Marisa Santos

Marisa Santos

orcid

Research Focus & Metrics

Academic Career Length

28Years (1999-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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22 October 2015 in Medical Decision Making
Verified
Journal Article
Closed access
MSMarisa Santos
Marisa Santos
MCMonica A. C. T. Cintra
Monica A. C. T. Cintra
AMAndrea L. Monteiro
Andrea L. Monteiro
BSBraulio Santos
Braulio Santos
FGFernando Gusmão-Filho
Fernando Gusmão-Filho
PKPaul Kind
Paul Kind
Background. Most EQ-5D-3L valuation studies include the same sample of health states that was used in the protocol of the original UK Measurement and Valuation of Health (MVH) study. Thus far, no studies using a time tradeoff utility elicitation method have been carried out using all 243 EQ-5D health states. Because the values and preferences regarding health outcomes differ among countries, it is essential to have country-specific data to enable local high-level decisions regarding resource allocation. This study developed a country-specific set of values for EQ-5D-3L health states. Methods. A multicentric study was conducted in 4 Brazilian areas. A probabilistic sample of the general population, aged 18 to 64 y, stratified by age and gender, was surveyed. The interview followed a revised version of the MVH protocol, in which all 243 health states were valued. Each respondent ranked and valued 7 health states using the TTO in a home interview. Results. Data were collected from 9148 subjects. The best-fitting regression model was an individual-level mixed-effects model without any interaction terms. The dimensions “Mobility” and “Usual Activities” were associated with higher losses in health state utility value. The “Anxiety/Depression” dimension was the domain that contributed to lower losses in health state utility value. Conclusions. This study generated significant insight into the Brazilian population’s health preferences that can be applied to health technology assessment and economic analyses in Brazil. This information represents an important new tool that can be used in Brazilian health policy creation and evaluation.

10 June 2021 in Health and Quality of Life Outcomes
Verified
Journal Article
Open access
PDF file
MSMarisa Santos
Marisa Santos
AMAndrea L. Monteiro
Andrea L. Monteiro
BSBráulio Santos
Bráulio Santos
Background: The EQ-5D-3L is a widely used generic health-related quality of life measure commonly applied to describe health outcomes and to measure disease burden. The aim of this study was to generate Brazilian population norms, stratified by age and gender, based on Brazilian preference weights for EQ-5D-3L.Methods: A multicenter cross-sectional study was conducted in three Brazilian urban areas. The final sample consisted of 5774 respondents, aged from 18 to 64 years. Amongst other information, respondents were asked to self-report their health status using the EQ-5D-3L descriptive system and visual analog scale (EQ-VAS). Data on socio-demographic characteristics was obtained through specific questionnaires. The Brazilian TTO scoring algorithm was used to derive the utility values. Multivariate logistic regression models were fitted to analyze the influence of age, sex, education status and sample site on the presence of any problem for each dimension of EQ5D.Results: Mean values were computed for both weighted index scores and self-rated health status (EQ-VAS), and stratified by gender and age groups. Health status declines with age, ranging between 0.87 for the youngest group 18–29 year-olds and 0.76 for 60–64-year-old. Men reported higher scores (0.85) than the woman (0.79). Lower education levels were associated with lower EQ-5D index score in most age groups.Conclusion: This study provides EQ-5D reference values for the Brazilian population. These values can be used by local decision-makers and researchers in economic evaluations and population health studies.

28 August 2019 in BMC Infectious Diseases
Verified
Journal Article
Open access
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LSLucia Teresa Côrtes da Silveira
Lucia Teresa Côrtes da Silveira
BTBernardo Tura
Bernardo Tura
MSMarisa Santos
Marisa Santos
Dengue is an arbovirus that has rapidly spread worldwide, and the incidence of dengue has greatly increased in recent decades. The actual numbers of dengue cases are underreported, and many cases are not classified correctly. Recent estimates indicate that 390 million dengue infections occur per year (95% CI, 284–528 million), of which 96 million (67–136 million) are symptomatic infections of any severity. One of the goals of the World Health Organization is to reduce dengue mortality by 50% by the year 2020. The use of a vaccine can be an important strategy to achieve this goal. Vaccines for dengue are in various stages of development; in Brazil, only one commercial formulation is available (CYD-TDV), which was developed by Sanofi Pasteur. To evaluate the efficacy of Dengue vaccine, a systematic review with a meta-analysis was conducted using randomized controlled clinical trials published between 2000 and 2017 that were identified in the MEDLINE databases via PubMed, LILACS, Cochrane Library, and EMBASE. The selection was performed by two reviewers independently, with disagreements resolved by a third reviewer. Seven clinical trials were included, with a total of 36,371 participants (66,511 person-years) between the ages of 2 and 45 years. The meta-analysis using the random-effects model estimated the efficacy of the vaccine at 44%, with a range from 25 to 59% and high heterogeneity (I2 = 80.1%). The serotype-stratified meta-analysis was homogeneous, except for serotype 2, with the heterogeneity of 64.5%. Most of the vaccinated individuals had previous immunity for at least one serotype, which generated safety concerns in individuals without previous immunity. Compared with other commercially available vaccines, the dengue vaccine showed poor efficacy.

11 July 2014 in Journal of Medical Virology
Verified
Journal Article
Closed access
PDF file
AGAna Carolina Ganime
Ana Carolina Ganime
FCFilipe A. Carvalho-Costa
Filipe A. Carvalho-Costa
MSMarisa Santos
Marisa Santos
RFRubens Costa Filho
Rubens Costa Filho
JLJosé Paulo G. Leite
José Paulo G. Leite
MMMarize P. Miagostovich
Marize P. Miagostovich

21 March 2022 in Value in Health Regional Issues
Verified
Journal Article
Closed access
RFRicardo Fernandes
Ricardo Fernandes
MSMarisa Santos
Marisa Santos
CMCarlos Alberto Da Silva Magliano
Carlos Alberto Da Silva Magliano
BTBernardo Rangel Tura
Bernardo Rangel Tura
LMLuana Schroeder Damico Nascimento Macedo
Luana Schroeder Damico Nascimento Macedo
ABAndressa Araujo Braga
Andressa Araujo Braga

14 November 2017 in PharmacoEconomics
Verified
Journal Article
Open access
PDF file
LLLivia Lemos
Livia Lemos
AJAugusto Afonso Guerra Junior
Augusto Afonso Guerra Junior
MSMarisa Santos
Marisa Santos
CMCarlos Alberto Da Silva Magliano
Carlos Alberto Da Silva Magliano
IDIsabela Diniz
Isabela Diniz
FAFrancisco de Assis Acurcio
Francisco de Assis Acurcio
In Brazil, inclusion and exclusion of health technologies within the Unified Health System (SUS) is the responsibility of the National Committee for Health Technology Incorporation (CONITEC). A recent Cochrane systematic review demonstrated that intramuscular interferon beta 1a (IFN-β-1a-IM) was inferior to the other beta interferons (IFN-βs) for multiple sclerosis (MS). As a result, CONITEC commissioned an analysis to review possible disinvestment within SUS. The objective of this paper is to describe the disinvestment process for IFN-β-1a-IM in Brazil. The first assessment comprised a literature review and mixed treatment comparison meta-analysis. The outcome of interest was the proportion of relapse-free patients in 2 years. This analysis confirmed the inferiority of IFN-β-1a-IM. Following this, CONITEC recommended disinvestment, with the decision sent for public consultation. More than 3000 contributions were made on CONITEC’s webpage, most of them against the preliminary decision. As a result, CONITEC commissioned a study to assess the effectiveness of IFN-β-1a-IM among Brazilian patients in routine clinical care. The second assessment involved an 11-year follow-up of a non-concurrent cohort of 12,154 MS patients developed by deterministic-probabilistic linkage of SUS administrative databases. The real-world assessment further demonstrated that IFN-β-1a-IM users had a statistically higher risk of treatment failure, defined as treatment switching or relapse treatment or death, with the assessment showing that IFN-β-1a-IM was inferior to the other IFN-βs and to glatiramer acetate in both direct and indirect analysis. In the drug ranking with 40,000 simulations, IFN-β-1a-IM was the worst option, with a success rate of only 152/40,000. Following this, CONITEC decided to exclude the intramuscular presentation of IFN-β from the current MS treatment guidelines, giving patients who are currently on this treatment the option of continuing until treatment failure. In conclusion, we believe this is the first example of this new disinvestment process in action, providing an exemplar for other treatments in Brazil as well as other countries.