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DOI: 10.1111/1471-0528.

15173 Systematic review


www.bjog.org

Clinical guidelines for prevention and


management of preterm birth: a systematic
review
N Medley,a B Poljak,a S Mammarella,b Z Alfirevica
a
Department of Women’s and Children’s Health, University of Liverpool, Liverpool Women’s Hospital, Liverpool, UK b Royal Victoria
Infirmary Hospital, Newcastle upon Tyne, UK
Correspondence: N Medley, Department of Women’s and Children’s Health, University of Liverpool, Liverpool Women’s Hospital, Crown
Street, Liverpool L8 7SS. 0151 795 9571. Email nmedley2@liv.ac.uk

Accepted 29 January 2018. Published Online 26 March 2018.

Background Clinical practice guidelines (CPG) endorse multiple Main results We identified 49 guidelines from 16 guideline
strategies to prevent or manage preterm birth (PTB). developers. We found consensus for several clinical practices:
cervical length screening for high-risk women; short-term tocolysis;
Objectives To summarise CPG recommendations for PTB and
steroids for fetal lung maturation; and magnesium sulphate for
identify areas of international consensus.
fetal neuroprotection. We found discrepant recommendations for
Search strategy In May 2017 we searched for all CPG relevant to progesterone and fibronectin. No guideline identified an effective
PTB without language restrictions. strategy for women with multiple pregnancy.
Selection criteria CPG were eligible if the following criteria were Conclusions We identified interventions for which there is an
met: (1) the guideline was published or current from June 2013; international consensus on benefit for PTB. Systematic reviews of
(2) the guideline recommended practices for the prevention or CPG using standardised methodology will help avoid duplication
management of PTB relevant to our prespecified clinical and target scarce resources for guideline developers globally.
questions for screening, medications or surgery and other
Keywords Clinical practice guideline, premature birth, preterm
interventions; (3) publications on methods of guideline
birth.
development for eligible CPG were included to enable quality
assessment. Tweetable abstract International clinical guidelines agree on the
benefits and harmful effects of several important interventions to
Data collection and analysis Two authors classified CPG
prevent preterm birth.
recommendations relevant to prespecified clinical questions. When
more than 70% of CPGs reporting on a topic recommended or Linked article This article is commented on by L Al-Hafez and SP
rejected an intervention, we regarded this as consensus. We Chauhan, p. 1370 in this issue. To view this mini commentary
summarised recommendations in tables. visit https://doi.org/10.1111/1471-0528.15228

Please cite this paper as: Medley N, Poljak B, Mammarella S, Alfirevic Z. Clinical guidelines for prevention and management of preterm birth: a systematic
review. BJOG 2018;125:1361–1369.

a key component of the global strategy to reduce newborn


Introduction
deaths, as set out in the United Nations’ Sustainable Devel-
Complications from preterm births (PTB) are a primary opment Goals to 2030.7
cause of neonatal deaths worldwide, with surviving infants Experts continue to debate the optimal clinical care of
at risk of serious neonatal complications and long-term pregnant women to prevent or manage PTB. Short- and
disability.1 The economic cost of PTB was estimated to be long-term effects of diverse interventions must be set
£2.9 billion for a single year in the UK,2,3 with the psycho- against women’s individual histories and preferences. Clini-
logical, social and financial costs to families no less cal setting also has an important impact on cost-effective-
profound.4,5 A World Health Organization (WHO) prior- ness. Even within the diverse individual, social and
ity-setting exercise identified PTB as a ‘top ten’ research economic structures that shape women’s antenatal care, it
priority to 2025.6 Discovery research to prevent PTB is also is now accepted that healthcare providers can improve

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Medley et al.

outcomes for pregnant women and their babies by follow-


Table 1. Clinical questions
ing evidence-based guidelines.8,9 There is also widespread
agreement that use of guidelines can improve efficient use 1. Should we use tocolysis long term to prolong pregnancy in
of resources,10 but implementation remains difficult.11 women with threatened preterm labour?
A recent study suggests that methods for guideline develop- 2. Should we use tocolysis short term to prolong pregnancy (up
to 48 hours) to allow for the administration of antenatal
ment have improved.12 As the need for up-to-date guidance
steroids?
continues, efforts to reduce duplication, improve collaboration 3. Should we use magnesium sulphate in women with
among guideline developers and establish methods for guide- threatened preterm labour?
line adaptation and more efficient updating have received 4. Should we use antibiotics as a prophylaxis in women with
wider consideration.13,14 The objectives of this study are to intact membranes but threatened preterm birth (PTB)?
propose a methodology for reviewing the content of practice 5. Should we use antibiotics in preterm prelabour rupture of
guidelines and, with this, to identify consensus and inconsis- membranes (PPROM) women?
6. Should we use steroids in preterm birth?
tency in recommendations across the PTB-related guidelines.
7. Should we use a second course of steroids?
8. Should we use elective cervical cerclage in women with more
Methods than three previous preterm births?
9. Should we use cervical cerclage in women with a history of
We based our review methods on two systematic reviews of one preterm birth before 34 weeks?
guidelines.8,9 10. Should we use cervical cerclage in women with a cervical
length <25 mm detected between 16 and 24 weeks and
without previous PTB?
Search strategy
11. Should we use cervical cerclage in women with a cervical
In June 2016 we searched six online databases including length <25 mm detected before 24 weeks and previous
Medline (Ovid) using a broad search strategy without lan- preterm birth?
guage restrictions. We checked references for additional 12. Should we use cervical cerclage in high-risk women (uterine
guidelines and hand-searched the websites of professional anomalies or cervical surgery as sole indication)?
societies. In May 2017 we repeated our hand searches and 13. Should we use cervical cerclage in twin pregnancy?
the Medline (Ovid) search, and we searched the online 14. Should we use transabdominal cerclage in women with a
history of cervix insufficiency with prior unsuccessful vaginal
database Literatura Latino Americana en Ci^encias da Sa ude
cervical cerclage?
virtual health library (LILACS). All search strategies com- 15. Should we use rescue or emergency cerclage in threatened
bined the keywords preterm or premature with birth, preterm labour before 34 weeks?
labour or delivery. Where possible, we limited the search 16. Should we use cervical length as universal screening in each
results of online databases to the article type ‘practice pregnancy?
guideline’. Full details of individual database search terms 17. Should we use cervical length as screening in high-risk
and results appear in Supporting Information Appendix S1 women?
18. Should we screen for bacterial vaginosis to prevent PTB in
and in a published protocol for this review.15
women without signs of preterm labour or PPROM?
We developed a list of clinical questions to inform the 19. Should we screen for asymptomatic bacteriuria to prevent
eligibility of practice guidelines and enable efficient searches PTB?
of guidelines. The list emerged from the Cochrane Preg- 20. Should we use vaginal progesterone supplementation
nancy and Childbirth review topic list and close readings of between 16 and 24 weeks in women with prior preterm
widely known practice guidelines; the process was iterative. birth but without short cervix?
The finalised list of 27 clinical questions delineates the 21. Should we use vaginal progesterone in asymptomatic women
with cervical length <20 mm before or at 24 weeks and
scope of this review (Table 1). We did not search for or
without history of PTB?
summarise topics relevant to PTB beyond those prespeci- 22. Should we use vaginal progesterone in twin pregnancy to
fied in our clinical questions. Eligible guidelines met the prevent preterm labour?
following criteria: 23. Should we use progesterone and cervical cerclage in women
 The guideline was published or assessed as current from at high risk of preterm labour?
June 2013. 24. Should we use pessary to prevent preterm labour?
 The guideline recommended clinical practices for the pre- 25. Should we use pessary to prevent preterm labour in twin
pregnancy?
vention or management of PTB relevant to our prespeci-
26. Should we use fibronectin as a screening in women at risk of
fied questions on screening, medications or surgery and preterm birth?
other interventions. 27. Should we use amnioinfusion in PPROM during labour?
 Guidelines targeted asymptomatic pregnant women,
women with risk factors or women presenting with

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Clinical practice guidelines for preterm birth

clinical signs of preterm labour or birth as defined by the For each clinical question we then reported the num-
guideline. Women had singleton or multiple pregnancy. ber of guidelines with relevant recommendations and
 Guidelines were written for single or multiple interven- used this number as a ‘denominator’. When a guideline’s
tions. recommendation for a specific clinical question was clas-
 Publications on the methodology of guideline develop- sified as ‘Yes’ or ‘Conditional yes’ for more than 70% of
ment for eligible CPG were included to enable quality guidelines reporting on the question, we understood this
assessment. as general support between guidelines and overall
Two researchers completed eligibility assessment indepen- endorsement. This logic also applied to recommendations
dently; we resolved conflicts through discussion. We sought against using an intervention to prevent or treat PTB. If
help from native speakers with clinical expertise to assess the more than 70% of reporting guidelines recommend that
eligibility of several guidelines not published in English, as a clinical strategy not be used with ‘No’ or ‘Not enough
documented below in Acknowledgements. We did not carry evidence’’ we recorded this as consensus on not using
out duplicate assessment of foreign language guidelines. the intervention. We did not summarise guideline recom-
mendations for health providers to ‘consider’ various
Quality assessment treatments, nor did we summarise unclear recommenda-
We assessed the adherence of guidelines to four of 13 Insti- tions. We note specific clinical questions with no or
tute of Medicine (IOM) Standards for a Trustworthy very few guideline recommendations in the discussion
Guideline.16,17 We chose four general standards prioritised below.
by this review team:
 Did the guideline describe a development and funding
Results
process that was publicly accessible?
 Did the guideline address gaps in evidence and sum- Of 750 screened records, 639 were excluded as being irrele-
marised evidence for benefits and harms related to each vant or duplications and 55 were not practice guidelines or
recommendation? were published before 2013. We included 56 articles (49
 Was the guideline based on a systematic review of avail- guidelines and seven methods papers) produced by the 16
able evidence? guideline developers listed below:
 Was the guideline developed by a multidisciplinary panel  American Congress of Obstetricians and Gynecologists
made up of clinical experts and patients or other health (ACOG)
consumers?  Belgium Healthcare Knowledge Centre (KCE)
Most included guideline developers contributed more  Chinese Society for Obstetrics and Gynecology
than one guideline to this review. Therefore, we sum-  National College of Gynecologists and Obstetricians -
marised adherence to IOM standards for each included France
guideline developer (based on methodological papers and  International Society of Ultrasound in Obstetrics and
select guidelines) rather than for each of the 49 included Gynecology (ISUOG)
guidelines. We conducted duplicate quality assessment with  Society of Obstetrics and Gynecology - Japan
disagreement resolved by discussion.  King Edward Memorial Hospital Western Australia (WA)
 National Institute for Clinical Excellence, UK (NICE)
Summarising evidence  New Zealand and Australian Clinical Practice Guidelines
To summarise guideline recommendations we divided the (NZA)
clinical questions into screening strategies, medications and  Queensland Australia
surgical or other interventions. Two authors independently  Royal College of Obstetrics and Gynaecology, UK
categorised recommendations according to the following (RCOG)
scheme:  Royal Women’s Hospital Australia
 Yes – the guideline recommends the practice  South Australia (SA)
 Conditional yes – the guideline recommends the practice  Society of Obstetricians and Gynaecologists of Canada
for specific subgroups of women (SOGC)
 Consider – the guideline states that the practice may be  University of Michigan Prenatal Care
considered under certain conditions or in subgroups  World Health Organization (WHO)
 No – the guideline advises against the practice We identified 29 current guidelines via hand searches;
 The guideline states further research is needed or there is such searches are particularly important for locating guide-
insufficient evidence to recommend line updates because some professional societies, such as
 The guideline does not mention the clinical question SOGC and ACOG, identified guidelines ‘reaffirmed as cur-
 The guideline recommendation is unclear rent’ only on their respective websites.18,19 Included

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Medley et al.

practice guidelines and reports on guideline methods are Five of our clinical questions related to screening practices
listed in the references to this paper.20–77 We documented (Table 2). We found consensus for two clinical scenarios.
search results and eligibility decisions in Supporting Infor- Guidelines reporting on cervical length (CL) screening for high-
mation Figure S1 (PRISMA flow diagram) and Supporting risk women endorsed the practice for this subgroup. No guide-
Information Appendix S2 (Excluded studies). line advised against using CL screening in high-risk women.
Sixteen of the 49 included guidelines were written specif- Just two guidelines reported on screening for asymptomatic
ically for the prevention or management of PTB. Other bacteriuria to prevent PTB; both recommended this strategy.
guidelines covered the following topics: obstetric, antenatal Most guidelines advised against using universal screening
or perinatal care (6); prelabour rupture of membranes of CL in each pregnancy; just two of the eight guidelines
(PROM) or preterm prelabour rupture of membranes that reported recommendations for this practice endorsed
(PPROM) (5); ultrasound in pregnancy (4); magnesium universal screening (Michigan; Japan). A similar number of
sulphate (4); multiple or twin pregnancy (3); screening guidelines advised against screening for bacterial vaginosis
during pregnancy (3); and cerclage (2). Single guidelines (BV) in pregnant women without signs of preterm labour
addressed antibiotics during pregnancy, nifedipine, tocoly- or PPROM. Two guidelines argued for BV screening for
sis and progesterone.
We assessed development methodologies for adherence
to four of 13 IOM indicators of quality.22,23 See Supporting Table 2. Screening strategies to prevent or manage preterm birth
Information Table S1 for complete assessments. (columns present number of guidelines that make
Seven guideline developers had clear and publicly acces- recommendations)

sible funding processes. Four additional developers replied Key Yes Conditional No Not enough
via email to describe their funding process (ACOG; China; recommendations Yes evidence to
SOGC; SA). Remaining guideline developers provided no recommend
clear information regarding funding attached to publica-
tions or websites. Guidelines endorsed. . .
All guideline developers made efforts to assess gaps in Cervical length as 5 3* 0 1
evidence and consider both benefits and harmful effects screening in high-risk
related to recommendations. Guideline developers based women only
Screening for 2 0 0 0
recommendations on formal systematic reviews of evidence,
asymptomatic
with the exception of two: both Michigan and The Royal bacteriuria to prevent
Women’s Hospital Australia drew evidence from literature PTB
searches (which included Cochrane systematic Guidelines advised against. . .
reviews).69,70,72 Finally, nine guideline developers included Cervical length as 2 0 4 2
patients or members of the public in interdisciplinary universal screening in
guideline panels. Two guideline developers reported (via each pregnancy
Screening for bacterial 0 2** 5 0
email) that they involved no members of the public or
vaginosis to prevent
patients [China; SOGC]; remaining guidelines had no PTB in women
details. without signs of PTL
The quality assessment validates our eligibility decisions. or PPROM
Included guidelines were overwhelmingly based on good- Guidelines found little consensus on . . .
quality methods, including systematic reviews of available Fibronectin as a 1 3*** 2 1
evidence and the consideration of harms as well as benefits screening method in
women at risk of PTB
of interventions. Just under half of the included guidelines
made their funding process publicly available. More than *ACOG advised against screening women with multiple
half of the included guideline developers involved patients pregnancy.27,28 SOGC also exempted twins.65 The ISUOG guideline
or members of the public. is written for twin pregnancy only (i.e. a high-risk group) and
endorsed the practice.75
**Queensland Australia targeted women with previous PTB57;
Recommendations for clinical practice SOGC targeted symptomatic women or those with risk factors for
We summarised recommendations for clinical practice in PTB.67
Tables 2–4 and Supporting Information Tables S3–S5). ***Belgium KCE targeted cervical length 16–29 mm.30 Western
Where we identified conditional recommendations, we Australia targeted symptomatic women 24–36 weeks, intact
membranes and cervical dilation <3 cm.43 SOGC targeted
included the parameters in footnotes. All recommendations
symptomatic women 22–36 weeks with dilation <3 cm.57
extracted for all included guidelines can be found in
Table S2A-C.

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Clinical practice guidelines for preterm birth

Table 3. Medications to prevent or manage preterm birth (columns Table 4. Surgical and other interventions (columns present number
present number of guidelines that make recommendations) of guidelines with recommendations)

Key recommendations Yes Conditional No Not Key recommendations Yes Conditional No Not
yes enough Yes enough
evidence evidence

Guidelines endorsed. . . Guidelines endorsed. . .


Tocolysis for short-term 4 3* 1 0 Elective cervical cerclage in 3 1* 0 0
prolongation of pregnancy women with more than
(up to 48 hours) to allow three PTB
for the administration of Cervical cerclage in women 5 0 0 0
antenatal steroids with cervical length of
Magnesium sulphate in 1 9** 0 0 <25 mm detected before
women in threatened PTB 24 weeks and previous
Antibiotics for women with 8 2*** 1 0 PTB
PPROM Transabdominal cerclage in 2 0 0 0
Vaginal progesterone in 8 0 0 0 women with history of
asymptomatic women cervical insufficiency with
without history of PTB prior unsuccessful vaginal
who have cervical length cervical cerclage
of <20 mm before or at
24 weeks’ gestation. *ACOG targets 1 or more painless losses due to cervical
Steroids for women with 1 11**** 0 1***** insufficiency and without abruption.24
threatened PTB

*WA targeted women without contraindications and < 34 weeks’


gestation43; The Royal Women’s Hospital Australia targeted for women without symptoms or history of PTB but with
PPROM69; France recommended atosiban or nifedipine for women
an evident short cervix before 24 weeks’ gestation; and ster-
with intact membranes.35
**NICE targeted 24–29 weeks plus 6 days.49 WA targeted singleton
oids for women with threatened PTB.
or multiple pregnancy <30 weeks.46 Queensland targeted 24 to Guidelines advised against using the following: antibiotic
30 weeks57; The Royal Women’s Hospital Australia targeted prophylaxis for women with intact membranes but threat-
imminent PTB, singleton or multiple pregnancy and <30 weeks.70 ened PTB, longer term tocolysis to prolong gestation and
WHO,74 Japan,20 S. Australia36 and France35 all targeted women
vaginal progesterone for women with twin pregnancy.
<30 weeks’ gestation, and China stated <32 weeks and use only for
<48 hours.34
For two clinical questions we found recommendations
***ACOG22 targeted <34 weeks. The Royal Women’s Hospital both for and against with no overall consensus. Guidelines
Australia targeted women up to 32 weeks without PTL or beyond were divided on whether or not to use vaginal progesterone
32 weeks if fetal lung maturity was not proven or delivery not in women with prior PTB but without short cervix. Ten
planned.69
guidelines reported recommendations on the use of a second
****Table S5 has details of conditions placed on steroid use.
*****Japan stated there was not enough evidence to recommend
dose of steroids for women who continue to be at risk of
use for pregnant women before 24 weeks’ gestation (at 22 and PTB; five guidelines endorsed a second dose and five did not.
23 weeks’ gestation). The guideline endorses use beyond 24 weeks Twelve clinical questions covered various surgical strate-
(20). gies to prevent or manage PTB (Tables 4 and S4). We
found consensus for three questions. All guidelines report-
ing on cerclage agreed the procedure should be performed
for women with short cervix and a previous PTB. Likewise,
women with a history of PTB or risk factors (Queensland; guidelines supported elective cerclage for women with mul-
SOGC). tiple prior losses. Two guidelines also endorsed transab-
Guidelines disagreed on the appropriate use of fibronec- dominal cerclage after failed cervical cerclage. No other
tin, with four guidelines endorsing its use in specific cir- circumstances warranted cerclage. Guidelines advised
cumstances and three advising against. against cerclage for women with short cervix but without
Ten clinical questions related to the use of medications prior PTB. Cerclage was not recommended for women with
to prevent or manage PTB (Tables 3 and S3). Guidelines a single prior loss. Guidelines advised against using cerclage
endorsed using active strategies for five of these: short-term for women with twin pregnancy and for women with uter-
tocolysis; magnesium sulphate for fetal neuroprotection; ine anomalies or cervical surgery as the sole indication.
antibiotics for women with PPROM; vaginal progesterone Guidelines advised against using cervical pessary for women

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Medley et al.

with singleton or multiple pregnancy; likewise, guidelines guidance is not exhaustive. Other author teams may have
advised against combining progesterone with cervical approached guidelines with different priorities. For example,
cerclage. peer reviewers of our paper felt strongly that we should have
There was very little guidance for two clinical questions: included diagnostic accuracy of tests for preterm labour and
no included guideline addressed amnioinfusion in preterm the role of low-dose aspirin among our clinical questions.
prelabour rupture of membranes and just two guidelines We chose not to deviate from the clinical questions described
stated that there was insufficient evidence to make a rec- in our published protocol, but this criticism highlights the
ommendation for the use of rescue or emergency cerclage. importance of a transparent method to determine the scope
of a review. For topics as wide-ranging as PTB prevention
and treatment, review teams may require significant input
Discussion
from a broad range of stakeholders to prioritise a clinical
Main findings topic list and, thereby, enable the structured review of guide-
This review of PTB-related guidelines aimed to identify lines. Another criticism was related to our failure to comply
areas of international consensus as well as contested or with the CROWN initiative and use the PTB core outcome
under-studied clinical strategies. We identified nine recom- set (COS) to structure data synthesis.76 The methodology
mendations with consensus regarding the benefit for PTB: proposed here summarises guideline recommendations for
CL screening for high-risk women; screening for asymp- interventions rather than for specific outcomes. However,
tomatic bacteriuria; vaginal progesterone for women with a there is no question that adherence of trials to COS domains
short cervix before 24 weeks’ gestation; short-term tocolysis would improve the quality of guidelines by strengthening the
for women at risk of PTB; antibiotics for women with evidence base for key interventions. Adoption of COS
PPROM; magnesium sulphate for fetal neuroprotection; domains may also improve consistency of guideline recom-
and steroids for women at risk of PTB. Guidelines also mendations.
endorsed cerclage for women with multiple prior losses There are several additional limitations to our synthesis.
and for women with prior PTB and a short cervix before Ambiguous wording obstructs the implementation of guide-
24 weeks’ gestation. Further, we found 12 interventions line recommendations.14 We took the view that guideline
deemed ineffective which should not be supported, includ- recommendations to ‘consider’ various treatments were too
ing antibiotics for women with intact membranes and signs vague to classify. We chose not to evaluate the feasibility of
of PTB, universal CL screening, and cerclage in women recommendations in different settings or to search for rele-
with a single prior loss, multiple pregnancy or no history vant cost-effectiveness data or implementation strategies. We
of PTB. We found no intervention endorsed to prevent or also did not summarise guidelines’ ratings of the quality of
manage PTB in multiple pregnancy. Importantly, for sev- evidence supporting recommendations.
eral clinical questions we found contradictory recommen-
dations – on the use of fibronectin, vaginal progesterone Interpretation in light of other evidence
and a second dose of steroids for women with continued To inform World Health Organization (WHO) guideline
risk of PTB. Recommendations for these clinical questions development, in 2016, Abalos et al.8 and Miller et al.9 sys-
deserve further scrutiny. Finally, we found few or no guide- tematically reviewed CPG recommendations for antenatal
line recommendations for cervical pessary, for amnioinfu- care and routine maternity care. Both reviews noted dis-
sion for women with ruptured membranes or for crepant recommendations. Miller et al.9 also used AGREE
emergency cerclage – these topics deserve further study. II scores to select higher-quality guidelines for further
analysis; they compared CPG recommendations to clinical
Strengths and limitations practice using coverage rates for several recommended
Strengths of this project include the comprehensiveness of and not recommended interventions. Neither WHO
searches (without language restrictions) and quality assess- review evaluated the quality of the evidence supporting
ment to confirm that we summarised the most relevant, recommendations. Other systematic reviews of CPG for
publicly available practice recommendations. In addition hypertension, sugar intake and antenatal infection screen-
we proposed methodology for guideline review to encour- ing reported similar methods [77-79]. However, no review
age research collaboration and reduce waste by identifying listed clinical questions a priori as we have done. Our
areas of international consensus. proposed methodology renders the scope of the
We based the scope of our review on prespecified clinical review transparent and reproducible, enables efficient
questions and followed transparent, replicable methods to searching of CPG and, importantly, eliminates post hoc or
reduce bias. Though we considered the Cochrane Pregnancy informal prioritisation of clinical questions.
& Childbirth topic list and well-known pregnancy guidelines For clinical areas such as PTB prevention and manage-
to prioritise 27 clinical questions, our review of PTB ment, where multiple clinical practice guidelines exist,

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funders should promote collaboration among guideline Takemoto, St. Luke’s International University Graduate
developers and encourage the adaptation of existing good- School of Nursing Science, Tokyo, Japan.
quality guidelines to suit local requirements.13,14 To facili-
tate this process, we urge funders and future guideline
developers to conduct a systematic review of all relevant Supporting Information
clinical practice guidelines before embarking on new, Additional Supporting Information may be found in the
resource-intense guideline development projects. online version of this article:
Figure S1. PRISMA study flow diagram.
Conclusion Table S1. Quality assessment
Table S2. (A-C) All guideline recommendations.
Effective strategies to avoid preterm birth are crucial for Table S3. Medications.
reducing newborn deaths worldwide. For clinical practice Table S4. Surgical and other therapy.
guidelines to improve health outcomes for women and babies, Table S5. Conditional recommendations for steroid use.
guidelines must present clear, credible and feasible recom- Appendix S1. Search strategies.
mendations. To avoid waste of scarce resources, we propose a Appendix S2. Excluded studies. &
method for systematic reviews of guidelines as a prudent first
step in the development of practice guidelines. We welcome
suggestions for improvement of these methods. Researchers
should also consider systematic reviews of guidelines as a References
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ª 2018 Royal College of Obstetricians and Gynaecologists 1369

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