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      Factors Associated with Not Breastfeeding and Delaying the Early Initiation of Breastfeeding in Mecca Region, Saudi Arabia

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          Abstract

          The objective of the study was to find the determinants related to not breastfeeding (BF) and others related to the delay in the early initiation of BF in the Mecca region, Saudi Arabia. A cross-sectional study in the Maternity and Children Hospital and primary healthcare centers was performed. A questionnaire was filled by dietitians to 814 asymptomatic Saudi mothers. Determinants related to not BF and the delay in the early initiation of BF were determined by binary logistic regression, and the odds ratio (OR) and 95% confidence interval (CI) were determined. Significant factors associated with not BF were not rooming-in infants in the mother’s room (OR: 2.37; 95% CI: 1.66–3.41) and using a pacifier (OR: 1.62; 95% CI: 1.13–2.33). The most significant determinant of the early initiation of BF was the initiation of bottle feeding (OR: 18.16; 95% CI: 10.51–31.4), followed by not rooming-in infants in the mother’s room (OR: 2.2; 95% CI: 1.52–3.18), initiation of partial feeding (OR: 1.89; 95% CI: 1.3–2.74), uninformed mothers regarding the importance of BF (OR: 1.56; 95% CI: 1.04–2.35), and cesarean sections (OR:1.42; 95% CI: 1.02–1.98). Risk factors affecting BF and the early initiation of BF in Mecca City should be highlighted in national campaigns to increase mothers’ awareness and promote BF practice.

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          Delayed breastfeeding initiation increases risk of neonatal mortality.

          Breastfeeding promotion is a key child survival strategy. Although there is an extensive scientific basis for its impact on postneonatal mortality, evidence is sparse for its impact on neonatal mortality. We sought to assess the contribution of the timing of initiation of breastfeeding to any impact. This study took advantage of the 4-weekly surveillance system from a large ongoing maternal vitamin A supplementation trial in rural Ghana involving all women of childbearing age and their infants. It was designed to evaluate whether timing of initiation of breastfeeding and type (exclusive, predominant, or partial) are associated with risk of neonatal mortality. The analysis is based on 10,947 breastfed singleton infants born between July 2003 and June 2004 who survived to day 2 and whose mothers were visited in the neonatal period. Breastfeeding was initiated within the first day of birth in 71% of infants and by the end of day 3 in all but 1.3% of them; 70% were exclusively breastfed during the neonatal period. The risk of neonatal death was fourfold higher in children given milk-based fluids or solids in addition to breast milk. There was a marked dose response of increasing risk of neonatal mortality with increasing delay in initiation of breastfeeding from 1 hour to day 7; overall late initiation (after day 1) was associated with a 2.4-fold increase in risk. The size of this effect was similar when the model was refitted excluding infants at high risk of death (unwell on the day of birth, congenital abnormalities, premature, unwell at the time of interview) or when deaths during the first week (days 2-7) were excluded. Promotion of early initiation of breastfeeding has the potential to make a major contribution to the achievement of the child survival millennium development goal; 16% of neonatal deaths could be saved if all infants were breastfed from day 1 and 22% if breastfeeding started within the first hour. Breastfeeding-promotion programs should emphasize early initiation as well as exclusive breastfeeding. This has particular relevance for sub-Saharan Africa, where neonatal and infant mortality rates are high but most women already exclusively or predominantly breastfeed their infants.
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            The changing concept of sudden infant death syndrome: diagnostic coding shifts, controversies regarding the sleeping environment, and new variables to consider in reducing risk.

            (2005)
            There has been a major decrease in the incidence of sudden infant death syndrome (SIDS) since the American Academy of Pediatrics (AAP) released its recommendation in 1992 that infants be placed down for sleep in a nonprone position. Although the SIDS rate continues to fall, some of the recent decrease of the last several years may be a result of coding shifts to other causes of unexpected infant deaths. Since the AAP published its last statement on SIDS in 2000, several issues have become relevant, including the significant risk of side sleeping position; the AAP no longer recognizes side sleeping as a reasonable alternative to fully supine sleeping. The AAP also stresses the need to avoid redundant soft bedding and soft objects in the infant's sleeping environment, the hazards of adults sleeping with an infant in the same bed, the SIDS risk reduction associated with having infants sleep in the same room as adults and with using pacifiers at the time of sleep, the importance of educating secondary caregivers and neonatology practitioners on the importance of "back to sleep," and strategies to reduce the incidence of positional plagiocephaly associated with supine positioning. This statement reviews the evidence associated with these and other SIDS-related issues and proposes new recommendations for further reducing SIDS risk.
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              Combined diet and exercise interventions for preventing gestational diabetes mellitus

              Gestational diabetes mellitus (GDM) is associated with a wide range of adverse health consequences for women and their infants in the short and long term. With an increasing prevalence of GDM worldwide, there is an urgent need to assess strategies for GDM prevention, such as combined diet and exercise interventions. This is an update of a Cochrane review that was first published in 2015. To assess the effects of diet interventions in combination with exercise interventions for pregnant women for preventing GDM, and associated adverse health consequences for the mother and her infant/child. We searched the Cochrane Pregnancy and Childbirth Group's Trials Register (27 November 2016) and reference lists of retrieved studies. We included randomised controlled trials (RCTs) and cluster‐RCTs, comparing combined diet and exercise interventions with no intervention (i.e. standard care), that reported on GDM diagnosis as an outcome. Quasi‐RCTs were excluded. Cross‐over trials were not eligible for inclusion. We planned to include RCTs comparing two or more different diet/exercise interventions, however none were identified. Two review authors independently assessed study eligibility, extracted data, assessed the risk of bias of the included trials and assessed quality of evidence for selected maternal and infant/child outcomes using the GRADE approach. We checked data for accuracy. In this update, we included 23 RCTs (involving 8918 women and 8709 infants) that compared combined diet and exercise interventions with no intervention (standard care). The studies varied in the diet and exercise programs evaluated and health outcomes reported. None reported receiving funding from a drug manufacturer or agency with interests in the results. Overall risk of bias was judged to be unclear due to the lack of methodological detail reported. Most studies were undertaken in high‐income countries. For our primary review outcomes, there was a possible reduced risk of GDM in the diet and exercise intervention group compared with the standard care group (average risk ratio (RR) 0.85, 95% confidence interval (CI) 0.71 to 1.01; 6633 women; 19 RCTs; Tau² = 0.05; I² = 42%; P = 0.07; moderate‐quality evidence ). There was also a possible reduced risk of caesarean section (RR 0.95, 95% CI 0.88 to 1.02; 6089 women; 14 RCTs; moderate ‐ quality evidence). No clear differences were seen between groups for pre‐eclampsia (RR 0.98, 95% CI 0.79 to 1.22; 5366 participants; 8 RCTs; low‐quality evidence ), pregnancy‐induced hypertension and/or hypertension (average RR 0.78, 95% CI 0.47 to 1.27; 3073 participants; 6 RCTs; Tau² = 0.19; I² = 62%; very low‐quality evidence ), perinatal mortality (RR 0.82, 95% CI 0.42 to 1.63; 3757 participants; 2 RCTs; low‐quality evidence ) or large‐for‐gestational age (RR 0.93, 95% CI 0.81 to 1.07; 5353 participants; 11 RCTs; low‐quality evidence ). No data were reported for infant mortality or morbidity composite. Subgroup analyses (based on trial design, maternal body mass index (BMI) and ethnicity) revealed no clear differential treatment effects. We were unable to assess the impact of maternal age, parity and specific features of the diet and exercise interventions. Findings from sensitivity analyses (based on RCT quality) generally supported those observed in the main analyses. We were not able to perform subgroup analyses based on maternal age, parity or nature of the exercise/dietary interventions due to the paucity of information/data on these characteristics and the inability to meaningfully group intervention characteristics. For most of the secondary review outcomes assessed using GRADE, there were no clear differences between groups, including for perineal trauma (RR 1.27, 95% CI 0.78 to 2.05; 2733 participants; 2 RCTs; moderate‐quality evidence ), neonatal hypoglycaemia (average RR 1.42, 95% CI 0.67 to 2.98; 3653 participants; 2 RCTs; Tau² = 0.23; I² = 77%; low quality evidence ); and childhood adiposity (BMI z score) (MD 0.05, 95% CI ‐0.29 to 0.40; 794 participants; 2 RCTs; Tau² = 0.04; I² = 59%; low‐quality evidence ). However, there was evidence of less gestational weight gain in the diet and exercise intervention group compared with the control group (mean difference (MD) ‐0.89 kg, 95% CI ‐1.39 to ‐0.40; 5052 women; 16 RCTs; Tau² = 0.37; I² = 43%; moderate‐quality evidence ). No data were reported for maternal postnatal depression or type 2 diabetes ; childhood/adulthood type 2 diabetes, or neurosensory disability . Moderate‐quality evidence suggests reduced risks of GDM and caesarean section with combined diet and exercise interventions during pregnancy as well as reductions in gestational weight gain, compared with standard care. There were no clear differences in hypertensive disorders of pregnancy, perinatal mortality, large‐for‐gestational age, perineal trauma, neonatal hypoglycaemia, and childhood adiposity ( moderate‐ to very low‐quality evidence) . Using GRADE methodology, the evidence was assessed as moderate to very low quality. Downgrading decisions were predominantly due to design limitations (risk of bias), and imprecision (uncertain effect estimates, and at times, small sample sizes and low event rates), however two outcomes (pregnancy‐induced hypertension/hypertension and neonatal hypoglycaemia), were also downgraded for unexplained inconsistency (statistical heterogeneity). Due to the variability of the diet and exercise components tested in the included studies, the evidence in this review has limited ability to inform practice. Future studies could describe the interventions used in more detail, if and how these influenced behaviour change and ideally be standardised between studies. Studies could also consider using existing core outcome sets to facilitate more standardised reporting. Review question What are the effects of combined diet and exercise for preventing gestational diabetes mellitus (GDM), and related health problems for mothers and their babies? This is an update of a Cochrane review that was first published in 2015. Background GDM is high blood sugar (hyperglycaemia) during pregnancy. Up to a quarter of pregnant women develop GDM, with some at a higher risk than others (such as overweight or obese women, older women, and those of particular ethnicities). GDM can lead to significant health problems for women and their babies. In the short term, women with GDM may develop pre‐eclampsia (high blood pressure (hypertension) and protein in the urine), or give birth by caesarean section. Their babies may grow large for their gestational age, and, as a result, be injured at birth, and/or cause injury to their mothers during birth. Babies of mothers with GDM often have low blood glucose (hypoglycaemia) and are overweight. Later in life, health problems such as neurosensory disabilities and type 2 diabetes can develop in these babies. Eating well and exercising is known to prevent type 2 diabetes and may be effective for preventing GDM. Study characteristics We searched for evidence in November 2016 and included 23 randomised controlled trials (RCTs) (involving 8918 women and their 8709 babies). Most studies were undertaken in high‐income countries. All of the studies compared women receiving diet and exercise programs with women receiving standard care without diet and exercise programs. The studies varied in the diet and exercise programs evaluated and health outcomes reported. None reported receiving funding from a drug manufacturer or agency with interests in the results. Key results Findings from 19 studies (6633 women) showed a possible reduction in GDM in women who received diet and exercise programs compared with women who received standard care. Fourteen studies (6089 women) showed a possible reduction in caesarean birth (14 studies; 6089 women) and 16 studies (5052 women) showed lower weight gain during pregnancy in women who received exercise programs. We found no differences between groups in other health problems for: pre‐eclampsia (8 studies; 5366 women); high blood pressure (6 studies; 3073 women); a large for age baby at birth (11 studies; 5353 babies); and perineal trauma (2 studies; 2733 women). Death of babies around birth (2 studies; 3757 babies), the baby having low blood glucose after birth (2 studies; 3653 babies), and infants being overweight (2 studies; 794 infants) did not differ in the two groups. Effects on depression or type 2 diabetes for mothers, a combined outcome of death or ill‐health for babies, or type 2 diabetes or neurosensory disability for babies as children were not reported. Participant views of programs were examined. The evidence suggests combined diet and exercise programs may be effective for preventing GDM though the optimum components of these programs are not yet clear. Future studies could describe the interventions used in more detail, if and how these influenced behaviour change and ideally be standardised between studies. Studies could also consider measuring similar maternal and infant outcomes and report them in a standardised way. Quality of the evidence The overall risk of bias was judged unclear due to lack of information on methods. We assessed evidence quality using GRADE considerations for selected key outcomes. Our assessments ranged from moderate to very low.
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                Author and article information

                Journal
                Children (Basel)
                Children (Basel)
                children
                Children
                MDPI
                2227-9067
                03 January 2018
                January 2018
                : 5
                : 1
                : 8
                Affiliations
                [1 ]Department of Clinical Nutrition, Collage of Applied Medical Sciences, Umm Al-Qura University, Makkah 21955, Saudi Arabia; hofe_66@ 123456hotmail.com (H.H.H.); Hywazzan@ 123456uqu.edu.sa (H.Y.W.); mtjoharji@ 123456uqu.edu.sa (M.T.J.); abdelelahj@ 123456yahoo.com (A.S.J.)
                [2 ]Department of Clinical Nutrition, Faculty of Applied Medical Sciences, University of Ha’il, Ha’il 21955, Saudi Arabia; awfa.yosef@ 123456gmail.com
                [3 ]Nutrition General Department, Awareness and Nutrition Education Division, Ministry of Health, Makkah 21955, Saudi Arabia; amfilimban@ 123456moh.gov.sa
                [4 ]Pediatric Department, Maternity and Children Hospital, Makkah 21955, Saudi Arabia; ahadi@ 123456moh.gov.sa
                [5 ]Medical Nutrition Therapy Department, Maternity and Children Hospital, Makkah 21955, Saudi Arabia; mlabani@ 123456moh.gov.sa (M.S.L.); Thasanain@ 123456moh.gov.sa (T.A.H.)
                [6 ]Department of Clinical Nutrition, Faculty of Applied Medical Sciences, Taibah University, Yanbu 21911, Saudi Arabia; aobeidat@ 123456taibahu.edu.sa
                Author notes
                [* ]Correspondence: fsazzeh@ 123456uqu.edu.sa ; Tel.: +966-5-4083-3661; Fax: +966-2572-0000-4227
                Author information
                https://orcid.org/0000-0002-1400-5465
                Article
                children-05-00008
                10.3390/children5010008
                5789290
                29301353
                50965335-d499-4180-8395-9a81eac78751
                © 2018 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 25 November 2017
                : 31 December 2017
                Categories
                Article

                breastfeeding,early initiation of breastfeeding,baby-friendly hospital initiative,mecca

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