APP Guidelines For GE
APP Guidelines For GE
Children
This practice parameter formulates recommenda- This practice parameter is not intended as a sole
tions for health care providers about the manage- source of guidance in the treatment of acute gastro-
ment of acute diarrhea in children ages 1 month to enteritis in children. It is designed to assist pedia-
5 years. It was developed through a comprehensive tnicians by providing an analytic framework for the
search and analysis of the medical literature. Expert evaluation and treatment of this condition. It is not
consensus opinion was used to enhance or formu- intended to replace clinical judgment or to estab-
late recommendations where data were insuffi- lish a protocol for all patients with this condition. It
cient. rarely will provide the only appropriate approach
The Provisional Committee on Quality Improve- to the problem. A technical report describing the
ment of the American Academy of Pediatrics (AAP) analyses used to prepare this parameter and a pa-
selected a subcommittee composed of pediatricians tient education brochure are available through the
with expertise in the fields of gastroenterology, Publications Department of the AAP.
infectious diseases, pediatric practice, and epidemi-
ology to develop the parameter. The subcommittee, BACKGROUND
the Provisional Committee on Quality Improve-
Although most children with gastroentenitis who
ment, a review panel of practitioners, and other
live in developed countries have mild symptoms and
groups of experts within and outside the AAP re-
little or no dehydration, a substantial number will
viewed and revised the parameter. Three specific
have more severe disease. In the United States, an
management issues were considered: (1) methods
average of 220 000 children younger than 5 years are
of rehydration, (2) refeeding after rehydration, and
hospitalized each year with gastroentenitis, account-
(3) the use of antidiarrheal agents. Main outcomes
ing for more than 900 000 hospital days. Approxi-
considered were success or failure of rehydration,
mately 9% of all hospitalizations of children younger
resolution of diarrhea, and adverse effects from
than 5 years are because of diarrhea.1 In addition,
various treatment options. A comprehensive bibli-
approximately 300 children younger than 5 years die
ography of literature on gastroenteritis and diar-
each year of diarrhea and dehydration (R. I. Glass,
rhea was compiled and reduced to articles amena-
written communication, February 1995). Clinicians
ble to analysis.
should be aware that young infants who were pre-
Oral rehydration therapy was studied in depth;
mature and children of teenaged mothers who have
inconsistency in the outcomes measured in the
not completed high school, had little or no prenatal
studies interfered with meta-analysis but allowed
care, and belong to minority groups are at higher risk
for formulation of strong conclusions. Oral rehy-
of death caused by diarrhea (R. I. Glass, written
dration was found to be as effective as intravenous
communication, February 1995).
therapy in rehydrating children with mild to mod-
In the United States, the incidence of diarrhea in
erate dehydration and is the therapy of first choice
children younger than 3 years has been estimated to
in these patients. Refeeding was supported by
be 1.3 to 2.3 episodes pen child per year; rates in
enough comparable studies to permit a valid meta-
children attending day care centers are higher.2 Hos-
analysis. Early refeeding with milk or food after
pitalization and outpatient care for pediatric diar-
rehydration does not prolong diarrhea; there is ev-
nhea result in direct costs of more than $2.0 billion
idence that it may reduce the duration of diarrhea
per year.5 There are also indirect costs to families.
by approximately half a day and is recommended
Surveys show that many health cane providers do
to restore nutritional balance as soon as possible.
not follow recommended procedures for manage-
Data on antidiarrheal agents were not sufficient to
ment of this disorder.6 This practice parameter is
demonstrate efficacy; therefore, the routine use of
intended to present current knowledge about the
antidiarrheal agents is not recommended, because
optimal treatment of children with diarrhea.
many of these agents have potentially serious ad-
verse effects in infants and young children.
Children Covered by the Parameter
In this practice parameter, acute gastroentenitis is
The recommendations in this statement do not indicate an exclusive course defined as dianrheal disease of rapid onset, with on
of treatment or serve as a standard of medical care. Variations, taking into
without accompanying symptoms and signs, such as
account individual circumstances, may be appropriate.
PEDIATRICS (ISSN 0031 4005). Copyright © 1996 by the American Acad- nausea, vomiting, fever, or abdominal pain. Al-
emy of Pediatrics. though the emphasis of this parameter is on diar-
have clinical signs on symptoms of malabsorption.7’39 sections. These recommendations are presented in
Infants fed human milk can be nursed safely during schematic form in the algorithm.
episodes of diarrhea.26 Full-strength animal milk on
animal milk formula usually is well tolerated by General Considerations
children who have mild, self-limited diarrhea.27’38
Evaluation of Dehydration
The combination of milk with staple foods, such as
Available published data have provided rigorous
cereal, is an appropriate and well-tolerated regimen
justification for the principles of ORT for diarrhea.
for children who are weaned.28’30’3437 In the past, the
Successful implementation of ORT starts with an
American Academy of Pediatrics (AAP) necom-
evaluation of the child’s degree of dehydration.
mended gradual reintroduction of milk-based for-
mulas or cow’s milk in the management of acute Guidelines for assessment of dehydration and nehy-
dration are listed in Table 3. If an accurate recent
diarrhea, beginning with diluted mixtures.4#{176} This nec-
weight is available, determination of the percentage
ommendation has been reevaluated in light of recent
of weight lost is an objective measure of dehydration.
data. If children are monitored to identify the few in
whom signs of malabsorption develop, a regular age- Capillary refill time can be a helpful adjunctive mea-
appropriate diet, including full-strength milk, can be sure to determine the degree of dehydration.41 Al-
used safely. though refill can be affected by fever, ambient tem-
perature, and age,42 the clinician should consider
The question of which foods are best for refeeding
delayed capillary refill to be a sign of significant
has been an issue of continuing study. Although
agreement is not universal, clinical experience based dehydration until proven otherwise. Urinary output
and specific gravity are helpful measures to confirm
on controlled clinical trials suggests that certain
the degree of dehydration and to determine that
foods, including complex carbohydrates (rice, wheat,
nehydration has been achieved. Parents should be
potatoes, bread, and cereals), lean meats, yogurt,
fruits, and vegetables, are better tolerated.24’25’36’37 taught the natural history of diarrhea and the signs
of dehydration.
Fatty foods or foods high in simple sugars (including
tea, juices, and soft drinks) should be avoided.7 Note
that this is not the classic BRAT diet, which consists Electrolyte Measurement
of bananas, rice, applesauce, and toast. Although Most episodes of dehydration caused by diarrhea
these foods can be tolerated, this limited diet is low are isonatremic, and serum electrolyte detenmina-
in energy density, protein, and fat. tions are unnecessary. Electrolyte levels should be
measured in moderately dehydrated children whose
REHYDRATION AND REFEEDING: MANAGEMENT histories or physical findings are inconsistent with
GUIDELINES straightforward diarrheal episodes and in all se-
The following therapeutic recommendations are verely dehydrated children. Clinicians should be
based on the evaluation of available literature aug- aware of the features of hypernatremic dehydration,
mented by expert opinion, as described in previous which can lead to neurologic damage and which
chloride channel blockers,83 calmodulin inhibitons,TM 2. Pickering LK, Hadler SC. Management and prevention of infectious
diseases in day care. In: Feigin RD. Cherry JC, eds. Textbook of Pediatric
octreotide acetate,85 and nonstenoidal antiinflamma-
Infectious Diseases. Philadelphia: WB Saunders; 1992:2308-2334
tory drugs. All of these agents must be considered 3. Glass RI, Ho MS. Lew J, Lebaron CW, Ing D. Cost-benefit studies of
experimental at this time. rotavirus vaccine in the United States. In: Sack DA, Freij L, eds. Prospects
Pediatr Infect Dis J. 1993;12:897-902 35. Isolauri E, Vesikari T. Oral rehydration, rapid refeeding and cholestyra-
5. Matson DO, Estes MK. Impact of rotavirus infection at a large pediatric mine for treatment of acute diarrhoea. J Pediatr Gastroenterol Nutr.
hospital. I Infect Dis. 1990;162:598-604 1985;4:366-374
6. Snyder JD. Use and misuse of oral therapy for diarrhea: comparison of 36. Brown KH, Perez F, Gastanaduy AS. Clinical trial of modified whole
US practices with American Academy of Pediatrics’ recommendations. milk, lactose-hydrolyzed whole milk, or cereal-milk mixtures for the
Pediatrics. 1991;87:28-33 dietary management of acute childhood diarrhea. J Pediatr Gastroenterol
7. Duggan C, Santosham M, Glass RI. The management of acute diarrhea Nutr. 1991;12:340-350
in children: oral rehydration, maintenance, and nutritional therapy. 37. Alarcon P, Montoya R, Perez F, Dongo JW, Peerson JM, Brown KH.
MMWR. 1992;41(RR-16):1-20 Clinical trial of home available, mixed diets versus a lactose-free, soy-
8. 51.83 Federal Register 16138 protein formula for the dietary management of acute childhood diar-
9. Pratt EL. Development of parenteral fluid therapy. I Pediatr. 1984;104: rhea. J Pediatr Gastroenterol Nutr. 1991;12:224-232
581-584 38. Brown KB, Peerson JM, Fontaine 0. Use of nonhuman milks in the
10. Powers GF. A comprehensive plan of treatment for the so-called intes- dietary management of young children with acute diarrhea: a meta-
tinal intoxication of children. Am J Dis Child. 1926;32:232-257 analysis of clinical trials. Pediatrics. 1994;93:17-27
39. Sunshine P. Kretchmer N. Studies of small intestine during develop-
11 . Darrow DC, Pratt EL, Heft J Jr. et al. Disturbances of water and elec-
ment, HI: infantile diarrhea associated with intolerance to disaccharides.
trolytes in infantile diarrhea. Pediatrics. 1949;3:129-156
Pediatrics. 1964;34:38-50
12. Hirschhorn NJ. The treatment of acute diarrhea in children: an historical
40. American Academy of Pediatrics, Committee on Nutrition. Use of oral
and physiological perspective. Am I C/in Nutr. 1980;33:637-663
fluid therapy and post-treatment feeding following enteritis in children
13. Hirschhorn NJ, Kinzie JL, Sachar DB, et al. Decrease in net stool output
in a developed country. Pediatrics. 1985;75:358-361
in cholera during intestinal perfusion with glucose-containing solu-
41 . Saavedra JM, Harris GD, Li 5, Finberg L. Capillary refilling (skin turgor)
tions. N Engi J Med. 1968;279:176-181
in the assessment of dehydration. Am I Dis Child. 1991;145:296-298
14. Pierce NF, Sack RB, Mitra RC, et al. Replacement of water and electro-
42. Schriger DL, Baraff L. Defining normal capillary refill: variation with
lyte losses in cholera by an oral glucose-electrolyte solution. Ann Intern
age, sex, and temperature. Ann E;nerg Med. 1988;17:932-935
Med. 1969;70:1173-1181
43. Shaw KN. Dehydration. In: Fleisher GR, Ludwig R, eds. Textbook of
15. Santosham M, Daum RS, Dillman L, et a!. Oral rehydration therapy of
Pediatric Emergency Medicine. 3rd ed. Baltimore, MD: Williams &
infantile diarrhea: a controlled study of well-nourished children hospi-
Wilkins; 1993:147-151
talized in the United States and Panama. N Engl I Med. 1982;306:
44. Silverman BK, ed. Advanced Pediatric Life Support. 2nd ed. Elk Grove
1070-1076
Village, IL: American Academy of Pediatrics, American College of
16. Tamer AM, Friedman LB. Maxwell SR. Cynamon HA, Perez HN, Cleve-
Emergency Physicians; 1993
land WW. Oral rehydration of infants in a large urban US medical
45. Chameides L, ed. Textbook of Pediatric Advanced Life Support. Dallas:
center. I Pediatr. 1985;107:14-19
American Heart Association, American Academy of Pediatrics; 1990
17. Listernick R, Zieserl E, Davis AT. Outpatient oral rehydration in the
46. Schiller LR, Santa Ana CA, Morawski 5G. Fordtran JS. Mechanism of
United States. Am J Dis Child. 1986;140:211-215
the antidiarrheal effect of loperamide. Gastroenterology. 1984;85:
18. Vesikari T, Isolauri E, Baer M. A comparative trial of rapid oral and
1475-1483
intravenous rehydration in acute diarrhoea. Acta Paediatr Scand. 1987;
47. Diarrhoeal Diseases Study Group (UK). Loperamide in acute diarrhoea
76:300-305
in childhood: results of a double-blind, placebo controlled multicentre
19. MacKenzie A, Barnes G. Randomized controlled trial comparing oral
clinical trial. Br Med J. 1984;289:1263-1267
and intravenous rehydration therapy in children with diarrhoea. Br Med
48. Motala C, Hill ID. Effect of loperamide on stool output and duration of
J. 1991;303:393-396
acute infectious diarrhea. I Pediatr. 1990;1 17:467-471
20. Santosham M, Burns B, Nadkami V, et al. Oral rehydration therapy for
49. Prakash P, Saxena 5, Sareen DK. Loperamide versus diphenoxylate in
acute diarrhea in ambulatory children in the United States: a double- the diarrhea of infants and children. Indian J Pediatr. 1980;47:303-306
blind comparison of four different solutions. Pediatrics. 1985;76:159-166
50. World Health Organization. The Rational Use of Drugs in the Management
21 . Carpenter CC, Greenough WB, Pierce NF. Oral rehydration therapy: the ofAcute Diarrhoea in Children. Geneva: World Health Organization; 1990
role of polymeric substrates. N Engl I Med. 1988;319:1346-1348
51. Bhutta TI, Tahir KI. Loperamide poisoning in children. Lancet. 1990;335:
22. Gore SM, Fontaine 0, Pierce NF. Impact of rice based oral rehydration 363
solution of stool output and duration of diarrhoea: meta-analysis of 13 52. Chow CB, Li SH, Leung NK. Loperamide associated necrotizing entero-
clinical trials. Br Med J. 1992;304:287-291 colitis. Acta Pediatr Scand. 1986;75:1034-1036
23. Pizarro D, Posada G, Sandi L, Moran JR. Rice-based oral electrolyte 53. Minton NA, Smith PGD. Loperamide toxicity in a child after a single
solutions for the management of infantile diarrhea. N Engl J Med. dose. Br Med J. 1987;294:1383
1991;324:517-521 54. Herranz J, Luzuriaga C, Sarralle R, Florez J. Neurological symptoms
24. Santosham M, Fayad I, Hashem M, et al. A comparison of rice-based precipitated by loperamide. Anales Espanoles Pediatr. 1980;13:1117-1120
oral rehydration solution and “early feeding” for the treatment of acute 55. Schwartz RH, Rodriguez WJ. Toxic delirium possibly caused by loper-
diarrhea in infants. J Pediatr. 1990;1 16:868-875 amide. J Pediatr. 1991;118:656-657
25. Fayad IM, Hashem M, Duggan C, Refat M, Bakir M, Fontame 0. 56. Ginsberg CM. Lomotil (diphenoxylate and atropine) intoxication. Am I
Comparative efficacy of rice-based
glucose-based oral rehydration and Dis Child. 1973;125:241-242
salts plus early reintroduction of food. Lancet. 1993;342:772-775 57. Rumack BH, Temple AP. Lomotil poisoning. Pediatrics. 1974;53:495-500
26. Khin MU, Nyunt-Nyunt W, Myokhin AJ, et al. Effect of clinical outcome 58. Curtis JAQ, Goel KM. Lomotil poisoning in children. Arch Dis Child.
of breast feeding during acute diarrhoea. Br Med J. 1985;290:587-589 1979;54:222-225
27. Margolis PA, Litteer T. Effects of unrestricted diet on mild infantile 59. Bala K, Khandpur 5, Gujral V. Evaluation of efficacy and safety of
diarrhea: a practice-based study. Am I Dis Child. 1990;144:162-164 lomotil in acute diarrheas in children. Indian Pediatr. 1979;16:903-907
28. Gazala E, Weitzman 5, Weitzman Z, et al. Early versus late refeeding in 60. DuPont HL, Hornick RB. Adverse effect of lomotil therapy in shigello-
acute infantile diarrhea. Isr J Med Sci. 1988;24:175-179 sis. JAMA. 1973;226:1525-1528
29. Fox R, Leen CL. Acute gastroenteritis in infants under 6 months old. 61 . Novak E, Lee JG, Seckman CE, Phillips JP, Disanto AR. Unfavorable
Arch Dis Child. 1990;65:936-938 effect of atropine-diphenoxylate (Lomotil) therapy in linomycin-caused
30. Rees L, Brook CGD. Gradual reintroduction of full-strength milk after diarrhea. JAMA. 1976;235:1451-1454
acute gastroenteritis in children. Lancet. 1979;1 :770-771 62. Pickering LK, Obrig TG, Stapleton FB. Hemolytic uremic syndrome and
31 . Placzek M, Walker-Smith JA. Comparison of two feeding regimens enterohemorrhagic E co/i. Pediatr Infect Dis J. 1994;13:459-475
following acute gastroenteritis in infancy. I Pediatr Gastroenterol Nutr. 63. Reves R, Bass P. DuPont HL, Sullivan P. Mendiola J. Failure to demon-
1984;3:245-248 strate effectiveness of an anticholinergic drug in the symptomatic treat-
32. Santosham M, Foster 5, Reid R, et al. Role of soy-based, lactose-free ment of acute traveler’s diarrhea. J C/in Gastroenterol. 1983;5:223-227
formula during treatment of acute diarrhea. Pediatrics. 1985;76:292-298 64. US Pharmacopeia. Anticholinergic/Antispasinodics System. Rockville, MD:
33. Brown KH, Gastanaduy AS, Saaverdra JM, et al. Effect of continued oral US Pharmacopeia Dispensing Information; 1992;1:312
432 DownloadedPARAMETER
PRACTICE from pediatrics.aappublications.org at King Fahad National Guard Hosp on March 1, 2015
65. Ericsson CD, Evans DG, DuPont HL, Evans DJ Jr. Pickering LK. Bis- 80. Kaila M, Isolauri E, Soppi E, Virtanen E, Lame 5, Arvilommi H. En-
muth subsalicylate activity inhibits
of crude toxins of Escherichia co/i and hancement of the circulating antibody secreting cell response in human
Vibrio cholerae. J Infect Dis. 1977;136:693-696 diarrhea by a human Lactobacillus strain. Pediatr Res. 1992;32:141-144
66. DuPont HL, Ericsson CD, Johnson PG. et al. Prevention of traveler’s 81 . Donowitz M, Levine 5, Watson A. New drug treatments for diarrhoea.
diarrhea by the tablet formulation of bismuth subsalicylate. JAMA. I Intern Med Suppl. 1990;228:155-163
1987;257:1347-1350 82. Schiller LR, Santa Ana CA, Morawski 5G. Fordtran JS. Studies of the
67. Steinhoff MC, Douglas RG Jr. Greenberg HB, Callahan DR. Bismuth antidiarrheal action of clonidine: effects on motility and intestinal ab-
subsalicylate therapy of viral gastroenteritis. Gastroenterology. 1980;78: sorption. Gastroenterology. 1985;89:982-988
1495-1499 83. BridgesRJ, Worrell RT, Frizzell RA, Benos DJ. Stilbene disulfonate
68. Soriano-Brucher H, Avendano P, O’Ryan M, et al. Bismuth subsalicylate blockadeof colonic secretory Cl-channels in planar lipid bilayers. Am I
in the treatment of acute diarrhea in children: a clinical study. Pediatrics. Physiol. 1989;256:907-912
1991;87:18-27 84. DuPont HL, Ericsson CD, Mathewson JJ, Marani 5, Knellwolf-Cousin
69. Figueroa-Quintanilla D, Salazar-Lmdo E, Sack RB, et al. A controlled AL, Martinez-Sandoval FG. alaride maleate, an intestinal calmodulin
trial of bismuth subsalicylate in infants with acute watery diarrheal inhibitor, in the therapy of traveler’s diarrhea. Gastroenterology. 1993;
disease. N EngI I Med. 1993;328:1653-1658 104:709-715
70. Feldman 5, Chen SL, Pickering LK, Cleary TG, Ericsson CD, Hulse M. 85. Cook DJ, Kelton JG, Stanisz AM, Collins SM. Somatostatin treatment for
Salicylate absorption from a bismuth subsalicylate preparation. Clin cryptosporidial diarrhea in a patient with the acquired immunodefi-
Pharmacol Ther. 1981;29:788-792 ciency syndrome (AIDS). Ann Intern Med. 1988;108:708-709
71 . Pickering LK, Feldman 5, Ericsson CD, Cleary TG. Absorption of salic-
ylate and bismuth from a bismuth subsalicylate-containing compound
(Pepto-Bismol). I Pediatr. 1981;99:654-656 GENERAL REFERENCES
72. Mendelowitz PC, Hoffman RS, Weber S. Bismuth absorption and myo-
clonic encephalopathy during bismuth subsalicylate therapy. Ann Intern Duggan C, Santosham M, Glass RI. The management of acute diarrhea in
Med. 1990;112:140-141 children: oral rehydration, maintenance, and nutritional therapy.
73. Parpia SH, Nix DE, Hejmanowski LG, Goldstein HR. Wilton JH, Schen- MMWR. 1992;41(RR-16):1-20
tag II. Sucralfate reduces the gastrointestinal absorption of norfloxacin. Pickering LK, Cleary TG. Approach to patients with gastrointestinal tract
Antimicrob Agents Chemother. 1989;33:99-102 infections and food poisoning. In: Feigin RD. Cherry JC, eds. Textbook of
74. Lidbeck A, Nord CE. Lactobacilli and the normal human anaerobic Pediatric Infectious Disease. 3rd ed. Philadelphia: WB Saunders; 1992:
microflora. Clin Infect Dis. 1993;16(suppl 4):5181-5187 565-596
75. Ramakrishna BS, Mathan VI. Colonic dysfunction in acute diarrhoea:
the role of luminal short chain fatty acids. Gut. 1993;34:1215-1218 Cohen MB, Balistreri WF. Diagnosing and treating diarrhea. Contemp Pedi-
atr. 1989;6:89-114
76. Clements ML, Levine MM, Black RE, et al. Lactobacillus prophylaxis for
diarrhea due to enterotoxigenic Escherichia co/i. Antimicrob Agents Che- Grisanti KA, Jaffe DM. Dehydration syndromes: oral rehydration and fluid
mother. 1981;20:104-108 replacement. Emerg Med C/in North Am. 1991;9:565-588
77. Reid G, Bruce AW, McGroorty JA, et al. Is there a role for lactobacilli in
Management of acute diarrheal disease. Proceedings of a symposium, 1990.
prevention of urogenital and intestinal infections? Clin Microbiol Rev.
I Pediatr. 1991;118:S25-S138
1993;3:335-344
78. Saavedra JM, Bauman NA, Oung I, Perman JA, Yolken RH. Feeding Guerrant RL, Bobak DA. Bacterial and protozoal gastroenteritis. N EngI I
Bifidobacterium bifidum and Streptococcus thermophilus to infants in hos- Med. 1991;325:327-340
pital for prevention of diarrhoea and shedding of rotavirus. Lancet.
Pickering LK, Matson DO. Therapy for diarrheal illness in children. In:
1994;334:1046-1049
Blaser MJ, Smith PD, Ravdin JI, Greenburg HB, Guerrant RL, eds. Infec-
79. Isolauri E, Juntunen M, Rautanen T, Sillanaukee P, Koivula T. A human
tions of the Gastrointestinal Tract. New York: Raven Press; 1995
Lactobacillus strain (Lactobacillus casei, sp strain GG) promotes recovery
from acute diarrhea in children. Pediatrics. 1991;88:90-97 Northrup RS, Flanigan iT. Gastroenteritis. Pediatr Rev. 1994;15:461-472
3
4
: :::r::::t0us;
is stable, as per Box 6.
______________________
(B)
No
5 6
_________________________________
No
8
spatien
therapy? oral
erating
ehydration Yes rehydration
hours or for
until 4-6 I
rehydrated.
(E)
No
11 12 $
(1) Institute intravenous
Patient with diarrhea is less therapy.
than 3% dehydrated by weight (2) Consider nasogastric
I loss or clinical
(F)
estimation.
] tube
14
13
(1) Resume breast feeding,
(1) Continue child’s regular diet. formula or milk.
(2) Consider added glucose-electrolyte (2) Resume recommended foods.
solution to replace stool losses, or (3) Replace ongoing losses with
give more usual dietary fluids. glucose-electrolyte solution.
(G) (H)
434 DownloadedPARAMETER
PRACTICE from pediatrics.aappublications.org at King Fahad National Guard Hosp on March 1, 2015
ANNOTATIONS FOR THE MANAGEMENT OF F. The type and intensity of therapy will vary with
ACUTE GASTROENTERITIS IN YOUNG CHILDREN the individual clinical situation.
Rehydration and Refeeding Algorithm G. Often, a child has diarrhea but remains ade-
quately hydrated. The parent can be reassured but
A. See Table 3 for guidance in the assessment of
should be taught to assess hydration and to identify
the degree of dehydration.
B. Restoration of cardiovascular stability is critical a worsening condition. If the stool output remains
modest, ORT might not be required if early, age-
and is accomplished by giving bolus IV therapy with
normal saline or Ringer’s lactate solution (see text). appropriate feeding is instituted and increased con-
In the patient who does not respond, consider the sumption of usual dietary fluids is encouraged. More
possibility of an underlying disorder, such as myo- significant stool losses can be replaced with an oral
canditis, myocardiopathy, penicanditis, septic shock, nehydrating solution at the rate of 10 mL/kg for each
or toxic shock syndrome. When the patient is in stool.
stable condition and has achieved satisfactory mental H. Bneastfeeding should be resumed. Nonlactose
status, ORT can be used according to the ORT guide- formula, milk-based formula, on milk may be given,
lines. although a small percentage of children will not to!-
C. Solutions containing 45 to 90 mmol/L sodium enate lactose-containing fluids. Lactose-containing
should be given in a volume of 100 mL/kg for mod- solutions seem to be tolerated better when combined
erate dehydration and 50 mL/kg for mild dehydra- with complex carbohydrates in weaned children.
tion. Giving the child these volumes requires pa- Children who are eating foods may resume eating,
tience and persistence, and progress must be although certain foods are tolerated better than oth-
monitored frequently. ens. Recommended foods include complex carbohy-
D. Intractable, severe vomiting, unconsciousness, drates (rice, wheat, potatoes, bread, and cereals), lean
and ileus are contraindications to ORT. Persistent meats, yogurt, fruits, and vegetables. Avoid fatty
refusal to drink may require a trial of IV therapy. foods and foods high in simple sugars (including
E. The rehydration phase usually can be com- juices and soft drinks). Supplement feeding with an
pleted in 4 hours; reevaluation should occur every 1 oral electrolyte solution, 10 mL/kg for each diarrheal
to 2 hours. See text for guidance to decide when stool and the estimated amount vomited for each
rehydnation has been achieved. emesis.
PEDIATRICS is the official journal of the American Academy of Pediatrics. A monthly publication, it
has been published continuously since 1948. PEDIATRICS is owned, published, and trademarked by the
American Academy of Pediatrics, 141 Northwest Point Boulevard, Elk Grove Village, Illinois, 60007.
Copyright © 1996 by the American Academy of Pediatrics. All rights reserved. Print ISSN: 0031-4005.
Online ISSN: 1098-4275.
Downloaded from pediatrics.aappublications.org at King Fahad National Guard Hosp on March 1, 2015
Practice Parameter: The Management of Acute Gastroenteritis in Young Children
Pediatrics 1996;97;424
The online version of this article, along with updated information and services, is located on
the World Wide Web at:
http://pediatrics.aappublications.org/content/97/3/424
PEDIATRICS is the official journal of the American Academy of Pediatrics. A monthly publication,
it has been published continuously since 1948. PEDIATRICS is owned, published, and trademarked
by the American Academy of Pediatrics, 141 Northwest Point Boulevard, Elk Grove Village,
Illinois, 60007. Copyright © 1996 by the American Academy of Pediatrics. All rights reserved. Print
ISSN: 0031-4005. Online ISSN: 1098-4275.
Downloaded from pediatrics.aappublications.org at King Fahad National Guard Hosp on March 1, 2015