RÉSUMÉ
Background: Anemia prevalence in young children con?nues to remain over 70% in most parts of India and Asia. In developing countries like India,anemia is a significant cause of mortality and morbidity in children under 5 years of age. In public health terms, Iron deficiency anemia (IDA) is a very important causa?ve factor for childhood anemia. Materials & Methods: A prospec?ve observa?onal study was conducted on hospitalized children in ter?ary care center. All children between 1 month to 18 years of age were admi?ed in Pediatric ward were taken to the study for 1.5 years study period. Results: Total number pa?ents admi?ed in pediatric ward were 1280 out of which 812 were enrolled for the study, out of which 522 pa?ents have been studied in detail as they had iron deficiency anemia. The total prevalence in our study period is 65.64%. Our analysis showed that males outnumbered females with sex ra?o of Male: Female is1.76:1. This study shows that the children of 1 month to 5 years is 361 which are 69.1%, children of age 5-12years are 123 which is 23.6%, children of age 12-18years are 38 which is 7.3%. We observed that the most common age group involved is less than 5 years which is significant. The e?ology of the hospitaliza?on has been studied, out of which Lower respiratory infec?ons were more common. Conclusion: This study revealed that the prevalence of IDA in under 5 years is more common than in other age groups. Children with anemia and those with iron deficiency anemia were found to be more suscep?ble to lower respiratory tract infec?ons.
RÉSUMÉ
Objective: To assess the cognitive development of nonhandicapped low birth weight (LBW) infants at 18 years. Design: Prospective cohort study. Setting: Infants born between 1987 - 1989 with birth weight less than 2000g and discharged from a neonatal special care unit were followed up till the age of 18 years. Methods: The intelligence quotient (IQ) was determined by Raven’s progressive matrices. Assessment of adjustment and aptitude was done. Results: The cohort of 161 LBW infants was divided into three groups according to their gestation - preterm SGA (n=61), full term SGA (n=30) and preterm AGA (n=70). 71 full term AGA infants served as controls. The IQ of the study group (Percentile 39.3) was significantly lower than that of controls (Percentile 54.9) (P=0.002). Preterm SGA subjects had the lowest IQ (Percentile 35.5), though just within normal limits. Males from the study group had significantly lower IQ than male controls (P=0.03). The IQ of PTSGA subjects of college educated mothers (P=0.004) and belonging to higher socio-economic class (P=0.04) was significantly higher. On the differential aptitude test, PTSGA subjects were poor in speed and mechanical reasoning. The 18 year IQ could be best predicted by IQ at 6 and 12 years. Conclusion: Preterm SGA children have the lowest IQ at 18 years, males have lower IQ. Maternal education and socioeconomic status have great impact on cognitive development. Good prediction of the 18 year IQ can be done by the 6 and 12 year IQ.
RÉSUMÉ
Objective: To assess the growth, adiposity and blood pressure of non-handicapped low birthweight children at 18 years. Design: Prospective cohort study. Setting: Infants born between 1987-1989 with birthweight less than 2000g, discharged from a neonatal special care unit of a referral hospital and followed up till the age of 18 years. Methods: The height, weight, and head circumference were measured. Measurements for adiposity, blood pressure, parental height and weight were recorded. Results: The cohort of 161 low birth weight (LBW) infants was divided into three groups according to their gestation – preterm SGA (n=61), full term SGA (n=30) and preterm AGA (n=70). 71 full term AGA infants served as controls. Preterm SGA males had height of 164.5 cms (162-166.9, 95% CI) which was significantly R E S E A R CH P A P E R INDIAN PEDIATRICS 727 VOLUME 49__SEPTEMBER 16, 2012 less (mean deficit = 5.7 cms) than that of controls (P=0.02). However, PTSGA children were short inspite of normal midparental height. Preterm SGA and AGA children had smaller head circumference. There was no evidence of adiposity and no child had hypertension. Mid-parental height was an important determinant of height in LBW children. Both parents’ weight and BMI were important determinants of weight and BMI, respectively in all LBW children. Conclusion: Preterm SGA males were short, but there was no difference in the weight of the LBW group and controls. Preterms had smaller head circumference. There was no evidence of adiposity or hypertension.
RÉSUMÉ
A long-term immunogenicity study of a single dose live attenuated H2 strain hepatitis A vaccine is being conducted in healthy Indian children at KEM Hospital, Pune. 131 of the original 143 children vaccinated in 2004, were evaluated for anti- HAV antibodies 30 months post vaccination (2007). Seroprotective antibody levels ≥20 mIU/mL were demonstrated in 87.8% subjects with an overall GMT of 92.02mIU/mL. No hepatitis like illness was recorded in any of the subjects since vaccination
Sujet(s)
Analyse chimique du sang , Études de suivi , Humains , Nouveau-né , Perfusions veineuses , Mâle , Radiographie thoracique , Maladies rares , Appréciation des risques , Indice de gravité de la maladie , Syndrome d'épidermolyse staphylococcique du nourrisson/diagnostic , Syndrome d'épidermolyse staphylococcique du nourrisson/traitement médicamenteux , Staphylococcus aureus/isolement et purification , Résultat thérapeutique , Vancomycine/administration et posologieRÉSUMÉ
OBJECTIVE: To study the circulation pattern of respiratory viruses in out patients department (OPD) and hospitalized children with acute respiratory tract infection. METHODS: Nasopharyngeal aspirates were collected from 385 children with acute respiratory tract infections attending the OPD (n=199, 51.7%) and admitted to pediatric ward (n=186, 43.2%). Specimens were screened for seven respiratory viruses by immunofluoresence test (IFT) using Respiratory panel 1 screening and identification kit. RESULTS: Viral antigens were detected in 57 (28.6%) and 86 (46.2%) patients from OPD and admitted cases respectively, giving an overall positivity of 143 (37.1%) for respiratory viruses. Of the six respiratory viruses, the most common was respiratory syncytial virus (RSV) in 100 (26%) patients, followed by influenza viruses in 21 (5.4%), parainfluenza in 8 (2.07%), adenovirus in 3 (0.8%). One patient had mixed infection of RSV and adenovirus. RSV was most frequently detected in the hospitalized children (39.8%). CONCLUSION: RSV appeared to be the most common respiratory viral infection in the age group 0-1 year causing hospitalization.
Sujet(s)
Adenoviridae/isolement et purification , Répartition par âge , Enfant , Enfant d'âge préscolaire , Études de cohortes , Femelle , Hospitalisation/statistiques et données numériques , Humains , Incidence , Inde/épidémiologie , Nourrisson , Mâle , Orthomyxoviridae/isolement et purification , Patients en consultation externe/statistiques et données numériques , Virus respiratoire syncytial humain/isolement et purification , Infections de l'appareil respiratoire/épidémiologie , Études rétrospectives , Indice de gravité de la maladie , Répartition par sexeRÉSUMÉ
OBJECTIVE: To assess the growth and sexual maturity of non-handicapped children with birth weight less than 2000 g at 12 years. DESIGN: Prospective cohort study. SETTING: Infants discharged from a Neonatal Special Care Unit of a referral hospital with birth weight less than 2000 g between 1987-1989 and followed up till the age of 12 years. METHODS: The height, weight and head circumference was measured. Sexual maturity was determined by Tanners score and age of menarche in girls was reported by parents. Parental height and weight was recorded. Intelligence quotient was determined by Weschslers Intelligence Scale. RESULTS: The cohort of 180 low birth weight (LBW) infants (birth weight less than 2000 g) was divided into 3 groups according to their gestation - preterm SGA (n=73), full term SGA (n=33) and preterm AGA (n=74). Ninety full term AGA infants served as controls. Preterm SGA children had significantly less height (mean deficit 5.8 cm), weight and head circumference (P<0.001). There was no significant difference in sexual maturity and onset of menarche between the study group and controls. There was a correlation between head circumference and IQ and preterm SGA children had the lowest mean IQ (85.4 +/- 17.7). Mothers height contributed 14% variance to a total variance of 25.3% for Z score of height at 12 years. Mothers weight contributed a variance 21.1% to a total variance of 29.4% for Z score of weight. CONCLUSION: Preterm SGA children were shorter, lighter and had the smallest head circumference, and also had the lowest IQ. Mothers height and weight was an important determinant of height and weight at 12 years.
Sujet(s)
Adiposité , Adolescent , Facteurs âges , Anthropométrie , Mensurations corporelles , Études cas-témoins , Enfant , Femelle , Troubles de la croissance/épidémiologie , Indicateurs d'état de santé , Humains , Nourrisson à faible poids de naissance , Nouveau-né , Nourrisson petit pour son âge gestationnel , Mâle , Études prospectives , Psychométrie , Maturation sexuelle , Échelles de WechslerRÉSUMÉ
Iron supplementation programs using pediatric tablets or drops have not been successful in the control of anemia amongst infants and children in India. Sprinkles is an innovative multi-micronutrient home fortification strategy to control iron deficiency and anemia. OBJECTIVE: We aimed to determine the hematologic response to different doses and forms of iron in Sprinkles and iron drops. SETTING: Twenty two villages of Vadu Rural Health Program, KEM Hospital, Pune. DESIGN: Double blind clustered randomized community-based trial. SUBJECTS: Children (n=432) aged 6 to 18 mo age with Hb between 70 to 100 g/L were enrolled. METHODS: Selected villages were randomized into 5 groups: Sprinkles 12.5, 20 or 30 mg ferrous fumarate, Sprinkles 20 mg micronized ferric pyrophosphate or drops 20 mg ferrous glycine sulphate (DROPS) for 8 weeks. Household socio-demographic information was collected at baseline. Side effects and compliance were monitored through weekly visits. Hemoglobin was estimated at baseline, 3 and 8 weeks. Ferritin was assessed at baseline and 8 weeks. RESULTS: Baseline characteristics were similar across all groups. Hemoglobin increased significantly (P<0.0001) in all groups at 8 weeks with no difference between groups. Ferritin increased (P<0.0001) significantly in all groups with no difference across the groups. Compliance (overall range: 42 to 62 %) was lowest for DROPS. Side effects were significantly higher among DROPS compared to Sprinkles (p>0.05). CONCLUSIONS: Sprinkles 12.5 mg FF dose is as efficacious as higher doses of iron in Sprinkles or DROPS in increasing hemoglobin. Sprinkles FF 12.5 mg is recommended as it has fewer reported side effects and better compliance compared to DROPS.
Sujet(s)
Anémie par carence en fer/sang , Compléments alimentaires/effets indésirables , Formes posologiques , Méthode en double aveugle , Ferritines/métabolisme , Hémoglobines/métabolisme , Humains , Nourrisson , Facteurs socioéconomiquesRÉSUMÉ
An open non comparative study of a live attenuated H2 strain Hepatitis A vaccine of Chinese origin was carried out in 143 healthy Indian children aged 1 to 12 years (mean age 4.87 2.76 years; 88 boys, 55 girls). At baseline, all were negative for IgG HAV antibodies and had normal hematological and biochemical indices. Two months after a single dose of the vaccine (given subcutaneously), 137 children (i.e. 95.8 %) developed protective antibodies of IgG > 20 mIU / mL. The hematological and biochemical parameters remained within normal limits. There were no adverse events in any except mild fever in one child. In conclusion, live attenuated H2 strain Hepatitis A vaccine in a single dose was found to be immunogenic and safe in Indian children.
Sujet(s)
Enfant , Enfant d'âge préscolaire , Femelle , Vaccins anti-hépatite A/effets indésirables , Anticorps de l'hépatite C/sang , Humains , Immunoglobuline G/sang , Inde , Nourrisson , Mâle , Sécurité , Vaccins atténuésRÉSUMÉ
OBJECTIVE: To study the transcutaneous absorption of traditionally massaged oil in newborns and to specifically compare the effects of (i) essential fatty acid (EFA) rich - safflower oil and (ii) saturated fat rich coconut oil, on fatty acid profiles of massaged babies. DESIGN: A short term randomised controlled study. SETTING: Tertiary care NICU of a large teaching hospital and a research laboratory of a University complex. METHODS: 120 study babies were randomly assigned to three oil groups (i) safflower oil (n = 40) (ii) coconut oil (n = 40) and (iii) no oil controls (n = 40). In each group, babies were selected in three subsets as per their gestational ages viz (a) less than 34 weeks, (b) 34-37 weeks, (c) greater than 37 weeks. 5 mL of the designated oil was massaged four times a day for five days under controlled conditions of temperature and feeding. Pre and post oil massage samples of blood were analysed for triglycerides and fatty acid profiles using gas chromatography. RESULTS: Post oil triglyceride values were significantly raised in both the oil groups and also in controls. However, the quantum of rise was significantly higher in oil groups as compared to controls. Fatty acid profiles (gas chromatography) showed significant rise in EFAs (linolenic acid and arachidonic acid) in safflower oil group and saturated fats in coconut oil group. Changes were more evident in term babies. There were no side effects associated with the massage. CONCLUSIONS: This study shows that topically applied oil can be absorbed in neonates and is probably available for nutritional purposes. The fatty acid constituents of the oil can influence the changes in the fatty acid profiles of the massaged babies.
Sujet(s)
Acides gras/administration et posologie , Acides gras indispensables/usage thérapeutique , Femelle , Humains , Phénomènes physiologiques nutritionnels chez le nourrisson , Nouveau-né , Mâle , Massage , Huiles végétales/administration et posologie , Huile de carthame/usage thérapeutique , Absorption cutanéeRÉSUMÉ
OBJECTIVE: To explore the contribution of biologic risk factors versus socio-demographic and environmental risk factors in cognitive development of children with birth weight less than 2000 g, at the age of 12 years. DESIGN: Prospective cohort study. SETTING: Infants discharged from a NICU of a referral hospital, with birth weight less than 2000 g between 1987-89 and followed up in the High Risk Clinic. METHODS: The children were assessed at the age of 12 years, with the Weschler's Intelligence Scale for IQ and by Wide Range Achievement Test for mathematics skills. Mother's education, father's education, socio-economic status, family structure, spaciousness of the house, the locality in which the child lived and the type of school the child attended, were all recorded. A stimulation score was determined at 6 and 12 months and 3 years. Family environment score was used at 12 years. RESULTS: The cohort consisted of 180 children, with 90 controls. The mean IQ of the study group was 89.5 +- 16.9, which was significantly lower than that of controls (97.2 +- 14.1) (P < 0.05). The mathematical skills of the study group were significantly poorer (P < 0.05) than that of controls. A multiple linear regression analysis was done using IQ as the dependent variable and all risk factors at birth, stimulation scores and socio-environmental factors as independent variables. Mothers education was the most important factor contributing to the total IQ, a variance of 25.2 % of the total variance 44.2 PERCENT. Fathers education emerged as an important factor for mathematics skills. School was the next important factor for IQ as well as academics. Controlling for all other background factors, birth weight was the only biologic factor of significance, and this had a very small contribution. CONCLUSION: Parental education and the type of school attended by the child were the most important factors influencing cognitive development. The only biologic factor of importance was birth weight, but this too had a very small contribution.
Sujet(s)
Poids de naissance , Enfant , Développement de l'enfant , Éducation de l'enfant , Enfant d'âge préscolaire , Cognition , Études de cohortes , Niveau d'instruction , Famille , Caractéristiques familiales , Humains , Nourrisson , Nourrisson à faible poids de naissance , Nouveau-né , Tests d'intelligence , Parents , Facteurs socioéconomiquesRÉSUMÉ
OBJECTIVE: To assess the intelligence, visuo-motor perception, motor competence and school performance of children with birth weight less than 2000 grams, at the age of 12 years. DESIGN: Prospective cohort study. SETTING: Infants discharged from a Neonatal Special Care Unit of a referral hospital with birth weight less than 2000 g between 1987-89 and followed up in the High Risk Clinic. METHODS: The children were assessed by the Weschler's Intelligence Scale, Bender Gestalt test for visuo-motor perception, Wide Range Achievement Test for specific learning disability, Draw-a-Person screening test for emotional problems and Movement Assessment Battery for motor competence. Academic achievement was also scrutinised. RESULTS: One hundred and eighty children weighing less than 2000 grams at birth and ninety control children were assessed. The mean IQ of the study group was normal (89.5 +/- 16.9), though significantly lower than that of controls (97.2 +/- 14.1; p<0.05). Pre term SGA children had the lowest mean IQ (85.4 +/- 17.7). In the 78 VLBW children, there were 12 (15.4%) mentally retarded children as compared to only 3 (3.3%) amongst controls (p<0.001). There were only 3 (3.8%) 'bright' children among the VLBW group, as compared to 20 (22.2%) in the control group (p<0.001). Visuo-motor perception and motor competence of the study group was poor, and they had writing and mathematics learning disability, especially the preterm SGA and VLBW group. Academic achievement was poor and the incidence of borderline intelligence was 24.4%, which has increased from 13.4% at 6 years. CONCLUSIONS: The intelligence and academic performance of the children weighing less than 2000 grams is significantly lower than that of controls, though within normal limits. They also have poor visuo-motor perception, motor incompetence, reading and mathematics learning disability. The preterm SGA and VLBW children had the poorest cognitive abilities.
Sujet(s)
Répartition par âge , Enfant , Développement de l'enfant/physiologie , Enfant d'âge préscolaire , Troubles de la cognition/épidémiologie , Études de cohortes , Femelle , Études de suivi , Humains , Incidence , Inde/épidémiologie , Nourrisson , Nourrisson à faible poids de naissance , Nouveau-né , Tests d'intelligence , Incapacités d'apprentissage/épidémiologie , Mâle , Tests neuropsychologiques , Probabilité , Études prospectives , Appréciation des risques , Répartition par sexe , Statistique non paramétrique , Facteurs tempsRÉSUMÉ
OBJECTIVE: To estimate frequency of acute bacterial meningitis (ABM) in early childhood in hospital admissions, to describe clinical and diagnostic features, and to analyze mortality, complications and long term sequelae. DESIGN: Prospective study. SETTING: Pediatric wards and Rehabilitation Center of KEM Hospital, Pune. METHOD: Study subjects between the ages of 1 months to 5 years with ABM were recruited. Clinical details were recorded. CSF was analysed by routine biochemical methods, antigen detection tests (Latex agglutination LAT) and microbiological studies on special media. Management was as per standard protocols. Survivors were followed up long term with neurodevelopmental studies and rehabilitation programmes. RESULTS: In a study period of 2 years, 54 children (1.5% of all admissions) satisfied the criteria of ABM in early childhood; 78% were below one year and 52% were under the age of six months. Chief presentation was high fever, refusal of feeds, altered sensorium and seizures. Meningeal signs were present in only 26%. CSF C-reactive protein was positive in 41%, gram stain was positive in 67% LAT in 78% and cultures grew causative organisms in 50% of the cases. The final etiological diagnosis (as per LAT and/or cultures) were Streptococcus pneumoniae 39% Hemophilus influenzae type b 26% and others in 35% The others included one case of Neisseria meningitidis and 10 who were LAT negative and culture sterile. 39% patients developed acute neurological complications during the hospital course. 31% children with ABM died in hospital or at home soon after discharge. Six were lost to follow up. Of the 31 children, available for long term follow up (1-3 years), 14 (45%) had no sequelae. The remaining had significant neurodevelopmental handicaps ranging from isolated hearing loss to severe mental retardation with multiple disabilities. CONCLUSION: ABM in early childhood has a considerable mortality, morbidity and serious long term sequelae. Neurodevelopmental follow up and therapy should begin early. Etiological diagnosis can be enhanced by LAT and good culture media. H. influenzae b and S. pneumoniae account for more than 60% of ABM in early childhood.
Sujet(s)
Maladie aigüe , Enfant d'âge préscolaire , Femelle , Humains , Inde/épidémiologie , Nourrisson , Nouveau-né , Mâle , Méningite bactérienne/diagnosticRÉSUMÉ
Wilson's disease (WD), an inborn error of copper (Cu) metabolism, is now one of the leading liver diseases in children in India. The clinical presentation can be extremely varied viz.,--all forms of acute and chronic liver disease, minimal to severe neurological disease, psychiatric problems, bony deformities, hemolytic anemia and endocrine manifestations. A high index of suspicion is necessary along with a judicious battery of investigations for diagnosis. Hepatic copper estimation is the most reliable test but is not easily available in India. Liver biopsy may not be possible because of bleeding problems and histological features are often not diagnostic of WD. In the absence of hepatic Cu, a low ceruloplasmin, high 24 hour urinary copper and presence of KF rings aid in making the diagnosis. The mainstay of initial therapy is Cu-chelators like D-Penicillamine, and Trientine for reduction in body copper to sub-toxic levels. Subsequent maintenance therapy is necessarily lifelong with D-Penicillamine, Trientine or Zinc. Children on therapy must be monitored regularly for response, side-effects, compliance and rehabilitation. Response to therapy may be unpredictable, but acute and early presentations like fulminant hepatic failures have a poor outcome. All siblings must be screened for WD as early diagnosis and treatment result in a good outcome. The identification of the WD gene on chromosome 13 has led to the possible use of molecular genetics (haplotype and mutational analyses) in the diagnosis of WD. Parent groups/associations must take active part in holistic management of WD.
Sujet(s)
Adolescent , Ponction-biopsie à l'aiguille , Analyse chimique du sang , Enfant , Enfant d'âge préscolaire , Association thérapeutique , Régime alimentaire , Femelle , Dégénérescence hépatolenticulaire/diagnostic , Humains , Inde , Transplantation hépatique , Mâle , Monitorage physiologique , Pénicillamine/administration et posologie , Pronostic , Indice de gravité de la maladie , Résultat thérapeutique , Trientine/administration et posologieRÉSUMÉ
OBJECTIVE: To assess the immune response of preterm and low birth weight babies (LBW) to hepatitis B (HB) vaccine. SETTING: Neonatal Intensive Care Unit (NICU), postnatal ward and follow up clinics of KEM Hospital, Pune. DESIGN: Open trial. METHODS: 100 babies were enrolled in four study groups. Group I - preterm, gestational age (GA) < 34 weeks; Group II - GA 34 to 36 weeks; Group III full term <2.5 kg (LBW babies); and Group IV full term >2.5 kg (controls). A recombinant DNA HB vaccine was given at 0, 1, 2 and 12 month schedule. The first injection was administered as soon as the neonate was stabilized. Immune response in terms of anti HBs titres (AUSAB EIA Diagnostic kit) was measured one month after each of the first three injections and at the time of one year booster. Adverse events were monitored. RESULTS: 88 and 62 babies completed the study till the third dose and one year booster dose respectively. Immune response of HB vaccine was uniformly good in all the study groups with 100 % sero-conversion after the second dose itself. By one year (i.e. before the booster dose), very high titres were recorded in all 100%, with 85% demonstrating titres >1000 mIU/ml. Preterm and LBW babies had higher GMT as compared to full term babies till one month after third dose. By one year (before booster), full term babies had higher GMT than preterm and LBW babies. However, these differences were not statistically significant. The vaccine was well tolerated and safe and there were no adverse reactions. CONCLUSION: Immune response of preterm, LBW and full term babies to the new generation recombinant DNA HB vaccine was uniformly good. High and long term seroprotective levels were achieved after the second dose itself.
Sujet(s)
Femelle , Vaccins anti-hépatite B/immunologie , Humains , Nourrisson à faible poids de naissance/immunologie , Nouveau-né , Prématuré/immunologie , MâleRÉSUMÉ
Liver has a central role in nutritional homeostasis and any liver disease leads to abnormalities in nutrient metabolism and subsequent malnutrition. All children with chronic liver disease (CLD) must undergo a periodic nutritional assessment--medical history, anthropometry esp. skinfold thickness and mid-arm circumference, and biochemical estimation of body nutrients. Nutritional rehabilitation is catered to the individual child but generally the caloric intake is increased to 130% of RDA by adding glucose polymers and/or MCT oil (coconut oil) with essential fatty acid supplementation (sunflower oil). The enteral route is preferred and occasionally nasogastric and/or nocturnal feeding are required to ensure an adequate intake. Proteins rich in branched chain amino acids are given in moderation (2-3 gm/kg/day) in compensated cirrhotics unless encephalopathy occurs when protein restriction may be necessary (1 gm/kg/day). Fat-soluble vitamins are supplemented in large quantities esp. in cholestasis along with other vitamins and minerals. Dietary therapy is the mainstay of management of some metabolic liver diseases and may be curative in disorders like galactosemia, fructosemia and glycogen storage disorders. Pre and postoperative nutritional support is an important factor in improving survival after liver transplantation.