"It is what I tell her that she will do": a mixed methods study of married men's knowledge and attitude towards supporting their wives' cervical cancer screening in rural South-East Nigeria.

INTRODUCTION: cervical cancer is a leading cause of death among Nigerian women. Women often require spousal support before attending cervical cancer screening services. This study assessed married men´s knowledge and attitude towards male involvement in cervical cancer screening of their wives. METHODS: a cross-sectional study using a mixed methods approach was conducted among 245 married men in Izzi, Local Government Area of Ebonyi State, South-East Nigeria. Quantitative data collected using structured, interviewer-administered questionnaires and qualitative data from focus group discussions were triangulated. Data analysis was done using IBM SPSS version 20. Qualitative findings were analysed using thematic analysis. RESULTS: the mean knowledge of cervical cancer was 2.06±0.55. Only 2.9% of the respondents had adequate knowledge of risk factors for cervical cancer. Up to 89.8% were willing to approve screening for their spouses. Majority (76.3%) considered screening important in cervical cancer prevention, while 91.4% were willing to pay for the screening test. Most of them exhibited patriarchal tendencies and insisted that their wives must obtain their consent before screening as depicted by the statement "It is what I tell her that she will do". Previous spousal screening was a predictor of good knowledge (OR = 10.94, 95% CI = 2.44-48.93; P=0.002). CONCLUSION: married men in this study had poor knowledge of cervical cancer. However, they were willing to support cervical cancer screening conditional on their pre-information and consent. Awareness creation activities on cervical cancer screening should incorporate active engagement of husbands in order to promote screening uptake by their wives.

Factors associated with organ donation by trauma patients in Nova Scotia.

BACKGROUND: Trauma patients represent a significant pool of potential organ donors (PODs), and previous research suggests that this population is underutilized for organ donation (OD). Our objective was to assess factors associated with OD in the trauma population. METHODS: We retrospectively analyzed OD in Nova Scotia over a 7-year period (2009-2016) using data from the Nova Scotia Trauma Registry and Nova Scotia Legacy of Life Donor Registry. All trauma patients who died in the hospital were included. Multiple logistic regression was used to assess factors associated with donation. We also evaluated characteristics, donation types, and reasons for nondonation among trauma PODs. RESULTS: There were 689 trauma-related deaths in all hospitals in NS during the study period, of which 39.8% (274 of 689) met the Nova Scotia Trauma Registry definition of a POD. Data on OD were available for 108 of these patients who were referred to the Legacy of Life Program. The conversion rate was 84%. Compared with nondonors, organ donors were significantly younger, had a higher Abbreviated Injury Scale head score and a lower scene Glasgow Coma Scale score, were more likely to suffer ischemia from drowning or asphyxia and to require air transport, and were less likely to have comorbidities. Regression analysis showed that donation was associated with younger age (odds ratio [OR], 0.97; 95% confidence interval [CI], 0.95-0.99) and lower Glasgow Coma Scale score at the scene (OR, 0.76; 95% CI, 0.66-0.88). Odds of donation were increased with air transport compared with land ambulance (OR, 8.27; 95% CI, 2.07-33.08) and injury within Halifax Regional Municipality compared with injury outside Halifax Regional Municipality (OR, 4.64; 95% CI, 1.42-15.10). Among the 60 referred PODs who did not donate, family refusal of consent was the most common reason (28 [46.7%] of 60). CONCLUSION: Younger age, greater severity of injury, and shorter time to tertiary care were associated with OD in trauma patients. LEVEL OF EVIDENCE: Prognostic and Epidemiological, Level III.

Voluntary participation and comprehension of informed consent in a genetic epidemiological study of breast cancer in Nigeria.

BACKGROUND: Studies on informed consent to medical research conducted in low or middle-income settings have increased, including empirical investigations of consent to genetic research. We investigated voluntary participation and comprehension of informed consent among women involved in a genetic epidemiological study on breast cancer in an urban setting of Nigeria comparing women in the case and control groups. METHODS: Surveys were administered in face-to-face interviews with 215 participants following their enrollment in the genetic study (106 patients, 109 controls). Audio-taped in-depth interviews were conducted with a sub-sample of 17 (8%) women who completed the survey. RESULTS: The majority of all participants reported being told that participation in the genetic study was voluntary (97%), that they did not feel pressured to participate in the study (99%), and that they could withdraw from the study (81%). The majority of the breast cancer patients (83%) compared to 58% of women in the control group reported that the study purpose was to learn about the genetic inheritance of breast cancer (OR 3.44; 95% CI =1.66, 7.14, p value = 0.001). Most participants reported being told about study procedures (95%) and study benefits (98%). Sixty-eight percent of the patients, compared to 47% of the control group reported being told about study risks (p-value <0.001). Of the 165 married women, 19% reported asking permission from their husbands to enroll in the breast cancer study; no one sought permission from local elders. In-depth interviews highlight the use of persuasion and negotiation between a wife and her husband regarding study participation. CONCLUSIONS: The global expansion of genetic and genomic research highlights our need to understand informed consent practices for studies in ethnically diverse cultural environments such as Africa. Quantitative and qualitative empirical investigations of the informed consent process for genetic and genomic research will further our knowledge of complex issues associated with communication of information, comprehension, decisional authority and voluntary participation. In the future, the development and testing of innovative strategies to promote voluntary participation and comprehension of the goals of genomic research will contribute to our understanding of strategies that enhance the consent process.

Comparative analysis of family consent to tissue donation according to two different donation form structures / Análise comparativa do consentimento familiar para doação de tecidos em função da mudança estrutural do termo de doação

Objective To define donors’ profile of an Organ and Tissue Procurement Center and compare the family consent for tissue donation before and after modification of the Donation Term. Methods A descriptive, documentary and quantitative study performed in an Organ and Tissue Procurement Center, analyzed 111 feasible donors’ charts in the period from March 13 to September 13, 2010 (1st period), and from September 14, 2010 to March 14, 2011 (2nd period), based on the modification date. Results The mean age of donors was 45.2 years, being 52.3% female. The causes of death included cerebral vascular accident (stroke) (64%), head trauma (27%), anoxic encephalopathy (2.7%), firearm injuries (2.7%) and others (3.6%). The notifications were predominantly of spontaneous origin (91%). Comparing the periods before and after the modification of the Donation Term, the donation consent for cornea increased by 17.2% and the consent for skin, bones, tendons and muscles had a discreet increase by 3.1%, 9.9% and 0.4%, respectively. On the other hand, there was decrease in consent for blood vessel (0.8%) and heart valves (4.1%) between the two periods. Conclusion There was increase in family consent for donation of most tissues, but it was statistically significant only for cornea donation. .

Objetivo Traçar o perfil dos doadores viabilizados por um Serviço de Procura de Órgãos e Tecidos e comparar o consentimento familiar para doação de tecidos antes e após esta modificação do Termo de Doação. Método Estudo descritivo, documental, quantitativo, realizado em um Serviço de Procura de Órgãos e Tecidos, analisou 111 prontuários de doadores viabilizados nos períodos de 13 de março a 13 de setembro de 2010 (1o Período) e de 14 de Setembro de 2010 a 14 de Março de 2011 (2o período), selecionados com base na data desta modificação. Resultado Foi encontrada média de idade de 45,2 anos entre os doadores, sendo 52,3% do sexo feminino. As causas de morte incluem acidente vascular encefálico (64%), traumatismos cranioencefálicos (27%), encefalopatias anóxicas (2,7%), ferimentos por arma de fogo (2,7%) e outras (3,6%). As notificações foram predominantemente de origem espontânea (91%). Comparando os períodos antes e após a modificação do Termo de Doação, o consentimento para doação de córneas apresentou aumento de 17,2% e para doação de pele, ossos, tendões e músculos, discreto aumento de 3,1%, 9,9% e 0,4% respectivamente. Por sua vez, apresentou discreta diminuição o consentimento de vasos sanguíneos, de 0,8%, e valvas cardíacas de 4,1%, entre os períodos. Conclusão Obteve-se um aumento do consentimento familiar para a doação da maioria dos tecidos, porém com significância estatística apenas para doação de córneas. .

[Consent to smoking in public places and at home the opinions of smokers and nonsmokers girls]. / Zgoda na palenie tytoniu w miejscach publicznych i w domu w opiniach dziewczat palacych i niepalacych.

The aim of this study was researching of dependence between current status of smoking and opinions about smoking tobacco in public places and at home of girls at the age 18. We examined 2246 girls who graduated junior high schools and were continuing their education in four types of schools: high schools, profiled high schools, technical secondary schools and vocational schools. Two-stage sampling method was used, with the team stratification by type of school. The study was conducted in November and December 2008, the auditorium method. The results show that although more than half of the girls, do not agree with smoking in various public places and by parents at home, about one quarter of them accept smoking in cafes, restaurants, pubs and bus stops, and less than 1/5 have no opinion on the subject. Applied analysis using logistic regression analysis indicate a close relationship between smoking trials undertaken by the girls examined, and their opinion about the approval for smoking by students at the school. The model attempts to smoking was a significant predictor of acceptance of smoking in cafes and pubs, and the model of the current consensus on tobacco smoking at bus stops. The presented results indicate the need for prevention activities among children and adolescents, which will contribute to the education of attitudes and skills necessary to take measures aimed at creating environments free from tobacco smoke.

Do participation rates change when active consent procedures replace passive consent.

Researchers face considerable ambiguity and controversy regarding the issue of informed consent. Decisions about consent procedures can affect study participation rates and prevalence estimates among specific populations. Changing from passive to active parental consent procedures was examined in a case study with an anonymous survey of sixth- through eighth-grade students' substance use. Four types of procedures for obtaining parental consent were examined. Results suggest that certain types of consent procedures can yield high levels of participation. This study also demonstrates that low participation rates with some active consent procedures can cause biases in sample characteristics and outcome data.

Experiencia del manejo de potenciales donantes cadáver en una UCI polivalente / Experience in the management of cadaver donors in an intensive care unit

Estudiamos a los pacientes que ingresaron con diagnóstico de muerte encéfalica a nuestra unidad entre 9/95 y 12/99: 24 pacientes, 18 varones (75 por ciento) y 6 mujeres (25 por ciento), con una mediana de edad de 33,5 años. El equipo de procuración de órganos no estaba involucrado en las decisiones terapéuticas. El diagnóstico de muerte encefálica fue certificado por un neurólogo ajeno a la procuración ante la ausencia persistente de funciones cerebrales por una etiología bien definida, descartando hipotermia, intoxicación por drogas, encefalopatía metabólica y shock. Las causas de muerte cerebral fueron: accidentes en 14 (10 del tránsito), 5 violencia, 3 accidente cerebro-vascular (ACV) y 2 trauma de cráneo (TEC) por mecanismo ignorado. Se logró la donación en 14 pacientes (58,3 por ciento), ambos riñones en todos y sólo en la mitad, otros órganos. Todos necesitaron ventilación mecánica y reanimación con volumen, 22 drogas vasoactivas y 6 transfusiones. Complicaciones fueron: hipotensión en poliuria en 19, 22, trastornos electrolíticos en 12, hipotermia en 11, oliguria en 7 y sangrado en 1. Concluimos que el porcentaje de potenciales donantes (PD) en los que se concretó la donación es similar a lo descrito en la literatura y el 16,6 por ciento de rechazo por familiares resulta inferior a lo descrito. Consideramos que este alto grado de consentimiento está influenciado por un sistema de procuración organizado y un equipo experimentado; soporte de PD con daño neurológico severo es una actividad que consume tiempo y recursos en una UCI, los que deberían considerarse en los programas de trasplante, y el número total de trasplantes podría incrementarse con la procuración de múltiples órganos de un mismo donante