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1.
Indian Pediatr ; 2019 Jun; 56(6): 485-488
Article | IMSEAR | ID: sea-199229

ABSTRACT

Objective: To study the effect of maternal pre-eclampsia on the short-term neurobehavioraloutcomes in late preterm neonates using Neurobehavioral Assessment of Preterm Infants(NAPI) score. Methods: 30 late preterm neonates born to mothers with preeclampsia, andthirty controls born to mothers without pre-eclampsia were enrolled, and followed up to 40weeks of post-menstrual age. They were evaluated by NAPI score of MDV (Motordevelopment-vigor) and AO (Alertness orientation) at 40 wk. Results: The mean NAPIscore of MDV in cases was 60.1 (9.56) as compared to 70.0 (11.48) in controls (P <0.001).The mean NAPI score of AO in cases was 37.45 (11.04) as compared to 45.6 (13.33) incontrols (P=0.006). Conclusions: Late preterm neonates born to mothers with pre-eclampsia have poor short term neurobehavioral outcomes.

2.
Indian Pediatr ; 2014 Mar; 51(3): 227-228
Article in English | IMSEAR | ID: sea-170550

ABSTRACT

Background: Perinatal asphyxia is known to precipitate myocardial dysfunction, rhythm abnormalities and congestive cardiac failure. Case characteristics: A 2-day old neonate with perinatal asphyxia. Observation: He developed shock secondary to ventricular tachycardia, and required synchronized cardioversion for reversion of abnormal rhythm. Outcome: Reversal of arrhythmia leading to recovery. Message: Early identification and management of ventricular tachycardia in neonate with perinatal asphyxia can be lifesaving.

3.
Indian J Pathol Microbiol ; 2011 Apr-Jun 54(2): 254-257
Article in English | IMSEAR | ID: sea-141960

ABSTRACT

Background: Conjunctivitis of the newborn is defined as hyperemia and eye discharge in the neonates and is a common infection occurring in the neonates in the first month of life. In the United States, the incidence of neonatal conjunctivitis ranges from 1-2%, in India, the prevalence is 0.5-33% and varies in the world from 0.9-21% depending on the socioeconomic status. Aim: To study the organisms causing conjunctivitis of the newborn and to correlate the etiology with the mode of delivery. Design: Single center, prospective, observational study. Materials and Methods: A total of 300 mothers and their newborns, born over a period of one year, were included in the study. Of these 200 newborns were delivered through vaginal route (Group A) and 100 (Group B) delivered by lower segment caesarean section (LSCS). At the time of labour, high vaginal swabs were taken from the mothers. Two conjunctival swabs each from both eyes of the newborn were collected at birth and transported to Microbiology department in a candle jar immediately. Results: Eight babies in Group A, developed conjunctivitis at birth. None of the babies in Group B developed conjunctivitis, this difference was statistically highly significant (P<0.000). The organisms found in the conjunctiva of the newborns in Group A were Coagulase negative Staphylococcus, α hemolytic Streptococcus, Escherichia coli and Pseudomonas spps. However, the commonest organism leading to conjunctivitis in the newborn in this study was Coagulase negative Staphylococcus. It was observed that the mothers of 5 out of 8 babies (60%) developing conjunctivitis gave history of midwife interference and premature rupture of membranes so the presence of risk factors contribute to the occurrence of conjunctivitis in the newborn. Conclusions: It is inferred that the mode of delivery and the presence of risk factors is responsible for conjunctivitis in the newborn.


Subject(s)
Adult , Bacteria/classification , Bacteria/isolation & purification , Bacterial Infections/epidemiology , Bacterial Infections/microbiology , Conjunctiva/microbiology , Conjunctivitis/epidemiology , Conjunctivitis/microbiology , Female , Humans , India , Infant, Newborn , Prevalence , Prospective Studies , Risk Factors , United States , Vagina/microbiology
4.
Indian J Pediatr ; 2009 Oct; 76(10): 1061-1062
Article in English | IMSEAR | ID: sea-142406

ABSTRACT

A newborn presented at 14 hrs of age with right sided clonic seizures and shrill cry. Magnetic Resonance Imaging of the brain showed left cerebral hemiatrophy with cystic changes in left fronto-parietal lobe and parasylvian region. The Magnetic Resonance Angiography revealed hypoplasia of left supraclinoid Internal Carotid Artery and hypoplasia and irregularity of vessel wall affecting the left Middle Cerebral Artery. Such an early presentation of this rare disorder has not been reported previously. Recognition of this anomaly has important implications during carotid and trans-sphenoidal surgery, in thromboembolic disease, and in the surveillance and detection of associated cerebral aneurysms.


Subject(s)
Apgar Score , Carotid Artery, Internal/abnormalities , Carotid Artery, Internal/pathology , Cerebral Angiography/methods , Follow-Up Studies , Humans , Imaging, Three-Dimensional/methods , Infant, Newborn , Magnetic Resonance Angiography/methods , Male , Phenobarbital/therapeutic use , Recurrence , Risk Assessment , Seizures/congenital , Seizures/diagnosis , Seizures/drug therapy , Seizures/etiology , Treatment Outcome , Vascular Malformations/complications , Vascular Malformations/diagnosis , Term Birth
6.
Indian J Pediatr ; 2007 Jun; 74(6): 585-6
Article in English | IMSEAR | ID: sea-83359

ABSTRACT

Parvovirus B19 is responsible for approximately 10% of all cases of nonimmune hydrops. An unusual case of perinatally acquired parvovirus infection in a neonate is reported who presented with nonimmune hydrops fetalis at D15 of life.


Subject(s)
Blood Transfusion/methods , Combined Modality Therapy , Female , Follow-Up Studies , Humans , Hydrops Fetalis/etiology , Immunoglobulins, Intravenous/therapeutic use , India , Infant, Newborn , Parvoviridae Infections/complications , Parvovirus B19, Human/isolation & purification , Rare Diseases , Risk Assessment , Severity of Illness Index , Treatment Outcome , Vitamin K/therapeutic use
7.
Indian J Pediatr ; 2007 Feb; 74(2): 197-8
Article in English | IMSEAR | ID: sea-84077

ABSTRACT

A large for gestational age male baby was born to a healthy young primigravida, on L-thyroxime, at 40 weeks by caesarean delivery in a tertiary care hospital. The baby had episodes of hypoglycemia during his immediate four postnatal days in the nursery that were successfully managed with intravenous glucose administration. The baby became unwell on day 5 and had a positive sepsis-screening test. Blood culture revealed a multidrug susceptible S. Paratyphi A strain, which he probably acquired on the first or second postnatal day from the contaminated expressed breast milk or the formula feed.


Subject(s)
Adult , Amikacin/administration & dosage , Anti-Bacterial Agents/administration & dosage , Bottle Feeding/adverse effects , Breast Feeding/adverse effects , Cesarean Section , Female , Follow-Up Studies , Humans , India , Infusions, Intravenous , Male , Ofloxacin/administration & dosage , Paratyphoid Fever/diagnosis , Pregnancy , Risk Assessment , Salmonella paratyphi A/isolation & purification , Sepsis/diagnosis , Treatment Outcome
9.
Indian J Pediatr ; 2005 May; 72(5): 441-2
Article in English | IMSEAR | ID: sea-80420

ABSTRACT

The combination of arthrogryposis multiplex congenita and osteogenesis imperfecta is extremely rare. This combination is named Bruck syndrome. A 34 week male baby weighing 1.7 kg at birth was noted to have multiple flexion contractures and pterygia at elbows, wrists and knees, in addition to right foot talipes equinovarus deformity. Postnatally the child developed multiple swellings involving both the upper and lower limbs. A plain radiograph revealed the presence of fractures involving the long bones of the upper and lower limbs. A diagnosis of osteogenesis imperfecta with arthrogryposis multiplex congenita was made, and the patient was labeled as a case of Bruck Syndrome. The aim of this report is to make the readers aware regarding this rare entity and to specifically look for presence of features suggestive of osteogenesis imperfecta when encountered with a neonate born with arthrogryposis multiplex congenita.


Subject(s)
Arthrogryposis/diagnosis , Humans , Infant, Newborn , Infant, Premature , Male , Osteogenesis Imperfecta/diagnosis , Syndrome
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