,
hospital records
Palauan (n = 1,171) LMP GA <37
weeks
Ministry of Health in
Republic of the Marshall
Islands, 2010 [55]
a
2007–2010 Descriptive
study
e
Republic of the Marshall Islands,
Vital Statistics Database
Women from Republic of the
Marshall Islands (n = 6,116)
Not reported Not reported
Ministry of Health in
Republic of the Marshall
Islands, 2016 [54]
a
2011–2016 Descriptive
study
e
Republic of the Marshall Islands,
Vital Statistics Database
Women from Republic of the
Marshall Islands (n = 7,515)
Not reported GA <37
weeks
New Zealand (N = 10:7 were used for prevalence estimate; 3 were used for risk comparison)
Cantwell et al., 1973 [63]
a, c
Not
reported
Prospective
cohort study
Hawkes Bay,
hospital records
Maori (n = 276, missing value
n = 21)
Not reported Not reported
Wright et al., 1998 [59]
a,
c
1987–1990 Cross-sectional
study
Cot Death Study Maori (n = 306)
Pacific Islander (n = 154)
Clinical estimate GA <37
weeks
Sadler et al., 2002 [61]
a, c
1992–1999 Retrospective
cohort study
e
Auckland,
hospital records
Maori (n = 4,361)
Pacific Islander (n = 8,197)
Not reported GA <37
weeks
Lawton et al., 2016 [62]
a,
c
1995–2009 Retrospective
cohort study
Wellington region,
hospital records
Maori (n = 6,960)
Pacific Islander (n = 5,697)
European (n = 33,386)
Not reported GA <36
weeks
Craig et al., 2004 [76]
b, d
1996–2001 Retrospective
cohort study
e
Data file from New Zealand
Health Information Service
Maori (n = 72,826, missing
value 6,729, 9.2%)
Pacific Islander (n = 32,713,
missing value 3,515, 10.7%)
European (n = 192,295,
missing value 18,042, 9.4%)
Ultrasound GA <37
weeks
Sundborn et al., 2011
[60]
a, c
2000 Cross-sectional
study
e
South Auckland,
Pacific Island Families Study
Samoan (n = 627)
Cook Island Maori (n = 230)
Niuean (n = 57)
Tongan (n = 278)
LMP GA <37
weeks
Berry et al., 2018 [64]
a, c
2005–2015 Retrospective
cohort study
The Department of Internal
Affairs and the Ministry of
Health’s National Minimum
Dataset
Maori (n = 129,300)
Pacific Islander (n = 72,435)
Ascertained by the
obstetric care provider
GA <37
weeks
Parry et al., 2011 [78]
b, d
2007–2010 Prospective
cohort study
Auckland,
hospital records
Maori (n = 13,647)
Pacific peoples (n = 6,625)
European (n = 33,957)
LMP GA <37
weeks
Edmonds et al., 2021
[77]
b, d
2010–2014 Retrospective
cohort study
Kaupapa Maori research Maori (n = 77,601)
Pasifika (n = 33,106)
European (n = 141,815)
Not reported GA <37
weeks
Ministry of Health et al.,
2019 [65]
a
2016 Descriptive
study
e
New Zealand Mortality
Collection
Maori (n = 17,329)
Pacific peoples (n = 5,976)
Not reported GA <37
weeks
Australia (N = 2)
(Continued)
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Preterm birth prevalence among Pacific Islanders: A meta-analysis
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95% HPDI 1.07–2.33, tau = 0.27, 95% HPDI 0–0.72), and Samoan (OR = 1.36, 95% HPDI
0.93–1.74, tau = 0.22, 95% HPDI 0.04–0.58) women were all more likely to experience preterm
birth compared to non-Hispanic White women in the US (S3 Fig).
Using data from three studies from New Zealand we determined that the pooled odds of
preterm birth were similar for Pacific Islander and European women (OR = 1.00, 95% HPDI
0.83–1.16, tau = 0.16, 95% HPDI 0.07–0.34, Fig 3B). Stratified by ethnicity subgroups, neither
Māori (OR = 1.10, 95% HPDI 0.77–1.41, tau = 0.16, 95% HPDI 0.03–0.54) nor other Pacific
Islanders (OR = 0.90, 95% HPDI 0.61–1.18, tau = 0.14, 95% HPDI 0.02–0.50) had higher odds
of preterm birth compared to European women.
Heterogeneity assessment
Checking the proportion of the studies with a smaller variance than the tau
2
[IV] suggests that
no heterogeneity existed in the prevalence meta-analysis in the US (0%) and New Zealand
(0%), however, meta-analyses conducted for the USAPI (100.0%), Australia (100.0%) and
Papua New Guinea (100.0%) all showed strong evidence of heterogeneity. When using the
same method to check the proportion of the studies with a smaller variance of log scale of the
ORs (Varlog[OR]) than the tau
2
[IV] there was strong evidence of heterogeneity in meta-
Table 1. (Continued )
Study Data
collection
Study design State/Setting, Dataset Pacific Islanders GA measurement
method
PTB
definition
Berman et al., 2021 [67]
a
2003–2016 Retrospective
cohort study
Linked birth, hospital and death
data from New South Wales
Oceania (n = 17,284) Not reported GA <37
weeks
(Included 32–
36 weeks
only)
Mozooni et al., 2018 [66]
a
2005–2013 Retrospective
cohort study
Dataset from Western Australia
Data Linkage System
Maori (n = 2,941) Not reported GA <37
weeks
Papua New Guinea (N = 4)
Garner et al., 1994 [69]
a
1984–1987 Cross-sectional
study
e
Wosera subdistrict,
hospital records
Women from Papua New
Guinea (n = 121)
Dubowitz assessment GA <37
weeks
Allen et al., 1998 [68]
a
1994–1996 Prospective
cohort study
Madang Province,
hospital records
Women from Papua New
Guinea (n = 987)
Ultrasound GA <38
weeks
Senn et al., 2009 [70]
a
2007–2008 Cross-sectional
study
Madang Province,
hospital records
Women from Papua New
Guinea (n = 310)
Not reported GA <37
weeks
Unger et al., 2019 [71]
a
2009–2013 Prospective
cohort study
Madang Province,
hospital records
Women from Papua New
Guinea (n = 1,229)
Ultrasound (65.5%);
fetal biometry for the
majority
GA <37
weeks
Other Pacific Island countries (N = 2)
Cafaro et al., 2015 [72]
f
2011–2013 Retrospective
cohort study
Records from KiraKira Hospital,
Makira-Ulawa Province,
Solomon Island
Solomon Islander (n = 1,233) Not reported GA<37 weeks
Therrien et al., 2021 [73]
f
2016 Cross-sectional
study
e
Records from Vila Central
Hospital on Efate Island,
Vanuatu.
Women from Vanuatu
(n = 187)
Not reported Not reported
GA, gestational age; LMP, last menstrual period; NHOPI, Native Hawaiian and Other Pacific Islanders; CA, California; HA, Hawaii
a
Labelled studies were included in preterm birth prevalence meta-analyses.
b
Labelled studies were included in the risk of preterm birth compared to White/European women meta-analysis.
c
Labelled studies were included in preterm birth prevalence subgroup meta-analysis.
d
Labelled studies were included in the risk of preterm birth compared to White/European women subgroup meta-analyses.
e
The study design was not reported and was decide by the first author’s judgement.
f
Labelled studies were not included in meat-analyses since there was only one study from each setting.
https://doi.org/10.1371/journal.pgph.0001000.t001
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Preterm birth prevalence among Pacific Islanders: A meta-analysis
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analyses comparing risk between Pacific Islander and White/European women in the US
(95.2%) and New Zealand (100.0%).
Publication bias assessment
For preterm birth prevalence meta-analyses, we did not identify any publication bias (Egger’s
test, US: P = 0.54, USAPI: P = 0.35, New Zealand: P = 0.53, Papua New Guinea: P = 0.27). This
Fig 2. Forest plots of preterm birth prevalence among Pacific Islanders stratified by country/territory: (A) the US, (B) the
USAPI, (C) New Zealand, (D) Australia, (E) Papua New Guinea
a
.
a
Prediction interval of Australia is not available.
https://doi.org/10.1371/journal.pgph.0001000.g002
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Preterm birth prevalence among Pacific Islanders: A meta-analysis
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assessment was not available for Australia since Egger’s test cannot be used with <3 studies.
For the risk comparison meta-analyses, the robust Bayesian model expressed weak evidence of
publication bias in the US (probability = 0.42, inclusion BF = 0.73) and New Zealand (proba-
bility = 0.48, inclusion BF = 0.93).
Discussion
Main findings
To our knowledge, this is the first systematic review and meta-analysis to summarize data
from both Pacific Islander immigrants in high income settings and those resident in the Pacific
Islands. Results indicate that US-resident Pacific Islanders had a relatively higher prevalence of
preterm birth than in New Zealand and Australia and experienced poorer birth outcomes than
White women, which was an inequity not observed in New Zealand. Estimates in other set-
tings were limited by sparse data.
Our Pacific Islander-specific findings mirror the most recent country level estimates
reported by the WHO. In 2014, among the three developed nations, the US had the highest
overall preterm birth prevalence (9.6%, uncertainty interval [UI] 10.3%-14.0%), while the
Fig 3. Forest plots of risk of preterm birth comparing Pacific Islander women to (A) non-Hispanic White women in the US and to (B) European women in
New Zealand.
https://doi.org/10.1371/journal.pgph.0001000.g003
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Preterm birth prevalence among Pacific Islanders: A meta-analysis
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estimates in New Zealand (7.5%, UI 7.0%-9.8%) and Australia (8.6%, UI 6.9%-9.5%) were sim-
ilar [82]. Notably, in our analysis we identified disparities between Pacific Islander and white
women that were present in the US, but not in New Zealand. In New Zealand, while Pacific
Islanders have become a minority group since European occupation, they make up a far
greater proportion (24.6% [7]) of the population than in the US (0.4%) [83]. As such, support-
ive and culturally-based health policies have been prioritized in New Zealand to care for popu-
lations with high need (including Māori and Pacific Islanders) [84], such as Very Low Cost
Access (VLCA), Te Tiriti o Waitangi (the Treaty of Waitangi) [85], which protects Māori
resources, and iwi (tribally)-based primary care consistent with Māori values, attitudes, and
aspirations [86,87]. In contrast, in the US Pacific Islander women have reported limited health
care access related to citizenship [16,17], discrimination [19], and mistrust of health profes-
sionals [1518]. Replicating New Zealand’s focus on primary health care, support for cultur-
ally-sensitive initiatives, and efforts to decrease structural racism [8789] may be important if
US disparities are to be addressed.
While Australia has among the largest absolute number of Pacific Islander migrants, they
make up a small proportion (0.9%) of the population
12
, which likely explains the limited num-
ber of Pacific Islander-related studies reporting preterm birth. Australia has continuously sup-
ported seven surrounding Pacific Island countries to promote universal health coverage since
1995, including Fiji, Kiribati, Nauru, Samoa, Solomon Islands, Tonga and Vanuatu [90], but
did not systematically record maternal ethnicity other than Caucasian and Indigenous
(Aboriginal and Torres Strait Islander) in their own health system before 1998 [91]. Studies
indicate that language barriers and inadequate health care access may increase the burden of
adverse pregnancy outcomes among Pacific Islander migrants to Australia [66], but further
data, with improved specificity in race/ethnicity reporting, is needed to better understand
their perinatal outcomes.
Data from the Pacific Islands themselves were sparse and limited conclusions about the
prevalence of preterm birth. While Pacific Islander women in the USAPI had a lower preterm
birth estimate than the US, the wider prediction interval should be noted. All of the USAPIs
are medically underserved [92] and, although prenatal/obstetric care is available [93,94], cov-
erage in different settings varies [94,95] limiting opportunities for systematic data collection.
Further data is sorely needed to adequately understand the needs of these territories, which are
heavily dependent on US grant funding to sustain their health care systems.
Although Papua New Guinea is the largest of the Pacific Islands, with 8.9 million residents
[96], studies were limited by design and response rate. For several reasons, the estimated prev-
alence may not accurately reflect the national burden of preterm birth. First, most of the
included studies were from Madang Province, where much research is concentrated since the
province is home to one of the country’s two medical schools and the Papua New Guinea Insti-
tute of Medical Research. The relatively higher prenatal care coverage (63%) in this setting [97,
98] compared to other regions may reduce maternal morbidity during or after pregnancy,
meaning that estimates for preterm birth prevalence may be lower than the whole nation. Sec-
ond, although malaria—a known risk factor for preterm birth—is endemic to Papua New
Guinea (86% of cases in WHO Western Pacific Region were from Papua New Guinea [14]),
most women in the included studies had either taken malaria prophylaxis before the recruit-
ment or were cured before giving birth [68,69,71] (one study did not report malaria related
information [70]). This also may not be the case for women residing in more rural and less
medically served settings. Finally, in one of the largest samples of women among the Papua
New Guinea studies [68], preterm birth was defined as less than 38 weeks, which may also
have influenced the estimate.
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Preterm birth prevalence among Pacific Islanders: A meta-analysis
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Strengths and Limitations
Limitations of our study should be noted. Beyond the USAPIs, Papua New Guinea and New
Zealand there was little data on perinatal health from the remaining Pacific Islands. We identi-
fied only one study from Vanuatu [73] (PTB prevalence: 8.0%), and one study from the Solo-
mon Islands in which the reported preterm birth prevalence was 23.8% in 2011–2013 [72]
indicating that there may be broad heterogeneity in preterm birth prevalence across the region
that was not captured here. Even within our studies, a large degree of heterogeneity was evi-
dent in prevalence meta-analyses for the USAPI, Australia, and Papua New Guinea. Potential
explanations could include the lack of consistency in GA measurement methods, the limited
publications, and quality of health care provided by local clinics. Similar heterogeneity in the
risk comparison meta-analysis in the US may be from different perinatal outcomes among
Pacific Islander subgroups, particularly the much higher risk and prevalence of preterm birth
among Marshallese women; in New Zealand, the heterogeneity may be from different study
designs, varied GA measurement methods (most were unclear), and the unavoidable heteroge-
neity for smaller meta-analyses [33]. The large proportion of included studies that did not
clearly state the methods used to estimated GA also should be noted.
Our study does, however, have several notable strengths. We systematically searched arti-
cles reporting preterm birth outcomes among Pacific Islanders, including grey literature and
comprehensively conducted backward and forward citation chaining. Second, we used tau for
the heterogeneity assessment instead of I
2
statistics, which have been questioned for their reli-
ability especially for prevalence meta-analysis [31] and meta-analyses with a small number of
included studies [33]. Additionally, to increase the accuracy of our risk comparison estimates,
we used a Bayesian meta-analysis approach that performs better than frequentist meta-analysis
approach when a small number of studies are included [35], and the corresponding robust
Bayesian modelling method for publication bias assessment.
Interpretation
Our findings have important public health implications. In developed nations like the US and
Australia, an improved record of race/ethnicity information and ethnicity-specific analyses are
the first steps to understanding the burden of adverse pregnancy outcomes among minority
groups. It is vital to identify related, contextually relevant risk factors to inform future polices
to decrease health disparities. Lessons may be learned from New Zealand’s culturally-sensitive
approach. In the USAPI, Papua New Guinea, and the other Pacific nations not represented
here, basic health care infrastructure improvements are likely needed before the true burden of
preterm birth can be understood.
Conclusion
Existing literature indicates that Pacific Islanders in the US had a higher prevalence of preterm
birth than in other global settings and experienced health inequities. Learning from New Zeal-
and’s culturally-sensitive approach to health care provision may provide a starting point for
addressing disparities. Data from other Pacific settings is sparse, limiting conclusions about
prevalence. More data is needed to understand the true burden of preterm birth in the Pacific
region.
Supporting information
S1 Checklist. PRISMA 2020 checklist.
(DOCX)
PLOS GLOBAL PUBLIC HEALTH
Preterm birth prevalence among Pacific Islanders: A meta-analysis
PLOS Global Public Health | https://doi.org/10.1371/journal.pgph.0001000 June 14, 2023 13 / 19
S1 Table. Search strategy for systematic review of the literature on MEDLINE ALL (Ovid).
(DOCX)
S2 Table. Screening questions.
(DOCX)
S3 Table. Articles excluded due to overlapping data (n = 31).
(DOCX)
S4 Table. Risk of bias assessment for the preterm birth prevalence meta-analysis using the
JBI checklist [26].
(DOCX)
S5 Table. Risk of bias assessment for the risk comparison of preterm birth meta-analysis
using the JBI checklist [27].
(DOCX)
S6 Table. Summary for adjustment methods and confounding factors (risk comparison of
preterm birth meta-analysis).
(DOCX)
S1 Fig. Forest plot of preterm birth prevalence subgroup analysis by Pacific Islander eth-
nicity in the US
a a
Please note, the overall estimate presented here is not expected to match
that in Fig 2A since these analyses are restricted to only a sub-sample of the overall study
population.
(TIF)
S2 Fig. Forest plot of preterm birth prevalence subgroup analysis by Pacific Islander eth-
nicity in the New Zealand
a a
Please note, the overall estimate presented here is not expected
to match that in Fig 2C since these analyses are restricted to only a sub-sample of the over-
all study population.
(TIF)
S3 Fig. Forest plot of risk of preterm birth comparing Pacific Islander women to non-His-
panic White women subgroup by ethnicity in the US.
(TIF)
S1 Appendix. R code for meta-analyses.
(DOCX)
Author Contributions
Conceptualization: Bohao Wu, Veronika Shabanova, Sarah Taylor, Nicola L. Hawley.
Data curation: Bohao Wu, Nicola L. Hawley.
Formal analysis: Bohao Wu, Veronika Shabanova, Elizabeth Izampuye.
Funding acquisition: Nicola L. Hawley.
Investigation: Bohao Wu, Veronika Shabanova, Kate Nyhan, Sarah Taylor, Nicola L. Hawley.
Methodology: Bohao Wu, Veronika Shabanova, Kate Nyhan, Nicola L. Hawley.
Project administration: Bohao Wu, Kendall Arslanian, Kate Nyhan, Nicola L. Hawley.
Resources: Bohao Wu, Kendall Arslanian, Kate Nyhan, Elizabeth Izampuye, Nicola L. Hawley.
Software: Bohao Wu, Veronika Shabanova, Kate Nyhan, Nicola L. Hawley.
PLOS GLOBAL PUBLIC HEALTH
Preterm birth prevalence among Pacific Islanders: A meta-analysis
PLOS Global Public Health | https://doi.org/10.1371/journal.pgph.0001000 June 14, 2023 14 / 19
Supervision: Bohao Wu, Veronika Shabanova, Sarah Taylor, Nicola L. Hawley.
Validation: Bohao Wu, Veronika Shabanova, Sarah Taylor, Bethel Muasau-Howard, Alec
Ekeroma, Nicola L. Hawley.
Visualization: Bohao Wu, Veronika Shabanova.
Writing original draft: Bohao Wu.
Writing review & editing: Bohao Wu, Veronika Shabanova, Kendall Arslanian, Kate
Nyhan, Elizabeth Izampuye, Sarah Taylor, Bethel Muasau-Howard, Alec Ekeroma, Nicola
L. Hawley.
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Article
Background Pacific Islander (PI) women in Australia have an increased risk of gestational diabetes (GDM); however, their perinatal outcomes are poorly understood. Aim The aim was to determine the maternal characteristics and perinatal outcomes of PI women with and without GDM compared to Australian/European (AE)–born women. Methods A retrospective analysis of perinatal outcomes of singleton deliveries >20 weeks’ gestation between 1 January 2011 and 31 December 2020 was conducted at a tertiary provider (Melbourne, Australia). Antenatal details and birth outcomes were extracted from the Birth Outcome Systems database. t ‐Tests and χ ² , univariate and multivariable logistic regression analyses assessed the relationship between ethnicity and outcomes. Results Of 52,795 consecutive births, 24,860 AE women (13.3% with GDM) and 1207 PI‐born women (20.1% with GDM) were compared. PI women had significantly greater pre‐pregnancy body mass index (BMI) and significantly lower rates of smoking and nulliparity. PI women with GDM had higher rates of pre‐eclampsia ( P < 0.001), large‐for‐gestational age (LGA) neonates ( P = 0.037) and neonatal hypoglycaemia ( P = 0.017) but lower rates of small‐for‐gestational age neonates ( P = 0.034). Neonatal intensive care unit (NICU)/special care nursery requirements did not increase. After having adjusted for covariates, PI women's risk of LGA neonates (adjusted odds ratio (aOR): 1.06, 95% confidence interval (CI): 0.86–1.31) was attenuated; however, risk of pre‐eclampsia (aOR: 1.49, 95% CI: 1.01–2.21) and neonatal hypoglycaemia (aOR: 1.40, 95% CI: 1.01–1.96) still increased. They were less likely to require a primary caesarean section (aOR: 0.86, 95% CI: 0.73–0.99). Conclusion PI women have higher BMI and GDM rates, contributing to an increased likelihood of adverse perinatal outcomes. BMI is a modifiable risk factor that could be addressed prenatally.
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Introduction Infants born alive <37 weeks are classified as premature. The global estimate of preterm birth in 2014 was 10.6%, and it is the leading cause of death of children under the age of 5 years. Preterm birth disproportionately affects women of minority populations, yet knowledge about the incidence and associated outcomes among Pacific Islanders is limited. The objectives of this scoping review are to identify studies that describe risk factors, maternal-child health outcomes and existing interventions to prevent preterm birth among Pacific Islanders, and to summarise the barriers and facilitators to decrease the burden. Methods and analysis We will follow the Joanna Briggs Institute Manual for Evidence Synthesis for scoping reviews and the Preferred Reporting Items for Scoping Reviews (PRISMA-ScR) to conduct this scoping review. The Covidence web application will be used for data management and consensus review. We will search on MEDLINE ALL (Ovid), EMBASE (Ovid), Web of Science Core Collection (as licensed at Yale), the Cochrane Library, CINAHL (EBSCOhost) and two non-indexed regional journals ( Pacific Journal of Reproductive Health and Pacific Health Dialog ). Title-abstract and full-text screening of eligible studies will be performed by two authors, and data will be extracted by the first author. Outcomes extracted will be presented using evidence mapping. Ethics and dissemination Findings will drive suggestions for new data collection needed to fill knowledge gaps and improve future study designs to decrease the burden of preterm birth among Pacific Islanders. There are no ethical concerns. This protocol will be disseminated in related peer-reviewed journals.
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Background Single group data present unique challenges for synthesises of evidence. Proportional meta-analysis is becoming an increasingly common technique employed for the synthesis of single group data. Proportional meta-analysis shares many similarities with the conduct and reporting of comparative, or pairwise, meta-analysis. While robust and comprehensive methods exist detailing how researchers can conduct a meta-analysis that compares two (or more) groups against a common intervention, there is a scarcity of methodological guidance available to assist synthesisers of evidence in the conduct, interpretation, and importance of proportional meta-analysis in systematic reviews. Main body This paper presents an overview targeted to synthesisers of evidence and systematic review authors that details the methods, importance, and interpretation of a proportional meta-analysis. We provide worked examples of how proportional meta-analyses have been conducted in research syntheses previously and consider the methods, statistical considerations, and presentation of this technique. Conclusion This overview is designed to serve as practical guidance for synthesisers of evidence in the conduct of proportional meta-analyses.
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Objective To explore preterm birth among Māori indigenous peoples through Kaupapa Māori research of preterm birth in Aotearoa New Zealand. Methods Linked maternity, mortality, and hospital data were analyzed for women and their infants born between January 1, 2010 and December 31, 2014. Relative risks (RR) were calculated for each ethnic group for preterm birth, small for gestational age (SGA), and mortality. Results Adjusted rates showed that compared with Māori women, European women were at significantly less risk of having extremely and very preterm infants (RR 0.86, 95% confidence interval [CI] 0.76–0.95). Preterm infants of European women had a significantly lower adjusted RR of early neonatal death (RR 0.65, 95% CI 0.45–0.93) or post‐neonatal death (RR 0.41, 95% CI 0.26–0.64). In addition to ethnicity, preterm rates were influenced by maternal age, body mass index, smoking status, and SGA status. Conclusion This study demonstrates that the Aotearoa New Zealand maternity system privileges whiteness, suggesting that clinical pathways for evidence‐based medical care are not delivered systemically and equitably for all. Health pathways that focus on equity as a fundamental right will enhance health outcomes for Māori women and their infants.
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This study quantifies the magnitude and persistence of differences in adverse birth outcomes between descendants of foreign-born and US-born women by race/ethnicity. Using 1978–2015 California birth records, I linked records of infants to those of their mothers to create an intergenerational sample (N = 501,323 second generation mothers and 633,102 third generation daughters). Prevalence of low birthweight and preterm birth were calculated in both generations by race/ethnicity, and foreign-born status. An initial foreign-born advantage in birth outcomes is present among most racial/ethnic groups with the exception of foreign-born Asian women. In the subsequent generation, the foreign-origin advantage diminishes for most groups and a foreign-origin disadvantage in low birthweight emerges for descendants of Asian women. Findings largely persist after adjustment for sociodemographic and healthcare-related characteristics. These results underscore the importance of disaggregating by race, ethnicity, and foreign origin when possible to better understand perinatal health disparities in the population.
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Background Preterm birth (PTB) accounts for the majority of perinatal morbidity and mortality in developed nations, accounting for 9.9% of all births in the U.S. in 2016. Prior research has primarily focused on disparities between Black and white mothers’ rates of PTB due to racial segregation. However, population health scholarship has been limited on the fastest growing population in the U.S., Asian and Pacific Islanders (API). Racial residential segregation has been well studied, but relatively little research examines the effects of economic segregation on perinatal health. This cross-sectional analysis examines how economic segregation modifies risk for PTB among various API ethnic groups. Methods U.S. natality data were used to identify 134 Metropolitan Statistical Areas (MSA) with >500 API births from 2015 to 2017 (n = 766,711). Economic segregation was calculated for each MSA using 2017 income data using the Rank-Order Information Theory Index (H Index). Generalized Estimating Equations estimated the log-odds of PTB, allowing for modification by ethnicity. Results There is heterogeneity in PTB prevalence by ethnicity and the association of economic segregation is non-linear. The risk for PTB is higher in MSAs with both high and low H Index for Chinese, Filipino, Japanese, Korean, Vietnamese, and Other Pacific Islander mothers. The risk for PTB follows highest in MSAs with mid-range values of standardized H Index for Indian, Hawaiian, Guamanian, and Samoan mothers. Filipino, Hawaiian, Guamanian, and Other Pacific Islander mothers had the highest predicted risk for PTB at mean levels of economic segregation while Chinese mothers had the lowest. Conclusion These findings are examined through the lens of immigration histories related to European colonialism, U.S. imperialism, and globalization. Importantly, the results suggest that current practices of aggregating API health data mask disparities in health and how socially stratifying processes like economic segregation may differ by ethnic group.
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Background Since the start of the COVID-19 outbreak, a large number of COVID-19-related papers have been published. However, concerns about the risk of expedited science have been raised. We aimed at reviewing and categorizing COVID-19-related medical research and to critically appraise peer-reviewed original articles. Methods The data sources were Pubmed, Cochrane COVID-19 register study, arXiv, medRxiv and bioRxiv, from 01/11/2019 to 01/05/2020. Peer-reviewed and preprints publications related to COVID-19 were included, written in English or Chinese. No limitations were placed on study design. Reviewers screened and categorized studies according to i) publication type, ii) country of publication, and iii ) topics covered. Original articles were critically appraised using validated quality assessment tools. Results Among the 11,452 publications identified, 10,516 met the inclusion criteria, among which 7468 (71.0%) were peer-reviewed articles. Among these, 4190 publications (56.1%) did not include any data or analytics (comprising expert opinion pieces). Overall, the most represented topics were infectious disease ( n = 2326, 22.1%), epidemiology ( n = 1802, 17.1%), and global health ( n = 1602, 15.2%). The top five publishing countries were China (25.8%), United States (22.3%), United Kingdom (8.8%), Italy (8.1%) and India (3.4%). The dynamic of publication showed that the exponential growth of COVID-19 peer-reviewed articles was mainly driven by publications without original data (mean 261.5 articles ± 51.1 per week) as compared with original articles (mean of 69.3 ± 22.3 articles per week). Original articles including patient data accounted for 713 (9.5%) of peer-reviewed studies. A total of 576 original articles (80.8%) showed intermediate to high risk of bias. Last, except for simulation studies that mainly used large-scale open data, the median number of patients enrolled was of 102 (IQR = 37–337). Conclusions Since the beginning of the COVID-19 pandemic, the majority of research is composed by publications without original data. Peer-reviewed original articles with data showed a high risk of bias and included a limited number of patients. Together, these findings underscore the urgent need to strike a balance between the velocity and quality of research, and to cautiously consider medical information and clinical applicability in a pressing, pandemic context. Systematic review registration https://osf.io/5zjyx/
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Introduction: Research suggests that neonatal morbidity differs by maternal region of birth at different gestational ages. This study aimed to determine the overall and gestation-specific risk of neonatal morbidity by maternal region of birth, after adjustment for maternal, infant and birth characteristics, for women giving birth in New South Wales, Australia, from 2003 to 2016. Material and methods: The study utilized a retrospective cohort study design using linked births, hospital and deaths data. Modified Poisson regression was used to determine risk with 95% confidence intervals (95% CI) of neonatal morbidity by maternal region of birth, overall and at each gestational age, compared with Australian or New Zealand-born women giving birth at 39 weeks. Results: There were 1 074 930 live singleton births ≥32 weeks' gestation that met the study inclusion criteria, and 44 394 of these were classified as morbid, giving a neonatal morbidity rate of 4.13 per 100 live births. The gestational age-specific neonatal morbidity rate declined from 32 weeks' gestation, reaching a minimum at 39 weeks in all maternal regions of birth. The unadjusted neonatal morbidity rate was highest in South Asian-born women at most gestations. Adjusted rates of neonatal morbidity between 32 and 44 weeks were significantly lower for babies born to East (adjusted relative risk [aRR] 0.65, 95% CI 0.62-0.68), South-east (aRR 0.76, 95% CI 0.73-0.79) and West Asian-born (aRR 0.93, 95% CI 0.88-0.98) mothers, and higher for babies of Oceanian-born (aRR 1.11, 95% CI 1.04-1.18) mothers, compared with Australian or New Zealand-born mothers. Babies of African, Oceanian, South Asian and West Asian-born women had a lower adjusted risk of neonatal morbidity than Australian or New Zealand-born women until 37 or 38 weeks' gestation, and thereafter an equal or higher risk in the term and post-term periods. Conclusions: Maternal region of birth is an independent risk factor for neonatal morbidity in New South Wales.
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In this paper, we analyze detailed maternal and paternal race information in a 25-year time series of birth record data to consider racial inequities in premature births experienced by women of color and women within interracial parent couples. We analyze birth outcomes within Utah, a historically racially homogeneous state experiencing growing racial diversity and interracial marriage over the past two decades. Our analyses consider disparities in preterm birth according to maternal race and the interracial status of couples for all birth certificate records within the Utah Population Database from 1989 to 2015 (N = 1,148,818). Our results, consistent with a dyadic perspective on minority stress, indicate that maternal race and interracial parent-couple status are each significantly associated with heightened risk of premature birth. The odds of preterm birth are significantly greater among all four racialized groups in the analyses (African Americans, Asians, Native Americans, and Native Hawaiian or Pacific Islanders) as compared to White women. Furthermore, we find that mothers in mixed-race parent couples with either a white or a black father experience a greater risk of preterm birth than mothers parenting with a father of the same race. Our results suggest that in order to capture the complete perspective on racial-ethnic disparities in adverse birth outcomes, outcomes pivotal for subsequent health outcomes over the life course, it is critical to address racism’s toxic effects across multiple levels of lived experience—from the individual level, to the parent dyad, to the local community and beyond.
Article
Background: Early prenatal care is vital for improving maternal health outcomes and health behaviors, but medically vulnerable and underserved populations are less likely to begin prenatal care in the first trimester. In 2017, the Health Center Program provided safety-net care to more than 27 million persons, including 573 026 prenatal patients, at approximately 12 000 sites across the United States and U.S. jurisdictions. As part of a mandatory reporting requirement, health centers tracked whether patients initiated prenatal care in their first trimester of pregnancy. Objective: To identify health center characteristics associated with the initiation of prenatal care in the first trimester, as well as actionable steps policymakers, providers, and health centers can take to promote early initiation of prenatal care. Design: Secondary analysis of cross-sectional data from the 2017 Uniform Data System. Setting: The United States and 8 U.S. jurisdictions. Participants: Health center grantees with prenatal patients (n = 1281). Measurements: Multinomial logistic regression (adjusted for state or jurisdiction clustering) was used to identify health center characteristics associated with achievement of the Healthy People 2020 baseline (77.1%) and target (84.8%) for women receiving prenatal care in the first trimester (Maternal, Infant, and Child Health Objective 10.1). Results: Overall, 57.4% of health centers met the Healthy People 2020 baseline (mean, 78%; median, 81%), and 37.9% met the Healthy People 2020 target. Several characteristics were positively associated with meeting the baseline (larger proportion of prenatal patients aged 20 to 24 years) and target (more total patients, prenatal care by referral only, a larger proportion of prenatal patients aged 25 to 44 or ≥45 years, and a larger proportion of White or privately insured patients). Other characteristics were negatively associated with the baseline (location outside New England, location in a rural area, and a large proportion of prenatal patients aged <15 years) and target (more prenatal patients, location outside New England, provision of prenatal care to women living with HIV, and more uninsured patients or patients eligible for both Medicare and Medicaid). Limitation: The data set is at the health center grantee level and does not contain information on timing or quality of follow-up prenatal care. Conclusion: Most health centers met the Healthy People 2020 baseline, but opportunities for improvement remain and the Healthy People 2020 target is still a challenge for many health centers. Policymakers, providers, and health centers can learn from high-achieving centers to promote early initiation of prenatal care among medically vulnerable and underserved populations. Primary funding source: Health Resources and Services Administration.
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In response to the coronavirus pandemic, several countries have imposed curfews, quarantines, and lockdowns to restrict the spread of the infection among people. India had initiated a nationwide lockdown to combat the pandemic starting from the last week of March until the end of May 2020. But, the lockdown had continued subsequently in several red zones across parts of the country for few months. However, scientists have criticized the government’s abrupt lockdown since it prevented people from preparing for the worst aftermath. Besides, the curfews have blocked millions of impoverished migrant workers from leaving cities to return to their homes in distant rural villages. As a result, the destitute workers have endured enormous hardship and outright discrimination desolately leading to their added physical and mental distress, pain, suffering, and death. Most of the victims of the lockdown have belonged to the economically distressed lower social classes of the Indian caste hierarchy. This article outlines their sufferings triggered by the long drawn-out lockdown episode.