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1.
J Pak Med Assoc ; 71(8): 1967-1971, 2021 Aug.
Article in English | MEDLINE | ID: mdl-34418011

ABSTRACT

OBJECTIVE: To determine the indications and threshold of haemoglobin levels for packed red blood cell transfusion and its association with outcomes in a paediatric intensive care setting. METHODS: The retrospective study was conducted in the paediatric intensive care unit of the Aga Khan University Hospital, Karachi, and comprised medical records of all inpatients with age between 1 month and 16 years who received packed red blood cell transfusions between January and December 2017. Data was retrieved from the hospital database and was analyzed using SPSS 22. RESULTS: Of the 147 subjects with a mean age of 67.89±65.8 months, 76(51.7%) were males. Mean paediatric risk of mortality score was 11.72±7.86. Major admitting diagnosis included sepsis and multiorgan dysfunction 50(34%), respiratory diseases 26(17.7%) and haematology/oncology diseases 22(15%). The indications for transfusion was low haemoglobin in 90(61.2%) patients, shock 29(19.7%) and hypoxia 28(19%). Acute transfusion reaction was observed in 1(0.7%) patient; 120(82%) required mechanical ventilation; and 94(64%) required inotropic support. Of the total, 88(59.9%) patients survived. Paediatric risk of mortality score, need for inotropic support and mechanical ventilation were associated with mortality (p<0.05). CONCLUSIONS: Packed red blood cell transfusion, which is frequently prescribed in intensive care settings, was not found to be associated with favourable outcome.


Subject(s)
Critical Illness , Erythrocyte Transfusion , Child , Humans , Infant , Intensive Care Units, Pediatric , Male , Respiration, Artificial , Retrospective Studies
4.
BMJ Case Rep ; 20172017 Jun 30.
Article in English | MEDLINE | ID: mdl-28667009

ABSTRACT

Congenital arteriovenous malformations (AVMs) of scalp are rare congenital vascular malformations. They are usually not symptomatic at birth and are often misdiagnosed as haemangiomas. To date, only two cases of symptomatic neonatal scalp AVM have been reported in literature. Pathophysiology of congenital AVM is not completely understood but genetic and acquired causes are implicated. Diagnosis and management are often difficult and require multidisciplinary approach. We report a rare case of symptomatic congenital scalp AVM in a 10-day-old neonate who was successfully managed at our unit.


Subject(s)
Arteriovenous Fistula , Intracranial Arteriovenous Malformations , Scalp/abnormalities , Arteriovenous Fistula/diagnosis , Arteriovenous Fistula/therapy , Diagnostic Errors , Embolization, Therapeutic , Hemangioma , Humans , Infant, Newborn , Intracranial Arteriovenous Malformations/diagnosis , Intracranial Arteriovenous Malformations/therapy , Male , Scalp/blood supply
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