Preterm labor and birth: Difference between revisions

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{{SK}} Preterm delivery, Premature labour, Early delivery, Premature birth, Premature labor, Pre term birth
==Overview==
==Overview==
[[Preterm birth]] is any birth that happens between 20 weeks of gestation and 36 6/7 weeks of gestation.<ref name="pmid27661654">{{cite journal| author=American College of Obstetricians and Gynecologists’ Committee on Practice Bulletins—Obstetrics| title=Practice Bulletin No. 171: Management of Preterm Labor. | journal=Obstet Gynecol | year= 2016 | volume= 128 | issue= 4 | pages= e155-64 | pmid=27661654 | doi=10.1097/AOG.0000000000001711 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27661654  }} </ref> In Europe it is defined after 22 weeks and before 37 weeks of gestation. The gestation can be dated using [[first trimester ultrasound]]. In the US, approximately 12% of the births are preterm, while in Europe it varies between 5-18%.<ref name="pmid28482713">{{cite journal| author=Di Renzo GC, Cabero Roura L, Facchinetti F, Helmer H, Hubinont C, Jacobsson B | display-authors=etal| title=Preterm Labor and Birth Management: Recommendations from the European Association of Perinatal Medicine. | journal=J Matern Fetal Neonatal Med | year= 2017 | volume= 30 | issue= 17 | pages= 2011-2030 | pmid=28482713 | doi=10.1080/14767058.2017.1323860 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28482713  }} </ref> The diagnosis is made based on clinical criteria which include: [[cervical dilation]] of at least 2cm and/or [[cervical effacement]], which happens with regular [[uterine contractions]]. It may happen with or without [[rupture of membrane]]. [[Preterm labor]] and delivery is associated to many risks for the babies such as: [[respiratory distress syndrome]], periventricular leukomalacia, [[intraventricular hemorrhage]], [[bronchopulmonary dysplasia]], [[necrotizing enterocolitis]], late-onset infection, [[retinopathy of prematurity]], [[cerebral palsy]] and other adverse neurological outcomes.<ref name="pmid25300768">{{cite journal| author=Tsimis ME, Abu Al-Hamayel N, Germaine H, Burd I| title=Prematurity: present and future. | journal=Minerva Ginecol | year= 2015 | volume= 67 | issue= 1 | pages= 35-46 | pmid=25300768 | doi= | pmc=4323881 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25300768  }} </ref> (25300768)
[[Preterm birth]] is any birth that happens between 20 weeks of [[gestation]] and 36 6/7 weeks of gestation. In Europe, it is defined after 22 weeks and before 37 weeks of [[gestation]]. The [[gestation]] can be dated using [[first-trimester ultrasound]]. In the US, approximately 12% of the births are preterm, while in Europe it varies between 5-18%.The [[diagnosis]] is made based on clinical criteria which include: [[cervical dilation]] of at least 2cm and/or [[cervical effacement]], which happens with regular [[uterine contractions]]. It may happen with or without [[rupture of membrane]]. [[Preterm labor]] and [[delivery]] is associated to many risks for the babies such as: [[respiratory distress syndrome]], periventricular leukomalacia, [[intraventricular hemorrhage]], [[bronchopulmonary dysplasia]], [[necrotizing enterocolitis]], late-onset infection, [[retinopathy of prematurity]], [[cerebral palsy]] and other adverse [[neurological]] outcomes.


==Historical Perspective==
==Historical Perspective==
[Disease name] was first discovered by [name of scientist], a [nationality + occupation], in [year]/during/following [event].


The association between [important risk factor/cause] and [disease name] was made in/during [year/event].
*In the 1930s, George Corner was the first to suggest the association between [[progesterone]] and the development of [[preterm labor]].<ref name="pmid28889957">{{cite journal| author=Talati AN, Hackney DN, Mesiano S| title=Pathophysiology of preterm labor with intact membranes. | journal=Semin Perinatol | year= 2017 | volume= 41 | issue= 7 | pages= 420-426 | pmid=28889957 | doi=10.1053/j.semperi.2017.07.013 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28889957  }} </ref>
 
*James Elgin Gill (born on [[20 May]] [[1987]] in [[Ottawa]], [[Canada]]) was the earliest premature baby in the world. He was 128 days premature (21 weeks and 5 days gestation) and weighed 1 lb. 6 oz.  (624 g). He survived and is quite healthy.<ref name="titlePowell's Books - Guinness World Records 2004 (Guinness Book of Records) by">{{cite web |url=http://www.powells.com/biblio?show=0553587129&page=excerpt? |title=Powell's Books - Guinness World Records 2004 (Guinness Book of Records) by |accessdate=2007-11-28 |format= |work=}}</ref><ref name="titleMiracle child">{{cite web |url=http://www.canada.com/topics/bodyandhealth/story.html?id=db8f33ab-33e9-429f-bedc-b6ca80f61bdc |title=Miracle child |accessdate=2007-11-28 |format= |work=}}</ref>
In the 1930s, George Corner was the first to suggest the association between progesterone and the development of preterm labor.<ref name="pmid28889957">{{cite journal| author=Talati AN, Hackney DN, Mesiano S| title=Pathophysiology of preterm labor with intact membranes. | journal=Semin Perinatol | year= 2017 | volume= 41 | issue= 7 | pages= 420-426 | pmid=28889957 | doi=10.1053/j.semperi.2017.07.013 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28889957  }} </ref>
 
In [year], [gene] mutations were first implicated in the pathogenesis of [disease name].
 
There have been several outbreaks of [disease name], including -----.
 
In [year], [diagnostic test/therapy] was developed by [scientist] to treat/diagnose [disease name].


==Classification==
==Classification==


[[Preterm labor]] may be classified according to the [[WHO]] into 3 subtypes/groups: extremely preterm (<28 weeks), very preterm (28 to 32 weeks), moderate to late preterm (32-37 weeks). https://www.who.int/news-room/fact-sheets/detail/preterm-birth
*[[Preterm labor]] may be classified according to the [[WHO]] into 3 groups: extremely preterm (<28 weeks), very preterm (28 to 32 weeks), moderate to late preterm (32-37 weeks).<ref name="urlPreterm birth">{{cite web |url=https://www.who.int/news-room/fact-sheets/detail/preterm-birth |title=Preterm birth |format= |work= |accessdate=2020-09-13}}</ref>


==Pathophysiology==
==Pathophysiology==
It is thought that [[preterm labor]] is the is mediated by either [[progesterone]], which promotes uterine relaxation to maintain pregnancy and [[inflammation]] of the gestational tissues, which acts as a key trigger opposing the effects of [[progesterone]] and inducing [[progesterone]] withdraw. Therefore, the occurrence of [[preterm labor]] with intact membranes depends on a balance between pro-labor/pro-inflammatory factors versus pro-pregnancy effects of [[progesterone]].<ref name="pmid28889957">{{cite journal| author=Talati AN, Hackney DN, Mesiano S| title=Pathophysiology of preterm labor with intact membranes. | journal=Semin Perinatol | year= 2017 | volume= 41 | issue= 7 | pages= 420-426 | pmid=28889957 | doi=10.1053/j.semperi.2017.07.013 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28889957  }} </ref>
 
[[Preterm premature rupture of membranes]] ([[PPROM]]) has unknown etiology and may lead to preterm labor. Some factors increase the risk of PPROM such as [[cervical shortening]] or [[intra-amniotic infection]].<ref name="pmid30016035">{{cite journal| author=Meller CH, Carducci ME, Ceriani Cernadas JM, Otaño L| title=Preterm premature rupture of membranes. | journal=Arch Argent Pediatr | year= 2018 | volume= 116 | issue= 4 | pages= e575-e581 | pmid=30016035 | doi=10.5546/aap.2018.eng.e575 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=30016035  }} </ref>
*It is thought that [[preterm labor]] is the is mediated by either [[progesterone]], which promotes uterine relaxation to maintain pregnancy and [[inflammation]] of the gestational tissues, which acts as a key trigger opposing the effects of [[progesterone]] and inducing [[progesterone]] withdraw.<ref name="pmid28889957">{{cite journal| author=Talati AN, Hackney DN, Mesiano S| title=Pathophysiology of preterm labor with intact membranes. | journal=Semin Perinatol | year= 2017 | volume= 41 | issue= 7 | pages= 420-426 | pmid=28889957 | doi=10.1053/j.semperi.2017.07.013 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28889957  }} </ref>
*The switch from a quiescent [[myometrium]] into an active one is mediated by [[inflammatory]] pathways that include [[IL-8]], [[IL-1]], [[IL-6]] and [[proteins]] such as [[oxytocin]] receptor, [[connexin]] 43 and [[prostaglandin]] receptor.<ref name="pmid25124429">{{cite journal| author=Romero R, Dey SK, Fisher SJ| title=Preterm labor: one syndrome, many causes. | journal=Science | year= 2014 | volume= 345 | issue= 6198 | pages= 760-5 | pmid=25124429 | doi=10.1126/science.1251816 | pmc=4191866 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25124429  }} </ref>
*Changes in the [[extracellular matrix protein]]s leads to cervical effacement and is the result of an increase in [[glycosaminoglycans]] and loss in [[collagen]] cross-linking results in a decrease in the tensile strength of the [[cervix]].<ref name="pmid30016035">{{cite journal| author=Meller CH, Carducci ME, Ceriani Cernadas JM, Otaño L| title=Preterm premature rupture of membranes. | journal=Arch Argent Pediatr | year= 2018 | volume= 116 | issue= 4 | pages= e575-e581 | pmid=30016035 | doi=10.5546/aap.2018.eng.e575 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=30016035  }} </ref>
*Increase in inflammatory factors such as [[TNF-alpha]] and [[IL-1]] lead to the activation of [[proteases]] ([[MMP-8]]) and dissolution of [[fibronectin]] which leads to withdrawal of [[Decidual cells|decidual]] support for [[pregnancy]]. This event causes separation of the [[chorioamniotic membranes]] from the [[decidua]] and eventually membrane rupture.<ref name="pmid25124429">{{cite journal| author=Romero R, Dey SK, Fisher SJ| title=Preterm labor: one syndrome, many causes. | journal=Science | year= 2014 | volume= 345 | issue= 6198 | pages= 760-5 | pmid=25124429 | doi=10.1126/science.1251816 | pmc=4191866 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25124429  }} </ref>
*Therefore, the occurrence of preterm labor with intact membranes depends on a balance between pro-labor/pro-[[inflammatory]] factors versus pro-pregnancy effects of [[progesterone]].<ref name="pmid28889957">{{cite journal| author=Talati AN, Hackney DN, Mesiano S| title=Pathophysiology of preterm labor with intact membranes. | journal=Semin Perinatol | year= 2017 | volume= 41 | issue= 7 | pages= 420-426 | pmid=28889957 | doi=10.1053/j.semperi.2017.07.013 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28889957  }} </ref>
*[[Preterm premature rupture of membranes]] ([[PPROM]]) has unknown etiology and may lead to preterm labor.
*Some factors increase the risk of PPROM such as [[cervical shortening]] or [[intra-amniotic infection]].<ref name="pmid30016035">{{cite journal| author=Meller CH, Carducci ME, Ceriani Cernadas JM, Otaño L| title=Preterm premature rupture of membranes. | journal=Arch Argent Pediatr | year= 2018 | volume= 116 | issue= 4 | pages= e575-e581 | pmid=30016035 | doi=10.5546/aap.2018.eng.e575 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=30016035  }} </ref>


==Causes==
==Causes==
Disease name] may be caused by [cause1], [cause2], or [cause3].
OR
Common causes of [disease] include [cause1], [cause2], and [cause3].


OR
*[[Preterm labor]] may be caused by [[infection]], [[uterine ovedistension]], [[decidual senescence]], [[vascular disorders]], [[stress]], [[cervical disease]], decline in [[progesterone]] action, or breakdown in [[maternal]]-[[fetal]] tolerance.
*So far, only [[intra-amniotic infection]] has been shown to cause preterm delivery. The other factors are being associated based on reports by clinical, [[epidemiologic]], placental [[Pathological|pathologic]], or experimental studies.
*[[Intra-amniotic infection|Intra-amniotic infections]] can be subclinical. One in four preterm [[infants]] are born due to this [[Causes|cause]].<ref name="pmid25124429">{{cite journal| author=Romero R, Dey SK, Fisher SJ| title=Preterm labor: one syndrome, many causes. | journal=Science | year= 2014 | volume= 345 | issue= 6198 | pages= 760-5 | pmid=25124429 | doi=10.1126/science.1251816 | pmc=4191866 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25124429  }} </ref>
**The most frequent route is the ascending pathway, but hematogenous dissemination can occur.
**[[Microorganisms]] are recognized by pattern recognition receptors, such as [[toll-like receptors]] (TLRs)
**[[TLR]]s stimulate the production of [[chemokines]] ([[IL-8]], [[C-C motif ligand 2]] (CCL2), etc.), [[cytokines]] ([[IL-1b]], [[TNF-a]], etc), [[prostaglandins]] and [[proteases]] which activate the quiescent [[myometrium]] and stimulates parturition.<ref name="pmid25124429">{{cite journal| author=Romero R, Dey SK, Fisher SJ| title=Preterm labor: one syndrome, many causes. | journal=Science | year= 2014 | volume= 345 | issue= 6198 | pages= 760-5 | pmid=25124429 | doi=10.1126/science.1251816 | pmc=4191866 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25124429  }} </ref>
**In 30% of cases of [[intra-amniotic infection]], [[bacteria]] can be found in the [[fetal circulation]] which causes [[fetal]] [[systemic inflammatory response]]. These fetuses are at risk for long-term [[complications]], such as [[cerebral palsy]] and [[chronic lung disease]], which emphasizes that these [[complications]] may not only occur due to immaturity but also [[inflammatory]] response.<ref name="pmid25124429">{{cite journal| author=Romero R, Dey SK, Fisher SJ| title=Preterm labor: one syndrome, many causes. | journal=Science | year= 2014 | volume= 345 | issue= 6198 | pages= 760-5 | pmid=25124429 | doi=10.1126/science.1251816 | pmc=4191866 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25124429  }} </ref>


The most common cause of [disease name] is [cause 1]. Less common causes of [disease name] include [cause 2], [cause 3], and [cause 4].
==Differentiating preterm labor from other Diseases==


OR
*Preterm labor [[diagnosis]] is not challenging and it must be investigated if it is caused by other diseases that also cause [[abdominal pain]], [[rupture of membranes]] and [[fetal distress]].
 
The cause of [disease name] has not been identified. To review risk factors for the development of [disease name], click [[Pericarditis causes#Overview|here]].
 
==Differentiating ((Page name)) from other Diseases==
[Disease name] must be differentiated from other diseases that cause [clinical feature 1], [clinical feature 2], and [clinical feature 3], such as [differential dx1], [differential dx2], and [differential dx3].
 
OR
 
[Disease name] must be differentiated from [[differential dx1], [differential dx2], and [differential dx3].


==Epidemiology and Demographics==
==Epidemiology and Demographics==
The incidence/prevalence of [disease name] is approximately [number range] per 100,000 individuals worldwide.
OR
In [year], the incidence/prevalence of [disease name] was estimated to be [number range] cases per 100,000 individuals worldwide.
OR
In [year], the incidence of [disease name] is approximately [number range] per 100,000 individuals with a case-fatality rate of [number range]%.
Patients of all age groups may develop [disease name].
OR
The incidence of [disease name] increases with age; the median age at diagnosis is [#] years.
OR
[Disease name] commonly affects individuals younger than/older than [number of years] years of age.
OR
[Chronic disease name] is usually first diagnosed among [age group].
OR
[Acute disease name] commonly affects [age group].
There is no racial predilection to [disease name].
OR
[Disease name] usually affects individuals of the [race 1] race. [Race 2] individuals are less likely to develop [disease name].
[Disease name] affects men and women equally.
OR
[Gender 1] are more commonly affected by [disease name] than [gender 2]. The [gender 1] to [gender 2] ratio is approximately [number > 1] to 1.


 
*The [[incidence]] of [[preterm labor]] is approximately 12% of the births in the United States.<ref name="pmid27661654">{{cite journal| author=American College of Obstetricians and Gynecologists’ Committee on Practice Bulletins—Obstetrics| title=Practice Bulletin No. 171: Management of Preterm Labor. | journal=Obstet Gynecol | year= 2016 | volume= 128 | issue= 4 | pages= e155-64 | pmid=27661654 | doi=10.1097/AOG.0000000000001711 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27661654  }} </ref>
 
*In Europe the [[incidence]] varies between 5-18% of the births.<ref name="pmid28482713">{{cite journal| author=Di Renzo GC, Cabero Roura L, Facchinetti F, Helmer H, Hubinont C, Jacobsson B | display-authors=etal| title=Preterm Labor and Birth Management: Recommendations from the European Association of Perinatal Medicine. | journal=J Matern Fetal Neonatal Med | year= 2017 | volume= 30 | issue= 17 | pages= 2011-2030 | pmid=28482713 | doi=10.1080/14767058.2017.1323860 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28482713  }} </ref>
The majority of [disease name] cases are reported in [geographical region].
*Approximately 17% of preterm births occur in the Americas (North, Central and South America, and the Caribbean), Europe and Australia.<ref name="pmid32107766">{{cite journal| author=Souza RT, Cecatti JG| title=A Comprehensive Integrative Review of the Factors Associated with Spontaneous Preterm Birth, Its Prevention and Prediction, Including Metabolomic Markers. | journal=Rev Bras Ginecol Obstet | year= 2020 | volume= 42 | issue= 1 | pages= 51-60 | pmid=32107766 | doi=10.1055/s-0040-1701462 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=32107766  }} </ref>
 
OR
 
[Disease name] is a common/rare disease that tends to affect [patient population 1] and [patient population 2].


==Risk Factors==
==Risk Factors==
There are no established risk factors for [disease name].


OR
*The most potent [[risk factor]] in the development of [[preterm labor]] are history of previous [[preterm birth]], [[smoking]], and [[multiple pregnancy]].<ref name="pmid32107766">{{cite journal| author=Souza RT, Cecatti JG| title=A Comprehensive Integrative Review of the Factors Associated with Spontaneous Preterm Birth, Its Prevention and Prediction, Including Metabolomic Markers. | journal=Rev Bras Ginecol Obstet | year= 2020 | volume= 42 | issue= 1 | pages= 51-60 | pmid=32107766 | doi=10.1055/s-0040-1701462 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=32107766  }} </ref>
 
*The earlier the [[preterm birth]], the higher the risk of having a new case.<ref name="pmid32107766">{{cite journal| author=Souza RT, Cecatti JG| title=A Comprehensive Integrative Review of the Factors Associated with Spontaneous Preterm Birth, Its Prevention and Prediction, Including Metabolomic Markers. | journal=Rev Bras Ginecol Obstet | year= 2020 | volume= 42 | issue= 1 | pages= 51-60 | pmid=32107766 | doi=10.1055/s-0040-1701462 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=32107766  }} </ref>
The most potent risk factor in the development of [disease name] is [risk factor 1]. Other risk factors include [risk factor 2], [risk factor 3], and [risk factor 4].
*Other [[risk factors]] include: low socio-economic status, [[ethnicity]], [[smoking]], maternal [[diabetes]]<ref name="pmid16118366">{{cite journal |author=Rosenberg TJ, Garbers S, Lipkind H, Chiasson MA |title=Maternal obesity and diabetes as risk factors for adverse pregnancy outcomes: differences among 4 racial/ethnic groups |journal=Am J Public Health |volume=95 |issue=9 |pages=1545–51 |year=2005 |pmid=16118366 |doi=10.2105/AJPH.2005.065680}}</ref>, short interpregnancy interval.<ref name="pmid16622143">{{cite journal| author=Conde-Agudelo A, Rosas-Bermúdez A, Kafury-Goeta AC| title=Birth spacing and risk of adverse perinatal outcomes: a meta-analysis. | journal=JAMA | year= 2006 | volume= 295 | issue= 15 | pages= 1809-23 | pmid=16622143 | doi=10.1001/jama.295.15.1809 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16622143  }} </ref> However, when the analysis is performed within women who have had at least three pregnancies (two intervals) and each woman serves as her own control, increased risk is found when the first pregnancy was preterm<ref name="pmid27367283">{{cite journal| author=Koullali B, Kamphuis EI, Hof MH, Robertson SA, Pajkrt E, de Groot CJ et al.| title=The Effect of Interpregnancy Interval on the Recurrence Rate of Spontaneous Preterm Birth: A Retrospective Cohort Study. | journal=Am J Perinatol | year= 2016 | volume=  | issue=  | pages=  | pmid=27367283 | doi=10.1055/s-0036-1584896 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27367283  }} </ref> but not among unselected women.<ref name="pmid25056260">{{cite journal| author=Ball SJ, Pereira G, Jacoby P, de Klerk N, Stanley FJ| title=Re-evaluation of link between interpregnancy interval and adverse birth outcomes: retrospective cohort study matching two intervals per mother. | journal=BMJ | year= 2014 | volume= 349 | issue=  | pages= g4333 | pmid=25056260 | doi=10.1136/bmj.g4333 | pmc=4137882 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25056260  }} </ref> [[low body mass index]], [[periodontitis]], cervical surgery ([[loop electrosurgical excision procedure]]/[[conization]]), [[uterus]] anomaly, [[pregnancy]] loss >16 weeks, gestational age, [[cervical insufficiency]], mode of conception ([[in-vitro fertilization]]), [[multiple pregnancy]], short [[cervix]] (the strongest predictor of premature birth).<ref>To MS, Skentou CA, Royston P, Yu CKH, Nicolaides KH. Prediction of patient-specific risk of early preterm delivery using maternal history and sonographic measurement of cervical length: a population-based prospective study. Ultra Obstet Gynecol 2006; 27: 362–367.</ref><ref>Fonseca et al. Progesterone and the risk of preterm birth among women with a short cervix. NEJM 2007; vol 357, no 5, pg 462-469.</ref><ref>Romero R. Prevention of spontaneous preterm birth: the role of sonographic cervical length in identifying patients who may benefit from progesterone treatment. Ultrasound Obstet Gynecol 2007; 30: 675-686. http://www3.interscience.wiley.com/journal/99020267/home free download</ref><ref name="pmid26906339">{{cite journal| author=Koullali B, Oudijk MA, Nijman TA, Mol BW, Pajkrt E| title=Risk assessment and management to prevent preterm birth. | journal=Semin Fetal Neonatal Med | year= 2016 | volume= 21 | issue= 2 | pages= 80-8 | pmid=26906339 | doi=10.1016/j.siny.2016.01.005 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26906339  }} </ref> Finally, use of [[tobacco]] and [[alcohol]] during pregnancy also increases the chance of preterm delivery. Tobacco is the most commonly abused drug during pregnancy and also contributes significantly to low birth weight delivery.<ref>Shiono, Patricia H., Mark A. Klebanoff, Robert P. Nugent, Mary F. Cotch, Diana G. Wilkins, Douglas E. Rollins, Christopher J. Carey, and Richard E. Behrman. "Fetus-Placenta-Newborn: the Impact of Cocaine and Marijuana Use on Low Birth Weight and Preterm Birth: a Multicenter Study." American Journal of Obsetrics and Gynecology 172 (1995): 19-27. [[1 May]] [[2007]] [http://pt.wkhealth.com/pt/re/ajog/abstract.00000447-199501000-00003.htm;jsessionid=GGQfDBDtJTWynh5ZX5cT2f1bw72GDVwyBbjh7q1rvNqj8b2L3mkQ!-1870145763!-949856144!8091!-1].
 
</ref> <ref>Parazzini, F, L. Chatenoud, M. Surace, L. Tozzi, B. Salerio, G. Bettoni, and G. Benzi. "Moderate Alcohol Drinking and Risk of Preterm Birth." European Journal of Clinical Nutrition 57 (2003): 1345. [[1 May]] [[2007]] [http://web.ebscohost.com/ehost/detail?vid=3&hid=3&sid=afc585c7-2d1e-43e5-87b5-f9c746caf1fc%40sessionmgr8].</ref>
OR
 
Common risk factors in the development of [disease name] include [risk factor 1], [risk factor 2], [risk factor 3], and [risk factor 4].
 
OR
 
Common risk factors in the development of [disease name] may be occupational, environmental, genetic, and viral.


==Screening==
==Screening==
There is insufficient evidence to recommend routine screening for [disease/malignancy].
OR
According to the [guideline name], screening for [disease name] is not recommended.


OR
*There is insufficient evidence to recommend routine screening for preterm labor.
 
According to the [guideline name], screening for [disease name] by [test 1] is recommended every [duration] among patients with [condition 1], [condition 2], and [condition 3].


==Natural History, Complications, and Prognosis==
==Natural History, Complications, and Prognosis==
If left untreated, [#]% of patients with [disease name] may progress to develop [manifestation 1], [manifestation 2], and [manifestation 3].


OR
*If left untreated, women in [[preterm labor]] will progress to delivery. [[Tocolysis]] can postpone the delivery in up to 48 hours.


Common complications of [disease name] include [complication 1], [complication 2], and [complication 3].
*Common [[complications]] of preterm delivery include [[respiratory distress syndrome]], periventricular leukomalacia, [[intraventricular hemorrhage]], [[bronchopulmonary dysplasia]], [[necrotizing enterocolitis]], late-onset infection, [[retinopathy of prematurity]], [[cerebral palsy]] and other adverse [[neurological]] outcomes.<ref name="pmid27661654">{{cite journal| author=American College of Obstetricians and Gynecologists’ Committee on Practice Bulletins—Obstetrics| title=Practice Bulletin No. 171: Management of Preterm Labor. | journal=Obstet Gynecol | year= 2016 | volume= 128 | issue= 4 | pages= e155-64 | pmid=27661654 | doi=10.1097/AOG.0000000000001711 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27661654  }} </ref>


OR
*[[Prognosis]] is generally dependent on [[gestational age]].
 
**[[Survival rate]] is about:
Prognosis is generally excellent/good/poor, and the 1/5/10-year mortality/survival rate of patients with [disease name] is approximately [#]%.
***40% for newborns at 24 weeks' gestation,
***50% for newborns at 25 weeks,
***60% for newborns at 26 weeks,
***70% for newborns at 27 weeks,
***80% newborns born at 28 weeks.<ref name="pmid8843835">{{cite journal| author=Koh T| title=Simplified way of counselling parents about outcome of extremely premature babies. | journal=Lancet | year= 1996 | volume= 348 | issue= 9032 | pages= 963 | pmid=8843835 | doi=10.1016/S0140-6736(05)65379-2 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8843835  }} </ref>


==Diagnosis==
==Diagnosis==
===Diagnostic Study of Choice===
===Diagnostic Study of Choice===
The diagnosis of [disease name] is made when at least [number] of the following [number] diagnostic criteria are met: [criterion 1], [criterion 2], [criterion 3], and [criterion 4].
OR
The diagnosis of [disease name] is based on the [criteria name] criteria, which include [criterion 1], [criterion 2], and [criterion 3].
OR
The diagnosis of [disease name] is based on the [definition name] definition, which includes [criterion 1], [criterion 2], and [criterion 3].
OR


There are no established criteria for the diagnosis of [disease name].
*The [[diagnosis]] of preterm labor is made when the patient presents with 20-36 6/7 weeks of [[gestation]] with [[uterine contractions]] occurring at a frequency of four per 20 minutes or eight per 60 minutes and at least 1 of the following 4 [[diagnostic criteria]] are met:
**[[Premature rupture of membranes]]
**[[Cervical dilation]] greater than 2 cm
**Effacement exceeding 50 percent
**Change in [[cervical dilation]] or effacement detected by serial examinations.<ref name="pmid9614414">{{cite journal| author=Von Der Pool BA| title=Preterm labor: diagnosis and treatment. | journal=Am Fam Physician | year= 1998 | volume= 57 | issue= 10 | pages= 2457-64 | pmid=9614414 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9614414  }} </ref>


===History and Symptoms===
===History and Symptoms===
The majority of patients with [disease name] are asymptomatic.


OR
*A positive history of regular [[uterine contraction]]s and loss of [[amniotic fluid]] through the [[vaginal canal]] before the 36th week of [[pregnancy]] is suggestive of [[preterm labor]]. The loss of fluid may be absent.
 
*[[Patients]] may also complain of frequent contractions (more than four per hour), [[cramping]], [[pelvic pressure]], excessive [[vaginal discharge]], [[back ache]] and [[low back pain]].<ref name="pmid9614414">{{cite journal| author=Von Der Pool BA| title=Preterm labor: diagnosis and treatment. | journal=Am Fam Physician | year= 1998 | volume= 57 | issue= 10 | pages= 2457-64 | pmid=9614414 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9614414  }} </ref>
The hallmark of [disease name] is [finding]. A positive history of [finding 1] and [finding 2] is suggestive of [disease name]. The most common symptoms of [disease name] include [symptom 1], [symptom 2], and [symptom 3]. Common symptoms of [disease] include [symptom 1], [symptom 2], and [symptom 3]. Less common symptoms of [disease name] include [symptom 1], [symptom 2], and [symptom 3].


===Physical Examination===
===Physical Examination===
Patients with [disease name] usually appear [general appearance]. Physical examination of patients with [disease name] is usually remarkable for [finding 1], [finding 2], and [finding 3].
OR
Common physical examination findings of [disease name] include [finding 1], [finding 2], and [finding 3].
OR
The presence of [finding(s)] on physical examination is diagnostic of [disease name].
OR


The presence of [finding(s)] on physical examination is highly suggestive of [disease name].
*Common physical examination findings of preterm labor include regular [[uterine contraction]]s, [[cervical dilation]] of at least 2cm, and it may present with or with our [[ruptured membranes]].
*The assessment of preterm [[delivery]] risk based on [[symptoms]] and physical examination alone is inaccurate.<ref name="pmid27661654">{{cite journal| author=American College of Obstetricians and Gynecologists’ Committee on Practice Bulletins—Obstetrics| title=Practice Bulletin No. 171: Management of Preterm Labor. | journal=Obstet Gynecol | year= 2016 | volume= 128 | issue= 4 | pages= e155-64 | pmid=27661654 | doi=10.1097/AOG.0000000000001711 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27661654  }} </ref>


===Laboratory Findings===
===Laboratory Findings===
An elevated/reduced concentration of serum/blood/urinary/CSF/other [lab test] is diagnostic of [disease name].
OR
Laboratory findings consistent with the diagnosis of [disease name] include [abnormal test 1], [abnormal test 2], and [abnormal test 3].
OR
[Test] is usually normal among patients with [disease name].
OR


Some patients with [disease name] may have elevated/reduced concentration of [test], which is usually suggestive of [progression/complication].
*Altered markers such as: cervical [[fibronectin]], [[HCG]], or [[phIGFBP-1]], presence of fetal [[fibronectin]] [[fFN]]/[[PAMG1]]/[[IGF-BP 1]] in cervical-vaginal secretions<ref name="pmid28482713">{{cite journal| author=Di Renzo GC, Cabero Roura L, Facchinetti F, Helmer H, Hubinont C, Jacobsson B | display-authors=etal| title=Preterm Labor and Birth Management: Recommendations from the European Association of Perinatal Medicine. | journal=J Matern Fetal Neonatal Med | year= 2017 | volume= 30 | issue= 17 | pages= 2011-2030 | pmid=28482713 | doi=10.1080/14767058.2017.1323860 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28482713  }} </ref>
 
*[[Serum]] [[C-reactive protein]], and [[amniotic fluid]] [[interleukin]]s may be useful for predicting spontaneous [[preterm birth]], but its accuracy is questionable.<ref name="pmid23099810">{{cite journal| author=Honest H, Hyde CJ, Khan KS| title=Prediction of spontaneous preterm birth:  no good test for predicting a spontaneous preterm birth. | journal=Curr Opin Obstet Gynecol | year= 2012 | volume= 24 | issue= 6 | pages= 422-33 | pmid=23099810 | doi=10.1097/GCO.0b013e328359823a | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23099810  }} </ref>
OR
 
There are no diagnostic laboratory findings associated with [disease name].


===Electrocardiogram===
===Electrocardiogram===
There are no ECG findings associated with [disease name].
OR


An ECG may be helpful in the diagnosis of [disease name]. Findings on an ECG suggestive of/diagnostic of [disease name] include [finding 1], [finding 2], and [finding 3].
*There are no [[ECG]] findings associated with preterm labor.


===X-ray===
===X-ray===
There are no x-ray findings associated with [disease name].
OR


An x-ray may be helpful in the diagnosis of [disease name]. Findings on an x-ray suggestive of/diagnostic of [disease name] include [finding 1], [finding 2], and [finding 3].
*There are no [[x-ray]] findings associated with preterm labor.
 
OR
 
There are no x-ray findings associated with [disease name]. However, an x-ray may be helpful in the diagnosis of complications of [disease name], which include [complication 1], [complication 2], and [complication 3].


===Echocardiography or Ultrasound===
===Echocardiography or Ultrasound===
There are no echocardiography/ultrasound  findings associated with [disease name].


OR
*[[Ultrasound]] imaging may be helpful in the [[diagnosis]] of preterm labor as well as in finding out [[risk factors]] for its development.
 
*Findings on an [[ultrasound]] suggestive of a higher risk for [[preterm labor]] include short [[cervical length]], especially if smaller than 25 mm.
Echocardiography/ultrasound  may be helpful in the diagnosis of [disease name]. Findings on an echocardiography/ultrasound suggestive of/diagnostic of [disease name] include [finding 1], [finding 2], and [finding 3].
*It can also be useful on identifying associated conditions with the [[fetus]] or [[placenta]], the fetus' position, the volume of [[amniotic fluid]], and estimate the fetus' weight.
 
OR
 
There are no echocardiography/ultrasound  findings associated with [disease name]. However, an echocardiography/ultrasound  may be helpful in the diagnosis of complications of [disease name], which include [complication 1], [complication 2], and [complication 3].


===CT scan===
===CT scan===
There are no CT scan findings associated with [disease name].
OR
[Location] CT scan may be helpful in the diagnosis of [disease name]. Findings on CT scan suggestive of/diagnostic of [disease name] include [finding 1], [finding 2], and [finding 3].


OR
*There are no [[CT scan]] findings associated with preterm labor.
 
There are no CT scan findings associated with [disease name]. However, a CT scan may be helpful in the diagnosis of complications of [disease name], which include [complication 1], [complication 2], and [complication 3].


===MRI===
===MRI===
There are no MRI findings associated with [disease name].
OR
[Location] MRI may be helpful in the diagnosis of [disease name]. Findings on MRI suggestive of/diagnostic of [disease name] include [finding 1], [finding 2], and [finding 3].
OR


There are no MRI findings associated with [disease name]. However, a MRI may be helpful in the diagnosis of complications of [disease name], which include [complication 1], [complication 2], and [complication 3].
*There are no [[MRI]] findings associated with preterm labor.


===Other Imaging Findings===
===Other Imaging Findings===
There are no other imaging findings associated with [disease name].
OR


[Imaging modality] may be helpful in the diagnosis of [disease name]. Findings on an [imaging modality] suggestive of/diagnostic of [disease name] include [finding 1], [finding 2], and [finding 3].
*There are no other imaging findings associated with preterm labor.


===Other Diagnostic Studies===
===Other Diagnostic Studies===
There are no other diagnostic studies associated with [disease name].
OR
[Diagnostic study] may be helpful in the diagnosis of [disease name]. Findings suggestive of/diagnostic of [disease name] include [finding 1], [finding 2], and [finding 3].


OR
*[[Uterine monitoring]] may be helpful in the diagnosis of preterm labor. Findings suggestive of [[preterm labor]] include [[tachysystole]] (greater than five contractions in 10 minutes).
 
Other diagnostic studies for [disease name] include [diagnostic study 1], which demonstrates [finding 1], [finding 2], and [finding 3], and [diagnostic study 2], which demonstrates [finding 1], [finding 2], and [finding 3].


==Treatment==
==Treatment==
===Medical Therapy===
===Medical Therapy===
There is no treatment for [disease name]; the mainstay of therapy is supportive care.
According to the American College of Obstetricians and Gynecologists guidelines<ref name="pmid27661654">{{cite journal| author=American College of Obstetricians and Gynecologists’ Committee on Practice Bulletins—Obstetrics| title=Practice Bulletin No. 171: Management of Preterm Labor. | journal=Obstet Gynecol | year= 2016 | volume= 128 | issue= 4 | pages= e155-64 | pmid=27661654 | doi=10.1097/AOG.0000000000001711 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27661654  }}</ref>:
 
OR
 
Supportive therapy for [disease name] includes [therapy 1], [therapy 2], and [therapy 3].
 
OR
 
The majority of cases of [disease name] are self-limited and require only supportive care.
 
OR
 
[Disease name] is a medical emergency and requires prompt treatment.
 
OR
 
The mainstay of treatment for [disease name] is [therapy].
 
OR
 
The optimal therapy for [malignancy name] depends on the stage at diagnosis.
 
OR


[Therapy] is recommended among all patients who develop [disease name].
*Pharmacologic medical therapy is recommended among [[patients]] with [[preterm labor]] in which a delay in delivery will be beneficial to the newborn. Such cases include [[patients]] presenting a [[gestational age]] no higher than 34 weeks.
*The medical therapy of delaying delivery is called [[tocolysis]], and it is effective for up to 48 hours.
*It is generally not indicated if there's no neonatal viability.
*Its use must be used only on women with preterm labor at high risk of spontaneous preterm birth.
*Administering [[corticosteroids]] (single course) is recommended for pregnant women between 24 weeks and 34 weeks of gestation who are at risk of delivery within 7 days.
*[[Antibiotics]] should not be used to prolong gestation or improve neonatal outcomes if membranes are intact.


OR
{| class="wikitable"
 
|+Tocolytic agents according to the American College of Obstetricians and Gynecologists<ref name="pmid27661654">{{cite journal| author=American College of Obstetricians and Gynecologists’ Committee on Practice Bulletins—Obstetrics| title=Practice Bulletin No. 171: Management of Preterm Labor. | journal=Obstet Gynecol | year= 2016 | volume= 128 | issue= 4 | pages= e155-64 | pmid=27661654 | doi=10.1097/AOG.0000000000001711 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27661654  }}</ref>
Pharmacologic medical therapy is recommended among patients with [disease subclass 1], [disease subclass 2], and [disease subclass 3].
| align="center" style="background: #4479BA; color: #FFFFFF " |Agent or Class
 
| align="center" style="background: #4479BA; color: #FFFFFF " |Maternal Side Effects
OR
| align="center" style="background: #4479BA; color: #FFFFFF " |Fetal or Newborn Adverse Effects
 
| align="center" style="background: #4479BA; color: #FFFFFF " |Contraindications
Pharmacologic medical therapies for [disease name] include (either) [therapy 1], [therapy 2], and/or [therapy 3].
|-
 
|[[Calcium channel blockers]]
OR
|[[Dizziness]], [[flushing]], and [[hypotension]]; suppression of [[heart rate]], [[contractility]], and [[left ventricular systolic pressure]] when used with [[magnesium sulfate]]; and elevation of [[hepatic]] [[transaminases]]
 
|No known adverse effects
Empiric therapy for [disease name] depends on [disease factor 1] and [disease factor 2].
|[[Hypotension]] and preload-dependent cardiac lesions, such as [[aortic insufficiency]]
 
|-
OR
|[[Nonsteroidal anti-inflammatory drugs]]
 
|[[Nausea]], [[esophageal reflux]], [[gastritis]], and [[emesis]]; [[platelet]] dysfunction is rarely of clinical significance in patients without underlying [[bleeding]] disorder
Patients with [disease subclass 1] are treated with [therapy 1], whereas patients with [disease subclass 2] are treated with [therapy 2].
|In utero constriction of [[ductus arteriosus]], [[oligohydramnios]], [[necrotizing enterocolitis]] in preterm [[newborns]], and [[patent ductus arteriosus]] in newborn
|[[Platelet]] dysfunction or [[bleeding]] disorder, [[hepatic dysfunction]], [[gastric ulcer]]s, [[renal injury]], and [[asthma]] (in women with [[hypersensitivity]] to [[aspirin]])
|-
|[[Beta-adrenergic receptor agonists]]
|[[Tachycardia]], [[hypotension]], [[tremor]], [[palpitations]], [[shortness of breath]], [[chest]] discomfort, [[pulmonary edema]], [[hypokalemia]], and [[hyperglycemia]]
|[[Fetal tachycardia]]
|[[Tachycardia]]-sensitive maternal cardiac disease and poorly controlled [[diabetes mellitus]]
|-
|[[Magnesium sulfate]]
|Causes [[flushing]], [[diaphoresis]], [[nausea]], loss of [[deep tendon reflexes]], [[respiratory depression]], and [[cardiac arrest]]; suppresses [[heart rate]], [[contractility]] and [[left ventricular systolic pressure]] when used with [[calcium channel blockers]]; and produces [[neuromuscular blockade]] when used with [[calcium channel blockers]]
|[[Neonatal depression]]
|[[Myasthenia gravis]]
|}


===Surgery===
===Surgery===
Surgical intervention is not recommended for the management of [disease name].


OR
*[[Surgery]] is [[ultrasound]]-indicated. The procedure is called [[cerclage]], made to prevent preterm labor.
 
*[[Cerclage]] is beneficial in women with [[cervical]] length <25 mm when placed between 16 and 24 weeks of gestation.<ref name="pmid26906339">{{cite journal| author=Koullali B, Oudijk MA, Nijman TA, Mol BW, Pajkrt E| title=Risk assessment and management to prevent preterm birth. | journal=Semin Fetal Neonatal Med | year= 2016 | volume= 21 | issue= 2 | pages= 80-8 | pmid=26906339 | doi=10.1016/j.siny.2016.01.005 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26906339  }} </ref>
Surgery is not the first-line treatment option for patients with [disease name]. Surgery is usually reserved for patients with either [indication 1], [indication 2], and [indication 3]
 
OR
 
The mainstay of treatment for [disease name] is medical therapy. Surgery is usually reserved for patients with either [indication 1], [indication 2], and/or [indication 3].
 
OR
 
The feasibility of surgery depends on the stage of [malignancy] at diagnosis.
 
OR
 
Surgery is the mainstay of treatment for [disease or malignancy].


===Primary Prevention===
===Primary Prevention===
There are no established measures for the primary prevention of [disease name].
OR
There are no available vaccines against [disease name].
OR
Effective measures for the primary prevention of [disease name] include [measure1], [measure2], and [measure3].


OR
*There are no established measures for the [[primary prevention]] of preterm labor.<ref name="pmid9614414">{{cite journal| author=Von Der Pool BA| title=Preterm labor: diagnosis and treatment. | journal=Am Fam Physician | year= 1998 | volume= 57 | issue= 10 | pages= 2457-64 | pmid=9614414 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9614414  }} </ref>
 
[Vaccine name] vaccine is recommended for [patient population] to prevent [disease name]. Other primary prevention strategies include [strategy 1], [strategy 2], and [strategy 3].


===Secondary Prevention===
===Secondary Prevention===
There are no established measures for the secondary prevention of [disease name].


OR
*[[Cerclage]] is a surgical procedure made in a certain group of patients to avoid the recurrence of preterm labor.
 
*Administration of progesterone is being investigated for high-risk patients, especially those who had an episode of preterm labor previously.<ref name="pmid23099810">{{cite journal| author=Honest H, Hyde CJ, Khan KS| title=Prediction of spontaneous preterm birth:  no good test for predicting a spontaneous preterm birth. | journal=Curr Opin Obstet Gynecol | year= 2012 | volume= 24 | issue= 6 | pages= 422-33 | pmid=23099810 | doi=10.1097/GCO.0b013e328359823a | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23099810  }} </ref>
Effective measures for the secondary prevention of [disease name] include [strategy 1], [strategy 2], and [strategy 3].


==References==
==References==
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Preterm labor and birth

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [3] Associate Editor(s)-in-Chief: José Eduardo Riceto Loyola Junior, M.D.[4]

Synonyms and keywords: Preterm delivery, Premature labour, Early delivery, Premature birth, Premature labor, Pre term birth

Overview

Preterm birth is any birth that happens between 20 weeks of gestation and 36 6/7 weeks of gestation. In Europe, it is defined after 22 weeks and before 37 weeks of gestation. The gestation can be dated using first-trimester ultrasound. In the US, approximately 12% of the births are preterm, while in Europe it varies between 5-18%.The diagnosis is made based on clinical criteria which include: cervical dilation of at least 2cm and/or cervical effacement, which happens with regular uterine contractions. It may happen with or without rupture of membrane. Preterm labor and delivery is associated to many risks for the babies such as: respiratory distress syndrome, periventricular leukomalacia, intraventricular hemorrhage, bronchopulmonary dysplasia, necrotizing enterocolitis, late-onset infection, retinopathy of prematurity, cerebral palsy and other adverse neurological outcomes.

Historical Perspective

  • In the 1930s, George Corner was the first to suggest the association between progesterone and the development of preterm labor.[1]
  • James Elgin Gill (born on 20 May 1987 in Ottawa, Canada) was the earliest premature baby in the world. He was 128 days premature (21 weeks and 5 days gestation) and weighed 1 lb. 6 oz. (624 g). He survived and is quite healthy.[2][3]

Classification

  • Preterm labor may be classified according to the WHO into 3 groups: extremely preterm (<28 weeks), very preterm (28 to 32 weeks), moderate to late preterm (32-37 weeks).[4]

Pathophysiology

Causes

Differentiating preterm labor from other Diseases

Epidemiology and Demographics

  • The incidence of preterm labor is approximately 12% of the births in the United States.[7]
  • In Europe the incidence varies between 5-18% of the births.[8]
  • Approximately 17% of preterm births occur in the Americas (North, Central and South America, and the Caribbean), Europe and Australia.[9]

Risk Factors

Screening

  • There is insufficient evidence to recommend routine screening for preterm labor.

Natural History, Complications, and Prognosis

  • If left untreated, women in preterm labor will progress to delivery. Tocolysis can postpone the delivery in up to 48 hours.
  • Prognosis is generally dependent on gestational age.
    • Survival rate is about:
      • 40% for newborns at 24 weeks' gestation,
      • 50% for newborns at 25 weeks,
      • 60% for newborns at 26 weeks,
      • 70% for newborns at 27 weeks,
      • 80% newborns born at 28 weeks.[20]

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

  • There are no ECG findings associated with preterm labor.

X-ray

  • There are no x-ray findings associated with preterm labor.

Echocardiography or Ultrasound

CT scan

  • There are no CT scan findings associated with preterm labor.

MRI

  • There are no MRI findings associated with preterm labor.

Other Imaging Findings

  • There are no other imaging findings associated with preterm labor.

Other Diagnostic Studies

Treatment

Medical Therapy

According to the American College of Obstetricians and Gynecologists guidelines[7]:

  • Pharmacologic medical therapy is recommended among patients with preterm labor in which a delay in delivery will be beneficial to the newborn. Such cases include patients presenting a gestational age no higher than 34 weeks.
  • The medical therapy of delaying delivery is called tocolysis, and it is effective for up to 48 hours.
  • It is generally not indicated if there's no neonatal viability.
  • Its use must be used only on women with preterm labor at high risk of spontaneous preterm birth.
  • Administering corticosteroids (single course) is recommended for pregnant women between 24 weeks and 34 weeks of gestation who are at risk of delivery within 7 days.
  • Antibiotics should not be used to prolong gestation or improve neonatal outcomes if membranes are intact.
Tocolytic agents according to the American College of Obstetricians and Gynecologists[7]
Agent or Class Maternal Side Effects Fetal or Newborn Adverse Effects Contraindications
Calcium channel blockers Dizziness, flushing, and hypotension; suppression of heart rate, contractility, and left ventricular systolic pressure when used with magnesium sulfate; and elevation of hepatic transaminases No known adverse effects Hypotension and preload-dependent cardiac lesions, such as aortic insufficiency
Nonsteroidal anti-inflammatory drugs Nausea, esophageal reflux, gastritis, and emesis; platelet dysfunction is rarely of clinical significance in patients without underlying bleeding disorder In utero constriction of ductus arteriosus, oligohydramnios, necrotizing enterocolitis in preterm newborns, and patent ductus arteriosus in newborn Platelet dysfunction or bleeding disorder, hepatic dysfunction, gastric ulcers, renal injury, and asthma (in women with hypersensitivity to aspirin)
Beta-adrenergic receptor agonists Tachycardia, hypotension, tremor, palpitations, shortness of breath, chest discomfort, pulmonary edema, hypokalemia, and hyperglycemia Fetal tachycardia Tachycardia-sensitive maternal cardiac disease and poorly controlled diabetes mellitus
Magnesium sulfate Causes flushing, diaphoresis, nausea, loss of deep tendon reflexes, respiratory depression, and cardiac arrest; suppresses heart rate, contractility and left ventricular systolic pressure when used with calcium channel blockers; and produces neuromuscular blockade when used with calcium channel blockers Neonatal depression Myasthenia gravis

Surgery

Primary Prevention

Secondary Prevention

  • Cerclage is a surgical procedure made in a certain group of patients to avoid the recurrence of preterm labor.
  • Administration of progesterone is being investigated for high-risk patients, especially those who had an episode of preterm labor previously.[22]

References

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  2. "Powell's Books - Guinness World Records 2004 (Guinness Book of Records) by". Retrieved 2007-11-28.
  3. "Miracle child". Retrieved 2007-11-28.
  4. "Preterm birth". Retrieved 2020-09-13.
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  6. 6.0 6.1 Meller CH, Carducci ME, Ceriani Cernadas JM, Otaño L (2018). "Preterm premature rupture of membranes". Arch Argent Pediatr. 116 (4): e575–e581. doi:10.5546/aap.2018.eng.e575. PMID 30016035.
  7. 7.0 7.1 7.2 7.3 7.4 American College of Obstetricians and Gynecologists’ Committee on Practice Bulletins—Obstetrics (2016). "Practice Bulletin No. 171: Management of Preterm Labor". Obstet Gynecol. 128 (4): e155–64. doi:10.1097/AOG.0000000000001711. PMID 27661654.
  8. 8.0 8.1 Di Renzo GC, Cabero Roura L, Facchinetti F, Helmer H, Hubinont C, Jacobsson B; et al. (2017). "Preterm Labor and Birth Management: Recommendations from the European Association of Perinatal Medicine". J Matern Fetal Neonatal Med. 30 (17): 2011–2030. doi:10.1080/14767058.2017.1323860. PMID 28482713.
  9. 9.0 9.1 9.2 Souza RT, Cecatti JG (2020). "A Comprehensive Integrative Review of the Factors Associated with Spontaneous Preterm Birth, Its Prevention and Prediction, Including Metabolomic Markers". Rev Bras Ginecol Obstet. 42 (1): 51–60. doi:10.1055/s-0040-1701462. PMID 32107766 Check |pmid= value (help).
  10. Rosenberg TJ, Garbers S, Lipkind H, Chiasson MA (2005). "Maternal obesity and diabetes as risk factors for adverse pregnancy outcomes: differences among 4 racial/ethnic groups". Am J Public Health. 95 (9): 1545–51. doi:10.2105/AJPH.2005.065680. PMID 16118366.
  11. Conde-Agudelo A, Rosas-Bermúdez A, Kafury-Goeta AC (2006). "Birth spacing and risk of adverse perinatal outcomes: a meta-analysis". JAMA. 295 (15): 1809–23. doi:10.1001/jama.295.15.1809. PMID 16622143.
  12. Koullali B, Kamphuis EI, Hof MH, Robertson SA, Pajkrt E, de Groot CJ; et al. (2016). "The Effect of Interpregnancy Interval on the Recurrence Rate of Spontaneous Preterm Birth: A Retrospective Cohort Study". Am J Perinatol. doi:10.1055/s-0036-1584896. PMID 27367283.
  13. Ball SJ, Pereira G, Jacoby P, de Klerk N, Stanley FJ (2014). "Re-evaluation of link between interpregnancy interval and adverse birth outcomes: retrospective cohort study matching two intervals per mother". BMJ. 349: g4333. doi:10.1136/bmj.g4333. PMC 4137882. PMID 25056260.
  14. To MS, Skentou CA, Royston P, Yu CKH, Nicolaides KH. Prediction of patient-specific risk of early preterm delivery using maternal history and sonographic measurement of cervical length: a population-based prospective study. Ultra Obstet Gynecol 2006; 27: 362–367.
  15. Fonseca et al. Progesterone and the risk of preterm birth among women with a short cervix. NEJM 2007; vol 357, no 5, pg 462-469.
  16. Romero R. Prevention of spontaneous preterm birth: the role of sonographic cervical length in identifying patients who may benefit from progesterone treatment. Ultrasound Obstet Gynecol 2007; 30: 675-686. http://www3.interscience.wiley.com/journal/99020267/home free download
  17. 17.0 17.1 Koullali B, Oudijk MA, Nijman TA, Mol BW, Pajkrt E (2016). "Risk assessment and management to prevent preterm birth". Semin Fetal Neonatal Med. 21 (2): 80–8. doi:10.1016/j.siny.2016.01.005. PMID 26906339.
  18. Shiono, Patricia H., Mark A. Klebanoff, Robert P. Nugent, Mary F. Cotch, Diana G. Wilkins, Douglas E. Rollins, Christopher J. Carey, and Richard E. Behrman. "Fetus-Placenta-Newborn: the Impact of Cocaine and Marijuana Use on Low Birth Weight and Preterm Birth: a Multicenter Study." American Journal of Obsetrics and Gynecology 172 (1995): 19-27. 1 May 2007 [1].
  19. Parazzini, F, L. Chatenoud, M. Surace, L. Tozzi, B. Salerio, G. Bettoni, and G. Benzi. "Moderate Alcohol Drinking and Risk of Preterm Birth." European Journal of Clinical Nutrition 57 (2003): 1345. 1 May 2007 [2].
  20. Koh T (1996). "Simplified way of counselling parents about outcome of extremely premature babies". Lancet. 348 (9032): 963. doi:10.1016/S0140-6736(05)65379-2. PMID 8843835.
  21. 21.0 21.1 21.2 Von Der Pool BA (1998). "Preterm labor: diagnosis and treatment". Am Fam Physician. 57 (10): 2457–64. PMID 9614414.
  22. 22.0 22.1 Honest H, Hyde CJ, Khan KS (2012). "Prediction of spontaneous preterm birth: no good test for predicting a spontaneous preterm birth". Curr Opin Obstet Gynecol. 24 (6): 422–33. doi:10.1097/GCO.0b013e328359823a. PMID 23099810.

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