What Is Known
- Gastroenteritis is still a major cause of death in children and of costs for societies and families worldwide.
- In addition, its epidemiology and other clinical and experimental data open new threats and new hopes for prevention and management.
What Is New
- This position paper provides a list of priorities that require attention and resources.
- Among the others, the composition of oral rehydration solution should be revised, anti-infective therapy should be better standardized, and guidelines should be reviewed and implemented.
- Research on pathogens and their mechanisms and new drugs is needed.
- Finally, at risk groups including malnourished children should be the target for prevention and management initiatives.
BRIEF SUMMARY OF THE PROBLEM AND FISPGHAN ACTIVITIES
Acute gastroenteritis (AGE) is a common cause of morbidity and mortality in infants and children. A child younger than 5 years may experience as many as 1 to 5 episodes of acute diarrhea each year. According to the Global Health Data Exchange in 2016, diarrhea was the eighth leading cause of death among all ages (1.65 million deaths) and the fifth leading cause of death among children younger than 5 years (446,000 deaths). Malnutrition, unsafe water, and sanitation continue to be leading risk factors for diarrhea (1). Almost 40% of these deaths have been putatively linked with rotavirus (RV) and most occur in low-income countries. AGE is, however, also an important health problem in developed countries as it leads to frequent emergency room visits, hospital admissions, and high costs to both society and families, and death is not exceptional (in western European countries approximately 300 children die annually due to gastroenteritis).
If AGE and dehydration are recognized and treated promptly and appropriately, the prognosis of diarrhea is good. Therapy is crucial, easy, and inexpensive. The major goal is to restore hydration and prevent dehydration, which can be achieved with oral rehydration solution (ORS). Avoiding fasting and continuing feeding are also important. In striking contrast, in rich countries and in private facilities in poor countries, unnecessary medical interventions are often applied, including inappropriate hospital admissions, microbiological investigations, diet restrictions, and medication administration.
In terms of prevention, hygiene measures (particularly the use of clean water and toilet systems) that can successfully reduce fecal contamination, and immunization particularly against RV, strongly reduce morbidity and mortality. Developing and applying the means of effective education of mothers in the early recognition of acute diarrhea as a potentially dangerous condition and what actions to take is extremely important particularly in developing countries.
The Federation of Pediatric Societies of Gastroenterology Hepatology and Nutrition (FISPGHAN) has prioritized AGE since its foundation. In 2012, a FISPGHAN expert working group (WG) identified priorities for medical intervention, education, and research to reduce the morbidity and mortality associated with AGE, which are still valid (2) (Table 1). Some have been achieved, also with the active intervention by FISPGHAN. In addition to indicating the priorities, the WG directly promoted important initiatives. An article that described a comparison of the recommendations for the management of gastroenteritis using available guidelines demonstrate major similarities (3). Based on this article, the WG formulated universal recommendations for the management of acute diarrhea (4), took an active role in education initiatives in developing countries, and tested the efficacy of e-learning programs (5). In addition, 2 informative videos were prepared by a group of young pediatric gastroenterologists targeting caretakers and social workers explaining the clinical signs, alarming conditions, and principles of management of gastroenteritis (https://www.youtube.com/watch?v=IYW9hpcAKwk). These videos have been translated in different languages.
In this report, a group of experts from all the societies forming FISPGHAN provide a global summary of AGE and indicate the major interventions needed to improve the health condition of children with a particular focus on low-income countries, which is the ultimate mission of FISPGHAN. Moreover, a list of unresolved problems, which should be the focus of future research and endeavors, is also included.
The article was not intended to produce recommendations on how to treat or prevent gastroenteritis. Rather it aims at briefly providing a picture of the current situation and open issues and provide a list of priorities for improving management and prevention. Priorities include recommendations for management, research issues, and further initiatives that FISPGHAN could engage or promote.
The article was constructed by agreeing on a list of topics that were handled either directly by the members appointed by the societies forming FISPGHAN or by outer experts that are included as authors. An extensive discussion took place among members which eventually led to the list of recommendations that are included in the last part of the article and reflect the position of the societies forming FISPGHAN about what needs to be done by political, scientific, and health care agencies and institutions (including FISPGHAN) to reduce the burden of gastroenteritis worldwide.
Changes and Novelties in the Epidemiology of Acute Diarrhea
Launched in the year 2000, the Millennium Development Goal 4 (MDG4) had the ambitious aim of reducing the global mortality rate of children younger than 5 years by 2015 by two-thirds. MDG4 was aimed at reducing childhood mortality due to acute diarrhea (6). The goal was, however, not fully achieved, and substantial challenges remain to be addressed.
In 2015, the MDGs were replaced by the more comprehensive, although less health-focused, Sustainable Development Goals. Sustainable Development Goal 3.2 is the main indicator for improving child survival, with the aim of reducing mortality of children below the age of 5 years to fewer than 25 deaths per 1000 live births, decreasing neonatal mortality to fewer than 12 deaths per 1000 live births, and eradicating preventable deaths of newborns and children younger than 5 years by 2030 (7).
In 2015, mortality due to diarrheal diseases and lower respiratory infections decreased in children younger than 5 years due to the continued expansion of routine immunization programs, improved sanitation, and better access to health services and care-seeking behaviors for childhood illnesses, particularly in lower-income countries. Diarrheal diseases, however, remain an important health problem globally and the results of MDG4 reduction have not been consistent across all regions, with Sub-Sahara Africa and South Asia reporting considerable mortality.
Viruses are the most common agents of AGE, accounting for >60% of pediatric cases, followed by bacteria and parasites (8–10). The prevalence of individual pathogens varies widely between geographic areas and different age groups but globally RV infection remains the leading cause of diarrhea in children younger than 5 years (10,11).
Molecular methods have substantially increased the sensitivity of pathogen detection and have expanded the understanding of etiologic agents in diarrhea (10–12). In a large cohort of children between 0 and 2 years with AGE, quantitative polymerase chain reaction identified pathogens in 65% of episodes, compared to 33% using traditional microbiologic studies (12). Thus, some pathogens such as heat-stable enterotoxin-producing Escherichia coli (ST-ETEC), Shigella, and Cryptosporidium were previously underestimated (13). These pathogens are common agents of moderate to severe diarrhea in young children in low-resource countries (9). Quantitative polymerase chain reaction determinations supported higher estimates of these pathogens and increased the attributable incidence for Shigella and Campylobacter jejuni/coli 2-fold, for ST-ETEC 1.5-fold, and for adenovirus 40 of 41 five-fold, compared with estimates based on culture or immunoassay (11).
Interestingly, enterotoxin-producing E coli was found to be a frequent agent of mild to moderate gastroenteritis also in high-income countries (13), raising the hypothesis that there may have differences in severity rather than the issue of distribution between low- and high-income countries.
Currently, several multiplex nucleic acid tests are available for the detection of a spectrum of enteric pathogens (14). The advantages of these tests include the breadth of pathogens discovered, the rapid turnaround, and the accuracy of their results. The challenges and setbacks include the high costs, limitations in identifying the true causative role of multiple pathogens in a stool sample of an affected patient, and the lack of bacterial isolates needed for antibiotic susceptibility and outbreak analysis. At present, the understanding of the prognostic, therapeutic, and pathogenic significance of multiple agents in a stool sample is limited, making it difficult for the clinician to evaluate the results of these special tests.
Vaccines for Prevention of Acute Diarrhea
Various enteric vaccines have been developed to reduce the incidence of acute diarrhea including cholera, typhoid, and RV vaccines (15–17). Because the efficacy rates of the currently available oral killed whole-cell oral cholera vaccine are between 50% and 60%, its inclusion in national immunization programs of endemic countries will depend on the prevalence of cholera, the frequency of outbreaks, and accessibility of healthcare services (15). A similar approach applies to typhoid vaccination. Thus, until further developments, wide-scale implementation of typhoid vaccinations will be evaluated in the light of efficacy rates and the burden of the disease in a particular country or setting (16).
EFFICACY OF VACCINES AND THEIR DIFFERENCES IN HIGH- AND LOW-INCOME AREAS
RV vaccine plays a major role in preventing AGE (18). The 2 commercially available RV vaccines, prequalified by the WHO, are the human monovalent vaccine and human-bovine reassortant pentavalent vaccine. Other 2 monovalent vaccines have been developed and made available in India and China. Differences in efficacy rates have been noticeably evident for high- and low-income countries (Table 2). The efficacy of RV vaccines is lower in low-income countries. The reasons are still unclear; however, differences in gut microbiome and human leukocyte antigen groups, titer of anti-RV IgA in mother's breast milk, and a possible interference of oral polio vaccine, may play a role in determining a lower efficacy in these settings. Due to the higher burden of diarrhea in these countries, more cases can, however, be prevented in these areas. No increased risk of serious adverse events has been observed for any RV vaccines in both the high- and low-income countries.
DISSEMINATION AND BARRIERS TO IMMUNIZATION
The efficacy of RV vaccines has been well established. A decade following the global dissemination, RV immunization has been included in the national and subnational immunization programs of 92 countries. A reduction of >80% and 50% in disease burden has since been observed in both high- and low-income countries, respectively (18). Recently, in a few European countries, targeted RV immunization has been proposed, for example, for preterm infants only, but the general conclusion is that RV immunization should be universally offered to all infants regardless of geography, age, and health condition (19)(European Academy of Paediatrics and ESPID, under review).
The FISPGHAN WG on AGE conducted a specific study on the barriers limiting RV immunization worldwide (20). The single most frequent barrier in this study was the cost. The lack of perception of severity of AGE is, however, also a significant barrier (20) (Fig. 1). Another major factor for the limited implementation of RV vaccination in countries with high disease burden remains the logistical support for the program. Failure to grasp the ease of disease transmission with a low viral load is another issue.
Several new vaccines are in the pipeline. Because there are no licensed vaccines against ETEC, the development of a suitable candidate vaccine could be beneficial for children in low-income countries and for travelers. Currently, an attenuated ETEC vaccine candidate, ACE527, that is co-administered with a mucosal adjuvant the double-mutant heat-labile toxin of ETEC, has demonstrated a protective efficacy rate of 66% against severe diarrhea among human volunteers challenged with virulent ETEC strain H10407 (21).
Comparison of Recommendations in Different Countries, Development of Universal Recommendations for Nonmalnourished Children, and Main Novelties About Management of Acute Diarrhea
Clinical practice guidelines universally recommend rapid assessment of dehydration and shock. Although most guidelines recommend that the actual loss of body weight be used to quantitatively estimate dehydration (4), prior data on the weight may be unavailable. Scoring systems based on clinical signs are suggested by the WHO and other institutions, although their reliability may be limited to selected settings (22). The Clinical Dehydration Scale is an easy tool supported by guidelines and is reliable in estimating diarrhea induced fluid losses (22). Mild to moderate uncomplicated AGE without underlying comorbidity or dysentery (as indicated by bloody stools) does not require routine microbiological or other laboratory work-up (4).
The management of AGE is based on 4 pillars: rehydration; anti-infective therapy; additional treatment of AGE/diarrhea to reduce its duration and severity; and nutritional management.
- The primary objective of management of diarrhea is to prevent potentially fatal complications including dehydration, metabolic acidosis, electrolyte disturbances, and sepsis. Achieving rehydration relies on the administration of rehydration solution via the oral or, in a small proportion of carefully selected children, the intravenous route (23). Most clinical guidelines recommend low osmolarity (≤75 mmol/L Na+) ORS3, but lower concentrations of Na+ have been used successfully. Thus, the optimal composition of ORS is debatable. The advantage of having a single ORS is quite clear and WHO ORS has been the most important preparation achieved by WHO since its formulation. On the contrary, the knowledge, epidemiology, and management of AGE have changed through the years and it may be timely to reconsider the composition of ORS taking into account efficacy, costs, stability, and palatability. Although palatability may be an issue in children with no or mild dehydration, Na+ concentration and its stoichiometric ratio with glucose should be optimized based on intestinal fluid absorption. Vomiting may impair oral rehydration. The use of ondansetron, particularly in emergency settings, may prove useful in overcoming a dangerous phase of AGE, and prevent hospital admission or the need of intravenous rehydration. This has been shown in interventions of improved clinical practice and in high-income and low-income countries (24). Nasogastric administration of ORS, although not widely used as a second-line treatment, is an effective alternative to intravenous fluids particularly in resource-poor settings (25).
- Anti-infective therapy is still an unresolved issue in AGE (26). There are 2 potential reasons for deciding on the use of antibiotic therapy in gastroenteritis: clinical conditions and host-related risk factors.Microbiological investigation is generally not indicated in AGE, unless anti-infective therapy is considered. Most guidelines recommend not giving antibiotics unless there is sepsis, cholera, or significant comorbidity. Children with suspected or confirmed invasive disease or with sepsis, demonstrated by blood culture or by an increase in inflammation markers, including C-reactive protein or neutrophilic leukocytosis should receive antibiotics once fecal samples have been obtained. In absence of sepsis, or immunosuppression, antibiotics should be used in response to culture results, or endemic infections specific to region of the world. “Dysentery,” and inflammation with elevated markers, do not always warrant antibiotic treatment, depending on the pathogen.
An example may be the isolation of Shiga toxin–producing E coli (E coli 0157:H7) in the stools, in that case the use of antibiotics in absence of sepsis or underlying conditions is contraindicated. The potential indications and choice of antibiotics for anti-infective therapy are listed in Table 3.
Hence the potential reasons for requiring a microbiological investigation of stools correspond to potential indications for anti-infective therapy, although the criteria for testing and treatment are difficult to develop. The etiology affects therapy and there is evidence of significant benefit for the use of antibiotics in diarrhea caused by Vibrio cholerae, and less strong evidence for Shigella and for persistent diarrhea (26–28). Children infected with Shiga toxin–producing E coli should not receive antibiotics. If Clostridium difficile is obtained from an otherwise healthy child with AGE, it should not be treated. For nontyphoidal Salmonellae, there are no universal recommendations and it is suggested to treat with antibiotics all infants less than 3 to 6 months of age due to an increased risk of invasive disease (29).
Severely immunocompromised children should be tested and, even if negative, considered for empirical antimicrobial treatment. Severe RV diarrhea in the hospital setting may be effectively treated with oral administration of human immunoglobulins given once at 400 mg/kg body weight (30). Severe acute malnutrition is also an indication for antibiotic therapy, independent of the presence of diarrhea (31). The choice of antibiotics and duration of treatment are far from being standardized. However, based on etiology and risks factors, the most common indications are listed in Table 4.
- Additional treatment of diarrhea aims at reducing the duration and severity of symptoms and encompasses a number of heterogeneous therapies.Oral administration of zinc and early refeeding with an age-appropriate diet are recommended in all clinical guidelines (3). In countries where many children are at risk of malnutrition, zinc is part of routine management of AGE. Zinc should be given as a therapy (usually tablet of 20 mg/day).
Several interventions have been proposed with the aim of reducing the duration and severity of symptoms. They should, however, always be considered as adjunct to rehydration and based on solid evidence. There is a discussion about the efficacy and importance of interventions put forward to reduce the duration and intensity of AGE. There is a fear that these interventions may detract from rehydration which is the basic therapy of AGE. In addition, not all interventions proposed as adjunct to oral rehydration are effective or are they necessarily a priority in terms of public health concern, particularly under resource-restricted conditions. On the contrary, the perspective of shortening the symptoms of an individual child and his/her family should not be neglected and if there is an affordable and effective intervention to shorten diarrhea even by 1 day, the intervention may be considered. The features of the ideal drug for AGE are reported in Table 5. Based on current available data, the physician may select effective intervention to be administered to shorten the duration of symptoms.
- Nutritional management. Nutrition is an important component in the management of AGE. The current recommendation is to continue feeding the child with AGE with a regular diet without restrictions. The nutritional approach, however, is considerably affected by local traditions and several dietary modifications are applied in many geographical locations, generally with little or no evidence of efficacy. The efficacy of a lactose-free diet in hospitalized children with AGE has been shown in a meta-analysis of 33 trials, of which 28 were performed in an inpatient setting. Lactose-free diet was associated with a shorter duration of diarrhea and reduced treatment failures. It may also be effective if diarrhea persist over 7/14 days. The data, however, did not include malnourished children nor were they performed in countries in which mortality is high (32). A trial of lactose-free feeding in malnourished children showed no impact on diarrhea (33). In conclusion, the management of AGE is simple as shown in the algorithm reported in Figure 2(34).
Paucity of Evidence in the Management of Diarrhea in Malnourished or At-risk or Immunocompromised Children
Diarrhea was the second leading cause of death in low-income countries in 2016, and most of these cases were children with severe malnutrition. AGE is a strong predictor of mortality in malnourished children (35,36). The treatment of AGE in the malnourished child is part of the updated WHO guideline on the management of severe acute malnutrition in infants and children (37). The evidence for the recommendations was low or very low, due to the limited availability of randomized controlled trials comparing existing WHO recommendations with new treatment options. Where direct evidence was not available, indirect evidence from different populations, or different intervention strategies were used. The review included clinical trials published up to 2011 (37).
Children with severe acute malnutrition who also have diarrhea and are dehydrated need special alternative fluids to treat dehydration. The current recommendations for the management of diarrheal disease are based on WHO guidelines.
- The management of gastroenteritis in malnourished children is different from that recommended in well-nourished children and it is broad and highly variable according to a recent survey by FISPGHAN WG (Lo Vecchio A et al, manuscript in preparation) and there is a need for specific guidelines.
The recommendations for the management of gastroenteritis need to be regularly updated in the light of new evidence available. They should be based on universal principles, but tailored to geographical, epidemiological, and organizational conditions.
Finally, there is nonconclusive evidence supporting a relationship between early AGE and subsequent functional disorders later in life (38). The cause-effect relationship is unknown and deserves attention.
Recommendations by the Working Group and Action Points
Reduction in mortality rates from diarrhea in Sub-Saharan countries and South Asia is still far from satisfactory. More resources should be directed at maternal health care services and educational programs for mothers and adolescents and at improving access to safe drinking water and sanitation (7) as indicated in the previous FISPGHAN report (2). In addition to immunization, AGE may be prevented much more effectively by socioeconomic, educational, and hygienic infrastructural interventions. Physicians and scientific societies should play a proactive role in lobbying, promoting education, and through other initiatives. FISPGHAN produced a video targeting mothers and field workers giving simple guidance in form of cartoons for early recognizing dehydration https://www.youtube.com/watch?v=IYW9hpcAKwk). Those initiatives should be conducted on a large scale using the available quad-media and mass communication, including social media.
Many questions on diarrhea management require interventions and active research.
- Recommendations needed
- Management of children treated at hospital because of AGE (this includes management in the emergency area and the inpatient facility)
- Specific management of children belonging to high risk groups, including malnourished children, those with chronic conditions, and neonates
- Evidence-based indications for anti-infective therapy
- Optimal composition of ORS for well-nourished and malnourished children
- Research issues
- Under what conditions is the detection of a diarrhea-associated microbe a diarrheal pathogen? Importance of qualitative, quantitative, and patient-based diagnostic approaches
- Stunting as a risk factor for diarrheal deaths
- Environmental enteric dysfunction as a diarrhea-independent process and its negative impact on the course of AGE
- First 1000 days (gut infections during pregnancy, lactation, and early childhood) as a risk for diarrhea and a target for prevention
- Efficacy and safety of specific drugs, antibiotics, probiotics, and diet to reduce the duration and intensity of diarrhea
- Efficacy of RV vaccine in different geographical settings
- Cause-effect relationships between intestinal infections and subsequent intestinal functional disorders
- Microbiome-directed refeeding during and following diarrheal episodes
- High-quality randomized controlled trials on drugs or other sustainable interventions that effectively reduce duration and intensity of AGE
- Future priorities of the Working Group
- Implementation of the universal guidelines for management of gastroenteritis based on evolving evidence, local resources, and data.
- Advocacy for research funding and implementation science for current best practices, informed by pragmaticism and resources
- New vaccines for high burden pathogens
- Broader dissemination of WHO recommendation for the treatment, prevention, and effective support to children who live in difficult conditions
1. GBD 2016 Diarrhoeal Disease Collaborators. Estimates of the global, regional, and national morbidity, mortality, and aetiologies of diarrhoea in 195 countries. Lancet Infect Dis
2. Guarino A, Winter H, Sandhu B, et al. Acute gastroenteritis
disease: report of the FISPGHAN Working Group. J Pediatr Gastroenterol Nutr
3. Lo Vecchio A, Dias JA, Berkley JA, et al. Comparison of recommendations in clinical practice guidelines for acute gastroenteritis
in children. J Pediatr Gastroenterol Nutr
4. Guarino A, Lo Vecchio A, Dias JA, et al. Universal recommendations for the management of acute diarrhea in non-malnourished children. J Pediatr Gastroenterol Nutr
5. Nicastro E, Lo Vecchio A, Liguoro I, et al. The impact of e-learning on adherence to guidelines for acute gastroenteritis
: a single-arm intervention study. PLoS One
6. Liu L, Za S, Hogan D, et al. Global, regional, and national causes of under-5 mortality in 2000-15: an updated systematic analysis with implications for the Sustainable Development Goals. Lancet
7. Acheampong M, Ejiofor C, Salinas-Miranda A. An analysis of determinants of under-5 mortality across countries: defining priorities to achieve targets in sustainable developmental goals. Matern Child Health J
8. Thongprachum A, Takanashi S, Kalesaran AF, et al. Four-year study of viruses that cause diarrhea in Japanese pediatric outpatients. J Med Virol
9. Kotloff KL, Nataro JP, Blackwelder WC, et al. Burden and aetiology of diarrhoeal disease in infants and young children in developing countries (the Global Enteric Multicenter Study, GEMS): a prospective, case-control study. Lancet
10. Operario DJ, Platts-Mills JA, Nadan S, et al. Etiology of severe acute watery diarrhea in children in the global Rotavirus
surveillance network using quantitative polymerase chain reaction. J Infect Dis
11. Liu J, Platts-Mills JA, Juma J, et al. Use of quantitative molecular diagnostic methods to identify causes of diarrhoea in children: a reanalysis of the GEMS case-control study. Lancet
12. Platts-Mills JA, Liu J, Rogawski ET, et al. Use of quantitative molecular diagnostic methods to assess the aetiology, burden, and clinical characteristics of diarrhoea in children in low-resource settings: a reanalysis of the MAL-ED cohort study. Lancet Glob Health
13. Guarino A, Alessio M, Tarallo L, et al. Heat stable enterotoxin produced by Escherichia coli
in acute diarrhoea. Arch Dis Child
14. Anderson NW, Tarr PI. Multiplex nucleic acid amplification testing to diagnose gut infections: challenges, opportunities, and result interpretation. Gastroenterol Clin North Am
15. Sinclair D, Abba K, Zaman K, et al. Oral vaccines for preventing cholera. Cochrane Database Syst Rev
16. Milligan R, Paul M, Richardson M, et al. Vaccines for preventing typhoid fever. Cochrane Database Syst Rev
17. Soares-Weiser K, Bergman H, Henschke N, et al. Vaccines for preventing rotavirus
diarrhoea: vaccines in use. Cochrane Database Syst Rev
18. Clark A, Van Zandvoort K, Flasche S, et al. Efficacy of live oral rotavirus
vaccines by duration of follow-up: a meta-regression of randomised controlled trials. Lancet Infect Dis
19. Vesikari T, Van Damme P, Giaquinto C, et al. European Society for Paediatric Infectious Diseases consensus recommendations for rotavirus
vaccination in Europe: update 2014. Pediatr Infect Dis J
20. Lo Vecchio A, Liguoro I, Dias JA, et al. Rotavirus
immunization: global coverage and local barriers for implementation
21. Harro C, Louis Bourgeois A, Sack D, et al. Live attenuated enterotoxigenic Escherichia coli
(ETEC) vaccine with dmLT adjuvant protects human volunteers against virulent experimental ETEC challenge. Vaccine
22. Falszewska A, Szajewska H, Dziechciarz P. Diagnostic accuracy of three clinical dehydration scales: a systematic review. Arch Dis Child
23. Anigilaje EA. Management of diarrhoeal dehydration in childhood: a review for clinicians in developing countries. Front Pediatr
24. Rutman L, Klein EJ, Brown JC. Clinical pathway produces sustained improvement in acute gastroenteritis
25. Rouhani S, Meloney L, Ahn R, et al. Alternative rehydration methods: a systematic review and lessons for resource-limited care. Pediatrics
26. Giannattasio A, Guarino A, Lo Vecchio A. Management of children with prolonged diarrhea [version 1; peer review: 3 approved]. F1000Res
27. Leibovici-Weissman Y, Neuberger A, Bitterman R, et al. Antimicrobial drugs for treating cholera. Cochrane Database Syst Rev
28. Tickell KD, Brander RL, Atlas HE, et al. Identification and management of Shigella
infection in children with diarrhoea: a systematic review and meta-analysis. Lancet Glob Health
29. Wen SCH, Best E, Nourse C. Non-typhoidal Salmonella infections in children: review of literature and recommendations for management. J Paediatr Child Health
30. Guarino A, Ashkenazi S, Gendrel D, et al. European society for pediatric gastroenterology, hepatology, and nutrition/European Society for Pediatric Infectious Diseases evidence-based guidelines for the management of acute gastroenteritis
in children in Europe: update 2014. J Pediatr Gastroenterol Nutr
31. Williams PCM, Berkley JA. Guidelines for the treatment of severe acute malnutrition: a systematic review of the evidence for antimicrobial therapy. Paediatr Int Child Health
32. MacGillivray S, Fahey T, McGuire W. Lactose avoidance for young children with acute diarrhoea. Cochrane Database Syst Rev
33. Bandsma RHJ, Voskuijl W, Chimwezi E, et al. A reduced-carbohydrate and lactose-free formulation for stabilization among hospitalized children with severe acute malnutrition: a double-blind, randomized controlled trial. PLoS Med
34. Lo Vecchio A, Vandenplas Y, Benninga M, et al. An international consensus report on a new algorithm for the management of infant diarrhoea. Acta Paediatr
36. WHO. World Health Statistics 2018: Monitoring Health for the SDGs. Geneva, Switzerland: WHO; 2018.
37. WHO. Guideline: Updates on the Management of Severe Acute Malnutrition in Infants and Children. Geneva, Switzerland: World Health Organization; 2013.
38. Cocciolillo S, Collins SM. The long-term functional consequences of acute infectious diarrhea. Curr Opin Gastroenterol