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1.
J Trop Pediatr ; 67(3)2021 07 02.
Artigo em Inglês | MEDLINE | ID: mdl-32778897

RESUMO

AIM: The aim of our study was to determine the factors associated with mortality in neonates with carbapenem-resistant Klebsiella pneumoniae (CRKP). MATERIAL AND METHODS: This retrospective, single-center study was conducted in the Neonatal Intensive Care Unit of Harran University Faculty of Medicine between January 2017 and July 2018 who had CRKP growth in their blood, urine or cerebrospinal fluid cultures. The discharged group was designated as the control group (Group 1), whereas the group that faced mortality was classified as the case group (Group 2). The demographic data, clinical findings and laboratory and microbiological results of the two groups were compared to identify risk factors. RESULTS: A total of 58 patients (36 in Group 1 and 22 in Group 2) exhibited CRKP growth during the study period. Low birth weight (p = 0.039), previous antifungal (p = 0.002) or amikacin use (p = 0.040), congenital anomalies (p = 0.002), total parenteral nutrition (TPN) administration (p = 0.002), surgery (p = 0.035), thrombocytopenia (p = 0.007), low platelet mass index (p = 0.011), elevated C-reactive protein (p = 0.004), high carbapenem minimum inhibitory concentration (MIC) (p = 0.029) and high amikacin MIC (p = 0.019) were associated with mortality. In a multivariate regression analysis, previous antifungal use (p = 0.028), congenital anomalies (p = 0.032) and TPN use (p = 0.013) were independent factors in predicting mortality. CONCLUSION: Previous antifungal use, congenital anomalies and TPN use were found to be independent risk factors for mortality in neonates with CRKP infection.


Assuntos
Infecções por Klebsiella , Klebsiella pneumoniae , Antibacterianos/uso terapêutico , Carbapenêmicos , Surtos de Doenças , Farmacorresistência Bacteriana , Humanos , Recém-Nascido , Unidades de Terapia Intensiva , Unidades de Terapia Intensiva Neonatal , Infecções por Klebsiella/tratamento farmacológico , Infecções por Klebsiella/epidemiologia , Estudos Retrospectivos , Fatores de Risco
2.
BMJ Case Rep ; 20182018 Sep 21.
Artigo em Inglês | MEDLINE | ID: mdl-30244227

RESUMO

Development of hypertrophic pyloric stenosis (HPS) after a few weeks of repair of an oesophageal atresia (OA) and tracheo-oesophageal fistula (TOF) is a rare condition in early infancy. Although vomiting or feeding intolerance in operated cases of OA+TOF are attributed to oesophageal stricture, gastro-oesophageal reflux and oesophageal dysmotility, it may also be caused by HPS. Herein, we report a newborn infant who had OA and TOF operation on day 2 of life and diagnosed to have HPS at 15th day of age. Even though it is a rare anomaly, HPS should be kept on mind in the presence of persistent vomiting following repair of OA.


Assuntos
Anastomose Cirúrgica/métodos , Atresia Esofágica/cirurgia , Cardiopatias Congênitas/diagnóstico por imagem , Atelectasia Pulmonar/diagnóstico , Estenose Pilórica Hipertrófica/diagnóstico , Fístula Traqueoesofágica/cirurgia , Antibacterianos/uso terapêutico , Atresia Esofágica/diagnóstico por imagem , Atresia Esofágica/fisiopatologia , Feminino , Cardiopatias Congênitas/fisiopatologia , Humanos , Recém-Nascido , Atelectasia Pulmonar/tratamento farmacológico , Atelectasia Pulmonar/fisiopatologia , Estenose Pilórica Hipertrófica/fisiopatologia , Estenose Pilórica Hipertrófica/cirurgia , Radiografia Torácica , Fístula Traqueoesofágica/diagnóstico por imagem , Fístula Traqueoesofágica/fisiopatologia , Resultado do Tratamento , Vômito
3.
Clin Case Rep ; 3(9): 731-4, 2015 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-26401276

RESUMO

We report the occurrence of supraventricular tachycardia during intravenous immunoglobulin (IVIG) infusion. Supraventricular tachycardia was observed in two newborn patients during IVIG infusion. Both of the babies responded to adenosine treatment. Cardiorespiratory monitoring during IVIG infusion can be recommended because of the possibility of this potentially lifethreatening adverse effect.

4.
J Child Neurol ; 28(1): 115-9, 2013 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-22451530

RESUMO

Macrocephaly-capillary malformation syndrome is characterized by cutaneous vascular malformations with associated anomalies as macrocephaly, macrosomia, hemihypertrophy, hypotonia, developmental delay, lax joints, loose skin, polysyndactyly, and neuroimaging abnormalities. We present a newborn with a prenatal diagnosis of macrosomia and tetralogy of Fallot. He also had macrocephaly; a high forehead; capillary hemangioma on the forehead, upper lip, and philtrum; generalized loose skin; postaxial polydactyly of both hands and feet, with neuroimaging findings of polymicrogyria and thrombosis in sagittal sinus and sinus rectus. His condition was diagnosed as macrocephaly-capillary malformation syndrome in the neonatal period and he died suddenly during sleep at 6 months of age. The clinical course in this syndrome is not as benign as was previously thought. Careful follow-up of these patients with particular emphasis on neuroradiologic and cardiologic evaluation might help decrease the risk of sudden death and to improve long-term outcome.


Assuntos
Megalencefalia/etiologia , Trombose do Seio Sagital/complicações , Anormalidades da Pele/etiologia , Tetralogia de Fallot/complicações , Encéfalo/patologia , Humanos , Lactente , Imageamento por Ressonância Magnética , Masculino , Megalencefalia/complicações , Anormalidades da Pele/complicações
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