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1.
J Ultrasound ; 26(1): 163-168, 2023 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-35567703

RESUMO

PURPOSE: Patients with COVID-19 have an increased risk for venous thrombo-embolism (VTE), especially pulmonary embolism. The exact prevalence of asymptomatic DVT is not known, as is the usefulness of screening for DVT in patients admitted to ward with COVID-19. We have studied the prevalence of asymptomatic DVT. METHODS: We performed a cross-sectional observational multi-center study at four university medical centers in The Netherlands. All adult patients admitted with COVID-19 to a medical ward were eligible for inclusion, including patients who were transferred back from the ICU to the ward. The study protocol consisted of weekly cross-sectional rounds of compression ultrasound. RESULTS: In total, 125 patients were included in the study. A significant proportion of patients (N = 34 (27%)) had developed a VTE during their admission for COVID-19 before the study ultrasound was performed. In most VTE cases (N = 27 (79%)) this concerned pulmonary embolism. A new asymptomatic DVT was found in 5 of 125 patients (4.0%; 95% CI 1.3-9.1%) (Table 2). Nine patients (7.2%; 95% CI 3.3-13.2%) developed a VTE (all PE) diagnosed within 28 days after the screening US was performed. CONCLUSION: We have shown a low prevalence (4%) of newly discovered asymptomatic DVT outside the ICU-setting in COVID-19 patients. Despite this low prevalence, nine patients developed PE (7%) within 28 days after ultrasound. This favors the hypothesis of local thrombus formation in the lungs. Based on our findings and literature, we do not recommend US-screening of asymptomatic patients with COVID-19 admitted to the ward.


Assuntos
COVID-19 , Embolia Pulmonar , Tromboembolia Venosa , Trombose Venosa , Adulto , Humanos , COVID-19/complicações , Trombose Venosa/diagnóstico por imagem , Trombose Venosa/epidemiologia , Tromboembolia Venosa/diagnóstico por imagem , Tromboembolia Venosa/epidemiologia , Tromboembolia Venosa/complicações , Estudos Transversais , Embolia Pulmonar/diagnóstico por imagem , Embolia Pulmonar/epidemiologia
2.
Antimicrob Resist Infect Control ; 11(1): 37, 2022 02 17.
Artigo em Inglês | MEDLINE | ID: mdl-35177128

RESUMO

BACKGROUND: We aimed to assess whether longer indwelling time of peripherally inserted central catheters (PICC) increases risk of central line associated bloodstream infections (CLABSI) in haematology patients. METHODS: Multicentre retrospective cohort study among haematology patients receiving PICCs between 2013 and 2015. Occurrence of CLABSI based on CDC definitions was assessed. We calculated incidence rates, determined risk factors for CLABSI and used Poisson regression models to assess the risk of developing CLABSI as a function of PICC dwell time. We compared diagnoses and treatment characteristics between 2013-2015 and 2015-2020. RESULTS: 455 PICCs placed in 370 patients were included, comprising 19,063 catheter days. Median indwelling time was 26 days (range 0-385) and CLABSI incidence was 4.0 per 1000 catheter days, with a median time to CLABSI of 33 days (range 18-158). Aplastic anaemia (AA) was associated with an increased risk of CLABSI; patients undergoing autologous stem cell transplantation (SCT) were less likely to develop CLABSI. In the unadjusted analysis, PICCs with an indwelling time of 15-28 days, 29-42 days, 43-56 days and > 56 days each had an increased CLABSI incidence rate ratio of 2.4 (1.2-4.8), 2.2 (0.95-5.0), 3.4 (1.6-7.5) and 1.7 (0.9-3.5), respectively, compared to PICCs in place for < 15 days. However, after adjusting for AA and SCT, there was no significant difference in incidence rates between dwell times (p 0.067). CONCLUSIONS: Our study shows that risk of CLABSI does not appear to increase with longer PICC indwelling time. Routine replacement of PICCs therefore is unlikely to prevent CLABSI in this population.


Assuntos
Infecções Relacionadas a Cateter , Cateterismo Venoso Central , Hematologia , Transplante de Células-Tronco Hematopoéticas , Sepse , Infecções Relacionadas a Cateter/prevenção & controle , Cateterismo Venoso Central/efeitos adversos , Catéteres/efeitos adversos , Estudos de Coortes , Transplante de Células-Tronco Hematopoéticas/efeitos adversos , Humanos , Incidência , Estudos Retrospectivos , Sepse/epidemiologia , Transplante Autólogo/efeitos adversos
3.
J Chir (Paris) ; 121(4): 245-51, 1984 Apr.
Artigo em Francês | MEDLINE | ID: mdl-6470065

RESUMO

Congenital absence of the vagina is the second cause of primary amenorrhea. Among 93 cases treated between 1956 and 1981, vulvar morphology was normal in only 37%. Partial bilateral absence of uterus was more frequent than total or than major asymmetric absence. 8 patients had a functional uterus. Ovaries were nearly always normal except in 5 cases of male hermaphroditism. Genetic abnormalities were exceptional. 30% patients had congenital abnormalities of urinary tract, especially when the uterus malformation was important and/or asymmetric. Unilateral renal absence was most common abnormality. 56 patients were treated by recto-vesical cleavage, without skin grafts with more than 90% anatomical and functional good results. 21 patients had been treated by Frank non operative method. Ileal and sigmoid plasties were performed five times. In absence of functional uterus, treatment of congenital absence of vagina must be simple. Frank method's when vulvar is normal; Recto-vesical cleavage, on the others cases.


Assuntos
Cirurgia Plástica/métodos , Vagina/anormalidades , Anormalidades Múltiplas/complicações , Feminino , Humanos , Útero/anormalidades , Vagina/cirurgia
4.
Ann Genet ; 21(4): 239-42, 1978 Dec.
Artigo em Francês | MEDLINE | ID: mdl-314264

RESUMO

A satellited Y chromosome (Yqs) occurred de novo in a boy born to first cousins. The child had severe mental retardation, facial dysmorphism, congenital heart disease, and amaurosis, and died at 6 months and of age. The chromosome rearrangement was confirmed by R-, G-, C-, Q-, and Ag-NOR banding. Its significance and the difficulty of genetic counseling are discussed.


Assuntos
Aberrações Cromossômicas , Cromossomos Sexuais , Cromossomo Y , Nucléolo Celular , Bandeamento Cromossômico , Humanos , Recém-Nascido , Masculino
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