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European Journal of Scientific Research - EuroJournals

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361 E. N. Al-kaissi, M. Makki and M. Al- Khoja<br />

Table 1: Comparison <strong>of</strong> Oral Rehydration Solutions<br />

Solutions<br />

Glucose Sodium<br />

Composition<br />

Potassium Chloride<br />

Commercial solutions<br />

(g per dL) (mEq per L) (mEq per L) (mEq per L)<br />

WHO solution 2.0 90 20 80<br />

Hydra-Lyte 1.2 84 10 59<br />

Rehydralyte 2.5 75 20 65<br />

Pedialyte 2.5 45 20 35<br />

Generic pediatric solution* 2.5 45 20 35<br />

Lytren 2.0 50 25 45<br />

Resol 2.0 50 20 50<br />

Infalyte 2.0 50 20 40<br />

Ricelyte Starch polymers 50 25 45<br />

Home remedies (not recommended)<br />

Jell-O(one-half strength) 8.0 6 to 17 0.2 --<br />

Gatorade 5.0 24 3 17<br />

S<strong>of</strong>t drinks 7.0 to 12.0 1 to 7 0.1 to 0.4 --<br />

Apple juice 12.0 0.1 to 3.5 24 to 43 --<br />

Broth -- 250 -- --<br />

WHO=World Health Organization.<br />

*--Similar to Pedialyte.<br />

Information from reference (MMWR2003).<br />

Materials and Methods<br />

200 cases admitted to the medical city hospital Baghdad/ Iraq for rehydration were included in this<br />

work, they were children between the age <strong>of</strong> 0-2 years and their diarrhoeas <strong>of</strong> less than 6 days duration<br />

prior to admission to hospital. The study extended for one year. Evaluation <strong>of</strong> the degree <strong>of</strong><br />

dehydration was performed on admission [19]. ORT (WHO formula- table 1) was <strong>of</strong>fered to all<br />

patients irrespective <strong>of</strong> age.<br />

Laboratory investigation<br />

A-Blood samples were sent to the Laboratory for biochemical investigation including: serum Na + , K + ,<br />

CL - , BUN, protein(by Technicon- Microlyzer) and acid-base study by Micro-Astup).)<br />

B-isolation <strong>of</strong> enteric pathogens<br />

A total <strong>of</strong> 200 stool specimens were collected from the children, the specimens were collected in sterile<br />

specimen bottles having the names and ages <strong>of</strong> the patients. All the samples were transferred<br />

immediately to the laboratory for analysis. General stool examinations were done as well as<br />

inoculation into standard appropriate culture media, Selective and differential solid media as well as<br />

enrichment broth were used for primary isolation <strong>of</strong> enteric organisms. These include: MacConkey's<br />

agar (Oxoid), deoxycholate citrate agar (Oxoid), and selenite F (Oxoid) as enrichment broth for<br />

entopathogenic Escherichia coli, Salmonella and Shigella as described [20], and Campylobacter<br />

selective agar, which contains vancomycin, polymyxinB sulphate and trimethoprim (WHO supply) for<br />

campylobacter species.All solid media plates were incubated aerobically at 35-37ºc for 18h except<br />

campylobacter selective agar plates which were incubated under microaerobic condition at 42ºc for 48h<br />

[21]. Biochemical tests such as methyl red, motility, kligler iron agar, indole, catalase, urease and<br />

oxidase were carried out on the bacterial isolates using conventional techniques <strong>of</strong> [22]. E. coli<br />

colonies from non inhibitory agar medium were screened for classical enteropathogenic serotypes by<br />

the slide agglutination tests using commercially available antisera (Wellcome Diagnostics, Temple

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