Preterm birth

Other names: Premature birth, preemies, premmies
Intubated preterm baby in an incubator
Specialty| Obstetrics, pediatrics
Symptoms| Birth of a baby at younger than 37 weeks' gestational age[1]
Complications| Cerebral palsy, delays in development, hearing problems, sight problems[1]
Causes| Often unknown[2]
Risk factors| Diabetes, high blood pressure, being pregnant with more than one baby, obesity or underweight, a number of vaginal infections, celiac disease, tobacco smoking, psychological stress[2][3][4]
Prevention| Progesterone[5]
Treatment| Corticosteroids, keeping the baby warm through skin-to-skin contact, supporting breastfeeding, treating infections, supporting breathing[2][6]
Frequency| ~15 million a year (12% of deliveries)[2]
Deaths| 805,800[7]

Preterm birth, also known as premature birth, is the birth of a baby at fewer than 37 weeks' gestational age, as opposed to the usual about 40 weeks.[1] These babies are known as preemies or premmies.[1] Symptoms of preterm labor include uterine contractions which occur more often than every ten minutes or the leaking of fluid from the vagina.[8] Premature infants are at greater risk for cerebral palsy, delays in development, hearing problems and sight problems.[1] The earlier a baby is born, the greater these risks will be.[1]

The cause of preterm birth is often not known.[2] Risk factors include diabetes, high blood pressure, being pregnant with more than one baby, being either obese or underweight, a number of vaginal infections, air pollution including tobacco smoking, and psychological stress.[2][3][9] It is recommended that labor not be medically induced before 39 weeks unless required for other medical reasons.[2] The same recommendation applies to cesarean section.[2] Medical reasons for early delivery include preeclampsia.[10]

In those at risk, the hormone progesterone, if taken during pregnancy, may prevent preterm birth.[5] Evidence does not support the usefulness of bed rest.[5][11] It is estimated that at least 75% of preterm infants would survive with appropriate treatment, and the survival rate is highest among the infants born the latest.[2] In women who might deliver between 24 and 37 weeks, corticosteroids improve outcomes.[6][12] A number of medications, including nifedipine, may delay delivery so that a mother can be moved to where more medical care is available and the corticosteroids have a greater chance to work.[13] Once the baby is born, care includes keeping the baby warm through skin-to-skin contact, supporting breastfeeding, treating infections and supporting breathing.[2]

Preterm birth is the most common cause of death among infants worldwide.[1] About 15 million babies are preterm each year (5% to 18% of all deliveries).[2] In the United Kingdom they are about 7.9% and in the United States they are about 12.3% of all births.[14][15] Approximately 0.5% of births are extremely early periviable births, and these account for most of the deaths.[16] In many countries, rates of premature births have increased between the 1990s and 2010s.[2] Complications from preterm births resulted in 0.81 million deaths in 2015 down from 1.57 million in 1990.[7][17] The chance of survival at 22 weeks is about 6%, while at 23 weeks it is 26%, 24 weeks 55% and 25 weeks about 72%.[18] The chances of survival without any long-term difficulties are lower.[19]

## Contents

* 1 Signs and symptoms
* 1.1 Complications
* 1.1.1 Mortality and morbidity
* 1.1.2 Specific risks for the preterm neonate
* 2 Risk factors
* 2.1 Maternal factors
* 2.2 Factors during pregnancy
* 2.3 Infection
* 2.4 Genetics
* 3 Diagnosis
* 3.1 Placental alpha microglobulin-1
* 3.2 Fetal fibronectin
* 3.3 Ultrasound
* 3.4 Classification
* 4 Prevention
* 4.1 Before pregnancy
* 4.2 During pregnancy
* 4.2.1 Screening during pregnancy
* 4.3 Reducing existing risks
* 4.3.1 Multiple pregnancies
* 4.3.2 Reducing indicated preterm birth
* 4.3.3 Reducing spontaneous preterm birth
* 4.3.3.1 Antibiotics
* 4.3.3.2 Progestogens
* 4.3.3.3 Cervical cerclage
* 5 Management
* 5.1 Steroids
* 5.2 Antibiotics
* 5.3 Tocolysis
* 5.4 Mode of delivery
* 5.5 Neonatal care
* 5.6 Nutrition
* 5.6.1 Human breast milk and formula
* 5.6.1.1 Fortified human breast milk and preterm/term formula
* 5.6.2 Timing of feeds
* 5.6.3 Intermittent feeding versus continuous feeding
* 5.6.4 High volume feeds
* 5.6.5 Parenteral (intraveneous) nutrition
* 5.6.6 Gastric residuals
* 5.7 Hearing assessment
* 6 Prognosis
* 7 Epidemiology
* 8 Society and culture
* 8.1 Economics
* 8.2 Notable cases
* 8.3 COVID19
* 9 Research
* 10 References
* 11 External links

## Signs and symptoms[edit | edit source]

A new mother holds her premature baby at Kapiolani Medical Center NICU in Honolulu, Hawaii

A preterm birth can be brought on by being induced, or can occur spontaneously. Preterm births can cause a range of problems.[20][21]

The main categories of causes of preterm birth are preterm labor induction and spontaneous preterm labor. Signs and symptoms of preterm labor include four or more uterine contractions in one hour. In contrast to false labour, true labor is accompanied by cervical dilatation and effacement. Also, vaginal bleeding in the third trimester, heavy pressure in the pelvis, or abdominal or back pain could be indicators that a preterm birth is about to occur. A watery discharge from the vagina may indicate premature rupture of the membranes that surround the baby. While the rupture of the membranes may not be followed by labor, usually delivery is indicated as infection (chorioamnionitis) is a serious threat to both fetus and mother. In some cases, the cervix dilates prematurely without pain or perceived contractions, so that the mother may not have warning signs until very late in the birthing process.

A review into using uterine monitoring at home to detect contractions and possible preterm births in women at higher risk of having a preterm baby found that it did not reduce the number of preterm births.[22] The research included in the review was poor quality but it showed that home monitoring may increase the number of unplanned antenatal visits and may reduce the number of babies admitted to special care when compared with women receiving normal antenatal care.[22]

### Complications[edit | edit source]

#### Mortality and morbidity[edit | edit source]

In the U.S. where many neonatal infections and other causes of neonatal death have been markedly reduced, prematurity is the leading cause of neonatal mortality at 25%.[23] Prematurely born infants are also at greater risk for having subsequent serious chronic health problems as discussed below.

The earliest gestational age at which the infant has at least a 50% chance of survival is referred to as the limit of viability. As NICU care has improved over the last 40 years, the limit of viability has reduced to approximately 24 weeks.[24][25] Most newborns who die, and 40% of older infants who die, were born between 20 and 25.9 weeks (gestational age), during the second trimester.[16]

As risk of brain damage and developmental delay is significant at that threshold even if the infant survives, there are ethical controversies over the aggressiveness of the care rendered to such infants. The limit of viability has also become a factor in the abortion debate.[26]

#### Specific risks for the preterm neonate[edit | edit source]

Preterm infants usually show physical signs of prematurity in reverse proportion to the gestational age. As a result, they are at risk for numerous medical problems affecting different organ systems.

* Neurological problems include apnea of prematurity, hypoxic-ischemic encephalopathy (HIE), retinopathy of prematurity (ROP),[27] developmental disability, transient hyperammonemia of the newborn, cerebral palsy and intraventricular hemorrhage, the latter affecting 25% of babies born preterm, usually before 32 weeks of pregnancy.[28] Mild brain bleeds usually leave no or few lasting complications, but severe bleeds often result in brain damage or even death.[28] Neurodevelopmental problems have been linked to lack of maternal thyroid hormones, at a time when their own thyroid is unable to meet postnatal needs.[29]
* Cardiovascular complications may arise from the failure of the ductus arteriosus to close after birth: patent ductus arteriosus (PDA).
* Respiratory problems are common, specifically the respiratory distress syndrome (RDS or IRDS) (previously called hyaline membrane disease). Another problem can be chronic lung disease (previously called bronchopulmonary dysplasia or BPD).
* Gastrointestinal and metabolic issues can arise from neonatal hypoglycemia, feeding difficulties, rickets of prematurity, hypocalcemia, inguinal hernia, and necrotizing enterocolitis (NEC).
* Hematologic complications include anemia of prematurity, thrombocytopenia, and hyperbilirubinemia (jaundice) that can lead to kernicterus.
* Infection, including sepsis, pneumonia, and urinary tract infection [1]

A study of 241 children born between 22 and 25 weeks who were currently of school age found that 46 percent had severe or moderate disabilities such as cerebral palsy, vision or hearing loss and learning problems. Thirty-four percent were mildly disabled and 20 percent had no disabilities, while 12 percent had disabling cerebral palsy.[30][31] Up to 15 out of 100 premature infants have significant hearing loss.[32]

## Risk factors[edit | edit source]

The exact cause of preterm birth is difficult to determine and it may be multi-factorial.[citation needed] Labor is a complex process involving many factors. Four different pathways have been identified that can result in preterm birth and have considerable evidence: precocious fetal endocrine activation, uterine overdistension (placental abruption), decidual bleeding, and intrauterine inflammation/infection.[33]

Identifying women at high risk of giving birth early would enable the health services to provide specialized care for these women to delay the birth or make sure they are in the best place to give birth (for example a hospital with a special care baby unit). Risk scoring systems have been suggested as a possible way of identifying these women. However, there is no research in this area so it is unclear whether the risk scoring systems would prolong pregnancy and reduce the numbers of preterm births or not.[34]

### Maternal factors[edit | edit source]

Risk factor | Relative risk[35] | 95% confidence
interval[35]

|
|

Fetal fibronectin | 4.0 | 2.9–5.5
Short cervical length | 2.9 | 2.1–3.9
Chlamydia | 2.2 | 1.0–4.8
Low socio-economic status | 1.9 | 1.7–2.2
Large or small pregnancy weight gain | 1.8 | 1.5–2.3
Short maternal height | 1.8 | 1.3–2.5
Periodontitis | 1.6 | 1.1–2.3
Celiac disease | 1.4[36] | 1.2–1.6[36]
Asymptomatic bacteriuria | 1.1 | 0.8–1.5
High or low BMI | 0.96 | 0.66–1.4
| odds ratio |
History of spontaneous preterm birth | 3.6 | 3.2–4.0
Bacterial vaginosis | 2.2 | 1.5–3.1
Black ethnicity/race | 2.0 | 1.8–2.2
Filipino ancestry[37] | 1.7 | 1.5–2.1
Unwanted pregnancy[38]:1 | 1.5 | 1.41-1.61
Unintended pregnancy[38]:1 | 1.31 | 1.09-1.58
Being single/unmarried[39] | 1.2 | 1.03–1.28
Percentage premature births in England and Wales 2011, by age of mother and whether single or multiple birth.

A number of factors have been identified that are linked to a higher risk of a preterm birth such as being less than 18 years of age.[40] Maternal height and weight can play a role.[41]

Further, in the U.S. and the UK, black women have preterm birth rates of 15–18%, more than double than that of the white population. Many Black women have higher preterm birth rates due to multiple factors but the most common is high amounts of chronic stress, which can eventually lead to premature birth.[42] Adult chronic disease isn't always the case with premature birth in Black women, which makes the main factor of premature birth challenging to identify.[42] Filipinos are also at high risk of premature birth, and it is believed that nearly 11–15% of Filipinos born in the U.S. (compared to other Asians at 7.6% and whites at 7.8%) are premature.[43] Filipinos being a big risk factor is evidenced with the Philippines being the 8th highest ranking in the world for preterm births, the only non-African country in the top 10.[44] This discrepancy is not seen in comparison to other Asian groups or Hispanic immigrants and remains unexplained.[40]

Pregnancy interval makes a difference as women with a six-month span or less between pregnancies have a two-fold increase in preterm birth.[45] Studies on type of work and physical activity have given conflicting results, but it is opined that stressful conditions, hard labor, and long hours are probably linked to preterm birth.[40]

A history of spontaneous (i.e., miscarriage) or surgical abortion has been associated with a small increase in the risk of preterm birth, with an increased risk with increased number of abortions, although it is unclear whether the increase is caused by the abortion or by confounding risk factors (e.g., socioeconomic status).[46] Increased risk has not been shown in women who terminated their pregnancies medically.[47] Pregnancies that are unwanted or unintended are also a risk factor for preterm birth.[38]

Adequate maternal nutrition is important. Women with a low BMI are at increased risk for preterm birth.[48] Further, women with poor nutrition status may also be deficient in vitamins and minerals. Adequate nutrition is critical for fetal development and a diet low in saturated fat and cholesterol may help reduce the risk of a preterm delivery.[49] Obesity does not directly lead to preterm birth;[50] however, it is associated with diabetes and hypertension which are risk factors by themselves.[40] To some degree those individuals may have underlying conditions (i.e., uterine malformation, hypertension, diabetes) that persist.

Women with celiac disease have an increased risk of the development of preterm birth.[36] The risk of preterm birth is more elevated when celiac disease remains undiagnosed and untreated.[4]

Marital status is associated with risk for preterm birth. A study of 25,373 pregnancies in Finland revealed that unmarried mothers had more preterm deliveries than married mothers (P=0.001).[39] Pregnancy outside of marriage was associated overall with a 20% increase in total adverse outcomes, even at a time when Finland provided free maternity care. A study in Quebec of 720,586 births from 1990 to 1997 revealed less risk of preterm birth for infants with legally married mothers compared with those with common-law wed or unwed parents.[51][needs update]

Genetic make-up is a factor in the causality of preterm birth. Genetics has been a big factor into why Filipinos have a high risk of premature birth as the Filipinos have a large prevalence of mutations that help them be predisposed to premature births.[43] An intra- and transgenerational increase in the risk of preterm delivery has been demonstrated.[52] No single gene has been identified.

Subfertility is associated with preterm birth. Couples who have tried more than 1 year versus those who have tried less than 1 year before achieving a spontaneous conception have an adjusted odds ratio of 1.35 (95% confidence interval 1.22-1.50) of preterm birth.[53] Pregnancies after IVF confers a greater risk of preterm birth than spontaneous conceptions after more than 1 year of trying, with an adjusted odds ratio of 1.55 (95% CI 1.30-1.85).[53]

Exposure to heat also appear to increase the risk of preterm birth, with this occurring in about 25,000 pregnancies per year.[54]

### Factors during pregnancy[edit | edit source]

Air pollution increases the risk of preterm birth.[9] One study attributed air pollution to 18% of premature births globally.[55] The countries with the highest air pollution associated preterm births were in South and East Asia, the Middle East, North Africa, and West sub-Saharan Africa. Living in an area with a high concentration of air pollution is a major risk factor, including living near major roadways or highways where vehicle emissions are high from traffic congestion or are a route for diesel trucks that tend to emit more pollution.[56][57]

The use of fertility medication that stimulates the ovary to release multiple eggs and of IVF with embryo transfer of multiple embryos has been implicated as an important factor in preterm birth. Maternal medical conditions increase the risk of preterm birth. Often labor has to be induced for medical reasons; such conditions include high blood pressure,[58] pre-eclampsia,[59] maternal diabetes,[60] asthma, thyroid disease, and heart disease.

In a number of women anatomical issues prevent the baby from being carried to term. Some women have a weak or short cervix[58] (the strongest predictor of premature birth)[61][62][63] Women with vaginal bleeding during pregnancy are at higher risk for preterm birth. While bleeding in the third trimester may be a sign of placenta previa or placental abruption – conditions that occur frequently preterm – even earlier bleeding that is not caused by these conditions is linked to a higher preterm birth rate.[64] Women with abnormal amounts of amniotic fluid, whether too much (polyhydramnios) or too little (oligohydramnios), are also at risk.[40] The mental status of the women is of significance. Anxiety[65] and depression have been linked to preterm birth.[40]

The use of tobacco, cocaine, and excessive alcohol during pregnancy increases the chance of preterm delivery. Tobacco is the most commonly abused drug during pregnancy and contributes significantly to low birth weight delivery.[66] Babies with birth defects are at higher risk of being born preterm.[67]

Passive smoking and/or smoking before the pregnancy influences the probability of a preterm birth. The World Health Organization published an international study in March 2014.[68]

Presence of anti-thyroid antibodies is associated with an increased risk preterm birth with an odds ratio of 1.9 and 95% confidence interval of 1.1–3.5.[69]

A 2004 systematic review of 30 studies on the association between intimate partner violence and birth outcomes concluded that preterm birth and other adverse outcomes, including death, are higher among abused pregnant women than among non-abused women.[70]

The Nigerian cultural method of abdominal massage has been shown to result in 19% preterm birth among women in Nigeria, plus many other adverse outcomes for the mother and baby.[71] This ought not be confused with massage conducted by a fully trained and licensed massage therapist or by significant others trained to provide massage during pregnancy, which has been shown to have numerous positive results during pregnancy, including the reduction of preterm birth, less depression, lower cortisol, and reduced anxiety.[72]

### Infection[edit | edit source]

The frequency of infection in preterm birth is inversely related to the gestational age. Mycoplasma genitalium infection is associated with increased risk of preterm birth, and spontaneous abortion.[73]

Infectious microorganisms can be ascending, hematogeneous, iatrogenic by a procedure, or retrograde through the Fallopian tubes. From the deciduas they may reach the space between the amnion and chorion, the amniotic fluid, and the fetus. A chorioamnionitis also may lead to sepsis of the mother. Fetal infection is linked to preterm birth and to significant long-term handicap including cerebral palsy.[74]

It has been reported that asymptomatic colonization of the decidua occurs in up to 70% of women at term using a DNA probe suggesting that the presence of micro-organism alone may be insufficient to initiate the infectious response.

As the condition is more prevalent in black women in the US and the UK, it has been suggested to be an explanation for the higher rate of preterm birth in these populations. It is opined that bacterial vaginosis before or during pregnancy may affect the decidual inflammatory response that leads to preterm birth. The condition known as aerobic vaginitis can be a serious risk factor for preterm labor; several previous studies failed to acknowledge the difference between aerobic vaginitis and bacterial vaginosis, which may explain some of the contradiction in the results.[75]

Untreated yeast infections are associated with preterm birth.[76]

A review into prophylactic antibiotics (given to prevent infection) in the second and third trimester of pregnancy (13–42 weeks of pregnancy) found a reduction in the number of preterm births in women with bacterial vaginosis. These antibiotics also reduced the number of waters breaking before labor in full-term pregnancies, reduced the risk of infection of the lining of the womb after delivery (endometritis), and rates of gonococcal infection. However, the women without bacterial vaginosis did not have any reduction in preterm births or pre-labor preterm waters breaking. Much of the research included in this review lost participants during follow-up so did not report the long-term effects of the antibiotics on mothers or babies. More research in this area is needed to find the full effects of giving antibiotics throughout the second and third trimesters of pregnancy.[77]

A number of maternal bacterial infections are associated with preterm birth including pyelonephritis, asymptomatic bacteriuria, pneumonia, and appendicitis. A review into giving antibiotics in pregnancy for asymptomatic bacteriuria (urine infection with no symptoms) found the research was of very low quality but that it did suggest that taking antibiotics reduced the numbers of preterm births and babies with low birth weight.[78] Another review found that one dose of antibiotics did not seem as effective as a course of antibiotics but fewer women reported side effects from one dose.[79] This review recommended that more research is needed to discover the best way of treating asymptomatic bacteriuria.[78]

A different review found that preterm births happened less for pregnant women who had routine testing for low genital tract infections than for women who only had testing when they showed symptoms of low genital tract infections.[80] The women being routinely tested also gave birth to fewer babies with a low birth weight. Even though these results look promising, the review was only based on one study so more research is needed into routine screening for low genital tract infections.[80]

Also periodontal disease has been shown repeatedly to be linked to preterm birth.[81][82] In contrast, viral infections, unless accompanied by a significant febrile response, are considered not to be a major factor in relation to preterm birth.[40]

### Genetics[edit | edit source]

There is believed to be a maternal genetic component in preterm birth.[83] Estimated heritability of timing-of-birth in women was 34%. However, the occurrence of preterm birth in families does not follow a clear inheritance pattern, thus supporting the idea that preterm birth is a non-Mendelian trait with a polygenic nature.[84]

## Diagnosis[edit | edit source]

### Placental alpha microglobulin-1[edit | edit source]

Placental alpha microglobulin-1 (PAMG-1) has been the subject of several investigations evaluating its ability to predict imminent spontaneous preterm birth in women with signs, symptoms, or complaints suggestive of preterm labor.[85][86][87][88][89][90] In one investigation comparing this test to fetal fibronectin testing and cervical length measurement via transvaginal ultrasound, the test for PAMG-1 (commercially known as the PartoSure test) has been reported to be the single best predictor of imminent spontaneous delivery within 7 days of a patient presenting with signs, symptoms, or complaints of preterm labor. Specifically, the PPV, or positive predictive value, of the tests were 76%, 29%, and 30% for PAMG-1, fFN and CL, respectively (P < 0.01).[91]

### Fetal fibronectin[edit | edit source]

Fetal fibronectin (fFN) has become an important biomarker—the presence of this glycoprotein in the cervical or vaginal secretions indicates that the border between the chorion and deciduas has been disrupted. A positive test indicates an increased risk of preterm birth, and a negative test has a high predictive value.[40] It has been shown that only 1% of women in questionable cases of preterm labor delivered within the next week when the test was negative.[92]

### Ultrasound[edit | edit source]

Further information: Cervical incompetence

Obstetric ultrasound has become useful in the assessment of the cervix in women at risk for premature delivery. A short cervix preterm is undesirable: A cervical length of less than 25 mm at or before 24 weeks of gestational age is the most common definition of cervical incompetence.[93]

### Classification[edit | edit source]

Stages in prenatal development, with weeks and months numbered from last menstruation.

In humans, the usual definition of preterm birth is birth before a gestational age of 37 complete weeks.[94] In the normal human fetus, several organ systems mature between 34 and 37 weeks, and the fetus reaches adequate maturity by the end of this period. One of the main organs greatly affected by premature birth is the lungs. The lungs are one of the last organs to mature in the womb; because of this, many premature babies spend the first days and weeks of their lives on ventilators. Therefore, a significant overlap exists between preterm birth and prematurity. Generally, preterm babies are premature and term babies are mature. Preterm babies born near 37 weeks often have no problems relating to prematurity if their lungs have developed adequate surfactant, which allows the lungs to remain expanded between breaths. Sequelae of prematurity can be reduced to a small extent by using drugs to accelerate maturation of the fetus, and to a greater extent by preventing preterm birth.

## Prevention[edit | edit source]

Historically efforts have been primarily aimed to improve survival and health of preterm infants (tertiary intervention). Such efforts, however, have not reduced the incidence of preterm birth. Increasingly primary interventions that are directed at all women, and secondary intervention that reduce existing risks are looked upon as measures that need to be developed and implemented to prevent the health problems of premature infants and children.[95] Smoking bans are effective in decreasing preterm births.[96] Different strategies are used in the administration of prenatal care, and future studies need to determine if the focus can be on screening for high-risk women, or widened support for low-risk women, or to what degree these approaches can be merged.[95]

### Before pregnancy[edit | edit source]

Adoption of specific professional policies can immediately reduce risk of preterm birth as the experience in assisted reproduction has shown when the number of embryos during embryo transfer was limited.[95] Many countries have established specific programs to protect pregnant women from hazardous or night-shift work and to provide them with time for prenatal visits and paid pregnancy-leave. The EUROPOP study showed that preterm birth is not related to type of employment, but to prolonged work (over 42 hours per week) or prolonged standing (over 6 hours per day).[97] Also, night work has been linked to preterm birth.[98] Health policies that take these findings into account can be expected to reduce the rate of preterm birth.[95] Preconceptional intake of folic acid is recommended to reduce birth defects. There is also some evidence that folic acid supplement preconceptionally (before becoming pregnant) may reduce premature birth.[99] Reducing smoking is expected to benefit pregnant women and their offspring.[95]

### During pregnancy[edit | edit source]

Self-care methods to reduce the risk of preterm birth include proper nutrition, avoiding stress, seeking appropriate medical care, avoiding infections, and the control of preterm birth risk factors (e.g. working long hours while standing on feet, carbon monoxide exposure, domestic abuse, and other factors).[100] Reducing physical activity during pregnancy has not been shown to reduce the risk of a preterm birth.[101] Healthy eating can be instituted at any stage of the pregnancy including nutritional adjustments and consuming suggested vitamin supplements.[95] Calcium supplementation in women who have low dietary calcium may reduce the number of negative outcomes including preterm birth, pre-eclampsia, and maternal death.[102] The World Health Organization (WHO) suggests 1.5–2 g of calcium supplements daily, for pregnant women who have low levels of calcium in their diet.[103] Supplemental intake of C and E vitamins have not been found to reduce preterm birth rates.[104]

While periodontal infection has been linked with preterm birth, randomized trials have not shown that periodontal care during pregnancy reduces preterm birth rates.[95] Smoking cessation has also been shown to reduce the risk.[105] The use of personal at home uterine monitoring devices to detect contractions and possible preterm births in women at higher risk of having a preterm baby have been suggested.[22] These home monitors may not reduce the number of preterm births, however, using these devices may increase the number of unplanned antenatal visits and may reduce the number of babies admitted to special care when compared with women receiving normal antenatal care.[22] Support from medical professionals, friends, and family during pregnancy may be beneficial at reducing caesarean birth and may reduce prenatal hospital admissions, however, these social supports alone may not prevent preterm birth.[106]

#### Screening during pregnancy[edit | edit source]

Screening for asymptomatic bacteriuria followed by appropriate treatment reduces pyelonephritis and reduces the risk of preterm birth.[107] Extensive studies have been carried out to determine if other forms of screening in low-risk women followed by appropriate intervention are beneficial, including screening for and treatment of Ureaplasma urealyticum, group B streptococcus, Trichomonas vaginalis, and bacterial vaginosis did not reduce the rate of preterm birth.[95] Routine ultrasound examination of the length of the cervix may identify women at risk of preterm labour and tentative evidence suggests ultrasound measurement of the length of the cervix in those with preterm labor can help adjust management and results in the extension of pregnancy by about 4 days.[108] Screening for the presence of fibronectin in vaginal secretions is not recommended at this time in women at low risk of preterm birth.[medical citation needed]

### Reducing existing risks[edit | edit source]

Women are identified to be at increased risk for preterm birth on the basis of their past obstetrical history or the presence of known risk factors. Preconception intervention can be helpful in selected patients in a number of ways. Patients with certain uterine anomalies may have a surgical correction (i.e. removal of a uterine septum), and those with certain medical problems can be helped by optimizing medical therapies prior to conception, be it for asthma, diabetes, hypertension, and others.

#### Multiple pregnancies[edit | edit source]

In multiple pregnancies, which often result from use of assisted reproductive technology, there is a high risk of preterm birth. Selective reduction is used to reduce the number of fetuses to two or three.[109][110][111]

#### Reducing indicated preterm birth[edit | edit source]

A number of agents have been studied for the secondary prevention of indicated preterm birth. Trials using low-dose aspirin, fish oil, vitamin C and E, and calcium to reduce preeclampsia demonstrated some reduction in preterm birth only when low-dose aspirin was used.[95] Even if agents such as calcium or antioxidants were able to reduce preeclampsia, a resulting decrease in preterm birth was not observed.[95]

#### Reducing spontaneous preterm birth[edit | edit source]

Reduction in activity by the mother—pelvic rest, limited work, bed rest—may be recommended although there is no evidence it is useful with some concerns it is harmful.[112] Increasing medical care by more frequent visits and more education has not been shown to reduce preterm birth rates.[106] Use of nutritional supplements such as omega-3 polyunsaturated fatty acids is based on the observation that populations who have a high intake of such agents are at low risk for preterm birth, presumably as these agents inhibit production of proinflammatory cytokines. A randomized trial showed a significant decline in preterm birth rates,[113] and further studies are in the making.

##### Antibiotics[edit | edit source]

While antibiotics can get rid of bacterial vaginosis in pregnancy, this does not appear to change the risk of preterm birth.[114] It has been suggested that chronic chorioamnionitis is not sufficiently treated by antibiotics alone (and therefore they cannot ameliorate the need for preterm delivery in this condition).[95]

##### Progestogens[edit | edit source]

Progestogens—often given in the form of vaginal[115] progesterone or hydroxyprogesterone caproate—relax the uterine musculature, maintain cervical length, and possess anti-inflammatory properties; all of which invoke physiological and anatomical changes considered to be beneficial in reducing preterm birth. Two meta-analyses demonstrated a reduction in the risk of preterm birth in women with recurrent preterm birth by 40–55%.[116][117]

Progestogen supplementation also reduces the frequency of preterm birth in pregnancies where there is a short cervix.[118] A short cervix is one that is less than 25mm, as detected during a transvaginal cervical length assessment in the midtrimester.[119] However, progestogens are not effective in all populations, as a study involving twin gestations failed to see any benefit.[120] Despite extensive research related to progestogen effectiveness, uncertainties remain concerning types of progesterone and routes of administration.[121]

##### Cervical cerclage[edit | edit source]

In preparation for childbirth, the woman's cervix shortens. Preterm cervical shortening is linked to preterm birth and can be detected by ultrasonography. Cervical cerclage is a surgical intervention that places a suture around the cervix to prevent its shortening and widening. Numerous studies have been performed to assess the value of cervical cerclage and the procedure appears helpful primarily for women with a short cervix and a history of preterm birth.[118][122] Instead of a prophylactic cerclage, women at risk can be monitored during pregnancy by sonography, and when shortening of the cervix is observed, the cerclage can be performed.[95]

## Management[edit | edit source]

Preterm birth at 32 weeks and 4 days with a weight of 2,000 g attached to medical equipment

About 75% of nearly a million deaths due to preterm deliver would survive if provided warmth, breastfeeding, treatments for infection, and breathing support.[123] If a baby has cardiac arrest at birth and is before 23 weeks or less than 400 g attempts at resuscitation are not indicated.[124]

Tertiary interventions are aimed at women who are about to go into preterm labor, or rupture the membranes or bleed preterm. The use of the fibronectin test and ultrasonography improves the diagnostic accuracy and reduces false-positive diagnosis. While treatments to arrest early labor where there is progressive cervical dilatation and effacement will not be effective to gain sufficient time to allow the fetus to grow and mature further, it may defer delivery sufficiently to allow the mother to be brought to a specialized center that is equipped and staffed to handle preterm deliveries.[125] In a hospital setting women are hydrated via intravenous infusion (as dehydration can lead to premature uterine contractions).[126]

### Steroids[edit | edit source]

Severely premature infants may have underdeveloped lungs because they are not yet producing their own surfactant. This can lead directly to respiratory distress syndrome, also called hyaline membrane disease, in the neonate. To try to reduce the risk of this outcome, pregnant mothers with threatened premature delivery prior to 34 weeks are often administered at least one course of glucocorticoids, a steroid that crosses the placental barrier and stimulates the production of surfactant in the lungs of the baby.[12] Steroid use up to 37 weeks is also recommended by the American Congress of Obstetricians and Gynecologists.[12] Typical glucocorticoids that would be administered in this context are betamethasone or dexamethasone, often when the pregnancy has reached viability at 23 weeks.

In cases where premature birth is imminent, a second "rescue" course of steroids may be administered 12 to 24 hours before the anticipated birth. There are still some concerns about the efficacy and side effects of a second course of steroids, but the consequences of RDS are so severe that a second course is often viewed as worth the risk. A 2015 Cochrane review supports the use of repeat dose(s) of prenatal corticosteroids for women still at risk of preterm birth seven days or more after an initial course.[127]

Beside reducing respiratory distress, other neonatal complications are reduced by the use of glucocorticosteroids, namely intraventricular bleeding, necrotising enterocolitis, and patent ductus arteriosus.[128] A single course of antenatal corticosteroids could be considered routine for preterm delivery, but there are some concerns about applicability of this recommendation to low-resource settings with high rates of infections.[128] It remains unclear whether one corticosteroid (or one particular regimen) has advantages over another.[129]

Concerns about adverse effects of prenatal corticosteroids include increased risk for maternal infection, difficulty with diabetic control, and possible long-term effects on neurodevelopmental outcomes for the infants. There is ongoing discussion about when steroids should be given (i.e. only antenatally or postnatally too) and for how long (i.e. single course or repeated administration). Despite these unknowns, there is a consensus that the benefits of a single course of prenatal glucocorticosteroids vastly outweigh the potential risks.[130][131][132]

### Antibiotics[edit | edit source]

The routine administration of antibiotics to all women with threatened preterm labor reduces the risk of the baby to get infected with group B streptococcus and has been shown to reduce related mortality rates.[133]

When membranes rupture prematurely, obstetrical management looks for development of labor and signs of infection. Prophylactic antibiotic administration has been shown to prolong pregnancy and reduced neonatal morbidity with rupture of membranes at less than 34 weeks.[134] Because of concern about necrotizing enterocolitis, amoxicillin or erythromycin has been recommended, but not amoxicillin + clavulanic acid (co-amoxiclav).[134]

### Tocolysis[edit | edit source]

A number of medications may be useful to delay delivery including: nonsteroidal anti-inflammatory drugs, calcium channel blockers, beta mimetics, and atosiban.[135] Tocolysis rarely delays delivery beyond 24–48 hours.[136] This delay, however, may be sufficient to allow the pregnant woman to be transferred to a center specialized for management of preterm deliveries and give administered corticosteroids to reduce neonatal organ immaturity. Meta-analyses indicate that calcium-channel blockers and an oxytocin antagonist can delay delivery by 2–7 days, and β2-agonist drugs delay by 48 hours but carry more side effects.[95][137] Magnesium sulfate does not appear to be useful to prevent preterm birth.[138] However the use of magnesium sulfate dose decrease the risk of cerebral palsy in those about to delivery premature.[139] Its use before delivery, however, does appear to decrease the risk of cerebral palsy.[140]

### Mode of delivery[edit | edit source]

The routine use of caesarean section for early delivery of infants expected to have very low birth weight is controversial,[141] and a decision concerning the route and time of delivery probably needs to be made on a case-by-case basis.

### Neonatal care[edit | edit source]

Incubator for preterm baby

After delivery, plastic wraps or warm mattresses are useful to keep the infant warm on their way to the neonatal intensive care unit (NICU).[142] In developed countries premature infants are usually cared for in an NICU. The physicians who specialize in the care of very sick or premature babies are known as neonatologists. In the NICU, premature babies are kept under radiant warmers or in incubators (also called isolettes), which are bassinets enclosed in plastic with climate control equipment designed to keep them warm and limit their exposure to germs. Modern neonatal intensive care involves sophisticated measurement of temperature, respiration, cardiac function, oxygenation, and brain activity. Treatments may include fluids and nutrition through intravenous catheters, oxygen supplementation, mechanical ventilation support,[143] and medications. In developing countries where advanced equipment and even electricity may not be available or reliable, simple measures such as kangaroo care (skin to skin warming), encouraging breastfeeding, and basic infection control measures can significantly reduce preterm morbidity and mortality. Bili lights may also be used to treat newborn jaundice (hyperbilirubinemia).

Water can be carefully provided to prevent dehydration but no so much to increase risks of side effects.[144]

In terms of respiratory support, there may be little or no difference in the risk of death or chronic lung disease between high flow nasal cannulae (HFNC) and continuous positive airway pressure (CPAP) or nasal intermittent positive pressure ventilation (NPPV).[145] For extremely preterm babies (born before 28 weeks' gestation), targeting a higher versus a lower oxygen saturation range makes little or no difference overall to the risk of death or major disability.[146] Babies born before 32 weeks' probably have a lower risk of death from bronchopulmonary dysplasia if they have CPAP immediately after being born, compared to receiving either supportive care or assisted ventilation.[147]

One review found that when premature infants are given osteopathic manipulations, they are less likely to require as lengthy of a hospital stay than if they are not manipulated.[148]

There is insufficient evidence for or against placing preterm stable twins in the same cot or incubator (co-bedding).[149]

### Nutrition[edit | edit source]

Meeting the appropriate nutritional needs of preterm infants is important for long-term health. Optimal care may require a balance of meeting nutritional needs and preventing complications related to feeding. The ideal growth rate is not known, however, preterm infants usually require a higher energy intake compared to babies who are born at term.[150] The recommended amount of milk is often prescribed based on approximated nutritional requirements of a similar aged fetus who is not compromised.[151] An immature gastrointestinal tract (GI tract), medical conditions (or co-morbidities), risk of aspirating milk, and necrotizing enterocolitis may lead to difficulties in meeting this high nutritional demand and many preterm infants have nutritional deficits that may result in growth restrictions.[151] In addition, very small preterm infants cannot coordinate sucking, swallowing, and breathing.[152] Tolerating a full enteral feeding (the prescribed volume of milk or formula) is a priority in neonatal care as this reduces the risks associated with venous catheters including infection, and may reduce the length of time the infant requires specialized care in the hospital.[151] Different strategies can be used to optimize feeding for preterm infants. The type of milk/formula and fortifiers, route of administration (by mouth, tube feeding, venous catheter), timing of feeding, quantity of milk, continuous or intermittent feeding, and managing gastric residuals are all considered by the neonatal care team when optimizing care. The evidence in the form of high quality randomized trials is generally fairly weak in this area, and for this reason different neonatal intensive care units may have different practices and this results in a fairly large variation in practice. The care of preterm infants also varies in different countries and depends on resources that are available.[151]

#### Human breast milk and formula[edit | edit source]

The American Academy of Pediatrics recommended feeding preterm infants human milk, finding "significant short- and long-term beneficial effects," including lower rates of necrotizing enterocolitis (NEC).[153] In the absence of evidence from randomised controlled trials about the effects of feeding preterm infants with formula compared with mother's own breast milk, data collected from other types of studies suggest that mother's own breast milk is likely to have advantages over formula in terms of the baby's growth and development.[154][150] When a mother's breast milk is not available, formula is probably better than donor breast milk for preterm babies in terms of weight gain, linear growth and head growth but there may be little or no difference in terms of neuro-developmental disability, death or necrotising enterocolitis.[155]

##### Fortified human breast milk and preterm/term formula[edit | edit source]

Breast milk or formula alone may not be sufficient to meet the nutritional needs of some preterm infants. Fortification of breast milk or formula by adding extra nutrients is an approach often taken for feeding preterm infants, with the goal of meeting the high nutritional demand.[150] High quality randomized controlled trials are needed in this field to determine the effectiveness of fortification.[156] It is unclear if fortification of breast milk improves outcomes in preterm babies, though it may speed growth.[156] Supplementing human milk with extra protein may increase short-term growth but the longer-term effects on body composition, growth and brain development are uncertain.[157][158] Higher protein formula (between 3 and 4 grams of protein per kilo of body weight) may be more effective than low protein formula (less than 3 grams per kilo per day) for weight gain in formula-fed low-birth-weight infants.[159] There is insufficient evidence about the effect on preterm babies' growth of supplementing human milk with carbohydrate,[160] fat,[161][162] and branched-chain amino acids.[163] Conversely, there is some indication that preterm babies who cannot breastfeed may do better if they are fed only with diluted formula compared to full strength formula but the clinical trial evidence remains uncertain.[164]

Individualizing the nutrients and quantities used to fortify enteral milk feeds in infants born with very low birth weight may lead to better short-term weight gain and growth but the evidence is uncertain for longer term outcomes and for the risk of serious illness and death.[165] This includes targeted fortification (adjusting the level of nutrients in response to the results of a test on the breast milk) and adjustable fortification (adding nutrients based on testing the infant).[165]

Multi-nutrient fortifier used to fortify human milk and formula has traditionally been derived from bovine milk.[166] Fortifier derived from humans is available, however, the evidence from clinical trials is uncertain and it is not clear if there are any differences between human-derived fortifier and bovine-derived fortifier in terms of neonatal weight gain, feeding intolerance, infections, or the risk of death.[166]

#### Timing of feeds[edit | edit source]

For very preterm infants, most neonatal care centres start milk feeds gradually, rather than starting with a full enteral feeding right away, however, is not clear if starting full enteral feeding early effects the risk of necrotising enterocolitis.[151] In these cases, the preterm infant would be receiving the majority of their nutrition and fluids intravenously. The milk volume is usually gradually increased over the following weeks.[151] Research into the ideal timing of enteral feeding and whether delaying enteral feeding or gradually introducing enteral feeds is beneficial at improving growth for preterm infants or low birth weight infants is needed.[151] In addition, the ideal timing of enteral feeds to prevent side effects such as necrotising enterocolitis or mortality in preterm infants who require a packed red blood cell transfusion is not clear.[167] Potential disadvantages of a more gradual approach to feeding preterm infants associated with less milk in the gut and include slower GI tract secretion of hormones and gut motility and slower microbial colonization of the gut.[151]

Regarding the timing of starting fortified milk, preterm infants are often started on fortified milk/formula once they are fed 100 mL/kg of their body weight. Other some neonatal specialists feel that starting to feed a preterm infant fortified milk earlier is beneficial to improve intake of nutrients.[168] The risks of feeding intolerance and necrotising enterocolitis related to early versus later fortification of human milk are not clear.[168] Once the infant is able to go home from the hospital there is limited evidence to support prescribing a preterm (fortified) formula.[169]

#### Intermittent feeding versus continuous feeding[edit | edit source]

For infants who weigh less than 1500 grams, tube feeding is usually necessary.[152] Most often, neonatal specialists feed preterm babies intermittently with a prescribed amount of milk over a short period of time. For example, a feed could last 10-20 minutes and be given every 3 hours. This intermittent approach is meant to mimic conditions of normal bodily functions involved with feeding and allow for a cyclic pattern in the release of gastrointestinal tract hormones to promote development of the gastrointestinal system.[152] In certain cases, continuous nasogastric feeding is sometimes preferred. There is low to very low certainty evidence to suggest that low birth weight babies who receive continuous nasogastic feeding may reach the benchmark of tolerating full enteral feeding later than babies fed intermittently and it is not clear if continuous feeding has any effect on weight gain or the number of interruptions in feedings.[152] Continuous feeding may have little to no effect on length of body growth or head circumference and the effects of continuous feeding on the risk of developing necrotising enterocolitis is not clear.[152]

#### High volume feeds[edit | edit source]

High-volume (more than 180 mL per Kg per day) enteral feeds of fortified or non-fortified human breast milk or formula may improve weight gain while the pre-term infant is hospitalized, however, there is insufficient evidence to determine if this approach improves growth of the neonate and other clinical outcomes including length of hospital stay.[150] The risks or adverse effects associated with high-volume enteral feeding of preterm infants including aspiration pneumonia, reflux, apnoea, and sudden oxygen desaturation episodes have not been reported in the trials considered in a 2021 systematic review.[150]

#### Parenteral (intraveneous) nutrition[edit | edit source]

For preterm infants who are born after 34 weeks of gestation ("late preterm infants") who are critically ill and cannot tolerate milk, there is some weak evidence that the infant may benefit from including amino acids and fats in the intravenous nutrition at a later time point (72 hours or longer from hospital admission) versus early (less than 72 hours from admission to hospital), however further research is required to understand the ideal timing of starting intravenous nutrition.[170]

#### Gastric residuals[edit | edit source]

For preterm infants in neonatal intensive care on gavage feeds, monitoring the volume and colour of gastric residuals, the milk and gastrointestinal secretions that remain in the stomach after a set amount of time, is common standard of care practice.[171] Gastric residual often contains gastric acid, hormones, enzymes, and other substances that may help improve digestion and mobility of the gastrointestinal tract. Analysis of gastric residuals may help guide timing of feeds.[171] Increased gastric residual may indicate feeding intolerance or it may be an early sign of necrotizing enterocolitis. Increased gastric residual may be caused by an underdeveloped gastrointestinal system that leads to slower gastric emptying or movement of the milk in the intestinal tract, reduced hormone or enzyme secretions from the gastrointestinal tract, duodenogastric reflux, formula, medications, and/or illness.[171] The clinical decision to discard the gastric residuals (versus re-feeding) is often individualized based on the quantity and quality of the residual.[171] Some experts also suggest replacing the fresh milk or curded milk and bile-stained aspirates, but not replacing haemorrhagic residual.[171] Evidence to support or refute the practice of re-feeding preterm infants with gastric residuals is lacking.[171]

### Hearing assessment[edit | edit source]

The Joint Committee on Infant Hearing (JCIH) state that for preterm infants who are in the neonatal intensive care unit (NICU) for a prolonged time should have a diagnostic audiologic evaluation before they are discharged from the hospital.[172] Well babies follow a 1-2-3 month benchmark timeline where they are screened, diagnosed, and receiving intervention for a hearing loss. However, very premature babies it might not be possible to complete a hearing screen at one month of age due to several factors. Once the baby is stable an audiologic evaluation should be performed. For premature babies in the NICU, auditory brainstem response (ABR) testing is recommended. If the infant doesn't pass the screen, they should be referred for an audiologic evaluation by an audiologist.[172] If the infant is on aminoglycosides such as gentamicin for less than five days they should be monitored and have a follow up 6–7 months of being discharged from the hospital to ensure there is no late onset hearing loss due to the medication.[172]

## Prognosis[edit | edit source]

Preterm infants survival rates[173][174][175][176][177][178]

The chance of survival at 22 weeks is about 6%, while at 23 weeks it is 26%, 24 weeks 55% and 25 weeks about 72% as of 2016.[18] With extensive treatment up to 30% of those who survive birth at 22 weeks survive longer term as of 2019.[179] The chances of survival without long-term difficulties is less.[19] Of those who survival following birth at 22 weeks 33% have severe disabilities.[179] In the developed world overall survival is about 90% while in low-income countries survival rates are about 10%.[123]

Some children will adjust well during childhood and adolescence,[20] although disability is more likely nearer the limits of viability. A large study followed children born between 22 and 25 weeks until the age of 6 years old. Of these children, 46 percent had moderate to severe disabilities such as cerebral palsy, vision or hearing loss and learning disabilities, 34 percent had mild disabilities, and 20 percent had no disabilities. Twelve percent had disabling cerebral palsy.[31]

As survival has improved, the focus of interventions directed at the newborn has shifted to reduce long-term disabilities, particularly those related to brain injury.[20] Some of the complications related to prematurity may not be apparent until years after the birth. A long-term study demonstrated that the risks of medical and social disabilities extend into adulthood and are higher with decreasing gestational age at birth and include cerebral palsy, intellectual disability, disorders of psychological development, behavior, and emotion, disabilities of vision and hearing, and epilepsy.[180] Standard intelligence tests showed that 41 percent of children born between 22 and 25 weeks had moderate or severe learning disabilities when compared to the test scores of a group of similar classmates who were born at full-term.[31] It is also shown that higher levels of education were less likely to be obtained with decreasing gestational age at birth.[180] People born prematurely may be more susceptible to developing depression as teenagers.[181] Some of these problems can be described as being within the executive domain and have been speculated to arise due to decreased myelinization of the frontal lobes.[182] Studies of people born premature and investigated later with MRI brain imaging, demonstrate qualitative anomalies of brain structure and grey matter deficits within temporal lobe structures and the cerebellum that persist into adolescence.[183] Throughout life they are more likely to require services provided by physical therapists, occupational therapists, or speech therapists.[20]

Despite the neurosensory, mental and educational problems studied in school age and adolescent children born extremely preterm, the majority of preterm survivors born during the early years of neonatal intensive care are found to do well and to live fairly normal lives in young adulthood.[184] Young adults born preterm seem to acknowledge that they have more health problems than their peers, yet feel the same degree of satisfaction with their quality of life.[185]

Beyond the neurodevelopmental consequences of prematurity, infants born preterm have a greater risk for many other health problems. For instance, children born prematurely have an increased risk for developing chronic kidney disease.[186]

## Epidemiology[edit | edit source]

Disability-adjusted life year for prematurity and low birth weight per 100,000 inhabitants in 2004.[187]

no data

less than 120

120-240

240-360

360-480

480-600

600-720

720-840

840-960

960-1080

1080-1200

1200-1500

more than 1500

Preterm birth complicates the births of infants worldwide affecting 5% to 18% of births.[76] In Europe and many developed countries the preterm birth rate is generally 5–9%, and in the USA it has even risen to 12–13% in the last decades.[188]

As weight is easier to determine than gestational age, the World Health Organization tracks rates of low birth weight (< 2,500 grams), which occurred in 16.5 percent of births in less developed regions in 2000.[189] It is estimated that one third of these low birth weight deliveries are due to preterm delivery. Weight generally correlates to gestational age, however, infants may be underweight for other reasons than a preterm delivery. Neonates of low birth weight (LBW) have a birth weight of less than 2500 g (5 lb 8 oz) and are mostly but not exclusively preterm babies as they also include small for gestational age (SGA) babies. Weight-based classification further recognizes Very Low Birth Weight (VLBW) which is less than 1,500 g, and Extremely Low Birth Weight (ELBW) which is less than 1,000 g.[190] Almost all neonates in these latter two groups are born preterm.

Complications from preterm births resulted in 740,000 deaths in 2013, down from 1.57 million in 1990.[17]

## Society and culture[edit | edit source]

### Economics[edit | edit source]

Preterm birth is a significant cost factor in healthcare, not even considering the expenses of long-term care for individuals with disabilities due to preterm birth. A 2003 study in the US determined neonatal costs to be $224,400 for a newborn at 500–700 g versus $1,000 at over 3,000 g. The costs increase exponentially with decreasing gestational age and weight.[191] The 2007 Institute of Medicine report Preterm Birth[192] found that the 550,000 premature babies born each year in the U.S. run up about $26 billion in annual costs, mostly related to care in neonatal intensive care units, but the real tab may top $50 billion.[193]

### Notable cases[edit | edit source]

James Elgin Gill (born on 20 May 1987 in Ottawa, Ontario, Canada) was the earliest premature baby in the world, until that record was broken in 2004. He was 128 days premature (21 weeks and 5 days' gestation) and weighed 1 pound 6 ounces (624 g). He survived.[194][195]

In 2014, Lyla Stensrud, born in San Antonio, Texas, U.S. became the youngest premature baby in the world. She was born at 21 weeks 4 days and weighed 410 grams (less than a pound). Kaashif Ahmad resuscitated the baby after she was born. As of November 2018, Lyla was attending preschool. She had a slight delay in speech, but no other known medical issues or disabilities.[196]

Amillia Taylor is also often cited as the most premature baby.[197] She was born on 24 October 2006 in Miami, Florida, U.S. at 21 weeks and 6 days' gestation.[198] This report has created some confusion as her gestation was measured from the date of conception (through in vitro fertilization) rather than the date of her mother's last menstrual period, making her appear 2 weeks younger than if gestation was calculated by the more common method.[181] At birth, she was 9 inches (22.9 cm) long and weighed 10 ounces (280 g).[197] She suffered digestive and respiratory problems, together with a brain hemorrhage. She was discharged from the Baptist Children's Hospital on 20 February 2007.[197]

The record for the smallest premature baby to survive was held for a considerable amount of time by Madeline Mann, who was born in 1989 at 26 weeks, weighing 9.9 ounces (280 g) and measuring 9.5 inches (241.3 mm) long.[199] This record was broken in September 2004 by Rumaisa Rahman, who was born in the same hospital, Loyola University Medical Center in Maywood, Illinois.[200] at 25 weeks' gestation. At birth, she was 8 inches (200 mm) long and weighed 261 grams (9.2 oz).[201] Her twin sister was also a small baby, weighing 563 grams (1 lb 3.9 oz) at birth. During pregnancy their mother had pre-eclampsia, requiring birth by caesarean section. The larger twin left the hospital at the end of December, while the smaller remained there until 10 February 2005 by which time her weight had increased to 1.18 kg (2.6 lb).[202] Generally healthy, the twins had to undergo laser eye surgery to correct vision problems, a common occurrence among premature babies.

In May 2019, Sharp Mary Birch Hospital for Women & Newborns in San Diego announced that a baby nicknamed "Saybie" had been discharged almost five months after being born at 23 weeks gestation and weighing 244 grams (8.6 oz). Saybie was confirmed by Dr. Edward Bell of the University of Iowa to be the new smallest surviving premature baby.[203]

The world's smallest premature boy to survive was born in February 2009 at Children's Hospitals and Clinics of Minnesota in Minneapolis, Minnesota, U.S. Jonathon Whitehill was born at 25 weeks' gestation with a weight of 310 grams (11 oz). He was hospitalized in a neonatal intensive care unit for five months, and then discharged.[204]

Historical figures who were born prematurely include Johannes Kepler (born in 1571 at seven months' gestation), Isaac Newton (born in 1642, small enough to fit into a quart mug, according to his mother), Winston Churchill (born in 1874 at seven months' gestation), and Anna Pavlova (born in 1885 at seven months' gestation).[205]

### COVID19[edit | edit source]

During the COVID-19 pandemic, a drop in the rate of premature births has been reported, ranging from 20% to 90%. There is no universally accepted explanation as of August 2020. Hypotheses include additional rest and support for expectant mothers staying at home, less air pollution due to shutdowns and reduced car fumes, and reduced likelihood to catch other diseases and viruses in general due to the lockdowns.[206]

## Research[edit | edit source]

Brain injury is common among preterms, ranging from white matter injury to intraventricular and cerebellar haemorrhages [207]. The characteristic neuropathology of preterms has been described as the “encephalopathy of prematurity”. [208] The number of preterms that receive special education is doubled compared to the general population. School marks are lower and so are verbal learning, executive function, language skills, and memory performance scores.[209] [210] [211] [212], as well as IQ scores [213] [214] [215] [216] [217] [218][219] Behaviourally, adolescents who were born very preterm and/or very low birth weight have similar self-reports of quality of life, health status and self-esteem as term controls.[220]

## References[edit | edit source]

1. ↑ 1.0 1.1 1.2 1.3 1.4 1.5 1.6 "Preterm Labor and Birth: Condition Information". National Institutes of Health. 3 November 2014. Archived from the original on 2 April 2015. Retrieved 7 March 2015.
2. ↑ 2.00 2.01 2.02 2.03 2.04 2.05 2.06 2.07 2.08 2.09 2.10 2.11 World Health Organization (November 2014). "Preterm birth Fact sheet N°363". who.int. Archived from the original on 7 March 2015. Retrieved 6 March 2015.
3. ↑ 3.0 3.1 "What are the risk factors for preterm labor and birth?". National Institutes of Health. 3 November 2014. Archived from the original on 5 April 2015. Retrieved 7 March 2015.
4. ↑ 4.0 4.1 Saccone G, Berghella V, Sarno L, Maruotti GM, Cetin I, Greco L, Khashan AS, McCarthy F, Martinelli D, Fortunato F, Martinelli P (February 2016). "Celiac disease and obstetric complications: a systematic review and metaanalysis". American Journal of Obstetrics and Gynecology. 214 (2): 225–234. doi:10.1016/j.ajog.2015.09.080. PMID 26432464.
5. ↑ 5.0 5.1 5.2 "What treatments are used to prevent preterm labor and birth?". National Institutes of Health. 3 November 2014. Archived from the original on 2 April 2015. Retrieved 7 March 2015.
6. ↑ 6.0 6.1 "What treatments can reduce the chances of preterm labor & birth?". National Institutes of Health. 11 June 2013. Archived from the original on 2 April 2015. Retrieved 7 March 2015.
7. ↑ 7.0 7.1 Wang H, Naghavi M, Allen C, Barber RM, Bhutta ZA, Carter A, et al. (GBD 2015 Mortality and Causes of Death Collaborators) (October 2016). "Global, regional, and national life expectancy, all-cause mortality, and cause-specific mortality for 249 causes of death, 1980-2015: a systematic analysis for the Global Burden of Disease Study 2015". Lancet. 388 (10053): 1459–1544. doi:10.1016/s0140-6736(16)31012-1. PMC 5388903. PMID 27733281.
8. ↑ "What are the symptoms of preterm labor?". National Institutes of Health. 11 June 2013. Archived from the original on 2 April 2015. Retrieved 7 March 2015.
9. ↑ 9.0 9.1 Korten, I; Ramsey, K; Latzin, P (January 2017). "Air pollution during pregnancy and lung development in the child". Paediatric Respiratory Reviews. 21: 38–46. doi:10.1016/j.prrv.2016.08.008. PMID 27665510.
10. ↑ "What causes preterm labor and birth?". National Institutes of Health. 3 November 2014. Archived from the original on 2 April 2015. Retrieved 7 March 2015.
11. ↑ Sosa CG, Althabe F, Belizán JM, Bergel E (March 2015). "Bed rest in singleton pregnancies for preventing preterm birth". The Cochrane Database of Systematic Reviews. 3 (3): CD003581. doi:10.1002/14651858.CD003581.pub3. PMC 7144825. PMID 25821121.
12. ↑ 12.0 12.1 12.2 "Antenatal Corticosteroid Therapy for Fetal Maturation". ACOG. October 2016. Archived from the original on 29 September 2016. Retrieved 27 September 2016.
13. ↑ Haram K, Mortensen JH, Morrison JC (March 2015). "Tocolysis for acute preterm labor: does anything work". The Journal of Maternal-Fetal & Neonatal Medicine. 28 (4): 371–8. doi:10.3109/14767058.2014.918095. PMID 24990666. S2CID 20078137.
14. ↑ Chow, Yuan Huang; Dattani, Nirupa (26 February 2009). "Estimating conception statistics using gestational age information from NHS Numbers for Babies data". Health Statistics Quarterly. 41 (1): 21–27. doi:10.1057/hsq.2009.5. ISSN 2040-1574. PMID 19320250. S2CID 23996035.
15. ↑ Mathews, T. J.; Minino, A. M.; Osterman, M. J. K.; Strobino, D. M.; Guyer, B. (20 December 2010). "Annual Summary of Vital Statistics: 2008". Pediatrics. 127 (1): 146–157. doi:10.1542/peds.2010-3175. ISSN 0031-4005. PMC 4079290. PMID 21173001.
16. ↑ 16.0 16.1 American College of Obstetricians Gynecologists; Society for Maternal-Fetal Medicine (October 2017). "Obstetric Care consensus No. 6: Periviable Birth". Obstetrics and Gynecology. 130 (4): e187–e199. doi:10.1097/AOG.0000000000002352. PMID 28937572.
17. ↑ 17.0 17.1 GBD 2013 Mortality and Causes of Death Collaborators (January 2015). "Global, regional, and national age-sex specific all-cause and cause-specific mortality for 240 causes of death, 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013". Lancet. 385 (9963): 117–71. doi:10.1016/S0140-6736(14)61682-2. PMC 4340604. PMID 25530442.
18. ↑ 18.0 18.1 Cloherty and Stark's Manual of Neonatal Care (8 ed.). Lippincott Williams & Wilkins. 2016. p. 161\. ISBN 9781496367495.
19. ↑ 19.0 19.1 Jarjour IT (February 2015). "Neurodevelopmental outcome after extreme prematurity: a review of the literature". Pediatric Neurology. 52 (2): 143–52. doi:10.1016/j.pediatrneurol.2014.10.027. PMID 25497122.
20. ↑ 20.0 20.1 20.2 20.3 Saigal S, Doyle LW (January 2008). "An overview of mortality and sequelae of preterm birth from infancy to adulthood". Lancet. 371 (9608): 261–9. doi:10.1016/S0140-6736(08)60136-1. PMID 18207020. S2CID 17256481.
21. ↑ Phillips, Courtney; Velji, Zain; Hanly, Ciara; Metcalfe, Amy (1 June 2017). "Risk of recurrent spontaneous preterm birth: a systematic review and meta-analysis". BMJ Open. 7 (6): e015402. doi:10.1136/bmjopen-2016-015402. PMC 5734267. PMID 28679674. Archived from the original on 20 December 2019. Retrieved 20 December 2019.
22. ↑ 22.0 22.1 22.2 22.3 Urquhart C, Currell R, Harlow F, Callow L (February 2017). "Home uterine monitoring for detecting preterm labour". The Cochrane Database of Systematic Reviews. 2: CD006172. doi:10.1002/14651858.CD006172.pub4. PMC 6464057. PMID 28205207.
23. ↑ Mathew TJ, MacDorman MF (2006). "Infant Mortality Statistics from the 2003 Period Linked Birth/Infant Death Data Set". National Vital Statistics Reports. 54 (16).
24. ↑ Kaempf JW, Tomlinson M, Arduza C, Anderson S, Campbell B, Ferguson LA, Zabari M, Stewart VT (January 2006). "Medical staff guidelines for periviability pregnancy counseling and medical treatment of extremely premature infants". Pediatrics. 117 (1): 22–9. doi:10.1542/peds.2004-2547. PMID 16396856. S2CID 20495326. Archived from the original on 18 March 2008. — in particular see TABLE 1 Survival and Neurologic Disability Rates Among Extremely Premature Infants Pediatrics -- Kaempf et al. 117 (1): 22 Table 1 at the Wayback Machine (archived 12 June 2008)
25. ↑ Morgan MA, Goldenberg RL, Schulkin J (February 2008). "Obstetrician-gynecologists' practices regarding preterm birth at the limit of viability". The Journal of Maternal-Fetal & Neonatal Medicine. 21 (2): 115–21. doi:10.1080/14767050701866971. PMID 18240080. S2CID 27735824.
26. ↑ Arzuaga BH, Lee BH (December 2011). "Limits of human viability in the United States: a medicolegal review". Pediatrics. 128 (6): 1047–52. doi:10.1542/peds.2011-1689. PMID 22065266. S2CID 31065615.
27. ↑ Lambert, Scott R.; Lyons, Christopher J. (31 October 2016). Taylor and Hoyt's pediatric ophthalmology and strabismus (Fifth ed.). Edinburgh. ISBN 9780702066160. OCLC 960162637.
28. ↑ 28.0 28.1 March of Dimes --> Neonatal Death Neonatal death at the Wayback Machine (archived 24 October 2014)(Positional parameters ignored) Retrieved on 11 November 2014
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98. ↑ Other Complications include:
* Jaundice of Prematurity
* Atrial septal defects commonly seen in babies with bronchopulmonary dysplasia because their lungs are so fragile.
* GER Gastroesophageal reflux
* Patent Ductus Arterosis
* Seizures
* Immature GI system so feeding from an (NG) tube or nasogastric tube may help make feeding easier on the babies' tummy. Also theirs[clarification needed] TPN feeding or Total Parenteral Nutrition is made up of lipids, calories, good fats calcium, magnesium sulfate and other vitamins including B and C. Neonatalogists work with the family as a whole instead of just the neonate or baby whose systems are to immature to actually swallow food so babies between 23-28 weeks are fed through a neonatal gastric tube from the babies nose to the stomach. In some neonates, there are disabilities from varying conditions of the baby this depends on the gestational age the babies delivered a.uUsually, women with severe enough preeclampsia will deliver earlier than normal and those mothers worry greatly because of all of their rumors about NICUs and babies needing wheelchairs glasses and also needing medicines for seizures and ADD/ADHD, Borderline Personality Disorder, anxiety disorders.
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208. ↑ Volpe, JJ (December 2009). "The encephalopathy of prematurity--brain injury and impaired brain development inextricably intertwined". Seminars in Pediatric Neurology. 16 (4): 167–78. doi:10.1016/j.spen.2009.09.005. PMC 2799246. PMID 19945651.
209. ↑ Nosarti, Chiara; Giouroukou, Elena; Healy, Elaine; Rifkin, Larry; Walshe, Muriel; Reichenberg, Abraham; Chitnis, Xavier; Williams, Steven C. R.; Murray, Robin M. (January 2008). "Grey and white matter distribution in very preterm adolescents mediates neurodevelopmental outcome". Brain. 131 (1): 205–217. doi:10.1093/brain/awm282. PMID 18056158.
210. ↑ Nosarti, Chiara; Nam, Kie Woo; Walshe, Muriel; Murray, Robin M.; Cuddy, Marion; Rifkin, Larry; Allin, Matthew P.G. (2014). "Preterm birth and structural brain alterations in early adulthood". NeuroImage: Clinical. 6: 180–191. doi:10.1016/j.nicl.2014.08.005. PMC 4215396. PMID 25379430.
211. ↑ Tanskanen, Päivikki; Valkama, Marita; Haapea, Marianne; Barnes, Anna; Ridler, Khanum; Miettunen, Jouko; Murray, Graham K.; Veijola, Juha M.; Jones, Peter B.; Taanila, Anja M.; Isohanni, Matti K. (January 2011). "Is Prematurity Associated With Adult Cognitive Outcome and Brain Structure?". Pediatric Neurology. 44 (1): 12–20. doi:10.1016/j.pediatrneurol.2010.07.002. PMID 21147382.
212. ↑ Orchinik, Leah J.; Taylor, H. Gerry; Espy, Kimberly Andrews; Minich, Nori; Klein, Nancy; Sheffield, Tiffany; Hack, Maureen (19 September 2011). "Cognitive Outcomes for Extremely Preterm/Extremely Low Birth Weight Children in Kindergarten". Journal of the International Neuropsychological Society. 17 (6): 1067–1079. doi:10.1017/S135561771100107X. PMC 3282051. PMID 21923973.
213. ↑ Allin, Matthew P. G.; Kontis, Dimitris; Walshe, Muriel; Wyatt, John; Barker, Gareth J.; Kanaan, Richard A. A.; McGuire, Philip; Rifkin, Larry; Murray, Robin M.; Nosarti, Chiara; Najbauer, Joseph (12 October 2011). "White Matter and Cognition in Adults Who Were Born Preterm". PLOS ONE. 6 (10): e24525. Bibcode:2011PLoSO...624525A. doi:10.1371/journal.pone.0024525. PMC 3192037. PMID 22022357. S2CID 3884637.
214. ↑ Bjuland, Knut Jørgen; Løhaugen, Gro Christine Christensen; Martinussen, Marit; Skranes, Jon (June 2013). "Cortical thickness and cognition in very-low-birth-weight late teenagers". Early Human Development. 89 (6): 371–380. doi:10.1016/j.earlhumdev.2012.12.003. PMID 23273486.
215. ↑ Cheong, JL; Anderson, PJ; Roberts, G; Burnett, AC; Lee, KJ; Thompson, DK; Molloy, C; Wilson-Ching, M; Connelly, A; Seal, ML; Wood, SJ; Doyle, LW (2013). "Contribution of brain size to IQ and educational underperformance in extremely preterm adolescents". PLOS ONE. 8 (10): e77475. Bibcode:2013PLoSO...877475C. doi:10.1371/journal.pone.0077475. PMC 3793949. PMID 24130887.
216. ↑ Hack, M.; Flannery, D. J.; Schluchter, M.; Cartar, L.; Borawski, E.; Klein, N. (2002). "Outcomes in young adulthood for very-low-birth-weight infants". The New England Journal of Medicine. 346 (3): 149–57. doi:10.1056/NEJMoa010856. PMID 11796848.
217. ↑ Nosarti, Chiara; Nam, Kie Woo; Walshe, Muriel; Murray, Robin M.; Cuddy, Marion; Rifkin, Larry; Allin, Matthew P.G. (2014). "Preterm birth and structural brain alterations in early adulthood". NeuroImage: Clinical. 6: 180–191. doi:10.1016/j.nicl.2014.08.005. PMC 4215396. PMID 25379430.
218. ↑ Orchinik, Leah J.; Taylor, H. Gerry; Espy, Kimberly Andrews; Minich, Nori; Klein, Nancy; Sheffield, Tiffany; Hack, Maureen (19 September 2011). "Cognitive Outcomes for Extremely Preterm/Extremely Low Birth Weight Children in Kindergarten". Journal of the International Neuropsychological Society. 17 (6): 1067–1079. doi:10.1017/S135561771100107X. PMC 3282051. PMID 21923973.
219. ↑ Weisglas-Kuperus, N; Hille, E T M; Duivenvoorden, H J; Finken, M J J; Wit, J M; van Buuren, S; van Goudoever, J B; Verloove-Vanhorick, S P (19 September 2008). "Intelligence of very preterm or very low birthweight infants in young adulthood". Archives of Disease in Childhood - Fetal and Neonatal Edition. 94 (3): F196–F200. doi:10.1136/adc.2007.135095. PMID 18805824. S2CID 16930851. Archived from the original on 29 August 2021. Retrieved 24 June 2020.
220. ↑ Zwicker, J. G.; Harris, S. R. (28 January 2008). "Quality of Life of Formerly Preterm and Very Low Birth Weight Infants From Preschool Age to Adulthood: A Systematic Review". Pediatrics. 121 (2): e366–e376. doi:10.1542/peds.2007-0169. PMID 18245409. S2CID 11674158.

## External links[edit | edit source]

Classification|

* ICD-10: O60.1, P07.3
* ICD-9-CM: 644, 765
* MeSH: D047928
* DiseasesDB: 10589

|

External resources|

* MedlinePlus: 001562
* eMedicine: ped/1889

* v
* t
* e

Infants and their care

Health (Pediatrics)|

* Baby food
* Birth weight
* Breast pump
* Breastfeeding
* Breastfeeding and medications
* Bottle feeding
* Colic
* Immunizations
* Cradle cap
* Cross eyed
* Failure to thrive
* Immunization
* Infant and toddler safety
* Infant bathing
* Infant food safety
* Infant formula
* Infant massage
* Infant food safety
* Infant nutrition
* Infant respiratory distress syndrome
* Infant sleep training
* Neo-natal intensive care unit
* Newborn care and safety
* Oral rehydration therapy
* Pedialyte
* Preterm birth
* Shaken baby syndrome
* Soy formula
* Sudden infant death syndrome
* Breastfeeding and mental health

Development|

* Attachment parenting
* Baby-led weaning
* Baby talk
* Babbling
* Childbirth
* Congenital disorder
* Crawling
* Infant visual development
* Diaper rash
* Gestational age
* Infant cognitive development
* Kangaroo care
* Mother
* Nursery Rhyme
* Object permanence
* Parent
* Parenting
* Peekaboo
* Play
* Prenatal development
* Prenatal development table
* Teething
* Types of crying
* Walking
* Weaning

Socialization and Culture|

* Attachment
* Babysitting
* Child abuse
* Child custody
* Child's rights
* UN Child rights
* Circumcision
* Daycare
* Foster care
* Grandparent visitation
* Infant swimming
* Milk bank
* Nanny
* Wet nurse

Infant care and equipment|

* Baby bouncer
* Baby gate
* Baby monitor/Hidden camera
* Baby powder
* Baby shampoo
* Baby toy
* Baby walker
* Bib
* Baby swing
* Baby transport
* Bassinet
* Car seat safety
* Cloth diaper
* Cradle board
* Diaper
* Diaper bag
* Baby wipes
* Haberman Feeder
* High chair
* Infant bed (American 'crib' and 'cradle', British 'cot')
* Infant carrier
* Infant clothing
* Pacifier
* Playpen
* Stroller
* Supplemental nursing system
* Swaddling
* Swim diaper
* Teether
* Travel cot

Other topics|

* Baby shower
* Babywearing
* Child neglect
* Closed adoption
* Cry room
* Infant ear piercing
* Open adoption
* Prenatal cocaine exposure
* Neonatal withdrawal syndrome
* Parental child abduction
* Parental responsibility
* Parenting plan
* Paternity
* Paternity fraud

* v
* t
* e

Pathology of pregnancy, childbirth, and the puerperium

Pregnancy|

| Pregnancy with
abortive outcome|

* Abortion
* Ectopic pregnancy
* Abdominal
* Cervical
* Interstitial
* Ovarian
* Heterotopic
* Embryo loss
* Fetal resorption
* Molar pregnancy
* Miscarriage
* Stillbirth

|

Edema, proteinuria, and
hypertensive disorders|

* Gestational hypertension
* Pre-eclampsia
* HELLP syndrome
* Eclampsia

Other, predominantly
related to pregnancy|

| Digestive system|

* Acute fatty liver of pregnancy
* Gestational diabetes
* Hepatitis E
* Hyperemesis gravidarum
* Intrahepatic cholestasis of pregnancy

|

Integumentary system /
dermatoses of pregnancy|

* Gestational pemphigoid
* Impetigo herpetiformis
* Intrahepatic cholestasis of pregnancy
* Linea nigra
* Prurigo gestationis
* Pruritic folliculitis of pregnancy
* Pruritic urticarial papules and plaques of pregnancy (PUPPP)
* Stretch marks

Nervous system|

* Chorea gravidarum

Blood|

* Gestational thrombocytopenia
* Pregnancy-induced hypercoagulability

Maternal care related to the
fetus and amniotic cavity|

* amniotic fluid
* Oligohydramnios
* Polyhydramnios
* Braxton Hicks contractions
* chorion / amnion
* Chorioamnionitis
* Chorionic hematoma
* Constriction ring syndrome
* Monoamniotic twins
* Prelabor rupture of membranes
* Obstetrical bleeding
* Antepartum
* placenta
* Circumvallate placenta
* Monochorionic twins
* Placenta accreta
* Placenta praevia
* Placental abruption
* Twin-to-twin transfusion syndrome

Labor|

* Amniotic fluid embolism
* Cephalopelvic disproportion
* Obstructed labour
* Shoulder dystocia
* Fetal distress
* Locked twins
* Nuchal cord
* Obstetrical bleeding
* Postpartum
* Pain management during childbirth
* placenta
* Placenta accreta
* Preterm birth
* Postmature birth
* Umbilical cord prolapse
* Uterine inversion
* Uterine rupture
* Vasa praevia
* Uterine atony

Puerperal|

* Breastfeeding difficulties
* Low milk supply
* Cracked nipples
* Breast engorgement
* Childbirth-related post-traumatic stress disorder
* Diastasis symphysis pubis
* Postpartum bleeding
* Peripartum cardiomyopathy
* Postpartum depression
* Postpartum infections
* Postpartum psychosis
* Postpartum thyroiditis
* Puerperal mastitis

Other|

* Concomitant conditions
* Diabetes mellitus
* Systemic lupus erythematosus
* Thyroid disorders
* Maternal death
* Sexual activity during pregnancy

* Category

* v
* t
* e

Conditions originating in the perinatal period / fetal disease

Maternal factors
complicating pregnancy,
labour or delivery|

| placenta|

* Placenta praevia
* Placental insufficiency
* Twin-to-twin transfusion syndrome

|

chorion/amnion|

* Chorioamnionitis

umbilical cord|

* Umbilical cord prolapse
* Nuchal cord
* Single umbilical artery

presentation|

* Breech birth
* Asynclitism
* Shoulder presentation

Growth|

* Small for gestational age / Large for gestational age
* Preterm birth / Postterm pregnancy
* Intrauterine growth restriction

Birth trauma|

* scalp
* Cephalohematoma
* Chignon
* Caput succedaneum
* Subgaleal hemorrhage
* Brachial plexus injury
* Erb's palsy
* Klumpke paralysis

Affected systems|

| Respiratory|

* Intrauterine hypoxia
* Infant respiratory distress syndrome
* Transient tachypnea of the newborn
* Meconium aspiration syndrome
* Pleural disease
* Pneumothorax
* Pneumomediastinum
* Wilson–Mikity syndrome
* Bronchopulmonary dysplasia

|

Cardiovascular|

* Pneumopericardium
* Persistent fetal circulation

Bleeding and
hematologic disease|

* Vitamin K deficiency bleeding

* HDN
* ABO
* Anti-Kell
* Rh c
* Rh D
* Rh E
* Hydrops fetalis
* Hyperbilirubinemia
* Kernicterus
* Neonatal jaundice

* Velamentous cord insertion
* Intraventricular hemorrhage
* Germinal matrix hemorrhage
* Anemia of prematurity

Gastrointestinal|

* Ileus
* Necrotizing enterocolitis
* Meconium peritonitis

Integument and
thermoregulation|

* Erythema toxicum
* Sclerema neonatorum

Nervous system|

* Perinatal asphyxia
* Periventricular leukomalacia

Musculoskeletal|

* Gray baby syndrome
* muscle tone
* Congenital hypertonia
* Congenital hypotonia

Infections|

* Vertically transmitted infection
* Neonatal infection
* rubella
* herpes simplex
* mycoplasma hominis
* ureaplasma urealyticum
* Omphalitis
* Neonatal sepsis
* Group B streptococcal infection
* Neonatal conjunctivitis

Other|

* Miscarriage
* Perinatal mortality
* Stillbirth
* Infant mortality
* Neonatal withdrawal

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