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1.
Curr Probl Cardiol ; 48(10): 101919, 2023 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-37402423

RESUMO

There is a paucity of data about the sex differences in acute coronary syndrome (ACS) outcomes in patients with prior mediastinal radiation. The National Inpatient Sample database from years 2009 to 2020 were queried for ACS hospitalizations of patients with prior mediastinal radiation. The primary outcome was MACCE (major cardiovascular events), and secondary outcomes included other clinical outcomes. A total of 23,385 hospitalizations for ACS with prior mediastinal radiation exposure ([15,904 (68.01%) females, and 7481 (31.99%) males]) were included in analysis. Males were slightly younger than females (median, age (70 [62-78] vs 72 [64-80]). Female patients with ACS had a higher burden of hypertension (80.82% vs 73.55%), diabetes mellitus (33% vs 28.35%), hyperlipidemia (66.09% vs 62.2%), obesity (17.02% vs 8.6%) however, males had a higher burden of peripheral vascular disease (18.29% vs 12.51%), congestive heart failure (41.8% vs 39.35%) and smoking (70.33% vs 46.92%). After propensity matching, primary outcome MACCE was higher in males (20.85% vs 13.29%, aOR: 1.80 95% CI (1.65-1.96), P < 0.0001) along with cardiogenic shock (8.74% vs 2.42%, aOR: 1.77 95% CI (1.55-2.02), P < 0.0001) and mechanical circulatory support use (aOR: 1.48 95% CI [1.29 -1.71], P < 0.0001). We observed no differences in the length of hospital stay, however total hospitalization cost was higher in males. This nationwide analysis showed significant disparities in outcomes among male and female ACS patients with prior mediastinal radiation history, with increasing trend in hospitalization for ACS among males and females but decreasing mortality among females.


Assuntos
Síndrome Coronariana Aguda , Humanos , Masculino , Feminino , Síndrome Coronariana Aguda/epidemiologia , Pacientes Internados , Caracteres Sexuais , Hospitalização , Tempo de Internação
2.
J Coll Physicians Surg Pak ; 26(6 Suppl): S21-3, 2016 06.
Artigo em Inglês | MEDLINE | ID: mdl-27376209

RESUMO

Feeding jejunostomy is one of the most widely used procedures for enteral nutrition. It is associated with several complications which can be grouped into mechanical, metabolic, nutritional, and infectious. Amongst mechanical complications, complete impulsive tube migration is rarely seen. We hereby report the case of a 60-year old woman, with advanced esophageal carcinoma, re-admitted in the ward with blocked and stuck Foley's catheter placed in the jejenum for feeding purpose. Within hours of admission, patient developed rapid peristalsis and catheter completely disappeared in the abdomen. Exploratory laparotomy was performed to retrieve the catheter, which revealed jejunal intussception and erosions. Migration of the feeding tube is infrequent complication; however, complete migration is even rarer and needs urgent intervention.


Assuntos
Cateteres de Demora/efeitos adversos , Nutrição Enteral/efeitos adversos , Nutrição Enteral/instrumentação , Migração de Corpo Estranho/etiologia , Intussuscepção/etiologia , Doenças do Jejuno/etiologia , Jejunostomia/efeitos adversos , Jejuno/cirurgia , Nutrição Enteral/métodos , Neoplasias Esofágicas/terapia , Feminino , Migração de Corpo Estranho/diagnóstico por imagem , Migração de Corpo Estranho/terapia , Humanos , Intussuscepção/cirurgia , Doenças do Jejuno/cirurgia , Laparotomia , Pessoa de Meia-Idade , Radiografia , Resultado do Tratamento
3.
J Ayub Med Coll Abbottabad ; 26(4): 625-7, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25672202

RESUMO

Laurence Moon Bardet Biedl Syndrome is a rare genetic disorder. Consanguineous marriage is usually the common cause. Principal features of Bardet Biedl Syndrome are red cone dystrophy, obesity, polydactyl, hypogonadism and renal anomalies. The diagnosis was overlooked in our patient until he came in our hospital. We here report an infrequent case of autosomal recessive disorder with Anaemia.


Assuntos
Ancilostomíase/complicações , Anemia/parasitologia , Síndrome de Bardet-Biedl/complicações , Síndrome de Bardet-Biedl/diagnóstico , Adolescente , Ancilostomíase/diagnóstico , Humanos , Masculino
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