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1.
Indian Pediatr ; 2019 Dec; 56(12): 1033-1036
Article | IMSEAR | ID: sea-199447

ABSTRACT

Objective: To describe the demographic, clinical, laboratory and bacteriological profile ofchildren with diagnosis of typhoid fever over a six-year period. Methods: Case recordanalysis of hospitalized children (≤5 y) with culture positive typhoid fever. Results: Bloodculture was positive in 100 (61%) of 166 suspected cases, with 78 isolates of SalmonellaTyphi and 22 Salmonella Paratyphi A. Only 12 children were aged below two years.Hepatomegaly (32), splenomegaly (44), eosinopenia (42), positive widal (15, 21.1%) andpositive Typhidot IgM (18, 28.1%) were not consistently observed. High susceptibility toAmpicillin, Chloramphenicol, Cotrimoxazole (87, 89, and 94, isolates, respectively), 100%susceptibility to third generation cephalosporins and Azithromycin, and high resistance toNalidixic Acid [(S. Typhi 48 (61.5%)], S. Paratyphi A 16 (72.7%)) were observed. Conclusion:We observed a high isolation rate of salmonella in blood culture, despite prior use ofantibiotics. Most salmonella isolates were susceptible in vitro to standard drugs, exceptnalidixic acid.

2.
Indian Pediatr ; 2019 Nov; 56(11): 939-950
Article | IMSEAR | ID: sea-199425

ABSTRACT

Hexavalent vaccines containing diphtheria, tetanus, pertussis, Haemophilus influenzae type b, poliomyelitis, and hepatitis B virusantigens have the potential to be used for the primary series in India (6, 10, 14 weeks of age) and the toddler booster dose. Threehexavalent vaccines are available in India: DTwP-Hib/HepB-IPV (wP-hexa), DTaP-IPV-HB-PRP~T(2aP-hexa), and DTaP-HBV-IPV/Hib(3aP-hexa). In the three published phase-3 Indian studies, pertussis ‘vaccine response’ rates 1 month after a 6-10-14-week primaryseries were 68.4-75.7% for wP-hexa, 93.8-99.3% for 2aP-hexa, and 97.0-100% for 3aP-hexa; seroprotection rates for the other fiveantigens were 88.2-100%, 49.6-100%, and 98.6-100%, respectively. Studies outside India show: good immunogenicity/safety afterboosting dosing; immune persistence to age 4.5 years (2aP-hexa), 7-9 years (3aP-hexa) (all antigens), and 9-10 and 14-15 years,respectively (hepatitis B); and successful co-administration with other vaccines. Hexavalent vaccines could reduce the number ofinjections, simplify vaccination schedules, and improve compliance.

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