| Literature DB >> 36147803 |
Jessica M Edney1, Sari Kovats1, Veronique Filippi2, Britt Nakstad3,4.
Abstract
Background: Increased rates of exclusive breastfeeding could significantly improve infant survival in low- and middle-income countries. There is a concern that increased hot weather due to climate change may increase rates of supplemental feeding due to infants requiring fluids, or the perception that infants are dehydrated. Objective: To understand how hot weather conditions may impact infant feeding practices by identifying and appraising evidence that exclusively breastfed infants can maintain hydration levels under hot weather conditions, and by examining available literature on infant feeding practices in hot weather.Entities:
Keywords: breastfeeding; climate; dehydration; heat stress; infant care; systematic review
Year: 2022 PMID: 36147803 PMCID: PMC9485728 DOI: 10.3389/fped.2022.930348
Source DB: PubMed Journal: Front Pediatr ISSN: 2296-2360 Impact factor: 3.569
Definitions used in this review.
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| Exclusive breastfeeding (EBF) | “No other food or drink, not even water, except breast milk (including milk expressed or from a wet nurse)” ( |
| High ambient temperatures | Air temperatures of ≥30°C: the midpoint between the range of air temperatures (25–35°C) that the WHO recommends infants to be exposed to avoid hyperthermia and hypothermia ( |
| High humidity | ≥60% relative humidity: the upper limit to the United States Occupational Safety and Health Administration recommendation for relative humidity for indoor air ( |
| Hot weather | Days where air temperatures exceed 30°C |
| Infant | A child up to the age of 12 months |
| Infant feeding practices | All methods of feeding infants food and water/other fluids, including exclusive breastfeeding, feeding infants expressed breastmilk or formula milk, feeding infants non-breast milk food and fluids, supplementing breast milk with water, tea, or other fluids, and supplementing breast milk with fluids and solid food |
| Low- middle-income country (LMIC) | As defined by the World Bank ( |
| Newborn | An infant aged up to 28 days |
| Partial breastfeeding/mixed methods feeding | Feeding an infant breast milk and other food and/or fluids (excluding oral rehydration solution, drops and syrups for medical purposes) ( |
| Prelacteal feeding | Giving a newborn food or drink prior to the first breast feed. It is not recommended by the WHO ( |
Figure 1PRISMA flow diagram of included and excluded records [adapted from (35)].
Summary of studies investigating infant hydration.
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| Almroth and Bidinger ( | India | Healthy infants aged 1–10 months ( | Quasi-experimental, using clinical measurements | USG and UO–cut-off values not reported | USG (of infants aged up to 6 months) = 1.004–1.036. UO = 66–1234 mml/l; mean = 1.011 (322 mml/l) | Under hot and dry conditions, healthy exclusively breast-fed infants do not require additional water. |
| Almroth ( | Jamaica | Healthy EBF infants aged 2 weeks−4 months ( | Quasi-experimental, using clinical measurements | USG and UO–cut-off values not reported | USG = 1.005–1.015 (mean = 1.009). UO = 103–468 mml/l (mean = 258 mml/). Mean USG for individuals = 1.006–1.012 (UO = 139–358 mml/l). | Healthy, exclusively breast-fed infants can remain hydrated without supplementary water in a hot humid climate. |
| Armelini and Gonzalez ( | Unknown “tropical” location | Healthy EBF infants aged 15–60 days | Cross-sectional, using clinical measurements | UO values below 200 mml/kg regarded as normal | Mean UO of samples collected at night = 137 mml/kg. Mean UO of samples collected in the afternoon = 171 mml/kg). Significant difference between means ( | Urine osmalality was lower at night but did not exceed 200 mosmol/kg of water even in the hottest temperatures so supplementary water is likely not necessary for healthy exclusively breastfed infants in a hot and humid climate. |
| Ashraf et al. ( | Pakistan | Healthy breastfed infants aged 2–4 months ( | Quasi-experimental, using clinical measurements | Water withheld for 8 days of study. Water given from day 8–15. DDAVP administered on day 15. USG values before and after the administration of DDAVP were compared. Haematocrit, sodium in breastmilk, and sodium in blood serum were compared at different stages to check for dehydration. | Significant increase in weight between day 1–8 and between day 8–15. No significant difference in haematocrit and serum sodium between day 8 and 1 and between day 15 and 8. No significant difference for USG between day 8 and 1. Significant increase in USG after infants received DDAVP. | Results indicate that the infants were not dehydrated when water was withheld and if needed, exclusively breastfed babies can concentrate urine when water is restricted |
| Brown et al. ( | Peru | Breastfed infants aged <6 months | Quasi-experimental, using clinical measurements | Maximum USG 1.015 in the first few days of life, then 1.025–1.030 by 5 months | Standardized milk intakes = 4.0–12.1 gm/kg body weight per hour. Urine volume = 0.9–6.3 ml per kg body weight per hour. Max. USG in each infant 1.003–1.017. No associations between ambient temperature and urinary measures. | Healthy infants can maintain adequate hydration while exclusively breastfeeding in hot and humid conditions |
| Cohen et al. ( | Honduras | EB LBW term male infants aged 0–4 months ( | Quasi-experimental, using clinical measurements | USG maximum below 1.018 | Maximum USG = 1.001–1.012. USG associated with max. daily temperature only at 2 weeks of age. No association with humidity. | Results indicate that exclusively breastfed LBW infants do not require supplementary water, even under hot and humid conditions |
| Goldberg and Adams ( | Unknown location in Sinai desert | Healthy EBF infants aged 40–150 days, from Bedouin villages ( | Cross-sectional, using clinical measurements | UO–cut-off values not reported | UO = 55–320 mmol/kg; mean = 164.5 mmol/kg | Supplementary water for breast-fed infants is not necessary to maintain hydration under hot and dry climatic conditions |
| Kusuma et al. ( | India | Newborn infants with a gestational age of 350/7 weeks to 376/7 weeks born in a tertiary care hospital (n=205) | Cohort study, using a questionnaire and clinical measurements | Cumulative weight loss equal to or more than 10% was taken as ‘significant'. USG below 1.020 taken as normal. | No significant difference in weight loss or hypernatremia among the exclusively breastfed babies and partially breastfed babies | Near-term-born infants who are exclusively breastfed can maintain similar hydration status to that of PBF newborns in the first week after birth, even in summer months |
| Sachdev et al. ( | Unknown “tropical” location | Healthy, male, exclusively breastfed babies aged 1–4 months attending a well-baby clinic ( | Quasi-experimental study using questionnaires, physical examinations, and clinical measurements | Breastmilk-intake, total fluid intake, urine output, UO, serum osmolality, weight change, rectal temperature. Cut-offs unclear. Compared study group (exclusively breastfed) with control group (partially breastfed) | Breastmilk intake and total fluid intake were significantly higher in the group that consumed only breastmilk compared to the control group after adjusting for confounders. No significant differences in urine output, urine or serum osmolality, weight change, or rectal temperature. | Exclusively breastfed babies don't require supplementary water in a tropical climate |
Summary of studies investigating determinants of infant feeding practices relating to hot seasons and high ambient temperatures.
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| Almroth et al. ( | Lesotho | Mothers with children aged under 5; grandmothers of children aged under 5; women paid to take care of children aged under 5; local health professionals | Cross-sectional study, using interviews, questionnaires, focus groups | Breastfeeding common but EBF was an unknown concept. | Hot weather may not have been a factor in giving water because Lesotho rarely experiences very high ambient temperatures |
| Ashraf et al. ( | Pakistan | Mothers of newborn infants in Lahore before 1993 ( | Cohort study, interviews | EBF rare and negatively associated with age. | Reasons for associations not explored |
| Forman et al. ( | Israel | Bedouin Arab mothers of apparently healthy newborn babies in the Negev in 1982 | Cohort study, interviews, questionnaires | Month at which infants reached 2 months of age modified association between social support and feeding practices. | 1. The month when infants reached two months old was independently associated with infant feeding practices–exclusive breastfeeding was less common at 2 months during the summer holidays (July/August), when mothers have a heavier workload with more childcare, and less support. |
| González-Chica et al. ( | Brazil | Hospital-born children in 1982, 1993, and 2004 (periodically followed-up for 2 years) ( | Cohort, using interviews, clinical measurements | Season of birth & temperatures in 1st month of life associated with duration of breastfeeding (colder temperatures associated with shorter duration). Early intro of fruits and vegetables sometimes associated with lower environmental temperature in 1st month of life. | 1. Reduced liquid intake on the part of the mother in colder seasons could affect infant feeding practices |
| 5. Maternal education and socio-economic status modified the effect - poor people less likely to have central heating and less educated mothers might be more inclined to believe supplementing with water is advisable | |||||
| Gray ( | Kenya | Turkana mothers and their breastfeeding infants in 1987 −1989 | Cohort study, using interviews, clinical measurements, nutritional assessments, observation | Consumption of supplementary foods increased with less rainfall in infants below 4 months. In infants aged 4–9 months, consumption of milk and butterfat common, especially after wet months. | Mothers use milk and butterfat to supplement the fat lost from breastmilk during leaner months, when rainfall is higher |
| Hossain et al. ( | Egypt | Singleton apparently healthy newborn children aged 0–47 weeks in 1987 | Cohort study, using interviews and questionnaires | Prelacteal feeding associated with warmer temperatures during the month of birth. Infants fed prelacteal food/drink less likely to be EBF in later months. | 1. The association between prelacteal feeding and warmer temperatures may be due to birth attendant recommendations that babies are given water in summer months |
| Jalil et al. ( | Pakistan | Infants born in an urban slum in 1964–1978 ( | Cohort study, using clinical measurements and observations | 50% of mothers introduced supplementary feeding within 1 month of birth. | 1. Cultural belief that milk comes in on the third day prevents early breastfeeding initiation. |
| Naggan et al. ( | Israel | Bedouin Arab mothers who delivered apparently healthy newborns in hospital or at home in 1981–1982 ( | Cohort study, using interviews, clinical measurements, clinical records | Babies born during wet cool months are EBF longer than babies born during the dry season. | Mothers may experience dehydration during the hot, dry season. There is no change in breast milk volume, but it becomes diluted so that enough nutrients are transferred to the baby. This may mean that they do not receive enough nutrients. This may be why exclusive breastfeeding occurs less in hot weather |
| Serdula et al. ( | Egypt | Children aged between 6 and 35 months in 1978 and 1980 | Cross-sectional study, using surveys | EBF (among infants aged 6–11 months) more prevalent in the hot season survey | 1. During the hot season, pregnancy rates were higher, which resulted in less breastfeeding |
Methodological problems identified in included studies.
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| Unclear if participants included in any comparisons were similar (except in exposure status) | 3 | Almroth et al. ( |
| Inclusion criteria for study subjects not defined | 3 | Almroth et al. ( |
| Study subjects and setting not adequately described | 5 | Almroth ( |
| Among intervention studies, true randomization was not used to assign participants to treatment groups | 4 (out of 4 intervention studies) | Almroth ( |
| Among intervention studies, unclear if participants were blind to exposure group | 4 (out of 4 intervention studies) – but impossible to blind participants given nature of intervention | Almroth ( |
| Outcome assessors were not blind to treatment assignment or to study hypothesis where control groups were not used | 17 | All studies but Forman et al. ( |
| “Cause" and “effect” unclear in the study | 2 | Almroth et al. ( |
| Unclear if exposures were measured in a consistent, valid, and reliable way | 3 | Almroth et al. ( |
| Unclear if outcomes were measured in a consistent, valid, and reliable way | 4 | Armelini and Gonzalez ( |
| Confounding factors not identified | 10 | Almroth ( |
| Unclear if strategies to address confounding were used | 10 | Almroth ( |
| Where applicable, no control group or control population studied | 11 (out of 16 applicable studies) | Almroth ( |
| Where applicable, follow-up time was incomplete, for which the reasons were not described or explored | 5 (out of 15 applicable studies) | Almroth ( |
| Where applicable, unclear if strategies to address incomplete follow-up were utilized | 10 (out of 15 applicable studies) | Almroth ( |
| Unclear if appropriate statistical analysis was | 7 | Almroth ( |
Critical appraisal of studies.
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| González-Chica et al. ( | Good |
| Hossain et al. ( | Good |
| Kusuma et al. ( | Good |
| Naggan et al. ( | Good |
| Sachdev et al. ( | Good |
| Armelini and Gonzalez ( | Fair |
| Ashraf et al. ( | Fair |
| Brown et al. ( | Fair |
| Cohen et al. ( | Fair |
| Forman et al. ( | Fair |
| Gray et al. ( | Fair |
| Jalil et al. ( | Fair |
| Serdula et al. ( | Fair |
| Almroth ( | Poor |
| Almroth and Bidinger ( | Poor |
| Almroth et al. ( | Poor |
| Ashraf et al. ( | Poor |
| Goldberg and Adams ( | Poor |