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1.
Int J Colorectal Dis ; 39(1): 128, 2024 Aug 08.
Artigo em Inglês | MEDLINE | ID: mdl-39115694

RESUMO

PURPOSE: To explore whether previous participation in clinical studies increases adherence to management guidelines in acute uncomplicated diverticulitis (AUD). METHODS: This retrospective cohort study was designed to give a SNAPSHOT of the management of AUD at six hospitals, three of which had participated in the AVOD trial comparing antibiotic versus non-antibiotic treatment of AUD. Patients with AUD were included from March 2019 through June 2020 and followed for 90 days. The primary outcome was treatment of AUD categorised by antibiotic treatment and inpatient or outpatient management compared between AVOD and non-AVOD hospitals. Descriptive statistics were compiled, and differences between hospitals were assessed with Pearson's chi-squared test. RESULTS: The cohort included 449 patients with AUD of which 63% were women and the median age was 63 (IQR: 52-73) years. Patient characteristics were comparable across the hospitals. Antibiotics were administered to 84 (19%) patients and 113 (25%) patients were managed as inpatients. Management varied significantly between AVOD and non-AVOD hospitals. The mean proportion of patients treated with antibiotics was 7% at AVOD hospitals compared to 38% at non-AVOD hospitals (p < 0.001). The mean proportion of in-hospital management was 18% at AVOD hospitals versus 38% at non-AVOD hospitals (p < 0.001). CONCLUSION: Most patients with AUD were managed according to current guidelines. However, the management varies between hospitals and previous participation in clinical studies may increase knowledge of and adherence to guidelines.


Assuntos
Antibacterianos , Diverticulite , Fidelidade a Diretrizes , Humanos , Feminino , Masculino , Pessoa de Meia-Idade , Idoso , Doença Aguda , Antibacterianos/uso terapêutico , Diverticulite/terapia , Diverticulite/tratamento farmacológico , Estudos Retrospectivos , Guias de Prática Clínica como Assunto , Resultado do Tratamento
2.
Ann Surg ; 274(1): e62-e69, 2021 07 01.
Artigo em Inglês | MEDLINE | ID: mdl-31365364

RESUMO

OBJECTIVE: The aim of this study was to investigate whether differences in postoperative outcome exist between open inguinal hernia repairs performed by surgical trainees and those performed by specialist surgeons. SUMMARY OF BACKGROUND DATA: Inguinal hernia repair is the prototype educational surgical procedure. The impact of trainee participation on postoperative outcome is still controversial and despite earlier studies no reliable hernia-specific data exist. METHODS: The study cohort was based on the Swedish Hernia Register and consisted of 61,161 cases of male patients aged 18 years and older with open anterior mesh repair of a primary inguinal hernia between January 1, 2002, and December 31, 2014. The study cohort was selected to represent the typical trainee procedure in Sweden. Primary outcome measures were reoperation due to hernia recurrence and postoperative 30-day complications. RESULTS: Procedures with longer operating times were at a higher risk for reoperation when performed by supervised trainees [57 to 72 minutes: hazard ratio (HR) 1.55, 99% confidence interval (99% CI) 1.05-2.27] or unsupervised trainees (57 to 72 minutes: HR 1.60, 99% CI 1.18-2.17; >72 minutes: HR 1.72, 99% CI 1.25-2.37). The same was true for specialist and trainee-assisted specialists with operating times <43 minutes (HR 1.63, 99% CI 1.25-2.13; HR 1.58, 99% CI 1.09-2.28). Postoperative 30-day complications were generally associated with longer operating times and occurred at all levels of experience. CONCLUSION: Trainee participation in open inguinal repair in combination with longer operating time is a risk factor associated with higher reoperation rates. This calls for a more structured supervision of trainees in an assumedly basic procedure.


Assuntos
Educação de Pós-Graduação em Medicina/métodos , Hérnia Inguinal/cirurgia , Herniorrafia/educação , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Estudos de Coortes , Herniorrafia/instrumentação , Herniorrafia/métodos , Humanos , Modelos Logísticos , Masculino , Pessoa de Meia-Idade , Duração da Cirurgia , Avaliação de Resultados em Cuidados de Saúde , Complicações Pós-Operatórias/epidemiologia , Complicações Pós-Operatórias/etiologia , Modelos de Riscos Proporcionais , Sistema de Registros , Reoperação/estatística & dados numéricos , Fatores de Risco , Telas Cirúrgicas , Suécia , Adulto Jovem
3.
J Clin Invest ; 109(6): 725-33, 2002 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-11901181

RESUMO

Deficiency of the Golgi enzyme UDP-Gal:N-acetylglucosamine beta-1,4-galactosyltransferase I (beta4GalT I) (E.C.2.4.1.38) causes a new congenital disorder of glycosylation (CDG), designated type IId (CDG-IId), a severe neurologic disease characterized by a hydrocephalus, myopathy, and blood-clotting defects. Analysis of oligosaccharides from serum transferrin by HPLC, mass spectrometry, and lectin binding revealed the loss of sialic acid and galactose residues. In skin fibroblasts and leukocytes, galactosyltransferase activity was reduced to 5% that of controls. In fibroblasts, a truncated polypeptide was detected that was about 12 kDa smaller in size than wild-type beta4GalT I and that failed to localize to the Golgi apparatus. Sequencing of the beta4GalT I cDNA and gene revealed an insertion of a single nucleotide (1031-1032insC) leading to premature translation stop and loss of the C-terminal 50 amino acids of the enzyme. The patient was homozygous and his parents heterozygous for this mutation. Expression of a corresponding mutant cDNA in COS-7 cells led to the synthesis of a truncated, inactive polypeptide, which localized to the endoplasmic reticulum.


Assuntos
Defeitos Congênitos da Glicosilação/enzimologia , Glicoproteínas/sangue , Transferrina/análise , Uridina Difosfato Galactose/deficiência , beta-N-Acetilglucosaminilglicopeptídeo beta-1,4-Galactosiltransferase/deficiência , Células Cultivadas , Pré-Escolar , Cromatografia de Afinidade , Defeitos Congênitos da Glicosilação/etiologia , Defeitos Congênitos da Glicosilação/metabolismo , Fibroblastos/citologia , Fibroblastos/enzimologia , Galactose/metabolismo , Complexo de Golgi/metabolismo , Humanos , Imuno-Histoquímica , Lactente , Leucócitos/enzimologia , Masculino , Transporte Proteico/fisiologia , Pele/citologia , Pele/metabolismo , Uridina Difosfato Galactose/metabolismo , beta-N-Acetilglucosaminilglicopeptídeo beta-1,4-Galactosiltransferase/genética , beta-N-Acetilglucosaminilglicopeptídeo beta-1,4-Galactosiltransferase/metabolismo
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