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1.
Health Secur ; 20(2): 147-153, 2022.
Article in English | MEDLINE | ID: mdl-35404146

ABSTRACT

Timely access to emergency funding has been identified as a bottleneck for outbreak response in Nigeria. In February 2019, a new revolving outbreak investigation fund (ROIF) was established by the Nigeria Centre for Disease Control (NCDC). We abstracted the date of NCDC notification, date of verification, and date of response for 25 events that occurred prior to establishing the fund (April 2017 to August 2019) and for 8 events that occurred after establishing the fund (February to October 2019). The median time to notification (1 day) and to verification (0 days) did not change after establishing the ROIF, but the median time to response significantly decreased, from 6 days to 2 days (P = .003). Response to disease outbreaks was accelerated by access to emergency funding with a clear approval process. We recommend that the ROIF should be financed by the national government through budget allocation. Finally, development partners can provide financial support for the existing fund and technical assistance for protocol development toward financial accountability and sustainability.


Subject(s)
Financial Management , Public Health , Disease Outbreaks/prevention & control , Emergencies , Humans , Nigeria/epidemiology
2.
BMC Public Health ; 22(1): 551, 2022 03 21.
Article in English | MEDLINE | ID: mdl-35313834

ABSTRACT

BACKGROUND: Health workers (HWs) in Africa face challenges accessing and learning from existing online training opportunities. To address these challenges, we developed a modular, self-paced, mobile-ready and work-relevant online course covering foundational infection prevention and control (IPC) concepts. Here, we evaluate the first pilot of this course, conducted with HWs in Nigeria. METHODS: We used a learner-centered design and prototyping process to create a new approach to delivering online training for HWs. The resulting course comprised 10 self-paced modules optimized for use on mobile devices. Modules presented IPC vignettes in which learning was driven by short assessment questions with feedback. Learners were recruited by distributing a link to the training through Nigeria-based email lists, WhatsApp groups and similar networks of HWs, managers and allied professionals. The course was open to learners for 8 weeks. We tracked question responses and time on task with platform analytics and assessed learning gains with pre- and post-testing. Significance was evaluated with the Wilcoxon signed-rank test, and effect size was calculated using Cohen's d. RESULTS: Three hundred seventy-two learners, with roles across the health system, enrolled in the training; 59% completed all 10 modules and earned a certificate. Baseline knowledge of foundational IPC concepts was low, as measured by pre-test scores (29%). Post-test scores were significantly higher at 54% (effect size 1.22, 95% confidence interval 1.00-1.44). Learning gains were significant both among learners with low pre-test scores and among those who scored higher on the pre-test. We used the Net Promoter Score (NPS), a common user experience metric, to evaluate the training. The NPS was + 62, which is slightly higher than published scores of other self-paced online learning experiences. CONCLUSIONS: High completion rates, significant learning gains and positive feedback indicate that self-paced, mobile-ready training that emphasizes short, low-stakes assessment questions can be an effective, scalable way to train HWs who choose to enroll. Low pre-test scores suggest that there are gaps in IPC knowledge among this learner population.


Subject(s)
Education, Distance , Health Personnel , Health Personnel/education , Health Workforce , Humans , Infection Control , Nigeria
3.
Blood Press Monit ; 27(1): 27-32, 2022 Feb 01.
Article in English | MEDLINE | ID: mdl-34992204

ABSTRACT

OBJECTIVE: Assessing the state of hypertension care remains the first step towards planning a robust health system needed to tackle the rising burden of hypertension. Prior to the commencement of the Community Action Against Non-Communicable Disease project, we assessed hypertension care using the hypertension care cascade (HCC). This will serve as a baseline to evaluate project performance upon completion. METHODS: Hypertensive subjects were grouped into a mutually exclusive care cascade of 5 categories including unscreened and undiagnosed; screened but undiagnosed; diagnosed but untreated; treated but uncontrolled and treated with controlled hypertension. RESULTS: Of the 372 participants, mean age 48.9 years, 161 (43.3%) were hypertensive, of whom only 12.0% had controlled blood pressure (BP). Among the 88.0% with uncontrolled BP,19.0% were unscreened and undiagnosed, 48.5% were screened but undiagnosed, 13.0% were diagnosed but untreated and 7.5% were treated but BP uncontrolled. The HCC demonstrates that 19% of the hypertensive patients were lost at the screening stage, 60% of those who were screened never diagnosed, 40% of those who were diagnosed did not receive treatment and 60% of those who were on treatment did not reach target BP. CONCLUSION: Unmet need of hypertension care is substantially high, thus underpinning the need for intervention with a multifaceted approach.


Subject(s)
Hypertension , Noncommunicable Diseases , Blood Pressure , Community Participation , Humans , Hypertension/diagnosis , Hypertension/epidemiology , Hypertension/therapy , Middle Aged , Nigeria , Noncommunicable Diseases/epidemiology , Noncommunicable Diseases/therapy
4.
BMJ Glob Health ; 6(6)2021 06.
Article in English | MEDLINE | ID: mdl-34083244

ABSTRACT

Healthcare workers (HCWs) are at increased risk of infection from SARS-CoV-2 and other disease pathogens, which take a disproportionate toll on HCWs, with substantial cost to health systems. Improved infection prevention and control (IPC) programmes can protect HCWs, especially in resource-limited settings where the health workforce is scarcest, and ensure patient safety and continuity of essential health services. In response to the COVID-19 pandemic, we collaborated with ministries of health and development partners to implement an emergency initiative for HCWs at the primary health facility level in 22 African countries. Between April 2020 and January 2021, the initiative trained 42 058 front-line HCWs from 8444 health facilities, supported longitudinal supervision and monitoring visits guided by a standardised monitoring tool, and provided resources including personal protective equipment (PPE). We documented significant short-term improvements in IPC performance, but gaps remain. Suspected HCW infections peaked at 41.5% among HCWs screened at monitored facilities in July 2020 during the first wave of the pandemic in Africa. Disease-specific emergency responses are not the optimal approach. Comprehensive, sustainable IPC programmes are needed. IPC needs to be incorporated into all HCW training programmes and combined with supportive supervision and mentorship. Strengthened data systems on IPC are needed to guide improvements at the health facility level and to inform policy development at the national level, along with investments in infrastructure and sustainable supplies of PPE. Multimodal strategies to improve IPC are critical to make health facilities safer and to protect HCWs and the communities they serve.


Subject(s)
COVID-19 , Health Personnel , Infectious Disease Transmission, Patient-to-Professional , Pandemics , Primary Health Care , Africa/epidemiology , COVID-19/epidemiology , COVID-19/prevention & control , COVID-19/transmission , Humans , Infectious Disease Transmission, Patient-to-Professional/prevention & control , Primary Health Care/organization & administration
5.
Ann Afr Med ; 20(1): 9-13, 2021.
Article in English | MEDLINE | ID: mdl-33727505

ABSTRACT

Background: The prevalence of obesity has risen to over 650 million adults in 2016, and accounts for 41 million deaths globally. It is a major contributor to the burden of noncommunicable diseases. We determined the prevalence and associated factors of obesity to inform policy decisions toward developing robust prevention and management strategies. Materials and Methods: We conducted a population-based cross-sectional study in July 2017 among 1265 adults in urban and rural communities in Benue State. We used multistage sampling technique in selecting the participants. The WHO standardized and validated tool were used to collect information on sociodemographic and anthropometric measurements. We calculated age standardized prevalence of obesity and determined factors associated with obesity using logistic regression at 5% level of significance. Results: The age standardized prevalence of obesity was 11.1% (rural 4.2%, urban 14.3%). The odds for obesity was higher among females (adjusted odds ratio [aOR]: 3.4; 95% confidence interval [CI]: 2.27-4.99), those with tertiary education (aOR: 3.3; 95% CI: 1.61-6.95), married (aOR: 2.1; 95% CI: 1.37-3.36), and those residing in urban areas (aOR: 3.0; 95% CI: 1.73-5.05) compared to rural dwellers. Conclusions: The prevalence of obesity was high among adults in Benue State. It is more prevalent among females, married, educated, and urban dwellers. Interventions targeted at healthy lifestyle choices should be directed at these populations for effective control.


RésuméContexte: La prévalence de l'obésité est passée à plus de 650 millions d'adultes en 2016 et représente 41 millions de décès dans le monde. C'est un majeur contribuant au fardeau des maladies non transmissibles. Nous avons déterminé la prévalence et les facteurs associés de l'obésité pour éclairer les décisions politiques vers l'élaboration de stratégies solides de prévention et de gestion. Matériel et méthodes: Nous avons réalisé une analyse transversale basée sur la population étude réalisée en juillet 2017 auprès de 1265 adultes des communautés urbaines et rurales de l'État de Benue. Nous avons utilisé une technique d'échantillonnage à plusieurs degrés pour sélectionner les participants. L'outil normalisé et validé de l'OMS a été utilisé pour collecter des informations sur les mesures sociodémographiques et anthropométriques. Nous avons calculé la prévalence standardisée selon l'âge de l'obésité et déterminé les facteurs associés à l'obésité en utilisant une régression logistique à un niveau de 5% de importance. Résultats: La prévalence de l'obésité normalisée selon l'âge était de 11,1% (rurale 4,2%, urbaine 14,3%). Les probabilités d'obésité étaient plus élevées chez femmes (rapport de cotes ajusté [aOR]: 3,4; intervalle de confiance à 95% [IC]: 2,27­4,99), celles ayant fait des études supérieures (aOR: 3,3; IC à 95%: 1,61­6,95), mariés (aOR: 2,1; IC à 95%: 1,37­3,36) et ceux résidant dans les zones urbaines (aOR: 3,0; IC à 95%: 1,73­5,05) par rapport aux habitants des zones rurales. Conclusions: La prévalence de l'obésité était élevée chez les adultes de l'État de Benue. Il est plus répandu chez les femmes mariées, instruites et citadins. Les interventions ciblées sur les choix de modes de vie sains devraient être dirigées vers ces populations pour un contrôle efficace.


Subject(s)
Obesity/epidemiology , Population Surveillance/methods , Residence Characteristics/statistics & numerical data , Adolescent , Adult , Age Distribution , Aged , Body Mass Index , Cross-Sectional Studies , Female , Humans , Male , Middle Aged , Nigeria/epidemiology , Prevalence , Rural Population , Sex Distribution , Socioeconomic Factors , Urban Population , Young Adult
6.
HIV Clin Trials ; 19(6): 209-224, 2018 12.
Article in English | MEDLINE | ID: mdl-30890061

ABSTRACT

BACKGROUND: IMPAACT PROMISE 1077BF/FF was a randomized study of antiretroviral therapy (ART) strategies for pregnant and postpartum women with high CD4+ T-cell counts. We describe postpartum outcomes for women in the study who were randomized to continue or discontinue ART after delivery. METHODS: Women with pre-ART CD4+ cell counts ≥350 cells/mm3 who started ART during pregnancy were randomized postpartum to continue or discontinue treatment. Women were enrolled from India, Malawi, South Africa, Tanzania, Uganda, Zambia, and Zimbabwe. The primary outcome was a composite of progression to AIDS-defining illness or death. Log-rank tests and Cox regression models assessed treatment effects. Incidence rates were calculated per 100 person-years. A post hoc analysis evaluated WHO Stage 2/3 events. All analyses were intent-to-treat. FINDINGS: 1611 women were enrolled (June 2011-October 2014) and 95% were breastfeeding. Median age at entry was 27 years, CD4+ count 728 cells/mm3 and the majority of women were Black African (97%). After a median follow-up of 1.6 years, progression to AIDS-defining illness or death was rare and there was no significant difference between arms (HR: 0·55; 95%CI 0·14, 2·08, p = 0.37). WHO Stage 2/3 events were reduced with continued ART (HR: 0·60; 95%CI 0·39, 0·90, p = 0.01). The arms did not differ with respect to the rate of grade 2, 3, or 4 safety events (p = 0.61). INTERPRETATION: Serious clinical events were rare among predominately breastfeeding women with high CD4+ cell counts over 18 months after delivery. ART had significant benefit in reducing WHO 2/3 events in this population.


Subject(s)
Anti-HIV Agents/therapeutic use , Antiretroviral Therapy, Highly Active , HIV Infections/drug therapy , Maternal Health , Adult , Breast Feeding , CD4 Lymphocyte Count , Disease Progression , Female , HIV Infections/virology , Humans , Postpartum Period , Pregnancy , Treatment Outcome , Young Adult
7.
J Acquir Immune Defic Syndr ; 67(5): 573-5, 2014 Dec 15.
Article in English | MEDLINE | ID: mdl-25247435

ABSTRACT

Recent human studies support historical animal studies that suggested an association between peripheral blood monocyte:lymphocyte (ML) ratio and tuberculosis (TB) disease. To evaluate generalizability of this finding, we modeled the association between peripartum ML ratio and incident TB disease within 18 months postpartum among 1202 HIV-infected women in South Africa, Tanzania, Uganda, and Zimbabwe. The ML ratio was associated with increased risk of TB disease independently to combination antiretroviral therapy, World Health Organization stage, or CD4 count (adjusted hazard ratio = 1.22, 95% confidence interval: 1.07 to 1.4, P = 0.003 per 0.1 unit increase in ML ratio).


Subject(s)
HIV Infections/complications , HIV Infections/immunology , Lymphocytes/immunology , Monocytes/immunology , Postpartum Period , Tuberculosis/epidemiology , Tuberculosis/immunology , Adult , Africa/epidemiology , Animals , Female , Humans , Leukocyte Count , Pregnancy , Risk Assessment , Young Adult
8.
AIDS ; 26(3): 325-33, 2012 Jan 28.
Article in English | MEDLINE | ID: mdl-22112598

ABSTRACT

OBJECTIVE: Nevirapine and cotrimoxazole are associated with hematologic toxicities and skin-rash. Safety of their concurrent use for prophylaxis over extended periods among HIV-exposed uninfected infants has not been previously assessed. DESIGN: Secondary data analysis of the 'HIV Prevention Trials Network-046 protocol' (version 2.0), a phase-III, randomized, placebo-controlled trial that assessed efficacy and safety of nevirapine prophylaxis against breast milk transmission of HIV-1. METHODS: Trial infants received 6-month study nevirapine/placebo, and standard-of-care peripartum single-dose nevirapine+/- zidovudine 'tail', and cotrimoxazole prophylaxis from 6 weeks through breastfeeding cessation. Adverse events were monitored using United States Division of AIDS Toxicity Tables (2004). Risk of neutropenia, anemia and skin-rash in the cotrimoxazole + nevirapine and the cotrimoxazole + placebo groups were compared using negative-binomial regression. RESULTS: Incidence of neutropenia and/or anemia, and skin-rash was highest during the first 6 weeks of life and declined, thereafter, regardless of study group. Time to first adverse event after 6 weeks was similar in cotrimoxazole + nevirapine and cotrimoxazole + placebo groups: hazard ratio (95% confidence interval) was 1.26 (0.96-1.66) for neutropenia and/or anemia (all grades), 1.27 (0.80-2.03) for neutropenia and/or anemia (grade ≥3) and 1.16 (0.46-2.90) for skin-rash (grade ≥2). There were no statistically significant differences in immediate (6 weeks-6 months) and long-term (6-12 months) adverse event risk among infants on cotrimoxazole + nevirapine versus cotrimoxazole + placebo. CONCLUSION: Extended nevirapine and cotrimoxazole prophylaxis through 6 months of age among HIV-exposed uninfected infants did not appear to increase the immediate or long-term risk of neutropenia, anemia or skin-rash. Concurrent use beyond 6 months, however, needs to be evaluated.


Subject(s)
Anemia/chemically induced , Anti-HIV Agents/administration & dosage , Exanthema/chemically induced , HIV Seropositivity/drug therapy , HIV-1/drug effects , Infectious Disease Transmission, Vertical/prevention & control , Neutropenia/chemically induced , Nevirapine/administration & dosage , Trimethoprim, Sulfamethoxazole Drug Combination/administration & dosage , Adult , Anti-HIV Agents/adverse effects , Blotting, Western , Breast Feeding/adverse effects , Drug Administration Schedule , Drug Eruptions/etiology , Female , HIV Seropositivity/epidemiology , HIV Seropositivity/transmission , Humans , Infant , Infant, Newborn , Male , Milk, Human/virology , Nevirapine/adverse effects , Pregnancy , Risk Factors , Time Factors , Treatment Outcome , Trimethoprim, Sulfamethoxazole Drug Combination/adverse effects , Uganda/epidemiology
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