Evidence map›Paper›PMID 33836175›Full record

ArticleThe Brazilian journal of infectious diseases : an official publication of the Brazilian Society of Infectious Diseases

A real-life study of the positive response to DAA-based therapies for hepatitis C in Brazil.

Simone Monzani Vivaldini, Rachel Abraão Ribeiro, Gláucio Mosimann Júnior, Karen Cristine Tonini, Gerson Fernando Mendes Pereira, Wildo Navegantes de Araújo

Open access · goldAbstract read
In one paragraph

Article in The Brazilian journal of infectious diseases : an official publication of the Brazilian Society of Infectious Diseases. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.2field-weighted citation impact, top 48% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 4 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Simone Monzani VivaldiniMinistry of Health, Secretariat for Health Surveillance, Department of Chronic Conditions Diseases and Other Sexually Transmitted Infections, Brasília, DF, Brazil; University of Brasília (UnB), Faculty of Medicine, Center for Tropical Medicine, Brasília, DF, Brazil. Electronic address: simonevivaldini@gmail.com.
Rachel Abraão RibeiroMinistry of Health, Secretariat for Health Surveillance, Department of Chronic Conditions Diseases and Other Sexually Transmitted Infections, Brasília, DF, Brazil.
Gláucio Mosimann JúniorMinistry of Health, Secretariat for Health Surveillance, Department of Chronic Conditions Diseases and Other Sexually Transmitted Infections, Brasília, DF, Brazil.
Karen Cristine ToniniMinistry of Health, Secretariat for Health Surveillance, Department of Chronic Conditions Diseases and Other Sexually Transmitted Infections, Brasília, DF, Brazil.
Gerson Fernando Mendes PereiraMinistry of Health, Secretariat for Health Surveillance, Department of Chronic Conditions Diseases and Other Sexually Transmitted Infections, Brasília, DF, Brazil.
Wildo Navegantes de AraújoUniversity of Brasília (UnB), Faculty of Medicine, Center for Tropical Medicine, Brasília, DF, Brazil; National Institute for Science and Technology for Health Technology Assessment, Porto Alegre, RS, Brazil; University of Brasília (UnB), Faculty of Ceilândia, Brasília, DF, Brazil.
Ministério da Saúde · BRUniversidade de Brasília · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A retrospective cohort of 11,308 chronic hepatitis C infected patients treated with regimens that included Sofosbuvir (SOF), Daclatasvir (DCV), Simeprevir (SMV), or an association of Ombitasvir, Veruprevir/Ritonavir and Dasabuvir (3D) with or without Ribavirin (RBV) were assessed for sustained virologic response (SVR) or viral cure after a 12-week treatment. Logistic regression analyses were used to identify factors independently associated with positive response to direct-acting antivirals (DAA)-based therapies. Overall 57.1% were male; 48.3% self-identified as white; 78.3% were over 50 years old; 44.1% were from the Southeast region; 47.7% had genotype 1b; and 84.5% were treated for 12 weeks. The SVR rates with DAAs ranged from 87% to 100%. Genotypes 1 and 4 had higher SVR rates (96.3-100%), and genotypes 2 and 3 had SVR of 90.6-92.2%, respectively. Treatment durations of 12 and 24 weeks were associated with an average SVR of 95.0% and 95.9%, respectively. Females were half as likely (OR 0.5; 95% CI 0.4-0.6) to have a negative response to therapy compared to males, and those with genotypes 2 and 3 were one and half fold more likely (OR 1.5-2.2; 95 CI% 0.7-2.9; 1.2-3.6 and OR 2.7-2.8; 95% CI 2.0-3.8, respectively) to not have SVR compared to genotype 1. Patients in the age-range of 50-69 years old were 1.2-fold (OR 1.2; 95% CI 0.7-1.9) more likely to not have SVR compared to other age groups, although not statistically significant. This study is the first of this magnitude to be held in a Latin-American country with high SVR results, supported by a free-of-charge universal and public health system. The high performance found in this study gives support to the Brazilian public health policy decision of adopting DAA-based therapies as a strategy to eliminate HCV by 2030.

Indexed as

Hepatitis CHepatitis C, ChronicAgedAntiviral AgentsBrazilDrug Therapy, CombinationFemaleGenotypeHepacivirusHumansMaleMiddle AgedRetrospective StudiesRibavirinTreatment OutcomeAntiviral AgentsRibavirinDirect-acting antiviralsHealth policyHepatitis CTreatment

Identifiers

PMID33836175
PMCPMC9392166
OpenAlexW3152484171

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.