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Essential pre-pregnancy and pregnancy interventions for improved maternal, newborn and child health
Reproductive Health volume 11, Article number: S2 (2014)
The statistics related to pregnancy and its outcomes are staggering: annually, an estimated 250000-280000 women die during childbirth. Unfortunately, a large number of women receive little or no care during or before pregnancy. At a period of critical vulnerability, interventions can be effectively delivered to improve the health of women and their newborns and also to make their pregnancy safe. This paper reviews the interventions that are most effective during preconception and pregnancy period and synergistically improve maternal and neonatal outcomes. Among pre-pregnancy interventions, family planning and advocating pregnancies at appropriate intervals; prevention and management of sexually transmitted infections including HIV; and peri-conceptual folic-acid supplementation have shown significant impact on reducing maternal and neonatal morbidity and mortality. During pregnancy, interventions including antenatal care visit model; iron and folic acid supplementation; tetanus Immunisation; prevention and management of malaria; prevention and management of HIV and PMTCT; calcium for hypertension; anti-Platelet agents (low dose aspirin) for prevention of Pre-eclampsia; anti-hypertensives for treating severe hypertension; management of pregnancy-induced hypertension/eclampsia; external cephalic version for breech presentation at term (>36 weeks); management of preterm, premature rupture of membranes; management of unintended pregnancy; and home visits for women and children across the continuum of care have shown maximum impact on reducing the burden of maternal and newborn morbidity and mortality. All of the interventions summarized in this paper have the potential to improve maternal mortality rates and also contribute to better health care practices during preconception and periconception period.
Although maternal mortality has decreased during the past decade, the proportion of births attended by a skilled health personnel still remains 68% in developing regions, often leading to tragic consequences . Annually, an estimated 250000-280000 women die during childbirth  while over 15 million are chronically afflicted with complications which occur during pregnancy . Adressing these issues in developing regions are critical forimproving maternal and neonatal health status and decreasing the associated morbidity and mortality.
In order to attain optimum level of health during pregnancy and the best possible maternal and neonatal health outcomes, effective interventions need to be delivered during preconception period and throughout pregnancy. In recent years, there has been increaased awareness regarding the importance of preconception period and efforts have been made to increase awareness and promote health right from childhood and adolescence onwards [4–12]. Research has also established linkages of preconception interventions with improved maternal, perinatal and neonatal health outcomes and it has been suggested that several proven interventions recommended during pregnancy may be even more effective if implemented before conception. On the other hand, interventions delivered during pregnancy also play a definitive beneficial role for improved maternal, fetal and neonatal health and survival. Maternal undernutrition, infections and chronic diseases carry a high risk for poor maternal and neonatal health and therefore, regular anatenatal checkups with improved screening can save many maternal and neonatal lives.
The motive of this review is to highlight the effectiveness of essential pre-pregnancy and pregnancy interventions that have an alleged impact on maternal, fetal and newborn outcomes and can be suitably delivered to low and middle income countries (LMIC) where minimal essential care is generally available.
The methodology has been described in detail elsewhere . In short, the review included all pre-pregnancy and pregnancy interventions based on current World Health Organization (WHO) guidelines and recent Lancet series which have an alleged impact on reducing maternal, neonatal and child mortality; suitable for delivery in LMICs, and those that can be delivered through the health sector (community level up to the referral level of health care) (Table 1). All relevant pre-pregnancy and pregnancy intervention reviews were identified from the electronic databases and were classified according to evidence and delivery strategies. Search was conducted in the following electronic databases: the Cochrane database of systematic reviews, the Cochrane database of abstract reviews of effectiveness (DARE), theCochrane database of systematic reviews of randomized control trials (RCT’s), and PubMed. The reference lists of the reviews and recommendations from experts in the field were also used as sources to obtain additional publications. The principal focus was on the existing systematic reviews and meta-analysis. Based on the efficiency of the interventions, these were then classisifed in categories from A to E (where A signified strongly beneficial effect while E indicated harmful effect) on different levels of health sector (community/outreach/referral).
There is a large unmet need for family planning as at least 200 million women desire safe and effective family planning methods.An estimated 21.6million unsafe abortions took place worldwide in 2008, almost all in LMICs. Numbers of unsafe abortions have increased from 19.7 million in 2003 although the overall unsafe abortion rate remains unchanged at about 14 unsafe abortions per 1000 women aged 15–44 years . Family planning prevents unwanted pregnancies and eliminates recourse to abortions. Both short and long inter-pregnancy intervals are associated with adverse perinatal outcomes [15–17] such as preterm birth, low birth weight (LBW), small for gestational age (SGA) and perinatal death. This link, however, may be confounded by different maternal characteristics and socio-economic status. To prevent these adverse events, birth spacing may be considered an intervention, especially in the developing world. Family planning is to plan when to have children and the use of birth control to delay pregnancy, including other techniques to implement such plans. Family planning services are defined as educational, comprehensive medical or social activities which enable individuals, including minors, to determine freely the number and spacing of their children and to select the means by which this may be achieved.
Short inter-pregnancy interval (IPIs) (less than 6 months) is associated with higher risk of preterm birth (odds ratio (OR) 1.40; 95% confidence interval (CI): 1.24, 1.58), LBW (OR 1.61; 95% CI: 1.39, 1.86), fetal death (OR 1.54, 95% CI: 1.06, 1.96) and SGA (OR 1.26; 95% CI: 1.18, 1.33) compared to IPI of 18 to 23 months. The risk is also significantly increased for these three adverse outcomes if the infant is conceived 60 months or more after a birth (preterm birth: OR 1.20; 95% CI: 1.17, 1.24; LBW: OR 1.43; 95% CI: 1.27, 1.62; fetal death OR 1.21, 95% CI: 1.07, 1.31 and SGA: OR 1.29; 95% CI: 1.20, 1.39) [18–20]. A recently published review with modified interval window reported the similar findings . Birth interval of shorter than 18 months was associated with increased odds of SGA (OR 1.51, 95% CI: 1.31, 1.75), preterm (OR: 1.58, 95% CI: 1.19, 2.10) and infant mortality (OR 1.83, 95% CI: 1.19, 2.81) as compared to IPI of 36 to <60 months. On the other hand, birth interval over 60 months had increased risk of SGA (OR: 1.22, 95% CI: 1.07, 1.39) and term-SGA (OR: 1.14, 95% CI: 1.03, 1.27) when compared with IPI of 36 to <60 months. The efficacy and effectiveness for different methods of contraception were also compared. The efficacy of the withdrawal method was found to be maximum (4%) and the least one was for the implant (0.1%), while the effectiveness was 21.6% for periodic abstinence and 15.1% for withdrawal . These findings suggest that short IPIs (less than 6 months) are associated with a significantly higher risk of preterm birth, LBW, fetal death and SGA infants compared to IPIs of 18 to 23 months. A recent review also reported higher risk of SGA, preterm births and infant mortality with IPIs of less than 18 months compared to 36 to <60 months. However, the risks were also higher if the infant is conceived 60 months or more after a birth. It is therefore advisable to plan pregnancies at appropriate intervals.
Prevention and management of sexually transmitted infections (STIs) including HIV
HIV was first declared as a pandemic in the early 1980s and the virus has become the leading cause of mortality across the globe, and the number of people it has infected and killed worldwide is astonishing. HIV is mainly spread in the population through sexual intercourse, needle sharing, blood transfusion or vertical transmission, which is the primary way by which children are infected. We looked at the role of mass media, behavioural interventions and biomedical interventions.
A review of observational studies found that antireteroviral therapy (ART) use in an HIV-infected member of an HIV-discordant couple is associated with lower risk of HIV transmission to the uninfected partner compared to untreated discordant couples (risk ratio (RR) 0.34; 95% CI 0.13, 0.92) . Mass treatment after three rounds of treatment of all community members for STIs indicated no effect of the intervention with the risk ratio (RR) for HIV incidence being 0.97 (95% CI 0.81, 1.2) . A combination of mass treatment and STI management trials showed a significant (12%) reduction in the prevalence of syphilis for those receiving a biomedical STI intervention (RR 0.88, 95% CI 0.80, 0.96) . These interventions also showed a significant 51% reduction in the prevalence of Gonorrhoea (RR 0.49, 95% CI 0.31, 0.77), while no improvement was observed in Chlamydia (RR 1.03, 95% CI 0.77, 1.4) . These findings suggest that effective interventions can prevent the spread of infection, if undertaken in reproductive age. Mass treatments and behavioural interventions to increase awareness can significantly reduce the incidence of STI while biomedical STI interventions can reduce the incidence of gonorrhoea, and chlamydia.
Peri-conceptual folic acid supplementation for preventing neural tube defects (NTDs)
Use of folic acid three months before conception to three months after conception, is known to reduce the risk of a first occurrence and a recurrence of NTDs [25, 26]. Folic acid deficiency has been linked to adverse outcomes of pregnancy like LBW, antepartum haemorrhage and perinatal mortality . It is recommended that all women of childbearing age should consume 0.4 mg of folic acid per day for the purpose of reducing the risk of a pregnancy with NTDs . During pregnancy, the requirement may go up to at least 600 mcg, or even more up to 1000mcg.
Studies suggest that the use of folic acid is highly effective for the prevention of recurrent NTDs (RR 0.30; 95% CI: 0.14, 0.65) . A Cochrane review also reported a protective effect of daily folic acid supplementation (alone or in combination with other vitamins and minerals) in preventing NTDs compared with no interventions/placebo or vitamins and minerals without folic acid (RR 0.28, 95% CI 0.15, 0.52) . It is also shown to have some non-significant impact on the reduction of miscarriage (RR 1.10; 95% CI: 0.97, 1.26)  and stillbirth (RR 0.96; 95% CI: 0.51, 1.83) . A meta-analysis of peri-conceptual folic acid fortification studies found reduction in primary incidence of NTDs by 41% (RR 0.59; 95% CI 0.52, 0.68] . Findings suggest that periconceptional folic acid have a significant protective effect on NTDs, particularly in women who had a previous pregnancy affected by it (recurrent NTDs). New methods for the provision of folic acid are underway which includes the addition of folic acid in oral contraceptives. All women with a history of baby with NTDs should be advised and given folate to prevent its recurrence. Evidence from Cochrane review is weak regarding the impact of folic acid supplementation on stillbirths and miscarriages.
Antenatal care visit model
The effectiveness of the content, frequency, and timing of visits in currently recommended programs for routine antenatal care is yet to be ascertained. Data from observational studies have shown that groups having more antenatal-care visits have lower maternal, fetal, and neonatal morbidity and mortality than those who have fewer antenatal-care visits . Earlier review found no association of perinatal mortality with reduced visits compared to standard care (OR 1.06; 95% CI: 0.82, 1.36) . However, a recent Cochrane review found that perinatal mortality was increased for those randomised to reduced visits rather than standard care (RR 1.14; 95% CI: 1.00, 1.31). In the subgroup analysis, for high-income countries (HICs) the association was non-significant (RR 0.90; 95% CI 0.45, 1.80); but for LMICs perinatal mortality was significantly higher in the reduced visits group (RR 1.15; 95% CI 1.01, 1.32) . Perception of mothers for the quality of prenatal care was not affected by the number of visits (RR 1.0; 95% CI 0.98, 1.01) . On the other hand, no difference in the rate of preterm birth (RR 0.87; 95% CI 0.47, 1.60) and LBW (less than 2500 g)(RR 1.03; 95% CI 0.73, 1.46) were found between women who received group antenatal care compared with women receiving standard one-to-one care . The number of antenatal care visits should be based of how effectively interventions can be delivered in a timely way during pregnancy because the purpose of routine antenatal care is to deliver effective and appropriate screening, preventive, or treatment interventions.
Iron and folic acid supplementation during pregnancy for maternal anaemia
During pregnancy, mothers who have iron deficiency anaemia have shown to have inadequate weight gain needed to maintain a healthy fetus; have weak immune system causing them to be more prone to infections; have heavy placentas; and are at a higher risk of neonates being born either prematurely or with LBW [36–39]. It is suggested that the high iron demand during pregnancy cannot be fulfilled from diet alone, so iron supplementation is vital in these months. Pregnant women are routinely provided with iron supplementation throughout pregnancy. Along with this, other interventions are now being employed in order to reduce iron deficiency and these include iron fortification, health and nutritional education and the control of parasitic infections along with increasing sanitation standards .
Maternal outcomes are shown to be greatly improved with iron supplementation. Women taking iron supplements were less likely to have LBW newborns (below 2500 g) compared to controls (RR 0.81; 95% CI 0.68, 0.97) with greater mean birth weight (mean difference (MD) 30.81g; 95% CI 5.94, 55.68) . Preventive iron supplementation reduces the risk of maternal anaemia at term by 70% (RR 0.30; 95% CI 0.19, 0.46) and iron deficiency at term by 57% (RR 0.43; 95% CI 0.27, 0.66) . Moderately significant evidence was found by Yakoob et al. stating that daily iron supplementation resulted in 73% reduction in the incidence of anaemia at term (RR 0.27; 95% CI: 0.17, 0.42) and 67% reduction in iron deficiency anaemia at term (RR 0.33; 95% CI: 0.16, 0.69) compared to no intervention/placebo . A review on folic acid supplementation during pregnancy showed no conclusive evidence for the impact on pregnancy outcomes such as preterm birth (RR 1.01; 95% CI 0.73, 1.38), and stillbirths/neonatal deaths (RR 1.33, 95% CI 0.96, 1.85). However, improvements were seen in the mean birth weight (MD 135.75g, 95% CI 47.85, 223.68) and reduction in the incidence of megaloblasticanaemia (RR 0.21, 95% CI 0.11, 0.38) . Exiting evidence suggests that providing mothers with iron supplementation during pregnancy reduces the risk of being anaemic near or at term. Although periconceptional folate supplementation has a clear protective benefit against occurrence of NTDs, antenatal folate supplementation in combination with iron or multivitamins has a limited role in prevention of perinatal mortality or morbidity. There are relatively few studies in this regard and a stronger recommendation can be made when results of more studies will be available.
Tetanus immunisation in pregnancy for preventing neonatal tetanus
Neonatal tetanus is a form of generalised tetanus that has a high fatality rate. It usually occurs through infection of the unhealed umbilical stump, particularly when the stump is cut with an unsterile instrument . Neonatal tetanus presents mostly (90%) during the first 3-14 days of life with the majority presenting at 6-8 days. The clinical presentation is very distressing and the case fatality rates tend to be very high even if full intensive care facilities are available. Therefore preventive measures are more effective than treatment options [45, 46].
A Cochrane review by Dimecheli 2013, found 2 very old trials (one on non-pregnant women). One trial compared the effectiveness of tetanus toxoid with influenza vaccine and reported a non-significant reduction in neonatal deaths (RR 0.57; 95% CI: 0.26, 1.24) and 43% vaccine effectiveness . Another trial assessed the effectiveness of tetanus-diphtheria toxoid in comparison with cholera toxoid in preventing neonatal mortality by 80% (RR 0.20; 95% CI 0.10, 0.40) with vaccine effectiveness as 80% .However, Blencowe 2010, added one well controlled cohort with one controlled trial and found a significant reduction in neonatal tetanus mortality by 94% (RR 0.06; 95% CI 0.02, 0.20) . Despite the available low cost immunisation and feasibility of reaching high coverage even in weak healthcare systems, the expected reduction in tetanus neonatal mortality has not been achieved yet. It is expected that with recent investments in the campaign for maternal and neonatal tetanus elimination, there will be substantial progress in reduction of mortality due to this illness.
Prevention and management of malaria in pregnancy
Prevention of malaria in pregnancy is especially important because most of these infections remain asymptomatic, and therefore remain undetected and untreated . There is a three-pronged approach to control malaria in pregnancy as suggested by WHO: it includes the use of insecticide-treated nets (ITNs) and antimalarial drugs, either through intermittent preventive therapy (IPT) or case management .
i) Prophylactic antimalarial for prevention of malaria in pregnancy
For malaria prophylaxis, IPTp with sulfadoxine-pyrimethamine (SP) is recommended for all pregnant women at each scheduled antenatal care visit. WHO recommends a schedule of four antenatal care visits.
The first IPTp-SP dose should be administered as early as possible during the 2ndtrimester of gestation
Each SP dose should be given at least 1 month apart
The last dose of IPTp with SP can be administered up to the time of delivery, without safety concerns
An unpublished meta-analysis by Kayentao et al. examined the number of IPTp doses that need to be administered during pregnancy to achieve the maximal beneficial effects of IPTp. The meta-analysis claimed that 3 or more doses (median of 4 doses) of IPTp with SP was superior to the standard 2 dose regimen in preventing LBW rates (reduction of 21% (95% CI 8, 32%) both in HIV infected and uninfected pregnant women and in all gravidity groups. Furthermore, women who received a median of 4 doses of IPTp-SP compared to those on the 2-dose regimen also had a lower risk of moderate-severe maternal anaemia, maternal malaria at delivery, and placental malaria. The meta-analysis, which included two trials in areas of Burkina Faso and Mali where the efficacy of SP remains high, showed that even in areas of high SP efficacy, 3 doses of SP were more effective than two doses . Antimalarial drugs did not show improvements in reducing maternal deaths (RR 0.34; 95% CI: 0.04, 3.27) or perinatal deaths (RR 1.02; 95% CI: 0.73, 1.43) . Routine antimalarial drugs reduce antenatal parasitaemia when given to pregnant women in malaria endemic areas. Greater benefit is seen in primi- and secundi-gravidas. SP regimen is feasible, though their regular use may precipitate increased risk of resistance. It is also associated with lower incidence of LBW (35%) and all-cause child mortality (18%). Two-dose IPT with SP when compared with placebo in women during their first or second pregnancy was found to reduce placental malaria (RR 0.48; 95% CI: 0.35, 0.68), LBW (RR 0.71; 95% CI: 0.55, 0.92), and anaemia (RR, 0.90; 95% CI: 0.81, 0.99) .
ii) Insecticide treated bed nets for preventing malaria in pregnancy
An insecticide-treated net (ITN) is a mosquito net that repel/disables and/or kills mosquitoes coming into contact with insecticide on the netting material. All mosquito nets act as a physical barrier, preventing access by vector mosquitoes and thus providing personal protection against malaria to the individual(s) using the nets. By reducing the vector population, ITNs, when used by a majority of the target population, provide protection for all people in the community, including those who do not themselves sleep under net. There are two categories of ITNs: conventionally treated nets and long-lasting insecticidal nets.
Langeler etal.conducted a review of five trials which showed that ITNs provided 17% protective efficacy (PE) compared to no nets (RR 0.83, 95% CI 0.76, 0.90), and 23% PE compared to untreated nets (RR 0.77, 95% CI 0.63, 0.95). About 5.5 lives (95% CI 3.39, 7.67) can be saved each year for every 1000 children protected with ITNs . Results by Gamble at al. show that ITNs, compared with no nets, reduced placental malaria in all pregnancies (RR 0.79, 95% CI 0.63, 0.98). They also reduced LBW (RR 0.77, 95% CI 0.61, 0.98) and fetal loss in the first to fourth pregnancy (RR 0.67, 95% CI 0.47, 0.97), but not in women with more than four previous pregnancies. It reduces peripheral and placental parasitaemia by 23% (RR 0.77; 95% CI 0.66, 0.90) [55, 56], increases mean birth weight by 55g (95% CI 21, 88) [55, 56], and decreases the risk of fetal loss in the by 33% (RR 0.67; 95% CI 0.47, 0.97) [55, 56]. Eisele et al. estimated that malaria prevention interventions in pregnancy (IPTp and ITNs) have a pooled PE of 35% (95% CI: 23-45%) for reducing the prevalence of LBW in the first or second pregnancy in areas of stable P. falciparum transmission . ITNs, therefore, should be an integral part of strategies to prevent malaria in pregnant women living especially in areas where malaria is endemic.
Smoking cessation in pregnancy for improving birth outcomes
Smoking during pregnancy has serious consequences on the health and wellbeing of the newborn child. It has important deleterious effects on the baby at birth and throughout the early development of the child. The smoking cessation strategies in pregnancy include provision of advice and counselling using various tools (written and electronic resources and telephone support), cognitive behavioural therapy (CBT) and motivational interviewing, advice and counselling based on feedback of fetal health status or measurement of by products of tobacco smoking in the mother, provision of pharmacological agents such as nicotine replacement therapy and bupropion, social support and encouragement, including the use of rewards for cessation and other interventions such as hypnosis.
Smoking cessation programs in pregnancy have shown to reduce smoking in late pregnancy (RR 0.94, 95% CI: 0.93 to 0.96) . This also has an impact on reducing LBW (RR 0.83, 95% CI 0.73 to 0.95) and preterm birth (RR 0.86, 95% CI 0.74 to 0.98), with a 53.91g (95% CI 10.44, 95.38 ) increase in mean birth weight . However, the difference in smoking cessation in later pregnancy after using nicotine replacement therapy was not significant when compared with placebo group (RR 1.33, 95% CI 0.93, 1.91) . It is important that smoking cessation programs be implemented in all maternity care settings. Smoking cessation and relapse prevention strategies should be routine parts of antenatal care as, for example, the measurement of blood pressure. Counselling and convincing patients for smoking cessation is a difficult job and it should be emphasized that midwives, general practitioners, and obstetricians support population-wide strategies for smoking control in the whole community to reduce/prevent/stop smoking by young people.
Prevention and management of syphilis
Maternal syphilis is related with adverse outcome in newborns. In 2008, the WHO estimated that 1.86 million cases of syphilis occur globally among pregnant women each year and that a large proportion of them are untreated or inadequately treated. Up to one third of the women attending antenatal care (ANC) clinics are not tested for syphilis .
Treatment of syphilis is associated with a reduction in preterm delivery (RR 0.36; 95% CI: 0.27, 0.47) . Observational studies have shown a reduction in stillbirths and neonatal mortality (RR 0.18; 95% CI: 0.10, 0.33 and RR 0.20; 95% CI: 0.13, 0.32 respectively) . Review by Walker at al.did not find studies that met predetermined criteria for comparison, however, they did conclude that penicillin are effective in treating syphilis but more studies are needed to establish the most effective dosage and duration of therapy . According to the CDC guidelines, the treatment of syphilis during pregnancy includes penicillin and the doses depend upon the stage of syphilis . For primary, secondary, and early latent syphilis the recommendation is to give benzathine penicillin-G 2.4 million units intramuscular in one dose. For females with late latent syphilis or latent syphilis with unknown duration the recommendation is for 7.2 million units of benzathine penicillin G administered as three doses (2.4 million units per dose) given intramuscularly for three weeks. The review on antibiotics given for the management of syphilis did not have any trial that met the eligibility criteria. However, observational studies showed benefits in lowering the incidence of neonatal mortality and preterm delivery.
Prevention and management of HIV and prevention of mother to child transmission (PMTCT) in pregnancy
Antiretroviral (ARV) drugs reduce viral replication and can reduce mother-to-child transmission of HIV either by lowering plasma viral load in pregnant women or through post-exposure prophylaxis in their newborns. In rich countries, highly active antiretroviral therapy (HAART) which usually comprises three drugs has reduced the mother-to-child transmission rates to around 1-2%. New evidence published in Lancet Infectious Diseases based on the Kesho Bora Studies state the giving a combination of three ARV drugs to pregnant mothers with HIV infection fromthelasttrimester, through delivery and six months of breastfeedingreducestheriskof transmitting HIV to the baby and improves survival. Infants of mothers whose virus is fully suppressed (undetectable) by triple-ARVs at the time of delivery have a very low risk of HIV infection (only 2.7% by the age of one year). It is therefore important to start ARVs early in pregnancy, ideally before pregnancy, for all women who require antiretroviral treatment (ART) (CD4 count at or below 350 cells/mm3). Giving HIV-positive pregnant women and that planning pregnancy priority access to HIV testing, CD4 count and ARVs will help eliminate mother-to-child transmission of HIV .
Vitamin A supplementation was found to reduce the risk of HIV infection in child (RR 1.04; 95% CI: 0.87, 1.24)  thus being useful for PMTCT. Vaginal disinfection, on the other hand, did not find any impact on reducing the transmission of HIV to child (RR 0.93; 95%CI 0.63, 1.38) .
A new study led by the WHO's Department of Reproductive Health and Research shows that if HIV-positive pregnant women are given a combination of antiretroviral (ARV) drugs from late in pregnancy until six months into breastfeeding, rather than a short course of drugs that ends at delivery, the likelihood of their babies becoming infected with HIV are over 40% lesser than with no such treatment .
The Kesho Bora study shows that a significant reduction in infant infection can be achieved when pregnant women with a CD4 immune cell count of 200-500 cells/ mm3 are given a combination of three ARVs to prevent transmission. This treatment should start in their last trimester of pregnancy, continuing through birth and six months of breastfeeding. This was shown to reduce the risk of transmitting HIV to the baby and improved survival compared with babies of mothers with HIV who are given the current WHO-recommended short-course ARV regimen in late pregnancy and around the time of delivery. An infant of mothers whose virus is fully suppressed undetectable by triple-ARVs at the time of delivery has a very low risk of HIV infection (only 2.7% by the age of one year). It is therefore important to start ARVs early in pregnancy, ideally before pregnancy, for all women who require antiretroviral treatment (ART) (CD4 count at or below 350 cells/mm3). Giving HIV-positive pregnant women and those planning pregnancy priority access to HIV testing, CD4 countand ARVs will help eliminate mother-to-child transmission of HIV .
The review by Read et al. identified 6 RCTs, of which, one RCT was on the efficacy of elective caesarean section (ECS) for prevention of MTCT of HIV-1. Among HIV-1-infected women not taking antiretroviral (ARVs) during pregnancy or taking only zidovudine, ECS was found to be efficacious for prevention of MTCT of HIV-1 .
Calcium for hypertension in pregnancy
Hypertension, with or without proteinuria, is an important cause of maternal and perinatal mortality and morbidity globally [69, 70]. It complicates pregnancy and is responsible for maternal deaths . Therefore, strategies to reduce the risk of these hypertensive disorders should be given high priority to save thousands of lives of mothers, especially in developing countries.Based on observations of communities in Guatemala and Ethiopia, it has been seen that women with a high calcium intake in their diet have a lower prevalence of pre-eclampsia and eclampsia . This was further supported by other epidemiological and clinical studies [72–75]. A possible mode of action of calcium could be that it reduces parathyroid hormone release and intracellular calcium, and so decreases smooth muscle contractility and, therefore, vasoconstriction [76, 77]. Calcium can also act directly on uterine smooth muscle to reduce contractility and prevent pre-term labour and delivery [76, 77].
Calcium supplementation can be an attractive, potential intervention to reduce the risk of a woman developing pre-eclampsia.
All studies showed that calcium supplementation has an effect on the reduction of pre-eclampsia (RR 0.45; 95% CI: 0.31, 0.65) .Hofmeyer 2007 also showed that high blood pressure was reduced with calcium supplementation when compared with placebo (RR 0.65, 95% CI 0.53, 0.81), as was pre-eclampsia (RR 0.48; 95% CI 0.33, 0.69) . The effect was greatest for women at high risk (RR 0.22; 95% CI 0.12, 0.42) and for those with low baseline calcium intake (RR 0.36; 95% CI 0.18, 0.70) [79, 80]. The composite outcome maternal death or serious morbidity was reduced (RR 0.80; 95% CI 0.65, 0.97). There was no overall effect on the risk of preterm birth or stillbirth or death before discharge from hospital [79, 80]. Jabeen et al. showed borderline reduction in stillbirths (RR 0.81, 95 % CI 0.63, 1.03)with calcium supplementation .
Calcium supplementation significantly reduced the risk of pre-eclampsia by 55% and by 64% in women with low dietary intake of calcium. It also had a significant protective effect on maternal mortality and serious morbidity and preterm birth. Its effect on, LBW or stillbirth was, however, non-significant. More large-scale trials need to be conducted to assess its safety profile before it can be routinely introduced into clinical practice.
Anti-platelet agents (low dose aspirin) for prevention of pre-eclampsia
Pre-eclampsia also leads to deficiency of prostacyclin, a vasodilator, and produces excessive amounts of thromboxane, which acts by stimulating platelet aggregation and causing platelet derived vasoconstriction . It is due to these observations that it is said the anti-platelet agents, especially low dose aspirin, can prevent or delay the development of pre-eclampsia.
The results show that that when anti-platelet agents are given during pregnancy, it leads to consistent reduction in the risk of preterm births (<34 weeks) (RR 0.92, 95%CI 0.88, 0.97), pre-eclampsia (RR 0.83, 95% CI 0.77, 0.89) and other adverse effect of pregnancy . Importantly for the fetus there was a significant reduction of 17% in all types of deaths (fetal, neonatal, infant) (RR 0.86, 95%CI 0.76, 0.98) . It is also noted that anti-platelet agents given to pregnant mothers who had gestational hypertension benefit even more with a significant reduction of 40% in the incidence of pre-eclampsia (RR 0.60 95%CI 0.45, 0.78) . On the other hand, a review Jabeen et al. did not show significant impact on reducing the risk of stillbirths (RR 1.15; 95% CI: 0.88, 1.49) . Another review also reported reduce incidence of pre-eclampsia with anti-platelet agents (RR 0.90, 95% CI 0.84, 0.97) .
We would recommend that anti-platelet agents should be given to pregnant women at high risk of pre-eclampsia or those with gestational hypertension, since they lead to reduction of vast adverse outcomes of pregnancy both for the mother and newborn.
Anti-hypertensive for treating severe hypertension
Hypertensive disorders of pregnancy, as a group, are a major cause of maternal and perinatal morbidity and mortality in both developing and the developed world [85, 86]. The International Society for the Study of Hypertension in Pregnancy defines hypertension as a diastolic blood pressure of 90 mmHg or above on two consecutive occasions at least four hours apart, or a single diastolic blood pressure of 110mmHg or more .
Women allocated calcium channel blockers rather than hydralazine were less likely to have persistent high blood (RR 0.37, 95% CI 0.21, 0.66) . Ketanserin was found to be associated with more persistent high blood pressure than hydralazine (RR 4.79, 95% CI 1.95, 11.73), but fewer side-effects (RR 0.32, 95% CI 0.19, 0.53). Both nimodipine and magnesium sulphate were associated witha high incidence of persistent high blood pressure, but a single study showed that this risk was lower for nimodipine compared to magnesium sulphate (RR 0.84, 95% CI 0.76 to 0.93) . Oral beta-blockers decrease the risk of severe hypertension (RR 0.37, 95% CI 0.26 to 0.53) and the need for additional antihypertensive (RR 0.44, 95% CI 0.31 to 0.62) .
The rationale for giving anti-hypertensive is that they will be dilatory in progression to severe disease with drastic complications for the mother and her baby. They may also reduce the risk of preterm delivery and placental abruption and improve fetal growth. Until better evidence is available, the choice of antihypertensive should depend on the clinician’s experience and familiarity with a particular drug and on what is known about adverse effects. Exceptions are diazoxide, ketanserin, nimodipine and magnesium sulphate, which are probably best avoided. The use of antihypertensive for treating severe hypertension in pregnant women is likely to bring an improvement in the neonatal and maternal outcomes.
Management of pregnancy-induced hypertension (PIH)/eclampsia
Pre-eclampsia is defined as a disorder during pregnancy with raised blood pressure and proteinuria, which may involve multiple systems including liver, kidneys, clotting system and brain. If it is complicated by convulsions (fits), then the condition is called eclampsia. Anticonvulsants like magnesium sulphate are used for eclamptic seizures and were introduced for women with pre-eclampsia in the belief that they would prevent the onset of seizures. This profile compares magnesium sulphate with other agents like diazepam, phenytoin and lytic cocktail for control of eclampsia; and also reviews the pros and cons of using it in women with pre-eclampsia as a prophylaxis vs. no anticonvulsants.
Magnesium sulphate therapy usually starts with an intravenous loading dose usually 4g but some advocate 6g, with therapy being continued either for 24 hours in total or until 12 to 24 hours after delivery. This is followed by either intramuscular (IM) or intravenous (IV) maintenance therapy. The IM maintenance regimen is usually 10 g given with the loading dose, and then 5 g every four hours. The IV infusion is usually 1 g/hour, although 2 g/hour is used by some.
Magnesium sulphate for pregnancies with pre-eclampsia had a significant impact on reducing stillbirths (RR 0.99; 95% CI: 0.87, 1.12) when compared with placebo/no treatment . When comparing magnesium sulphate to diazepam, magnesium sulphate was associated with a reduction in maternal death (RR 0.59, 95% CI 0.38, 0.92) and recurrence of seizures (RR 0.43, 95% CI 0.33, 0.55) . When compared with phenytoin, magnesium sulphate was associated with a substantial reduction in the recurrence of seizures (RR 0.34, 95% CI 0.24, 0.49). The trend in maternal mortality favours magnesium sulphate, but the difference does not reach statistical significance (RR 0.50, 95% CI 0.24, 1.05) . On the other hand, when magnesium sulphate was compared with placebo or no anticonvulsant, it led to halved the risk of eclampsia (RR 0.41, 95% CI 0.29, 0.58), with a non-significant reduction in maternal death (RR 0.54, 95% CI 0.26, 1.10) but no clear difference in serious maternal morbidity (RR 1.08, 95% CI 0.89, 1.32) . Magnesium sulphate was also compared with lytic cocktail and it was associated with fewer maternal deaths (RR 0.14, 95% CI 0.03, 0.59) and was better at preventing further seizures (RR 0.06, 95% CI 0.03, 0.12) than lytic cocktail .
Magnesium sulphate is an inexpensive drug and can be conveniently used in low income countries. Our review indicates that this drug significantly reduces the progress to eclampsia when given to women with pre-eclampsia compared to placebo. It should, therefore, be considered for those pre-eclamptic cases where there is a concern about the development of eclampsia. Clinical monitoring is necessary and can be achieved if trained staff is available. Serum monitoring is not necessary. For eclampsia, magnesium sulphate is now preferred over diazepam, phenytoin or lytic cocktail. It is significantly better in preventing maternal mortality and recurrence of seizures.
External cephalic version for breech presentation at term (>36 weeks)
Malpresentation places a healthy fetus and mother at increased risk of a complicated vaginal birth or caesarean section. It is not surprising that, over the years, the possibility of turning the baby from the breech to the cephalic presentation (ECV) has intrigued some obstetric caregivers. Before the mid-1970s, ECV was usually attempted before term because of the belief that the procedure would seldom be successful at term. Subsequent studies showed that with the use of tocolysis, ECV could be achieved in a substantial proportion of women with breech presentation at term (37 completed weeks of pregnancy or more). Predictors of unsuccessful version include engaged presenting part, fetal head not easily palpable and tense uterus .
Tocolytic drugs, in particular beta stimulants, were effective in increasing cephalic presentations in labour by 38% (RR 1.38, 95% CI 1.03,1.85) and in reducing the number of caesarean sections by 18% (RR 0.82, 95% CI 0.71, 0.94) . Initially, successful ECV at a late stage of pregnancy was considered to have become possible only because of the use of tocolytic drugs to relax the uterus. However, later studies showed that ECV at term was frequently possible without tocolysis. The overall success rate was 60% in a systematic review of RCTs where some trials included facilitation and others did not .
When postural management with pelvic elevation for breech presentation was compared with a control group reported the similar rates for non-cephalic births, caesarean section and Apgar scores below 7 at one minute, regardless of whether ECV was attempted or not(RR 0.98; 95% CI 0.84, 1.15; RR 1.10; 95% CI 0.89, 1.37; RR 0.88; 95% CI 0.50, 1.55 respectively). When comparing births with ECV for term births, no significant differences in the incidence of Apgar score ratings below seven at one minute (RR 0.95, 95% CI 0.47, 1.89) or five minutes (RR 0.76, 95% CI 0.32, 1.77), low umbilical artery pH levels (RR 0.65, 95% CI 0.17, 2.44), neonatal admission (RR 0.36, 95% CI 0.04, 3.24), perinatal death (RR 0.34, 95% CI 0.05, 2.12), nor time from enrolment to delivery (Weighted Mean Difference (WMD) -0.25 days, 95% CI -2.81 to 2.31) were found . For term breech delivery, perinatal or neonatal death (excluding fatal anomalies) or serious neonatal morbidity was reduced with planned caesarean section (RR 0.33, 95% CI 0.19, 0.56). This reduction was less for countries with high national perinatal mortality rates . Evidence exists in which moxibustion has no impact in reducing the need for ECV (RR 0.67 95% CI 0.34, 1.32)  but there is a need for well-designed RCTs to establish further evidence of the effectiveness of the intervention.
During an external cephalic version, practitioners use their hands on the woman’s abdomen to gently try to turn the baby from the breech position. There is sufficient evidence to conclude that external cephalic version at term reduces the chances of non-cephalic births and caesarean sections. There is lack of evidence from RCTs to assess the complication of cephalic version at term. Insufficient evidence exists to support the use of moxibustion to correct breech presentation.
Management of preterm, premature rupture of membranes
A) Management of premature rupture of membranes (PROM) (induction of labour)
Rupture of membranes before the onset of labour complicates 5-10% of all pregnancies, referred to as PROM (premature rupture of the membranes) . A minimum of 60% of these cases occur in pregnant women at term. Infection can be cause or a consequence of PROM. One way to prevent infections after PROM at term would be to expedite delivery by inducing labour, in which case pre-labour antibiotics may not be indicated. But in situations where expectant management is preferred, antibiotics may be beneficial in terms of reducing the likelihood of infection in the mother and her baby. This review compiles the existing evidence on the benefits and risks of the use of antibiotics in PROM at or near term.
Early delivery increased the incidence of caesarean section (RR 1.51; 95% CI 1.08, 2.10). There was no difference in the overall perinatal mortality (RR 0.98, 95% CI 0.41, 2.36), intrauterine deaths (RR 0.26;95% CI 0.04, 1.52) or neonatal deaths (RR 1.59, 95% CI 0.61, 4.16) when comparing early delivery with expectant management .
There is insufficient evidence to guide clinical practice on the benefits and harms of immediate delivery compared with expectant management for women with PPROM.
B) Management of preterm, premature rupture of membranes (PPROM) (use of antibiotic)
Management of PROM includes administration of any antibiotic for women with PPROM, inculcating all beta-lactam antibiotics (including penicillin) and macrolides.
The use of antibiotics was associated with a statistically significant reduction in chorioamnionitis(RR 0.66, 95% CI 0.46, 0.60) , preterm birth (RR 0.79, 95% CI 0.71, 0.89)  and neonatal infections including pneumonia (RR 0.67, 95% CI 0.52, 0.85) , which would support their routine clinical use in cases of pPROM. It did not, however, significantly impact perinatal mortality and neonatal mortality. Cousenset al. included 18 RCTs from high-income countries and provided strong evidence that antibiotics for pPROM reduce the risk of respiratory distress syndrome (RR 0.88; 95% CI 0.80, 0.97), and early onset postnatal infection (RR 0.61; 95% CI 0.48, 0.77) . The data was also found to be consistent with a reduction in neonatal mortality (RR 0.90; 95% CI 0.72, 1.12) .
Any antibiotics, administered as prophylaxis, by any route, to women at gestational age 36 weeks or beyond, with premature rupture of the membranes, can be used to manage this condition. There is not enough evidence to recommend routine use of antibiotics in women with PROM at term, although there was a 36% reduction in chorioamnionitis. Antibiotics may be reserved only for women that develop clinical indications of an infection, rather than prescribing it for all women in general. There were no clear neonatal advantages either. More trials are needed to evaluate their use, especially in women with PROM with expectant management or with a policy of delayed induction.
C) Corticosteroid use in preterm labour
One of the gravest outcomes of preterm labour is babies being born with respiratory distress syndrome (RDS), as this is the primary cause of early neonatal death and disability . RDS occurs as a complication of preterm delivery and it is present in about 20% of LBW babies (<2500g) and about 66% of extremely LBW babies (<1500g) . The reason for the development of RDS is a combination of poor lung development, immaturity of organs and a deficiency of surfactant. The role of corticosteroids when given prior to preterm birth shows that they can decrease the incidence of RDS and neonatal mortality in babies . This occurs from the theory that steroids can cause premature liberation of surfactant by alveoli and the surfactant produced will help in preventing the alveoli from collapsing. In the absence of surfactant the alveoli collapse during expiration and the following inspiration needs more effort to open the alveoli. If there is no surfactant this cycle of the alveoli collapsing continues and finally leads to fatigue, decreased respiratory effort, hypoxia, cyanosis, acidosis, and eventually death .
Antenatal steroids decrease neonatal mortality among preterm infants (<36 weeks gestation) by 31% (RR 0.69; 95% CI 0.58, 0.81). RCTs from middle-income countries suggests 53% mortality reduction (RR 0.47; 95% CI 0.35, 0.64) and 37% morbidity reduction (RR 0.63; 95% CI 0.49, 0.81) . Treatment with corticosteroids showed a statistically significant reduction of 23% in combined incidence of fetal and neonatal deaths (RR 0.77, 95%CI 0.67, 0.89), and this result was mainly due to the reduction seen in neonatal deaths (RR 0.69, 95% CI 0.58, 0.81). Antenatal corticosteroids were tested for the reduction ofmaternal death but the result failed to reach statistical significance (RR 0.98, 95% CI 0.06, 15.50) .There was also a significant reduction in the incidence of RDS (RR 0.66, 95% CI 0.59,0.73),moderate to severe RDS(RR 0.55, 95% CI0.43, 0.71),cerebroventricular haemorrhage (CVH) and severe CVH (RR 0.54, 95% CI 0.43, 0.69) . A Cocharane review of 10 trials showed that dexamethasone decreased the incidence of intraventricular haemorrhage compared with betamethasone (RR 0.44, 95%CI 0.21, 0.92) .
Management of unintended pregnancy
Numbers of unsafe abortions have increased from 19.7million in 2003 although the overall unsafe abortion rate remains unchanged at about 14 unsafe abortions per 1000 women aged 15–44 years . WHO defines these abortions as procedures that women undergo in order to terminate an unwanted pregnancy either in surroundings that are far below the medical standards or done by unskilled individuals, or both . The reasons for high rates of unsafe abortions in the developing world are that in some countries abortions are considered illegal or legal abortions are not offered, forcing females with unplanned pregnancy to either obtain secret abortions by untrained medical workers or self-induce abortions leading to the risk of complications. Females who undergo unsafe abortions are at the risk of developing complications which in most cases lead to long hospital stay and can also lead to mortality. It is stated that the commonest causes of mortality in females undergoing unsafe abortions are haemorrhage, infections and, in some cases, poisons that were used in self-inducing abortions . It is reason like these that makes it vital for clinics and hospitals, especially those in the developing countries, to have proper post-abortion care for patients. The fundamentals of post-abortion care should include having a medical staff skilled enough to handle all types of complications, along with having facilities for uterine evacuation procedures, along with referral of all patients to advanced sexual and reproductive health services. Lastly, females should be provided with counselling on contraceptives, family planning and told about the risks of unsafe abortions .
Another option to decrease the number of unsafe abortions and its complications would be by legalizing abortions, along with promoting the use of contraceptives or providing females proper counselling on these topics. It is seen that in those countries where abortion is legalized, mortality has considerably declined. This notion would be highly recommended for all developing nations where abortion is still not legalized, especially countries where religious prohibition and social norms do not allow this to occur.
According to the WHO guidelines on safe abortion 2003 , abortion services should be provided by well-trained health personnel to pregnant women who elect for the procedure. It must be supported by policies, regulations and a health systems infrastructure, including equipment and supplies, so that women can have rapid access to these services.
Cross cutting interventions
Home visits for women and children across the continuum of care
It is difficult to provide expert medical care to each and every person at community level especially in developing countries. To support the basic primary health care infrastructure, different community based intervention packages have been introduced to train persons in the society who has some background medical knowledge e.g. community health workers. These individuals with proper training, can function as community activists, opinion leaders, or health promoters, and can share their knowledge with community members, including pregnant women and their families. However as the background of each community health worker is different, a particular integrated approach could not be developed with public sector programs to target a particular goal. Different community based intervention packages have been developed to train community health workers for specific tasks like antenatal and postnatal care etc. [114, 115].
Improved perinatal care practices led to a drop in maternal mortality rate (OR 0.62; 95% CI 0.39, 0.98) . Home based Neonatal care packages led to a decrease in perinatal mortality (RR 0.71; 95% CI 0.61, 0.84) ; as well as incidence of stillbirths (RR 0.87; 95% CI 0.73, 1.03) . Another review showed a reduction in neonatal mortality (RR 0.76; 95% CI 0.68, 0.84) as well as incidence of stillbirths (RR 0.84; 95% CI 0.74, 0.97) and perinatal mortality (RR 0.80; 95% CI 0.71, 0.91) . The intervention packages included home visits during the neonatal period, home-based treatment for illness and community mobilization efforts showed a reduced risk of neonatal death (RR: 0.62; 95% CI 0.44, 0.87) and stillbirth (RR: 0.76; 95% CI 0.65, 0.89) .
The available data suggests that introduction of community based intervention packages can improve maternal and neonate survival. The results from Cochrane review are very promising and showed impact on reducing stillbirths, perinatal mortality and neonatal mortality.
The review aimed to document the essential pre-pregnancy and pregnancy interventions for improved maternal, newborn and child health. It covers pre-pregnancy interventions including family planning, prevention and management of STI and HIV and folic acid suuplementation prior to pregnancy amongst other interventions. In order to achieve maximum impact of pre-pregnancy interventions, these interventions should be appropriately timed . With regards to antenatal care, calcium and magnesium supplementation for prevention and management of pre-eclampsia and prophylactic and therapeutic uterotonics for prevention of postpartum heamorrahge are a couple of effective interventions that have the potential to save many maternal lives and prevent poor pregnancy outcomes. The implementation of the interventions reviewed in this paper will provide to be of paramount importance to improving the maternal and neonatal statistics especially in the developing countries, where there is a lot of potential work to be done. It is vital to understand that these interventions are central for LMIC where maternal and child health indicators are still not up to the standards and many lives are either lost or their quality compromised owing to a dearth of provision of essential interventions .
This review was designed to serve as a comprehensive and thorough document of essential pre-pregnancy and pregnancy interventions which could be used by both clinicians and policy makers. The review included all the recent Cochrane and non Cochrane reviews on specific interventions and the exercise included all essential pre-pregnancy and pregnancy interventions for maternal, newborn and child health. The data was summarized in a logical manner that can be utilized for further implementation and policy making to enable improvement in current health care system of LMICs. However, at times the quality of all included randomized controlled trials could not be ensured which limited the quality of the data obtained. Some reviews that were included were not updated recently and the data extracted from them might reflect facts that are not up to date. However, those reviews which had been updated by the authors were revised and the data extracted from within them was made up to date.
As stated earlier, the review is meant to be useful for health care practitioners as well as policy makers so that they may integrate and plan these interventions not only during the course of the pregnancy but also before pregnancy. It is essential to make policies and ensure that these essential interventions are delivered in a timely and effective manner.The integration of these interventions in the existing health services can not only improve outcomes presently but also lead to a better future of health care settings for both mothers and neonates. Long term sustainment of these improvements are necessary, therefore, it is essential to evaluate the impact of these interventions once streamlined into existing packages and programs. The transition to improved health care system must be made soon as it is becoming increasingly important to deliver these interventions at a large scale. With the deadlines of MDGs approaching upon us, immediate action is required to discuss these issues at policy making levels as well, so that we can find a way forward. Unless these problems are actively pursed and the suggestions given a thought, the issues related to maternal and newborn health care will keep on lingering upon us. Therefore, the review focuses on the approach which is critical to achieving the MDGs 4 and 5 – ensuring that we not only save lives to also address overall health and well-being.
Needless to say,the global cost for maternal disability is very high, therefore, ensuring the prompt and effective delivery of these interventions will be an effective strategy at moving towards the achievement of the millennium development and it would also lead to a much needed decrease in the burden of disease related to chronic complications of pregnancy and childbirth. Quite promisingly, a decline of 47% is seen in the statistics related to maternal mortality since the 1990s around the globe. Most encouraging is the fact that since 1990, some countries in Asia and Northern Africa have more than halved the numbers related to maternal mortality. These advancements herald atime when the achievement of MDGS 4 and 5 is closer than it has ever been before. With the proper implementation of a set of essential interventions recommended in this paper, we can hope to see the promising status of both improved and sustained maternal, neonatal and child helath outcomes.The integration of the basic care recommended and discussed in this paper with the global healthcare settings will be an effective strategy towards attaining a better health care setting for mothers and their children.With each passing day, we must aim to build a future in which each mother and child receives the best of health care regardless of their financial status or the area in which they reside. This could only be possible if there is a global knowledge and implementation of thelife saving interventions mentioned in this review.
The reviewer reports for this article can be found in Additional File 1.
McCall EM, Alderdice F, Halliday HL, Jenkins JG, Vohra S: Interventions to prevent hypothermia at birth in preterm and/or low birthweight infants. Cochrane Database Syst Rev. 2010, 3 (3): CD004210-
WHO: WHO recommendations for the prevention and treatment of postpartum haemorrhage. 2012, Geneva, Switzerland: World Health Organisation
Lozano R, Wang H, Foreman KJ, Rajaratnam JK, Naghavi M, Marcus JR, Dwyer-Lindgren L, Lofgren KT, Phillips D, Atkinson C: Progress towards Millennium Development Goals 4 and 5 on maternal and child mortality: an updated systematic analysis. Lancet. 2011, 378 (9797): 1139-1165. 10.1016/S0140-6736(11)61337-8.
Bhutta ZA, Memon ZA, Soofi S, Salat MS, Cousens S, J M: Implementing community-based perinatal care: results from a pilot study in rural Pakistan. Bulletin of the World Health Organization. 2008, 86: 452-459.
Manandhar DS, Osrin D, Shrestha BP, Mesko N, Morrison J, Tumbahangphe , KM TS, Thapa S, Shrestha D, Thapa B: Effect of participatory intervention with women’s groups on birth outcomes in Nepal: cluster randomised control trial. Lancet. 2004, 364: 970-979. 10.1016/S0140-6736(04)17021-9.
Azad K, Barnett S, Banerjee B, Shaha S, Khan K, Rega AR, Barua S, Flatman D, Pagel C, Prost A: Effect of scaling up women's groups on birth outcomes in three rural districts in Bangladesh: a cluster-randomised controlled trial. Lancet. 2010, 375:
Tripathy P, Nair N, Barnett S, Mahapatra R, Borghi J, Rath S, Gope R, Mahto D, Sinha R, Lakshminarayana R: Effect of participatory intervention with women's groups on birth outcomes and maternal depression in Jharkhand and Orissa, India: a cluster-randomised controlled trial. [In press]. Lancet. 2010, 375:
Rosato M, Mwansambo CW, Kazembe PN, Phiri T, Soko QS, Lewycka S, Kunyenge BE, Vergnano S, Osrin D, Newell ML: Women's groups' perceptions of maternal health issues in rural Malawi. The Lancet. 2006, 368 (9542): 1180-1188. 10.1016/S0140-6736(06)69475-0.
Osrin D, Mesko N, Shrestha BP, Shrestha D, Tamang S, Thapa S, Tumbahangphe KM, Shrestha JR, Manandhar MK, Manandhar DS: Implementing a community-based participatory intervention to improve essential newborn care in rural Nepal. TRANSACTIONS-ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE. 2003, 97 (1): 18-21. 10.1016/S0035-9203(03)90008-3.
Baqui AH, El-Arifeen S, Darmstadt GL, Ahmed S, Williams EK, Seraji HR, Mannan I, Rahman SM, Shah R, Saha SK: Effect of community-based newborn-care intervention package implemented through two service-delivery strategies in Sylhet district, Bangladesh: a cluster-randomised controlled trial. The Lancet. 2008, 371 (9628): 1936-1944. 10.1016/S0140-6736(08)60835-1.
Kumar V, Mohanty S, Kumar A, Misra RP, Santosham M, Awasthi S, Baqui AH, Singh P, Singh V, Ahuja RC: Effect of community-based behaviour change management on neonatal mortality in Shivgarh, Uttar Pradesh, India: a cluster-randomised controlled trial. The Lancet. 2008, 372 (9644): 1151-1162. 10.1016/S0140-6736(08)61483-X.
Wade A, Osrin D, Shrestha BP, Sen A, Morrison J, Tumbahangphe KM: Behaviour change in perinatal care practices among rural women exposed to a women's group intervention in Nepal. BMC Pregnancy and Childbirth. 2006, 6: 20-10.1186/1471-2393-6-20.
Lassi ZS, Salam RA, Dai JK, Bhutta ZA: Essential interventions for maternal, newborn and child health: background and methodology. Reproductive Health. 2014, 11 (Suppl 1): S1-
World Health Organization: Unsafe abortion Global and regional estimates of the incidence of unsafe abortion and associated mortality in 2008. 2011, EDITION S, [http://whqlibdoc.who.int/publications/2011/9789241501118_eng.pdf]
King JC: The risk of maternal nutritional depletion and poor outcomes increases in early or closely spaced pregnancies. J Nutr. 2003, 133 (5): 1732S-1736S.
Rousso D, Panidis D, Gkoutzioulis F, Kourtis A, Mavromatidis G, Kalahanis I: Effect of the interval between pregnancies on the health of mother and child. Eur J Obstet Gynecol Reprod Biol. 2002, 105 (1): 4-6. 10.1016/S0301-2115(02)00077-5.
Winikoff B: The effects of birth spacing on child and maternal health. Stud Fam Plann. 1983, 14 (10): 231-245. 10.2307/1965748.
Conde-Agudelo A, Belizan JM, Breman R, Brockman SC, Rosas-Bermudez A: Effect of the interpregnancy interval after an abortion on maternal and perinatal health in Latin America. Int J Gynecol Obstet. 2005, 89: S34-S40.
Conde-Agudelo A, Rosas-Bermudez A, Kafury-Goeta AC: Birth spacing and risk of adverse perinatal outcomes. JAMA. 2006, 295 (15): 1809-1823. 10.1001/jama.295.15.1809.
Conde-Agudelo A, Rosas-Bermudez A, Kafury-Goeta AC: Effects of birth spacing on maternal health: a systematic review. Am Obstet Gynecol. 2007, 196 (4): 297-308. 10.1016/j.ajog.2006.05.055.
Kozuki N, Lee ACC, Silveira MF, Victora CG, Adair L, Humphrey J, Ntozini R, Black RE, Katz J: The associations of birth intervals with small-for-gestational-age, preterm, and neonatal and infant mortality: a meta-analysis. BMC Public Health. 2013, 13 (Suppl 3): S3-
Steiner MJ, Dalebout S, Condon S, Dominik R, Trussell J: Understanding risk: a randomized controlled trial of communicating contraceptive effectiveness. Obstet Gynecol. 2003, 102 (4): 709-717. 10.1016/S0029-7844(03)00662-8.
Anglemyer A, Rutherford GW, Horvath T, Baggaley RC, Egger M, Siegfried N: Antiretroviral therapy for prevention of HIV transmission in HIV-discordant couples. Cochrane Database Syst Rev. 2013, 4 (4): CD009153-
Ng B, Butler L, Horvath T, Rutherford G: Population-based biomedical sexually transmitted infection control interventions for reducing HIV infection. Cochrane Database Syst Rev. 2011, 3 (3): CD00122-
Czeizel AE: Prevention of congenital abnormalities by periconceptional multivitamin supplementation. BMJ. 1993, 306 (6893): 1645-10.1136/bmj.306.6893.1645.
Prevention of neural tube defects: results of the Medical Research Council Vitamin Study. MRC Vitamin Study Research Group. Lancet. 1991, 338 (760): 131-137.
Scholl TO, Johnson WG: Folic acid: influence on the outcome of pregnancy. Am J Clin Nutr. 2000, 71 (5): 1295s-1303s.
CDC centers for disease control: Recommendations for the use of folic acid to reduce the number of cases of spina bifida and other neural tube defects; MMWR 1992; 41(No. RR-14). 1992
Blencowe H, Cousens S, Modell B, Lawn J: Folic acid to reduce neonatal mortality from neural tube disorders. Int J Epidemiol. 2010, 39 (Supplement 1): i110-10.1093/ije/dyq028.
De-Regil LM, Fernández-Gaxiola AC, Dowswell T, Peña-Rosas JP: Effects and safety of periconceptional folate supplementation for preventing birth defects. Cochrane Database Syst Rev. 2010, 10 (Issue): CD007950-
Imdad A, Yakoob MY, Bhutta ZA: The effect of folic acid, protein energy and multiple micronutrient supplements in pregnancy on stillbirths. BMC Public Health. 2011, 11 (Suppl 3): S4-10.1186/1471-2458-11-S3-S4.
Villar J, Carroli G, Khan-Neelofur D, Piaggio G, Gulmezoglu M: Patterns of routine antenatal care for low-risk pregnancy. Cochrane Database Syst Rev. 2001, 4 (4): CD000934-
Carroli G, Villar J, Piaggio G, Khan-Neelofur D, Gulmezoglu M, Mugford M, Lumbiganon P, Farnot U, Bersgo P: WHO systematic review of randomised controlled trials of routine antenatal care. Lancet. 2001, 357 (9268): 1565-1570. 10.1016/S0140-6736(00)04723-1.
Dowswell T, Carroli G, Duley L, Gates S, Gulmezoglu AM, Khan-Neelofur D, Piaggio GGP: Alternative versus standard packages of antenatal care for low-risk pregnancy. Cochrane Database Syst Rev. 2010, 10 (10): CD000934-
Homer CSE, Ryan C, Leap N, Foureur M, Teate A, Catling-Paull CJ: Group versus conventional antenatal care for women. Cochrane Database Syst Rev. 2012, 11 (11): CD007622-
Garn SM, Ridella SA, Petzold AS, Falkner F: Maternal hematologic levels and pregnancy outcomes. Semin Perinatol. 1981, 5: 155-
Kandoi A, Bhatia BD, Pandey LK, Pandey S, Sen PC, Satya K: Cellular immunity status in anaemia in pregnancy. Indian J Med Res. 1991, 94: 11-
Prema K, Ramalakshmi BA, Madhavapeddi R, Babu S: Immune status of anaemic pregnant women. BJOG. 1982, 89 (3): 222-225. 10.1111/j.1471-0528.1982.tb03619.x.
Scholl TO, Hediger ML, Fischer RL, Shearer JW: Anemia vs iron deficiency: increased risk of preterm delivery in a prospective study. Am J Clin Nutr. 1992, 55 (5): 985-988.
International Nutritional Anemia Consultative G: Guidelines for the eradication of iron deficiency anemia: a report. 1977, Nutrition Foundation
Pena-Rosas J, De-Regil L, Dowswell T, Viteri F: Daily oral iron supplementation during pregnancy. Cochrane Database Syst Rev. 2012, 12 (12): CD004736-
Yakoob M, Bhutta Z: Effect of routine iron supplementation with or without folic acid on anemia during pregnancy. BMC Public Health. 2011, 11 (3): s21-
Lassi Z, Salam R, Haider B, Bhutta Z: Folic acid supplementation during pregnancy formaternal health and pregnancyoutcomes. Cochrane Database Syst Rev. 2013, 3 (3): CD006896-
Demicheli V, Barale A, Rivetti A: Vaccines for women to prevent neonatal tetanus. Cochrane Database Syst Rev. 2005, 4 (12): CD002959-
Patel JC, Mehta BC: Tetanus: Study of 8697 cases*. Indian J Med Sci. 1999, 53 (9): 393-
WHO: Expanded programme on immunization: Prevention of neonatal tetanus. Weekly Epidemiological Record. 1982, WHO, 57:
Demicheli V, Barale A, Rivetti A: Vaccines for women to prevent neonatal tetanus. Cochrane Database Syst Rev. 2013, 5 (5): CD002959-
Blencowe H, Lawn J, Vandelaer J, Roper M, Cousens S: Tetanus toxoid immunization to reduce mortality from neonatal tetanus. Int J Epidemiol. 2010, 39 (suppl 1): i102-i109.
van Geertruyden J-P, Thomas F, Erhart A, D Alessandro U: The contribution of malaria in pregnancy to perinatal mortality. Am J Trop Med Hyg. 2004, 71 (2 suppl): 35-40.
World Health Organization: The African summit on Roll Back Malaria. 2000, Abuja, Nigeria, [http://savekids.dzopus.org/pdfs/African%20Summit%20on%20Roll%20Back%20Malaria.pdf]
Kayentao K, Garner P, van Eijk AM, Naidoo I, Roper C, Mulokozi A, MacArthur JR, Luntamo M, Ashorn P, Doumbo OK: Intermittent Preventive Therapy for Malaria During Pregnancy Using 2 vs 3 or More Doses of Sulfadoxine-Pyrimethamine and Risk of Low Birth Weight in AfricaSystematic Review and Meta-analysisMalaria Prophylaxis and Risk of Low Birth Weight. JAMA. 2013, 309 (6): 594-604. 10.1001/jama.2012.216231.
Garner P, Gulmezoglu AM: Drugs for preventing malaria in pregnant women. Cochrane Database Syst Rev. 2006, 4 (4): CD000169-
Ter Kuile FO, van Eijk AM, Filler SJ: Effect of sulfadoxine-pyrimethamine resistance on the efficacy of intermittent preventive therapy for malaria control during pregnancy. JAMA. 2007, 297 (23): 2603-2616. 10.1001/jama.297.23.2603.
Lengeler C: Insecticide-treated bed nets and curtains for preventing malaria. Cochrane Database Syst Rev. 2004, 2 (2): CD000363-
Gamble C, Ekwaru PJ, Garner P, ter Kuile FO: Insecticide-treated nets for the prevention of malaria in pregnancy: a systematic review of randomised controlled trials. PLoS Med. 2007, 4 (3): e107-10.1371/journal.pmed.0040107.
Gamble C, Ekwaru JP, ter Kuile FO: Insecticide-treated nets for preventing malaria in pregnancy. Cochrane Database Syst Rev. 2006, 2 (2): CD003755-
Eisele TP, Larsen D, Steketee RW: Protective efficacy of interventions for preventing malaria mortality in children in Plasmodium falciparum endemic areas. Int J Epidemiol. 2010, 39 (suppl 1): i88-i101.
Lumley J, Chamberlain C, Dowswell T, Oliver S, Oakley L, Watson L: Interventions for promoting smoking cessation during pregnancy. Cochrane Database Syst Rev. 2009, 3 (3): CD001055-
Coleman T, Chamberlain C, Davey M-A, Cooper SE, Leonardi-Bee J: Pharmacological interventions for promoting smoking cessation during pregnancy. Cochrane Database Syst Rev. 2012, 9 (9): CD010078-
Who U, Unicef: Global HIV/AIDS response: epidemic update and health sector progress towards universal access. Progress report November. 2011
Blencowe H, Cousens S, Kamb M, Berman S, Lawn JE: Lives Saved Tool supplement detection and treatment of syphilis in pregnancy to reduce syphilis related stillbirths and neonatal mortality. BMC Public Health. 2011, 11 (Suppl 3): S9-10.1186/1471-2458-11-S3-S9.
Walker GJ: Antibiotics for syphilis diagnosed during pregnancy. Cochrane Database Syst Rev. 2001, 4 (4): CD001143-
Centers for Disease Control and Prevention (CDC): Sexually transmitted diseases treatment guidelines. Morbidity and Mortality Weekly Report. 2002, 51 (RR-6): 1-80.
De Vincenzi I: Triple-antiretroviral (ARV) prophylaxis during pregnancy and breastfeeding compared to short-ARV prophylaxis to prevent mother-to-child transmission of HIV-1 (MTCT): the Kesho Bora randomized controlled clinical trial in five sites in Burkina Faso, Kenya. 5th International AIDS Society Conference on HIV Pathogenesis, Treatment and Prevention, Cape Town, 19-22 July 2009: 2009. 2009
Wiysonge CS, Shey M, Kongnyuy EJ, Sterne JA, Brocklehurst P: Vitamin A supplementation for reducing the risk of mother-to-child transmission of HIV infection. Cochrane Database Syst Rev. 2011, 1 (1): CD003648-
Shey WCU, Brocklehurst P, Sterne JAC: Vaginal disinfection during labour for reducing the risk of motherâ€ toâ€ child transmission of HIV infection. Cochrane Database Syst Rev. 2002, 3 (3): CD003651-
Kesho Bora Study G: Triple-antiretroviral prophylaxis during pregnancy and breastfeeding compared to short-ARV prophylaxis to prevent mother-to-child transmission of HIV-1: the Kesho Bora randomized controlled clinical trial in five sites in Burkina Faso, Kenya and South Africa. Fifth International AIDS Society Conference on HIV Treatment, Pathogenesis and Prevention: 2009. 2009
Read J, Newell M: Efficacy and safety of cesarean delivery for prevention of mother-to-child transmission of HIV-1. Cochrane Database Syst Rev. 2005, 4 (4): CD005479-
NHMRC: Report on Maternal Deaths in Australia 1988-1990. Canberra, Australia: Government Publising Service. 1993
HMSO: Report on Confidential Enquiries into Maternal Deaths in the United Kingdom 1988-1990. London: HMSO: Department of Health Welsh Office, Scottish Office Home and Health Department, Department of Health and Social Security, Northern Ireland. 1994
Villar J, Say L, Shennan A, Lindheimer M, Duley L, Conde-Agudelo A, Merialdi M: Methodological and technical issues related to the diagnosis, screening, prevention, and treatment of pre-eclampsia and eclampsia. Int J Gynaecol Obstet. 2004, 85: S28-S41.
Belizán JM, Villar J: The relationship between calcium intake and edema, proteinuria and hypertension gestosis. A hypothesis. American Journal of Clinical Nutrition. 1980, 33: 2202-2210.
Belizán JM, Villar J, Bergel E, González L, Campodónico L: Calcium supplementation to prevent hypertensive disorders of pregnancy. New England Journal of Medicine. 1991, 325: 1399-1405. 10.1056/NEJM199111143252002.
Belizán JM, Villar J, Zalazar A, Rojas L, Chan D, Bryce GF: Preliminary evidence of the effect of calcium supplementation on blood pressure in normal pregnant women. American Journal of Obstetrics and Gynecology. 1983, 146: 175-180.
Hofmeyr GJ, Lawrie TA, Atallah AN, Duley L: Calcium supplementation during pregnancy for preventing hypertensive disorders and related problems. Cochrane Database of Systematic Reviews. 2013, Issue 11:
Belizán JM, Villar J, Repke J: The relationship between calcium intake and pregnancy-induced hypertension: up-to-date evidence. Am J Obstet Gynecol. 1988, 158 (4): 898-10.1016/0002-9378(88)90091-9.
Belizán JM, Villar J, Self S, Pineda O, González I, Sainz E: The mediating role of the parathyroid gland in the effect of low calcium intake on blood pressure in the rat. Archivos Latinoamericanos de Nutrición. 1984, 34: 666-675.
Imdad A, Jabeen A, Bhutta ZA: Role of calcium supplementation during pregnancy in reducing risk of developing gestational hypertensive disorders: a meta-analysis of studies from developing countries. BMC Public Health. 2011, 11 (Suppl 3): S18-10.1186/1471-2458-11-S3-S18.
Hofmeyr GJ, Lawrie TA, Atallah lN, Duley L: Calcium supplementation during pregnancy for preventing hypertensive disorders and related problems. Cochrane Database Syst Rev. 2010, 8 (8): CD001059-
Hofmeyr GJ, Duley L, Atallah A: Dietary calcium supplementation for prevention of pre-eclampsia and related problems: a systematic review and commentary. BJOG. 2007, 114 (8): 933-943. 10.1111/j.1471-0528.2007.01389.x.
Jabeen M, Yakoob MY, Imdad A, Bhutta ZA: Impact of interventions to prevent and manage preeclampsia and eclampsia on stillbirths. BMC Public Health. 2011, 11 (Suppl 3): S6-10.1186/1471-2458-11-S3-S6.
Bussolino F, Benedetto C, Massobrio M, Camussi G: Maternal vascular prostacyclin activity in pre-eclampsia. Lancet. 1980, 316 (8196): 702-10.1016/S0140-6736(80)92746-4.
Duley L, Henderson-Smart DJ, Meher S, King JF: Antiplatelet agents for preventing pre-eclampsia and its complications. Cochrane Database Syst Rev. 2007, 4 (4): CD004659-
Askie LM, Duley L, Henderson-Smart DJ, Stewart LA: Antiplatelet agents for prevention of pre-eclampsia: a meta-analysis of individual patient data. Lancet. 2007, 369 (9575): 1791-1798. 10.1016/S0140-6736(07)60712-0.
DH: Department of Health, Welsh Office, Scottish Home and Health Department, Department of Health and Social Security, Northern Ireland. Report on Confidential Inquiries into Maternal Deaths in the United Kingdom 1994-96. London: HMSO. 1998
Duley L: Maternal mortality associated with hypertensive disorders of pregnancy in Africa, Asia, Latin America and the Caribbean. BJOG. 1992, 99 (7): 547-553. 10.1111/j.1471-0528.1992.tb13818.x.
Davey DA, MacGillivray I: The classification and definition of the hypertensive disorders of pregnancy. Am J Obstet Gynecol. 1988, 158 (4): 892-898. 10.1016/0002-9378(88)90090-7.
Duley L, Meher S, Jones L: Drugs for treatment of very high blood pressure during pregnancy. Cochrane Database Syst Rev. 2013, 7 (7): CD001449-
Magee LA, Duley L: Oral beta-blockers for mild to moderate hypertension during pregnancy. Cochrane Database Syst Rev. 2003, 3 (3): CD002863-
Duley L, Henderson-Smart DJ, Walker GJ, Chou D: Magnesium sulphate versus diazepam for eclampsia. Cochrane Database Syst Rev. 2010, 12 (12): CD000127-
Duley L, Henderson-Smart DJ, Chou D: Magnesium sulphate versus phenytoin for eclampsia. Cochrane Database Syst Rev. 2010, 10 (10): CD000128-
Duley L, Gulmezoglu AM, Henderson-Smart DJ, Chou D: Magnesium sulphate and other anticonvulsants for women with pre-eclampsia. Cochrane Database Syst Rev. 2010, 11 (11): CD000025-
Duley L, Gulmezoglu AM, Chou D: Magnesium sulphate versus lytic cocktail for eclampsia. Cochrane Database Syst Rev. 2010, 9 (9): CD002960-
Lau TK, Lo KWK, Wan D, Rogers MS: Predictors of successful external cephalic version at term: a prospective study. BJOG. 1997, 104 (7): 798-802. 10.1111/j.1471-0528.1997.tb12023.x.
Cluver C, Hofmeyr GJ, Gyte GM, Sinclair M: Interventions for helping to turn term breech babies to head first presentation when using external cephalic version. Cochrane Database Syst Rev. 2012, 1 (1): CD000184-
Hutton EK, Hofmeyr GJ: External cephalic version for breech presentation before term. Cochrane Database Syst Rev. 2006, 1 (1): CD000084-
Hofmeyr G, Kulier R: Cephalic version by postural management for breech presentation. Cochrane Database Syst Rev. 2012, 10 (10): CD000051-
Hofmeyr GJ, Kulier R: External cephalic version for breech presentation at term. Cochrane Database Syst Rev. 2012, 10 (10): CD000083-
Hofmeyr GJ, Hannah ME, Lawrie TA: Planned caesarean section for term breech delivery. Cochrane Database Syst Rev. 2003, 2 (2): CD000166-
Coyle ME, Smith CA, Peat B: Cephalic version by moxibustion for breech presentation. Cochrane Database Syst Rev. 2012, 5 (5): CD003928-
Duff P: Premature rupture of the membranes at term. N Engl J Med. 1996, 334 (16): 1053-1054. 10.1056/NEJM199604183341609.
Buchanan SL, Crowther CA, Levett KM, Middleton P, Morris J: Planned early birth versus expectant management for women with preterm prelabour rupture of membranes prior to 37 weeks' gestation for improving pregnancy outcome. Cochrane Database Syst Rev. 2010, 3 (3): CD004735-
Kenyon S, Boulvain M, Neilson JP: Antibiotics for preterm rupture of membranes. Cochrane Database Syst Rev. 2010, 8 (8): CD001058-
Cousens S, Blencowe H, Gravett M, Lawn JE: Antibiotics for pre-term pre-labour rupture of membranes: prevention of neonatal deaths due to complications of pre-term birth and infection. Int J Epidemiol. 2010, 39 (suppl 1): i134-i143.
Roberts D, Dalziel S: Antenatal corticosteroids for accelerating fetal lung maturation for women at risk of preterm birth. Cochrane Database Syst Rev. 2006, 3 (3): CD004454-
Crowley P, Chalmers I, Ke1Rse MJ: The effects of corticosteroid administration before preterm delivery: an overview of the evidence from controlled trials. BJOG. 1990, 97 (1): 11-25. 10.1111/j.1471-0528.1990.tb01711.x.
Purandare C: FETAL LUNG MATURITY. J Obstet Gynecol India. 2005, 55 (3): 215-217.
Mwansa-Kambafwile J, Cousens S, Hansen T, Lawn JE: Antenatal steroids in preterm labour for the prevention of neonatal deaths due to complications of preterm birth. Int J Epidemiol. 2010, 39 (suppl 1): i122-i133.
Brownfoot FC, Crowther CA, Middleton P: Different corticosteroids and regimens for accelerating fetal lung maturation for women at risk of preterm birth. Cochrane Database Syst Rev. 2008, 4 (4): CD006764-
World Health Organization: The prevention and management of unsafe abortion.Report of a Technical Working Group. 1992, [http://whqlibdoc.who.int/hq/1992/WHO_MSM_92.5.pdf]
Stephenson P, Wagner M, Badea M, Serbanescu F: Commentary: the public health consequences of restricted induced abortion--lessons from Romania. Am J Public Health. 1992, 82 (10): 1328-1331. 10.2105/AJPH.82.10.1328.
Kestler E, Valencia L, Del Valle V, Silva A: Scaling up post-abortion care in Guatemala: initial successes at national level. Reprod Health Matters. 2006, 14 (27): 138-147. 10.1016/S0968-8080(06)27235-5.
World Health Organization: Safe abortion: technical and policy guidance for health systems. 2003, World Health Organization
Bhutta ZA, Ali S, Cousens S, Ali TM, Haider BA, Rizvi A, Okong P, Bhutta SZ, Black RE: Alma-Ata: Rebirth and Revision 6 Interventions to address maternal, newborn, and child survival: what difference can integrated primary health care strategies make?. Lancet. 2008, 372 (9642): 972-989. 10.1016/S0140-6736(08)61407-5.
Bhutta ZA, Darmstadt GL, Haws RA, Yakoob MY, Lawn JE: Delivering interventions to reduce the global burden of stillbirths: improving service supply and community demand. BMC Pregnancy and Childbirth. 2009, 9 (Supplement 1): S7-
Kidney E, Winter HR, Khan KS, Gumezoglu AM, Meads CA, Deeks JJ, MacArthur C: Systematic review of effect of community-level interventions to reduce maternal mortality. BMC Pregnancy and Childbirth. 2009, 9 (1): 2-10.1186/1471-2393-9-2.
Lassi ZS, Haider BA, Bhutta ZA: Community-based intervention packages for reducing maternal and neonatal morbidity and mortality and improving neonatal outcomes. Cochrane Database Syst Rev. 2010, 11 (11): CD007754-
Gogia S, Sachdev HS: Home visits by community health workers to prevent neonatal deaths in developing countries: a systematic review. Bull World Health Organ. 2010, 88 (9): 658-666. 10.2471/BLT.09.069369.
Campbell OM, Graham WJ: Strategies for reducing maternal mortality: getting on with what works. Lancet. 2006, 368 (9543): 1284-1299. 10.1016/S0140-6736(06)69381-1.
Bhutta ZA, Darmstadt GL, Hasan BS, Haws RA: Community-based interventions for improving perinatal and neonatal health outcomes in developing countries: a review of the evidence. Pediatrics. 2005, 115 (Supplement 2): 519-617.
The publication of these papers and supplement was supported by an unrestricted grant from The Partnership for Maternal, Newborn and Child Health.
This article has been published as part of Reproductive Health Volume 11 Supplement 1, 2014: Essential intervention for maternal, newborn and child health. The full contents of the supplement are available online at http://www.reproductive-health-journal.com/supplements/11/S1. Publication charges for this collection were funded by the Partnership for Maternal, Newborn & Child Health (PMNCH).
We do not have any financial or non-financial competing interests for this review.
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Lassi, Z.S., Mansoor, T., Salam, R.A. et al. Essential pre-pregnancy and pregnancy interventions for improved maternal, newborn and child health. Reprod Health 11, S2 (2014). https://0-doi-org.brum.beds.ac.uk/10.1186/1742-4755-11-S1-S2
- essential interventions