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1.
Epidemiol Infect ; 151: e114, 2023 06 20.
Article in English | MEDLINE | ID: mdl-37337304

ABSTRACT

Although Africa is home to about 14% of the global population (1.14 billion people), it is growing three times faster than the global average [1]. The continent carries a high burden of disease, but there has been real progress in eradication, elimination, and control since 2015. Examples are the eradication of wild polio in 2020 [2] and the eradication or elimination of neglected tropical diseases, such as dracunculiasis in Kenya in 2018; Human African trypanosomiasis in Togo in 2022; and trachoma in Togo, Gambia, Ghana, and Malawi in 2022 [3]. New HIV infections reduced by 44% in 2021 compared to 2010 [4], and in 2021 the African region passed the 2020 milestone of the End TB Strategy, with a 22% reduction in new infections compared with 2015 [5].


Subject(s)
Dracunculiasis , HIV Infections , Poliomyelitis , Humans , HIV Infections/epidemiology , HIV Infections/prevention & control , Dracunculiasis/epidemiology , Ghana/epidemiology , Poliomyelitis/epidemiology , Poliomyelitis/prevention & control , Cost of Illness , Disease Eradication
2.
Emerg Infect Dis ; 25(2): 249-255, 2019 02.
Article in English | MEDLINE | ID: mdl-30500321

ABSTRACT

Ebola virus (EBOV) can persist in immunologically protected body sites in survivors of Ebola virus disease, creating the potential to initiate new chains of transmission. From the outbreak in West Africa during 2014-2016, we identified 13 possible events of viral persistence-derived transmission of EBOV (VPDTe) and applied predefined criteria to classify transmission events based on the strength of evidence for VPDTe and source and route of transmission. For 8 events, a recipient case was identified; possible source cases were identified for 5 of these 8. For 5 events, a recipient case or chain of transmission could not be confidently determined. Five events met our criteria for sexual transmission (male-to-female). One VPDTe event led to at least 4 generations of cases; transmission was limited after the other events. VPDTe has increased the importance of Ebola survivor services and sustained surveillance and response capacity in regions with previously widespread transmission.


Subject(s)
Disease Outbreaks , Ebolavirus , Hemorrhagic Fever, Ebola/epidemiology , Hemorrhagic Fever, Ebola/transmission , Survivors , Adolescent , Adult , Africa, Western/epidemiology , Ebolavirus/classification , Ebolavirus/genetics , Ebolavirus/isolation & purification , Female , Hemorrhagic Fever, Ebola/virology , Humans , Male , Middle Aged , Public Health Surveillance , Young Adult
3.
N Engl J Med ; 373(25): 2448-54, 2015 Dec 17.
Article in English | MEDLINE | ID: mdl-26465384

ABSTRACT

A suspected case of sexual transmission from a male survivor of Ebola virus disease (EVD) to his female partner (the patient in this report) occurred in Liberia in March 2015. Ebola virus (EBOV) genomes assembled from blood samples from the patient and a semen sample from the survivor were consistent with direct transmission. The genomes shared three substitutions that were absent from all other Western African EBOV sequences and that were distinct from the last documented transmission chain in Liberia before this case. Combined with epidemiologic data, the genomic analysis provides evidence of sexual transmission of EBOV and evidence of the persistence of infective EBOV in semen for 179 days or more after the onset of EVD. (Funded by the Defense Threat Reduction Agency and others.).


Subject(s)
Ebolavirus/genetics , Hemorrhagic Fever, Ebola/transmission , Semen/virology , Adult , Coitus , Ebolavirus/isolation & purification , Female , Genome, Viral , Hemorrhagic Fever, Ebola/virology , Humans , Liberia , Male , RNA, Viral/blood , Reverse Transcriptase Polymerase Chain Reaction , Unsafe Sex
4.
Emerg Infect Dis ; 23(4): 714-715, 2017 04.
Article in English | MEDLINE | ID: mdl-28287374

ABSTRACT

Ebola virus is known to persist in semen of male survivors of Ebola virus disease (EVD). However, maximum duration of, or risk factors for, virus persistence are unknown. We report an EVD survivor with preexisting HIV infection, whose semen was positive for Ebola virus RNA 565 days after recovery from EVD.


Subject(s)
Ebolavirus/isolation & purification , HIV Infections/complications , Hemorrhagic Fever, Ebola/virology , RNA, Viral/isolation & purification , Semen/virology , Humans , Male , Middle Aged , RNA, Viral/chemistry , Time Factors , Viral Core Proteins/chemistry , Viral Matrix Proteins/chemistry
6.
N Engl J Med ; 371(16): 1481-95, 2014 10 16.
Article in English | MEDLINE | ID: mdl-25244186

ABSTRACT

BACKGROUND: On March 23, 2014, the World Health Organization (WHO) was notified of an outbreak of Ebola virus disease (EVD) in Guinea. On August 8, the WHO declared the epidemic to be a "public health emergency of international concern." METHODS: By September 14, 2014, a total of 4507 probable and confirmed cases, including 2296 deaths from EVD (Zaire species) had been reported from five countries in West Africa--Guinea, Liberia, Nigeria, Senegal, and Sierra Leone. We analyzed a detailed subset of data on 3343 confirmed and 667 probable Ebola cases collected in Guinea, Liberia, Nigeria, and Sierra Leone as of September 14. RESULTS: The majority of patients are 15 to 44 years of age (49.9% male), and we estimate that the case fatality rate is 70.8% (95% confidence interval [CI], 69 to 73) among persons with known clinical outcome of infection. The course of infection, including signs and symptoms, incubation period (11.4 days), and serial interval (15.3 days), is similar to that reported in previous outbreaks of EVD. On the basis of the initial periods of exponential growth, the estimated basic reproduction numbers (R0 ) are 1.71 (95% CI, 1.44 to 2.01) for Guinea, 1.83 (95% CI, 1.72 to 1.94) for Liberia, and 2.02 (95% CI, 1.79 to 2.26) for Sierra Leone. The estimated current reproduction numbers (R) are 1.81 (95% CI, 1.60 to 2.03) for Guinea, 1.51 (95% CI, 1.41 to 1.60) for Liberia, and 1.38 (95% CI, 1.27 to 1.51) for Sierra Leone; the corresponding doubling times are 15.7 days (95% CI, 12.9 to 20.3) for Guinea, 23.6 days (95% CI, 20.2 to 28.2) for Liberia, and 30.2 days (95% CI, 23.6 to 42.3) for Sierra Leone. Assuming no change in the control measures for this epidemic, by November 2, 2014, the cumulative reported numbers of confirmed and probable cases are predicted to be 5740 in Guinea, 9890 in Liberia, and 5000 in Sierra Leone, exceeding 20,000 in total. CONCLUSIONS: These data indicate that without drastic improvements in control measures, the numbers of cases of and deaths from EVD are expected to continue increasing from hundreds to thousands per week in the coming months.


Subject(s)
Epidemics/statistics & numerical data , Hemorrhagic Fever, Ebola/epidemiology , Adolescent , Adult , Africa, Western/epidemiology , Child , Ebolavirus , Female , Hemorrhagic Fever, Ebola/diagnosis , Hemorrhagic Fever, Ebola/transmission , Humans , Incidence , Infectious Disease Incubation Period , Male , Middle Aged , Mortality , Young Adult
7.
Bull World Health Organ ; 95(7): 526-530, 2017 Jul 01.
Article in English | MEDLINE | ID: mdl-28670017

ABSTRACT

PROBLEM: The lack of proper water and sanitation infrastructures and poor hygiene practices in health-care facilities reduces facilities' preparedness and response to disease outbreaks and decreases the communities' trust in the health services provided. APPROACH: To improve water and sanitation infrastructures and hygiene practices, the Liberian health ministry held multistakeholder meetings to develop a national water, sanitation and hygiene and environmental health package. A national train-the-trainer course was held for county environmental health technicians, which included infection prevention and control focal persons; the focal persons acted as change agents. LOCAL SETTING: In Liberia, only 45% of 701 surveyed health-care facilities had an improved water source in 2015, and only 27% of these health-care facilities had proper disposal for infectious waste. RELEVANT CHANGES: Local ownership, through engagement of local health workers, was introduced to ensure development and refinement of the package. In-county collaborations between health-care facilities, along with multisectoral collaboration, informed national level direction, which led to increased focus on water and sanitation infrastructures and uptake of hygiene practices to improve the overall quality of service delivery. LESSONS LEARNT: National level leadership was important to identify a vision and create an enabling environment for changing the perception of water, sanitation and hygiene in health-care provision. The involvement of health workers was central to address basic infrastructure and hygiene practices in health-care facilities and they also worked as stimulators for sustainable change. Further, developing a long-term implementation plan for national level initiatives is important to ensure sustainability.


Subject(s)
Health Facility Administration/standards , Hygiene/standards , Sanitation/methods , Water Supply/methods , Attitude of Health Personnel , Cooperative Behavior , Developing Countries , Humans , Infection Control/organization & administration , Interinstitutional Relations , Leadership , Liberia , Program Development , Program Evaluation , Sanitation/standards , Water Supply/standards
8.
J Infect Dis ; 213 Suppl 3: S116-23, 2016 May 01.
Article in English | MEDLINE | ID: mdl-26912379

ABSTRACT

BACKGROUND: Following the 65th World Health Assembly (WHA) resolution on intensification of the Global Poliomyelitis Eradication Initiative (GPEI), the Nigerian government, with support from the World Health Organization (WHO) and other partners, implemented a number of innovative strategies to curb the transmission of wild poliovirus (WPV) in the country. One of the innovations successfully implemented since mid 2012 is the WHO's engagement of surge capacity personnel. METHODS: The WHO reorganized its functional structure, adopted a transparent recruitment and deployment process, provided focused technical and management training, and applied systematic accountability framework to successfully manage the surge capacity project in close collaboration with the national counterparts and partners. The deployment of the surge capacity personnel was guided by operational and technical requirement analysis. RESULTS: Over 2200 personnel were engaged, of whom 92% were strategically deployed in 11 states classified as high risk on the basis of epidemiological risk analysis and compromised security. These additional personnel were directly engaged in efforts aimed at improving the performance of polio surveillance, vaccination campaigns, increased routine immunization outreach sessions, and strengthening partnership with key stakeholders at the operational level, including community-based organizations. DISCUSSION: Programmatic interventions were sustained in states in which security was compromised and the risk of polio was high, partly owing to the presence of the surge capacity personnel, who are engaged from the local community. Since mid-2012, significant programmatic progress was registered in the areas of polio supplementary immunization activities, acute flaccid paralysis surveillance, and routine immunization with the support of the surge capacity personnel. As of 19 June 2015, the last case of WPV was reported on 24 July 2014. The surge infrastructure has also been instrumental in building local capacity; supporting other public health emergencies, such as the Ebola outbreak response and measles and meningitis outbreaks; and strengthening the integrated disease surveillance and response. Due to weak health systems in the country, it is vital to maintain a reasonable level of the surge capacity for successful implementation of the 2013-2018 global polio endgame strategy and beyond.


Subject(s)
Disease Eradication , Immunization Programs , Poliomyelitis/prevention & control , Surge Capacity , Health Plan Implementation , History, 21st Century , Humans , Nigeria/epidemiology , Poliomyelitis/epidemiology , Poliomyelitis/history , Population Surveillance , Retrospective Studies , Vaccination , World Health Organization
9.
Emerg Infect Dis ; 22(2): 169-77, 2016 Feb.
Article in English | MEDLINE | ID: mdl-26811980

ABSTRACT

The severe epidemic of Ebola virus disease in Liberia started in March 2014. On May 9, 2015, the World Health Organization declared Liberia free of Ebola, 42 days after safe burial of the last known case-patient. However, another 6 cases occurred during June-July; on September 3, 2015, the country was again declared free of Ebola. Liberia had by then reported 10,672 cases of Ebola and 4,808 deaths, 37.0% and 42.6%, respectively, of the 28,103 cases and 11,290 deaths reported from the 3 countries that were heavily affected at that time. Essential components of the response included government leadership and sense of urgency, coordinated international assistance, sound technical work, flexibility guided by epidemiologic data, transparency and effective communication, and efforts by communities themselves. Priorities after the epidemic include surveillance in case of resurgence, restoration of health services, infection control in healthcare settings, and strengthening of basic public health systems.


Subject(s)
Hemorrhagic Fever, Ebola/epidemiology , Hemorrhagic Fever, Ebola/prevention & control , Disease Management , Health Communication , Health Personnel , Hemorrhagic Fever, Ebola/diagnosis , Hemorrhagic Fever, Ebola/history , History, 21st Century , Humans , Liberia/epidemiology , Patient Isolation , Population Surveillance
10.
MMWR Morb Mortal Wkly Rep ; 65(36): 963-6, 2016 Sep 16.
Article in English | MEDLINE | ID: mdl-27632552

ABSTRACT

According to World Health Organization (WHO) data, the Ebola virus disease (Ebola) outbreak that began in West Africa in 2014 has resulted in 28,603 cases and 11,301 deaths (1). In March 2015, epidemiologic investigation and genetic sequencing in Liberia implicated sexual transmission from a male Ebola survivor, with Ebola virus detected by reverse transcription-polymerase chain reaction (RT-PCR) 199 days after symptom onset (2,3), far exceeding the 101 days reported from an earlier Ebola outbreak (4). In response, WHO released interim guidelines recommending that all male survivors, in addition to receiving condoms and sexual risk reduction counseling at discharge from an Ebola treatment unit (ETU), be offered semen testing for Ebola virus RNA by RT-PCR 3 months after disease onset, and every month thereafter until two consecutive semen specimens collected at least 1 week apart test negative for Ebola virus RNA (5). Male Ebola survivors should also receive counseling to promote safe sexual practices until their semen twice tests negative. When these recommendations were released, testing of semen was not widely available in Liberia. Challenges in establishing and operating the first nationwide semen testing and counseling program for male Ebola survivors included securing sufficient resources for the program, managing a public health semen testing program in the context of ongoing research studies that were also collecting and screening semen, identification of adequate numbers of trained counselors and appropriate health communication messages for the program, overcoming Ebola survivor-associated stigma, identification and recruitment of male Ebola survivors, and operation of mobile teams.


Subject(s)
Counseling/organization & administration , Disease Outbreaks/prevention & control , Hemorrhagic Fever, Ebola/prevention & control , Mass Screening/organization & administration , Survivors , Ebolavirus/isolation & purification , Hemorrhagic Fever, Ebola/epidemiology , Humans , Liberia/epidemiology , Male , Program Development , Semen/virology , Survivors/statistics & numerical data
11.
MMWR Morb Mortal Wkly Rep ; 64(35): 979-80, 2015 Sep 11.
Article in English | MEDLINE | ID: mdl-26355323

ABSTRACT

Following 42 days since the last Ebola virus disease (Ebola) patient was discharged from a Liberian Ebola treatment unit (ETU), September 3, 2015, marks the second time in a 4-month period that the World Health Organization (WHO) has declared Liberia free of Ebola virus transmission (1). The first confirmed Ebola cases in West Africa were identified in southeastern Guinea on March 23, 2014, and within 1 week, cases were identified and confirmed in Liberia (1). Since then, Liberia has reported 5,036 confirmed and probable Ebola cases and 4,808 Ebola-related deaths. The epidemic in Liberia peaked in late summer and early fall of 2014, when more than 200 confirmed and probable cases were reported each week .


Subject(s)
Disease Eradication , Disease Outbreaks/prevention & control , Hemorrhagic Fever, Ebola/prevention & control , Ebolavirus/isolation & purification , Hemorrhagic Fever, Ebola/epidemiology , Humans , Liberia/epidemiology
12.
MMWR Morb Mortal Wkly Rep ; 64(17): 479-81, 2015 May 08.
Article in English | MEDLINE | ID: mdl-25950255

ABSTRACT

On March 20, 2015, 30 days after the most recent confirmed Ebola Virus Disease (Ebola) patient in Liberia was isolated, Ebola was laboratory confirmed in a woman in Monrovia. The investigation identified only one epidemiologic link to Ebola: unprotected vaginal intercourse with a survivor. Published reports from previous outbreaks have demonstrated Ebola survivors can continue to harbor virus in immunologically privileged sites for a period of time after convalescence. Ebola virus has been isolated from semen as long as 82 days after symptom onset and viral RNA has been detected in semen up to 101 days after symptom onset. One instance of possible sexual transmission of Ebola has been reported, although the accompanying evidence was inconclusive. In addition, possible sexual transmission of Marburg virus, a filovirus related to Ebola, was documented in 1968. This report describes the investigation by the Government of Liberia and international response partners of the source of Liberia's latest Ebola case and discusses the public health implications of possible sexual transmission of Ebola virus. Based on information gathered in this investigation, CDC now recommends that contact with semen from male Ebola survivors be avoided until more information regarding the duration and infectiousness of viral shedding in body fluids is known. If male survivors have sex (oral, vaginal, or anal), a condom should be used correctly and consistently every time.


Subject(s)
Ebolavirus/isolation & purification , Hemorrhagic Fever, Ebola/diagnosis , Hemorrhagic Fever, Ebola/transmission , Sexually Transmitted Diseases, Viral , Adult , Disease Outbreaks , Female , Hemorrhagic Fever, Ebola/epidemiology , Humans , Liberia/epidemiology , Male , Middle Aged , RNA, Viral , Semen/virology , Survivors , Unsafe Sex
13.
MMWR Morb Mortal Wkly Rep ; 64(7): 188-92, 2015 Feb 27.
Article in English | MEDLINE | ID: mdl-25719682

ABSTRACT

West Africa is experiencing its first epidemic of Ebola virus disease (Ebola). As of February 9, Liberia has reported 8,864 Ebola cases, of which 3,147 were laboratory-confirmed. Beginning in August 2014, the Liberia Ministry of Health and Social Welfare (MOHSW), supported by CDC, the World Health Organization (WHO), and others, began systematically investigating and responding to Ebola outbreaks in remote areas. Because many of these areas lacked mobile telephone service, easy road access, and basic infrastructure, flexible and targeted interventions often were required. Development of a national strategy for the Rapid Isolation and Treatment of Ebola (RITE) began in early October. The strategy focuses on enhancing capacity of county health teams (CHT) to investigate outbreaks in remote areas and lead tailored responses through effective and efficient coordination of technical and operational assistance from the MOHSW central level and international partners. To measure improvements in response indicators and outcomes over time, data from investigations of 12 of 15 outbreaks in remote areas with illness onset dates of index cases during July 16-November 20, 2014, were analyzed. The times to initial outbreak alerts and durations of the outbreaks declined over that period while the proportions of patients who were isolated and treated increased. At the same time, the case-fatality rate in each outbreak declined. Implementation of strategies, such as RITE, to rapidly respond to rural outbreaks of Ebola through coordinated and tailored responses can successfully reduce transmission and improve outcomes.


Subject(s)
Disease Outbreaks/prevention & control , Ebolavirus/isolation & purification , Hemorrhagic Fever, Ebola/prevention & control , Rural Population , Adolescent , Adult , Aged , Aged, 80 and over , Child , Child, Preschool , Disease Outbreaks/statistics & numerical data , Female , Hemorrhagic Fever, Ebola/epidemiology , Humans , Infant , Liberia/epidemiology , Male , Middle Aged , Rural Population/statistics & numerical data , Time Factors , Young Adult
14.
J Infect Dis ; 210 Suppl 1: S23-39, 2014 Nov 01.
Article in English | MEDLINE | ID: mdl-25316840

ABSTRACT

A renewed commitment at the regional and the global levels led to substantial progress in the fight for polio eradication in the African Region (AFR) of the World Health Organization (WHO) during 2008-2012. In 2008, there were 912 reported cases of wild poliovirus (WPV) infection in 12 countries in the region. This number had been reduced to 128 cases in 3 countries in 2012, of which 122 were in Nigeria, the only remaining country with endemic circulation of WPV in AFR. During 2008-2012, circulation apparently ceased in the 3 AFR countries with reestablished WPV transmission-Angola, the Democratic Republic of the Congo, and Chad. Outbreaks in West Africa continued to occur in 2008-2010 but were more rapidly contained, with fewer cases than during earlier years. This progress has been attributed to better implementation of core strategies, increased accountability, and implementation of innovative approaches. During this period, routine coverage with 3 doses of oral polio vaccine in AFR, as measured by WHO-United Nations Children's Fund estimates, increased slightly, from 72% to 74%. Despite this progress, challenges persist in AFR, and 2013 was marked by new setbacks and importations. High population immunity and strong surveillance are essential to sustain progress and assure that AFR reaches its goal of eradicating WPV.


Subject(s)
Disease Eradication/methods , Disease Eradication/organization & administration , Poliomyelitis/epidemiology , Poliomyelitis/prevention & control , Africa/epidemiology , Endemic Diseases , Humans , Incidence , Poliomyelitis/transmission , Poliomyelitis/virology , Poliovirus Vaccine, Oral/administration & dosage , Topography, Medical , Vaccination/statistics & numerical data
15.
J Infect Dis ; 210 Suppl 1: S341-6, 2014 Nov 01.
Article in English | MEDLINE | ID: mdl-25316853

ABSTRACT

BACKGROUND: To assess the quality of supplementary immunization activities (SIAs), the Global Polio Eradication Initiative (GPEI) has used cluster lot quality assurance sampling (C-LQAS) methods since 2009. However, since the inception of C-LQAS, questions have been raised about the optimal balance between operational feasibility and precision of classification of lots to identify areas with low SIA quality that require corrective programmatic action. METHODS: To determine if an increased precision in classification would result in differential programmatic decision making, we conducted a pilot evaluation in 4 local government areas (LGAs) in Nigeria with an expanded LQAS sample size of 16 clusters (instead of the standard 6 clusters) of 10 subjects each. RESULTS: The results showed greater heterogeneity between clusters than the assumed standard deviation of 10%, ranging from 12% to 23%. Comparing the distribution of 4-outcome classifications obtained from all possible combinations of 6-cluster subsamples to the observed classification of the 16-cluster sample, we obtained an exact match in classification in 56% to 85% of instances. CONCLUSIONS: We concluded that the 6-cluster C-LQAS provides acceptable classification precision for programmatic action. Considering the greater resources required to implement an expanded C-LQAS, the improvement in precision was deemed insufficient to warrant the effort.


Subject(s)
Health Services Research , Immunization, Secondary/methods , Lot Quality Assurance Sampling/methods , Poliomyelitis/prevention & control , Poliovirus Vaccines/administration & dosage , Poliovirus Vaccines/immunology , Child, Preschool , Female , Humans , Infant , Infant, Newborn , Male , Nigeria
16.
J Infect Dis ; 210 Suppl 1: S523-30, 2014 Nov 01.
Article in English | MEDLINE | ID: mdl-25316876

ABSTRACT

BACKGROUND: Efforts are underway to strengthen Nigeria's routine immunization system, yet measuring impact poses a challenge. We document limitations in using administrative data from 12 states in Nigeria and explore alternative approaches. METHODS: We compared state-reported coverage with the third dose of diphtheria-tetanus-pertussis vaccine (DTP3) to district-reported coverage and data from coverage surveys conducted during 2006-2013. We used district-reported data during 2010-2013 to calculate the annual change in immunization coverage, the percentage of the target population that was unimmunized, and the number of vaccine doses administered. Data quality indicators were also assessed. RESULTS: State-reported DTP3 coverage was 66%-102% in 2010, 49%-98% in 2011, 38%-84% in 2012, and 75%-123% in 2013 and was a median 46%-114% greater than survey coverage during 2006-2013. The mean local government area (LGA)-reported coverage varied substantially (standard deviation range, 10%-33% across years). For 2010-2013, the mean annual percentage change in LGA-reported DTP3 coverage was -15% from 2010 to 2011, -9% from 2011 to 2012, and 74% from 2012 to 2013; the mean annual percentage change in the percentage of the target population unimmunized was -62%, 426%, and -62%, respectively; and the mean annual percentage change in the number of doses administered was -13%, -7%, and 90%, respectively. Annually, a mean 14% of LGAs reported DTP3 coverage of >100%. DISCUSSION: Assessing immunization system performance by using administrative data has notable limitations. In addition to long-term improvements in administrative data management, alternatives for measuring routine immunization performance should be considered.


Subject(s)
Data Collection/methods , Diphtheria-Tetanus-Pertussis Vaccine/administration & dosage , Health Services Research/methods , Immunization/statistics & numerical data , Female , Humans , Infant , Infant, Newborn , Male , Nigeria
17.
J Infect Dis ; 210 Suppl 1: S91-7, 2014 Nov 01.
Article in English | MEDLINE | ID: mdl-25316881

ABSTRACT

BACKGROUND: As 1 of 3 remaining poliovirus-endemic countries, Nigeria has become key to the global polio eradication effort. We evaluated supplemental immunization activities, including team performance, communications/mobilization activities, and vaccine acceptance, in 3 high-risk states. METHODS: We used structured survey and observation instruments, document review, and stakeholder interviews. RESULTS: Observations or surveys were conducted at 1697 households. Vaccine acceptance ranged from 87%-94%; among households rejecting polio vaccine, 38% of mothers sought measles vaccine for their children. Teams performed between 4%-42% of assigned tasks. CONCLUSIONS: Acceptance is high but teams have a critical role in surmounting residual vaccine resistance.


Subject(s)
Patient Acceptance of Health Care/statistics & numerical data , Poliomyelitis/prevention & control , Poliovirus Vaccines/administration & dosage , Vaccination/statistics & numerical data , Child, Preschool , Female , Humans , Infant , Infant, Newborn , Male , Nigeria/epidemiology , Patient Acceptance of Health Care/psychology , Poliomyelitis/epidemiology
18.
J Infect Dis ; 210 Suppl 1: S98-101, 2014 Nov 01.
Article in English | MEDLINE | ID: mdl-25316882

ABSTRACT

The application of geospatial data to public health problems has expanded significantly with increased access to low-cost handheld global positioning system (GPS) receivers and free programs for geographic information systems analysis. In January 2010, we piloted the application of geospatial analysis to polio supplementary immunization activities (SIAs) in northern Nigeria. SIA teams carried GPS receivers to compare hand-drawn catchment area route maps with GPS tracks of actual vaccination teams. Team tracks overlaid on satellite imagery revealed that teams commonly missed swaths of contiguous households and indicated that geospatial data can improve microplanning and provide nearly real-time monitoring of team performance.


Subject(s)
Geographic Information Systems , Poliomyelitis/prevention & control , Poliovirus Vaccines/administration & dosage , Vaccination , Female , Humans , Male , Nigeria/epidemiology , Pilot Projects , Poliomyelitis/epidemiology , Vaccination/statistics & numerical data
19.
J Infect Dis ; 210 Suppl 1: S40-9, 2014 Nov 01.
Article in English | MEDLINE | ID: mdl-25316862

ABSTRACT

BACKGROUND: Transmission of wild poliovirus (WPV) has never been interrupted in Afghanistan, Pakistan, and Nigeria. Since 2003, infections with WPV of Nigerian origin have been detected in 25 polio-free countries. In 2012, the Nigerian government created an emergency operations center and implemented a national emergency action plan to eradicate polio. The 2013 revision of this plan prioritized (1) improving the quality of supplemental immunization activities (SIAs), (2) implementing strategies to reach underserved populations, (3) adopting special approaches in security-compromised areas, (4) improving outbreak response, (5) enhancing routine immunization and activities implemented between SIAs, and (6) strengthening surveillance. This report summarizes implementation of these activities during a period of unprecedented insecurity and violence, including the killing of health workers and the onset of a state of emergency in the northeast zone. METHODS: This report reviews management strategies, innovations, trends in case counts, vaccination and social mobilization activities, and surveillance and monitoring data to assess progress in polio eradication in Nigeria. RESULTS: Nigeria has made significant improvements in the management of polio eradication initiative (pei) activities with marked improvement in the quality of SIAs, as measured by lot quality assurance sampling (LQAS). Comparing results from February 2012 with results from December 2013, the proportion of local government areas (LGAs) conducting LQAS in the 11 high-risk states at the ≥90% pass/fail threshold increased from 7% to 42%, and the proportion at the 80%-89% threshold increased from 9% to 30%. During January-December 2013, 53 polio cases were reported from 26 LGAs in 9 states in Nigeria, compared with 122 cases reported from 13 states in 2012. No cases of WPV type 3 infection have been reported since November 2012. In 2013, no polio cases due to any poliovirus type were detected in the northwest sanctuaries of Nigeria. In the second half of 2013, WPV transmission was restricted to Kano, Borno, Bauchi, and Taraba states. Despite considerable progress, 24 LGAs in 2012 and 7 LGAs in 2013 reported ≥2 cases, and WPV continued to circulate in 8 LGAs that had cases in 2012. Campaign activities were negatively impacted by insecurity and violence in Borno and Kano states. CONCLUSIONS: Efforts to interrupt transmission remain impeded by poor SIA implementation in localized areas, anti-polio vaccine sentiment, and limited access to vaccinate children because of insecurity. Sustained improvement in SIA quality, surveillance, and outbreak response and special strategies in security-compromised areas are needed to interrupt WPV transmission in 2014.


Subject(s)
Disease Eradication/methods , Disease Eradication/organization & administration , Poliomyelitis/epidemiology , Poliomyelitis/prevention & control , Poliovirus Vaccine, Oral/administration & dosage , Vaccination/statistics & numerical data , Adolescent , Animals , Child , Child, Preschool , Endemic Diseases , Epidemiological Monitoring , Female , Health Policy , Humans , Incidence , Infant , Infant, Newborn , Male , Nigeria/epidemiology , Poliomyelitis/transmission , Poliomyelitis/virology , Poliovirus Vaccine, Oral/supply & distribution
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