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1.
Neth J Med ; 77(1): 19-24, 2019 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-30774100

RESUMO

BACKGROUND: Patients with a chronic hepatitis B virus (HBV) infection or patients who have recovered from an HBV infection are at risk for HBV reactivation (HBVr), especially if they need treatment with chemotherapy. International guidelines recommend routine HBV screening for all patients starting with chemotherapy. This study evaluates the implementation of a routine HBV screening protocol. METHODS: A retrospective study was performed between January 2015 and October 2016 at the Medical Centre Slotervaart Amsterdam. All patients with a solid or hematological malignancy starting intravenous chemotherapy were included. In September 2015, a protocol for routine HBV screening was introduced. HBV screening results were evaluated before and after implementation of the screening protocol. RESULTS: In total, 184 patients were included, of which 129 patients were actually screened; 37 of the 70 (53%) patients were screened in the group before implementation of the protocol and 92 of the 114 (81%) after implementation. Before routine HBV screening, 8/37 (21.6%) patients tested anti-HBc positive; after introduction of routine screening, 13/92 (14.1%) patients tested anti-HBc positive. After implementation of the screening protocol, no HBVr occurred. CONCLUSION: Implementation of routine HBV screening in patients starting chemotherapy increases identification of the number of patients identified as at risk for HBVr and contributes to prevention of HBVr. A high prevalence of anti-HBc positive patients was found during routine HBV screening, indicating the importance of screening. Awareness and implementation of routine HBV screening, together with knowledge of existing guidelines is necessary to increase the HBV screening rate in patients treated with chemotherapy.


Assuntos
Antineoplásicos/efeitos adversos , Hepatite B/diagnóstico , Hepatite B/prevenção & controle , Programas de Rastreamento/métodos , Ativação Viral/efeitos dos fármacos , Idoso , Antineoplásicos/uso terapêutico , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Neoplasias/tratamento farmacológico
2.
Fam Cancer ; 17(3): 371-380, 2018 07.
Artigo em Inglês | MEDLINE | ID: mdl-28936633

RESUMO

Identifying a hereditary colorectal cancer (CRC) syndrome or familial CRC (FCC) in a CRC patient may enable the patient and relatives to enroll in surveillance protocols. As these individuals are insufficiently recognized, we evaluated an online family history tool, consisting of a patient-administered family history questionnaire and an automated genetic referral recommendation, to facilitate the identification of patients with hereditary CRC or FCC. Between 2015 and 2016, all newly diagnosed CRC patients in five Dutch outpatient clinics, were included in a trial with a stepped-wedge design, when first visiting the clinic. Each hospital continued standard procedures for identifying patients at risk (control strategy) and then, after a predetermined period, switched to offering the family history tool to included patients (intervention strategy). After considering the tool-based recommendation, the health care provider could decide on and arrange the referral. Primary outcome was the relative number of CRC patients who received screening or surveillance recommendations for themselves or relatives because of hereditary CRC or FCC, provided by genetic counseling. The intervention effect was evaluated using a logit-linear model. With the tool, 46/489 (9.4%) patients received a screening or surveillance recommendation, compared to 35/292 (12.0%) in the control group. In the intention-to-treat-analysis, accounting for time trends and hospital effects, this difference was not statistically significant (p = 0.58). A family history tool does not necessarily assist in increasing the number of CRC patients and relatives enrolled in screening or surveillance recommendations for hereditary CRC or FCC. Other interventions should be considered.


Assuntos
Neoplasias Colorretais/diagnóstico , Neoplasias Colorretais/genética , Detecção Precoce de Câncer/métodos , Predisposição Genética para Doença/genética , Inquéritos e Questionários , Adulto , Idoso , Feminino , Aconselhamento Genético/métodos , Humanos , Masculino , Anamnese/métodos , Pessoa de Meia-Idade , Sistemas On-Line
3.
J Viral Hepat ; 23(12): 950-954, 2016 12.
Artigo em Inglês | MEDLINE | ID: mdl-27405785

RESUMO

Chronic hepatitis C virus (HCV) infection is a major cause of chronic liver disease and liver-related death. Recently, multiple regimens of different direct-acting antiviral agents (DAAs) have been registered. Although treatment with sofosbuvir (SOF) and simeprevir (SMV) is registered for the treatment of genotype 4 patients in some countries, data on efficacy of this combination are lacking. We aimed to assess the efficacy of SOF and SMV with or without RBV during 12 weeks in a real-life cohort of genotype 4 HCV patients. A retrospective multicentre observational study was conducted in 4 hospitals in Amsterdam, the Netherlands, including patients with advanced liver fibrosis or liver cirrhosis treated with SOF plus SMV with or without RBV during 12 weeks for a genotype 4 chronic HCV infection from 1 January 2015 to 1 August 2015. Sustained viral response (SVR) was established at week 12 after end of treatment. A total of 53 patients with genotype 4 HCV infection, treatment naïve and experienced, were included. SVR was achieved in 49 of 53 patients (92%). The four failures all had a virological relapse and did not receive ribavirin. Three were nonresponder to earlier interferon-based treatment, and one was treatment naive. In this real-life cohort of patients with HCV genotype 4 infection and advanced liver fibrosis/cirrhosis, we show that treatment with SOF and SMV is effective. The addition of RBV could be considered in treatment-experienced patients as recommended in guidelines.


Assuntos
Antivirais/uso terapêutico , Genótipo , Hepacivirus/genética , Hepatite C Crônica/tratamento farmacológico , Cirrose Hepática/patologia , Simeprevir/uso terapêutico , Sofosbuvir/uso terapêutico , Adulto , Idoso , Feminino , Hepacivirus/classificação , Hepacivirus/isolamento & purificação , Hepatite C Crônica/complicações , Hepatite C Crônica/virologia , Humanos , Cirrose Hepática/virologia , Masculino , Pessoa de Meia-Idade , Países Baixos , Inibidores de Proteases , Recidiva , Estudos Retrospectivos , Resultado do Tratamento
4.
Eur J Radiol ; 84(1): 19-25, 2015 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-25455410

RESUMO

OBJECTIVES: To evaluate patient burden and preferences for MR colonography with a limited bowel preparation and automated carbon dioxide insufflation in comparison to conventional colonoscopy. METHODS: Symptomatic patients were consecutively recruited to undergo MR colonography with automated carbon dioxide insufflation and a limited bowel preparation followed within four weeks by colonoscopy with a standard bowel cleansing preparation. Four questionnaires regarding burden (on a five-point scale) and preferences (on a seven-point scale) were addressed after MR colonography and colonoscopy and five weeks after colonoscopy. RESULTS: Ninety-nine patients (47 men, 52 women; mean age 62.3, SD 8.7) were included. None of the patients experienced severe or extreme burden from the MR colonography bowel preparation compared to 31.5% of the patients for the colonoscopy bowel preparation. Colonoscopy was rated more burdensome (25.6% severe or extreme burden) compared to MR colonography (5.2% severe or extreme burden) (P<0.0001). When discarding the bowel preparations, the examinations were rated equally burdensome (P=0.35). The majority of patients (61.4%) preferred MR colonography compared to colonoscopy (29.5%) immediately after the examinations and five weeks later (57.0% versus 39.5%). CONCLUSION: MR colonography with a limited bowel preparation and automated carbon dioxide insufflation demonstrated less burden compared to colonoscopy. The majority of patients preferred MR colonography over colonoscopy.


Assuntos
Dióxido de Carbono , Colonoscopia , Neoplasias Colorretais/patologia , Efeitos Psicossociais da Doença , Insuflação/métodos , Espectroscopia de Ressonância Magnética , Preferência do Paciente , Adulto , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Preferência do Paciente/estatística & dados numéricos , Estudos Prospectivos , Inquéritos e Questionários
5.
Eur J Radiol ; 83(5): 743-50, 2014 May.
Artigo em Inglês | MEDLINE | ID: mdl-24560199

RESUMO

OBJECTIVES: To evaluate the diagnostic performance of MR colonography using automated carbon dioxide (CO2) insufflation for colonic distension, with colonoscopy serving as the reference standard. METHODS: Ninety-eight symptomatic patients underwent MR colonography with faecal tagging and automated CO2 insufflation. Three readers (one expert (reader 1), and two less experienced (readers 2 and 3)) evaluated the images for the presence of colorectal lesions. Bowel distension was evaluated on a 4-point scale. Results were verified with colonoscopy and histopathological analysis. RESULTS: Per-patient sensitivity for lesions ≥10mm was 91.7% (11 of 12) (reader 1), 75.0% (9 of 12) (reader 2), and 75% (9 of 12) (reader 3). Specificity was 96.5% (82 of 85) (reader 1), 97.7% (83 of 85) (reader 2), 95.3% (81 of 85) (reader 3). Per-patient sensitivity for lesions ≥6mm was 85.7% (18 of 21) (reader 1), 57.1% (12 of 21) (reader 2), and 57.1% (12 of 21) (reader 3). Specificity was 86.8% (66 of 76), 98.7% (75 of 76), 90.8% (69 of 76), respectively. Per-patient sensitivity for advanced neoplasia of ≥10mm and ≥6mm was 88.9% (8 of 9) for all readers. Specificity for ≥10mm and ≥6mm was 98.9% (87 of 88) (reader 1), 97.7% (86 of 88) (reader 2), 96.6% (85 of 88) (reader 3). 94.4% of the colon segments were adequate to optimal distended with dual positioning. CONCLUSION: MR colonography can accurately detect lesions ≥10mm, and advanced neoplasia ≥6mm. Sufficient distension was achieved using automated CO2 insufflation for colonic distension in MR colonography.


Assuntos
Dióxido de Carbono , Neoplasias Colorretais/patologia , Aumento da Imagem/métodos , Interpretação de Imagem Assistida por Computador/métodos , Insuflação/métodos , Imageamento por Ressonância Magnética/métodos , Adulto , Idoso , Idoso de 80 Anos ou mais , Dióxido de Carbono/administração & dosagem , Colonoscopia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Variações Dependentes do Observador , Reprodutibilidade dos Testes , Sensibilidade e Especificidade , Método Simples-Cego
6.
Euro Surveill ; 15(15): 19539, 2010 Apr 15.
Artigo em Inglês | MEDLINE | ID: mdl-20429995

RESUMO

Many individuals with hepatitis C virus (HCV) infection are undiagnosed. This study evaluates a risk assessment questionnaire, developed for use online to target blood-screening for HCV. Two hundred and eighty-nine patients with known HCV status completed a written questionnaire on prominent HCV risk factors. Questionnaires generated advice to seek testing if at least one risk factor was reported. Agreement of the testing advice with the HCV status of respondents was evaluated. Subsequently, we validated our questionnaire among 985 patients of an outpatient clinic for sexually transmitted infections. The post-test-probability-of-disease (PTPD) and diagnostic gain (PTPD minus prior probability of disease) were calculated. The questionnaire's sensitivity and specificity were 84.6% and 63.8%, respectively, and higher in the STI clinic patients. The PTPD of positive testing advice was 72.5% given HCV prevalence of 53.0%, yielding a diagnostic gain of 19.5%. Applying the estimated prevalence in the general Dutch population (0.1-0.4%), and the anticipated prevalence in the online project (1.0-6.0%), yielded diagnostic gains of 0.13-0.53% and 1.3-7.0%, respectively. We conclude that our questionnaire succeeded in selecting at-risk individuals as its testing advice agreed well with the HCV status. We suggest that the questionnaire be used online as a selection tool for HCV blood-screening in the general population.


Assuntos
Hepacivirus/isolamento & purificação , Hepatite C/diagnóstico , Programas de Rastreamento/métodos , Medição de Risco/métodos , Inquéritos e Questionários , Adulto , Feminino , Hepatite C/epidemiologia , Humanos , Masculino , Pessoa de Meia-Idade , Países Baixos/epidemiologia , Sensibilidade e Especificidade
8.
Neth J Med ; 40(1-2): 53-61, 1992 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-1579186

RESUMO

UNLABELLED: The objective was to study the usefulness of routine measurement of liver enzymes (ASAT, ALAT, alkaline phosphatase, gamma-GT), and total protein (TP) and albumin (Alb) in a general medicine outpatient clinic. A prospective study was made of consecutive patients who were classified according to whether or not an indication for the tests was present. All six tests were measured in all patients. Physicians were kept unaware of the results of tests in patients with no indication for ordering the test. The setting was a general internal medicine outpatient clinic in a 850-bed teaching hospital which serves as a referral clinic for general practitioners. There were 615 consecutive patients who were all new referrals to the outpatient clinic. The results of all patients with no indication for the test but who had abnormal results were presented to a panel of three experienced internists who decided whether the results had any clinical importance. Repeat measurements of the tests or follow-up results were obtained in all these patients. Seventy-eight of 320 patients in whom no indication for the test for liver enzymes existed had abnormal results. In only six of these (1.9%) were the abnormalities of clinical significance. In 56 of 449 patients in whom no indications were present for TP and Alb measurement the results were abnormal. In only 2 (0.4%) was this clinically important. CONCLUSION: the routine measurement of these six tests in general medicine outpatient clinics should be abandoned because of the low yield.


Assuntos
Proteínas Sanguíneas/análise , Testes Diagnósticos de Rotina/estatística & dados numéricos , Fígado/enzimologia , Albumina Sérica/análise , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Criança , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Países Baixos , Ambulatório Hospitalar , Estudos Prospectivos
9.
Neth J Med ; 37(1-2): 32-6, 1990 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-2215831

RESUMO

This report is about a 71-yr-old woman who suffered from acute liver failure, induced by the nonsteroidal antiinflammatory drug, pirprofen. She presented with jaundice 6 weeks after starting treatment with 800 mg pirprofen daily. She is the fifth patient described in the literature to die from pirprofen-induced hepatotoxicity.


Assuntos
Anti-Inflamatórios não Esteroides/efeitos adversos , Doença Hepática Induzida por Substâncias e Drogas/etiologia , Fenilpropionatos/efeitos adversos , Adulto , Idoso , Anti-Inflamatórios não Esteroides/administração & dosagem , Doença Hepática Induzida por Substâncias e Drogas/mortalidade , Doença Hepática Induzida por Substâncias e Drogas/patologia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Fenilpropionatos/administração & dosagem
11.
Hepatogastroenterology ; 37(1): 90-1, 1990 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-2312047

RESUMO

Patients with monosymptomatic celiac disease (CD) can escape diagnosis for a long period. Anemia is a common finding in CD, although anemia as the sole symptom is relatively unknown. We report on three patients who presented with iron deficiency anemia and no other symptom, in whom CD was considered and diagnosed several to many years after the anemia was documented.


Assuntos
Anemia Hipocrômica/diagnóstico , Doença Celíaca/diagnóstico , Anemia Hipocrômica/etiologia , Anemia Hipocrômica/terapia , Doença Celíaca/complicações , Doença Celíaca/dietoterapia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade
12.
Digestion ; 44 Suppl 1: 63-7, 1989.
Artigo em Inglês | MEDLINE | ID: mdl-2691311

RESUMO

A case is described with pathological gastro-oesophageal reflux and nighttime bronchial asthma. Treatment with omeprazole resulted not only in improvement of gastro-oesophageal reflux but also in alleviation of asthmatic symptoms and increases in expiratory peak flow values. The possible pathophysiological mechanisms whereby gastro-oesophageal reflux may induce or aggravate asthmatic symptoms are discussed. At present it is not yet possible to predict which patients with bronchial asthma will benefit from antireflux therapy with respect to their pulmonary condition, but such treatment is warranted in all patients with bronchial asthma and proven pathological gastro-oesophageal reflux.


Assuntos
Asma/tratamento farmacológico , Refluxo Gastroesofágico/tratamento farmacológico , Omeprazol/administração & dosagem , Esquema de Medicação , Seguimentos , Humanos , Pico do Fluxo Expiratório/efeitos dos fármacos , Capacidade Vital/efeitos dos fármacos
13.
Eur Respir J ; 1(10): 966-8, 1988 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-3224694

RESUMO

A 25-yr-old man suffered from severe nocturnal asthma, which was shown to be provoked by pathological gastro-oesophageal reflux. A dramatic, immediate improvement of his pulmonary condition was achieved by treatment with omeprazole after failure of other therapeutic measures, including high doses of ranitidine.


Assuntos
Asma/tratamento farmacológico , Refluxo Gastroesofágico/tratamento farmacológico , Omeprazol/uso terapêutico , Adulto , Asma/etiologia , Domperidona/uso terapêutico , Refluxo Gastroesofágico/complicações , Humanos , Masculino , Ranitidina/uso terapêutico , Recidiva
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