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Hepatitis C treatment in a district Hospital

dc.contributor.authorEspírito Santo, Margarida
dc.contributor.authorGuerreiro, Luisa
dc.contributor.authorNascimento, Tânia
dc.date.accessioned2019-01-23T11:07:09Z
dc.date.available2019-01-23T11:07:09Z
dc.date.issued2015-10
dc.descriptionPublicação sob a forma de Posterpt_PT
dc.description.abstractThe aim of this study was the characterization of patients with Hepatitis C (HCV) under treatment. Patients included in this study were followed in a Portuguese District Hospital between January 2012 and September 2014, have received treatment for HCV and who had at least one infectiology consultation in this period. Data were collected from the hospital computer system, and patient´s data were collected anonymously, without patient identification. Data analysis was performed using SPSS v22.0. Were included in this study 87 patients who met the inclusion criteria, 75% (n=65) were males and 25% (n=22) female, with a mean age of 45±10 years. Most patients included in this study were Portuguese, resident in the Hospital district and nearby districts. Patients were diagnosed with HCV with a mean age of 3311 years, were followed on average for 53.5 years in this Hospital, and were diagnosed with HCV on average 126.9 years ago. Among these patients, 44% (n=38) had genotype 1, 2% (n=2) genotype 2, 17% (n=15) genotype 3, 13% (n=11) genotype 4 and 24% (n=21) with unknown genotype. Most frequent treatment regimens used by patients included in the study were the association of pegylated interferon alfa 2b (100mcg/week) and ribavirin (1000 mg/day) (52%; n=45); pegylated interferon alpha 2a (180mcg/week) and ribavirin (1000 mg/day) (42%; n=36). Other associations were used but less frequently: pegylated interferon alfa 2a + ribavirin + boceprevir (2%; n=2); pegylated interferon alfa 2b + ribavirin + boceprevir (3%; n=3); and pegylated interferon alfa 2a + ribavirin + telaprevir (1%; n=1). Among included patients, 55 (63%) have performed, to date, one treatment for HCV, 19 (22%) have performed two treatments for HCV (using two different regimens or by using the same regimen twice), 9 (10%) already underwent treatment three times, 3 (3%) already underwent treatment four times and only one patient (1%) has conducted five treatments for HCV. Excluding patients who were receiving treatment at the time of data collection (September 2014), the average length of all other treatments performed by the patients was 82 months, and most (40%; n=51) of treatments performed by patients had a duration from 6 to 9 months. From the results, the standard treatment for patients with HCV appears to be in accordance with the existing guidelines for the treatment of this pathology. In the future it would be advisable further analysis and extended to other hospitals to assess the degree of compliance with currently existing national guidelines for the treatment of this pathology.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.urihttp://hdl.handle.net/10400.1/12302
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherOrdem dos Farmacêuticospt_PT
dc.subjectHepatitis Cpt_PT
dc.subjectTreatmentpt_PT
dc.titleHepatitis C treatment in a district Hospitalpt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceCentro de Congressos de Lisboapt_PT
oaire.citation.titleCongresso Nacional dos Farmacêuticospt_PT
person.familyNameNeto Espírito-Santo
person.familyNameNascimento
person.givenNameMargarida de Fátima
person.givenNameTânia
person.identifier2191220
person.identifier.ciencia-id6215-22B3-56BF
person.identifier.ciencia-id8F1D-1FFE-9777
person.identifier.orcid0000-0002-2200-0015
person.identifier.orcid0000-0003-2429-7374
person.identifier.scopus-author-id57150665300
rcaap.rightsopenAccesspt_PT
rcaap.typeconferenceObjectpt_PT
relation.isAuthorOfPublication34f3dbba-01c4-4cb3-b3a9-f6d05fac2753
relation.isAuthorOfPublicationf975caa2-7c09-4dca-ab01-23d4dcc587a2
relation.isAuthorOfPublication.latestForDiscovery34f3dbba-01c4-4cb3-b3a9-f6d05fac2753

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