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1.
Indian Pediatr ; 2008 Jan; 45(1): 17-23
Article de Anglais | IMSEAR | ID: sea-10468

RÉSUMÉ

OBJECTIVE: To compare the effect of Kangaroo mother care (KMC) and conventional methods of care (CMC) on growth in LBW babies (> 2000 g). STUDY DESIGN: Randomized controlled trial. SETTING: Level III NICU of a teaching institution in western India. SUBJECTS: 206 neonates with birth weight < 2000 g. INTERVENTION: The subjects were randomized into two groups: the intervention group (KMC-103) received Kangaroo mother care. The control group (CMC: 103) received conventional care. OUTCOME MEASURES: Growth, as measured by average daily weight gain and by other anthropometrical parameters at 40 weeks postmenstrual age in preterm babies and at 2500 g in term SGA infants was assessed. RESULTS: The KMC babies had better average weight gain per day (KMC: 23.99 g vs CMC: 15.58 g, P< 0.0001). The weekly increments in head circumference (KMC: 0.75 cm vs CMC: 0.49 cm, P = 0.02) and length (KMC: 0.99 cm vs CMC: 0.7 cm, P = 0.008) were higher in the KMC group. A significantly higher number of babies in the CMC group suffered from hypothermia, hypoglycemia, and sepsis. There was no effect on time to discharge. More KMC babies were exclusively breastfed at the end of the study (98% vs 76%). KMC was acceptable to most mothers and families at home. CONCLUSION: Kangaroo mother care improves growth and reduces morbidities in low birth weight infants. It is simple, acceptable to mothers and can be continued at home.


Sujet(s)
Allaitement naturel , Développement de l'enfant , Comorbidité , Humains , Soins du nourrisson , Nourrisson à faible poids de naissance , Nouveau-né , Prématuré , Maladies du prématuré/épidémiologie , Études prospectives , Prise de poids
2.
Indian J Pediatr ; 2005 Apr; 72(4): 367
Article de Anglais | IMSEAR | ID: sea-79226

RÉSUMÉ

Sirenomelia is an exceptionally rare congenital malformation characterized by complete or near complete fusion of lower limbs. A newborn with clinical features of sirenomelia including fused lower limbs in medial position, absent fibula, anal atresia, complete absence of urogenital system (bilateral renal agenesis, absent ureters, urinary bladder, absent internal and external genitalia), a single umbilical artery and a vestigial tail is reported. Association of vestigial tail with sirenomelia is not described in the literature.


Sujet(s)
Autopsie , Coccyx/malformations , Ectromélie/complications , Femelle , Humains , Nouveau-né
3.
Indian Pediatr ; 2005 Mar; 42(3): 285-7
Article de Anglais | IMSEAR | ID: sea-13526

RÉSUMÉ

Fanconi's anemia (FA) is a paradigm for congenital anomalies, aplastic anemia and predisposition to malignancies. Identification of the disease at birth is based on characteristic physical malformations, as hematologic manifestations at birth are extremely rare. We report a case of FA in a newborn who presented with anophthalmia, unilateral radial ray defect, hemivertebrae and thrombocytopenia.


Sujet(s)
Malformations multiples/génétique , Anophtalmie/génétique , Anémie de Fanconi/diagnostic , Humains , Nouveau-né , Mâle , Thrombopénie/génétique
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