Literature DB >> 25988350

Oral Cholera Vaccine Coverage, Barriers to Vaccination, and Adverse Events following Vaccination, Haiti, 2013.

Rania A Tohme, Jeannot François, Kathleen Wannemuehler, Preetha Iyengar, Amber Dismer, Paul Adrien, Terri B Hyde, Barbara J Marston, Kashmira Date, Eric Mintz, Mark A Katz.   

Abstract

In 2013, the first government-led oral cholera vaccination (OCV) campaign in Haiti was implemented in Petite Anse and Cerca Carvajal. To evaluate vaccination coverage, barriers to vaccination, and adverse events following vaccination, we conducted a cluster survey. We enrolled 1,121 persons from Petite Anse and 809 persons from Cerca Carvajal, categorized by 3 age groups (1-4, 5-14, >15 years). Two-dose OCV coverage was 62.5% in Petite Anse and 76.8% in Cerca Carvajal. Two-dose coverage was lowest among persons >15 years of age. In Cerca Carvajal, coverage was significantly lower for male than female respondents (69% vs. 85%; p<0.001). No major adverse events were reported. The main reason for nonvaccination was absence during the campaign. Vaccination coverage after this campaign was acceptable and comparable to that resulting from campaigns implemented by nongovernmental organizations. Future campaigns should be tailored to reach adults who are not available during daytime hours.

Entities:  

Keywords:  Haiti; bacteria; cholera; coverage survey; oral cholera vaccine; vaccination campaigns

Mesh:

Substances:

Year:  2015        PMID: 25988350      PMCID: PMC4451924          DOI: 10.3201/eid2106.141797

Source DB:  PubMed          Journal:  Emerg Infect Dis        ISSN: 1080-6040            Impact factor:   6.883


Since October 2010, Haiti has endured one of the largest cholera epidemics ever recorded in a single country, accounting for 54% of all cholera cases and 41% of all cholera deaths reported to the World Health Organization (WHO) during 2010–2013 (–). Contributing to this sustained, ongoing epidemic were inadequate drinking water and sanitation infrastructure, worsened by the 2010 earthquake, and an immunologically naive population. In February 2013, the Haiti Ministry of Health and Population launched the 2013–2022 national plan of action for elimination of cholera (). The plan outlined long-term interventions such as improving water quality, sanitation, and waste management. However, because these interventions will require years to implement, the Haitian government proposed vaccinating 600,000 persons during 2013–2015 as a short-term approach to help control the cholera epidemic (). This decision was consistent with World Health Assembly Resolution 64.15, which calls for implementation of an integrated and comprehensive approach to cholera control that includes the use of oral cholera vaccine (OCV) (). OCVs are increasingly being used as part of preemptive and reactive vaccination strategies (–). Before 2011, Dukoral vaccine (Crucell, Stockholm, Sweden), licensed for use in persons >2 years of age (2 doses given 7 days to 6 weeks apart), was the only available WHO-prequalified vaccine approved for purchase by United Nations agencies on the basis of safety and efficacy. However, its use in vaccination campaigns was limited by the need to mix the vaccine in a buffer solution diluted in clean water and by its relatively high cost (US$3–6/dose). In September 2011, Shanchol vaccine (Shantha Biotechnics, Hyderabad, India) was prequalified by WHO (2 doses given 14 days apart). Shanchol offered several advantages over Dukoral, including approval for use in persons >1 year of age, administration without buffer or water, and lower price (US$1.85/dose). Recent data from Kolkata, India, indicated that the 5-year protective efficacy of 2 doses of Shanchol was 65% (95% CI 52%–74%) (), and effectiveness 6 months after a vaccination campaign for outbreak control in Guinea was 86% (95% CI 56.7%–95.8%) (). These findings further support the use of OCV in response to epidemic and endemic cholera. In 2012, the first pilot OCV campaign was conducted in Haiti by 2 Haitian nongovernmental organizations (NGOs) in a rural area in Artibonite Department (target population for vaccination 50,000) and in an urban area in Port-au-Prince (target population 69,185) (,). In 2013, the Haiti Ministry of Health and Population conducted the first government-run OCV campaign as part of the national plan for the elimination of cholera. Shanchol was used, and the target population included (per manufacturer recommendations) persons >1 year of age, with the exception of pregnant women. Because only 200,000 doses of the vaccine were available, the Ministry of Health and Population chose to target Petite Anse, an urban area in the commune of Cap Haitian in the North Department (estimated target population 86,989), and Cerca Carvajal, a rural area in the Centre Department (estimated target population 20,917). These areas were chosen because they had the required target population for the available OCV doses, poor water and sanitation infrastructure, difficult access to health care services, and historically high cholera attack rates (10.1%–37%) () (Figure). The first vaccination round was conducted August 5–9, 2013. The second round was conducted August 26–30 in Cerca Carvajal and was split between August 26–28 and September 9−10 in Petite Anse because of depleted vaccine supplies and the time needed to receive additional doses. The campaign was conducted at fixed and mobile sites and through house-to-house visits. Vaccination cards specific for the campaign were used to document vaccination. Printed pamphlets including information about water, sanitation, and hygiene (WASH) and the need to receive 2 doses of the vaccine were distributed during the campaign. However, messages delivered orally varied between areas and included no details about the vaccine. Administrative coverage (coverage reported by the country) with 2 OCV doses was 92% in Petite Anse and 104% in Cerca Carvajal. Previously, administrative vaccination coverage estimates have been shown to be unreliable in Haiti because the number of persons in the target populations was not always known (,).
Figure

Areas selected for the first government-implemented oral cholera vaccination campaign in Haiti, 2013. Data source: Haiti Ministry of Health and Population, Centre National de l’Information Géo-Spatiale, and Institut Haïtien de Statistique et d’Informatique, OpenStreetMap.

Areas selected for the first government-implemented oral cholera vaccination campaign in Haiti, 2013. Data source: Haiti Ministry of Health and Population, Centre National de l’Information Géo-Spatiale, and Institut Haïtien de Statistique et d’Informatique, OpenStreetMap. To inform planning for future OCV campaigns in Haiti and other countries, we conducted a vaccination coverage survey. Compared with use of administrative coverage results, this method enables better assessment of the success of vaccination campaigns (evaluation of vaccine coverage, barriers to vaccination, and adverse events reported following vaccination).

Methods

Sampling and Study Population

We conducted a multistage cluster survey by using the 2011 household and population estimates provided by the Haitian Institute of Statistics and Information. The sampling frame consisted of 116 enumeration areas in Petite Anse and 25 in Cerca Carvajal. Enumeration areas are the primary sampling units, clearly delineated and mapped by the census bureau in Haiti, and are used as a sampling frame for major surveys in Haiti, including the Demographic and Health Survey. Sample size was calculated to estimate coverage by age group (1–4, 5–14 and >15 years) by using the following assumptions: 1) a desired precision of ±0.05, 2) an expected 2-dose OCV coverage of 85%, 3) a child 1–4 years of age in 65% of households, 4) a nonparticipation rate of 5%, and 5) a design effect of 1.7 in Petite Anse and 1.5 in Cerca Carvajal. These age groups were chosen for the purpose of comparison with OCV surveys conducted in other countries (,,,). A total of 564 households were needed in Petite Anse, and 353 households were needed in Cerca Carvajal. We selected 30 (26%) enumeration areas from Petite Anse and 18 (72%) from Cerca Carvajal by systematic random sampling without replacement. In each enumeration area, 20 households were selected by systematic sampling. Finally, in each selected household, 1 person in each age group, if available, was randomly selected (by use of a random number table) for interview. A household was defined as a group of persons who ate together and lived under the same roof. Persons in households were eligible to participate if they 1) were >1 year of age and not pregnant during the OCV campaign, 2) resided in a selected household during the OCV campaign, and 3) gave oral consent (for participants <18 years of age, consent was provided by a responsible adult member of the household). Responses for children were provided by the mother and the child if child was >5 years of age. The protocol was approved by the national ethics committee in Haiti. It was classified as a program evaluation activity by the Centers for Disease Control and Prevention.

Data Collection

Team members (2 interviewers and 1 supervisor) who had experience with Demographic and Health Surveys were trained on survey and household selection methods, interviewing, use of smartphones for data collection, and use of global positioning system units. The survey was conducted during September 13–27, 2013, <1 month after campaign completion. Interviews were initiated with the first household in 1 of the corners of the enumeration area noted on the global positioning system device. Subsequent households were selected by using the systematic method of traversing the enumeration area by moving in a clockwise manner and skipping households according to a precalculated sampling interval (estimated total number of households in cluster divided by 20). Contact was initiated with an adult, usually the female head of household, who was interviewed by use of a standardized questionnaire. Information collected included general household information: access to treated water and health care facilities, previous history of cholera infection in the household, awareness of the OCV campaign, and the number of eligible persons in the household who were vaccinated with OCV during the campaign and the number of doses received. Next, for each household, 1 person was randomly chosen from each of the 3 age groups for an in-depth interview (for younger children, the mother provided the information). Each interview collected information about the interviewee’s age, sex, previous history of cholera, number of OCV doses received during the campaign (documented by card or by recall if the card was not available), vaccine administration (route, location, and whether person spat out the vaccine), adverse events within 14 days of receipt of the first and second OCV dose, and general knowledge about OCV (duration of protection, need for other measures for protection against cholera). Those who had not received the first or second dose were asked their reasons for not being vaccinated. Interviewers asked all questions without prompting for answers. Interviews were conducted in Haitian Creole, and answers were recorded on smartphones. Households were visited at least 2 times if no one was at home or if a randomly selected person was unavailable during the first visit. Selected households were not replaced if they were not eligible or if no one was at home (no response) after at least 2 attempted visits.

Statistical Analyses

Estimated percentages and 95% CIs were calculated by using SAS-callable SUDAAN version 10.01 (RTI International, Research Triangle Park, NC, USA) to account for the finite population at the first stage cluster sampling. Statistical weights for each household were based on the sampling probabilities of the first 2 stages, and statistical weights for each person were based on the sampling probabilities of all 3 stages. For each area, we estimated 1- and 2-dose OCV campaign coverage (including 95% CI) by age group and sex. Satterthwaite-adjusted χ2 tests were used to compare coverage between subpopulations. For each area we also calculated rates of dropout between receipt of first and second vaccine doses, reports of any adverse events, and reasons for not receiving vaccine.

Results

Household Characteristics

Of 960 visited households, 925 (96%) consented to participate (568 in Petite Anse, 357 in Cerca Carvajal). Of the participating households, 79% in Petite Anse and 46% in Cerca Carvajal were within a 15-minute walking distance of a drinking water source. In Petite Anse, the most common source of drinking water was bottled water or water purchased from a company (84%); in Cerca Carvajal, it was unprotected spring water (42%) and public piped water (34%). For 56% and 21% of households in Petite Anse and Cerca Carvajal, respectively, the closest heath facility was located within 30 minutes of travel by the mode of transportation available in the household (walking, driving, motorcycle, or other). Overall, for 11% and 59% of the households in Petite Anse and Cerca Carvajal, respectively, the nearest health facility was >1 hour away. For ≈16% and 27% of households in Petite Anse and Cerca Carvajal, respectively, at least 1 household member had been infected with cholera during the past 2 years. At least 1 person had died of cholera in ≈3% of households (3.4% in Petite Anse and 3.2% in Cerca Carvajal).

Campaign Awareness and Vaccination of Household Members

Of the 568 households in Petite Anse and 357 in Cerca Carvajal, 511 (91%, 95% CI 87%–93%) and 335 (93%, 95% CI 89%–96%), respectively, were aware of the 2013 OCV campaign. Of those who were aware, the principal sources of information were social mobilizers who used megaphones, followed by health care workers and friends/family. In Petite Anse, 79.9% (95% CI 75.5%–83.7%) of households had at least 1 eligible person who had received 2 OCV doses; in Cerca Carvajal, 89% (95% CI 83%–93%) of households had at least 1 person who had received 2 doses. All eligible household members had received 2 OCV doses in 23% (95% CI 17.4%–28.7%) of households in Petite Anse and 37% (95% CI 31%–44%) of households in Cerca Carvajal.

Vaccination among Enrolled Household Members

A total of 1,121 and 809 persons in Petite Anse and Cerca Carvajal, respectively, who were eligible for vaccination were enrolled and categorized into 1 of the 3 age groups (Table 1). Overall, 62.5% (95% CI 57.9%–66.9%) of eligible persons from selected households in Petite Anse and 76.8% (95% CI 71.1%–81.8%) from Cerca Carvajal received both doses of OCV (Table 2). Of those who received 2 doses, 51% from Petite Anse and 70% from Cerca Carvajal had card documentation of both doses. In Petite Anse, the dropout rate between the first and second OCV dose was 9.6% (95% CI 7.1%–12.9%) and was significantly higher among persons >15 years of age (12.0%) than among children 1–4 years of age (3.4%; p = 0.008). In Cerca Carvajal, the dropout rate between the first and second OCV dose was 8.4% (95% CI 5.5%–12.6%) and was significantly higher among male than female respondents (12.6% vs. 4.5%; p = 0.002). For both regions, 2-dose coverage was significantly lower among persons >15 years of age than among younger persons (p<0.01). In Cerca Carvajal, coverage was significantly lower among male than among female respondents overall (69.0% vs. 84.9%; p<0.001), among those 5–14 years of age compared with those in other age groups (76.5% vs. 92.9%; p = 0.005), and among those >15 years of age compared with those in other age groups (57.9% vs. 82.7%; p<0.001).
Table 1

General characteristics of participants in oral cholera vaccine coverage survey, Haiti, 2013

CharacteristicArea
Petite Anse, n = 1,121Cerca Carvajal, n = 809
Sex, no. (%)
M499 (43.1)407 (50.6)
F622 (56.9)402 (49.4)
Age, y, no. (%)
1–4206 (10.3)192 (13.8)
5–14353 (24.8)263 (35.0)
>15562 (64.9)354 (51.1)
History of cholera, % (95% CI)38 3.5 (2.4–5.2)48 6.6 (4.5–9.6)
Table 2

Estimated oral cholera vaccination coverage, Haiti, 2013*

No. doses ReceivedArea, % (95% CI)
Petite Anse
Cerca Carvajal
Total, n = 1,118Male, n = 497Female, n = 621Total, n = 808Male, n = 407Female, n = 401
Total
2 62.5 (57.9–66.9)59.8 (53.9–65.5)64.5 (58.8–69.7)76.8 (71.1–81.8)69.0 (60.4–76.4)84.9 (80.0–88.8)
1 6.6 (4.9–8.9)7.1 (4.7–10.4)6.3 (3.8–10.2)7.0 (4.7–10.5)10.0 (6.3–15.4)4.0 (2.4–6.8)
030.9 (26.8–35.3)33.1 (27.6–39.1)29.2 (24.8–34.1)16.1 (12.4–20.6)21.1 (15.3–28.3)11.0 (7.9–15.2)
Age group, y
1–4n = 206n = 102n = 104n = 191n = 91n = 100
267.9 (60.2–74.8)†63.9 (52.8–73.6)71.8 (62.5–79.5)81.6 (72.9–88.0)†87.5 (75.5–94.1)76.1 (63.1–85.6)
12.4 (0.8–6.9)4.5 (1.4–13.4)0.3 (0.0–2.4)5.8 (2.7–12.0)3.5 (0.8–13.9)7.9 (3.2–18.5)
029.7 (23.3–37.0)31.6 (22.3–42.5)27.9 (20.3–37.1)12.6 (7.9–19.6)9.1 (4.1–18.8)16.0 (9.1–26.5)
5–14n = 351n = 163n = 188n = 263n = 148n = 115
277.9 (71.7–83.0)†75.5 (65.1–83.6)79.8 (72.4–85.6)83.8 (75.0–89.9)†76.5 (63.6–85.9)92.9 (85.1–96.7)
15.8 (3.7–9.0)6.1 (3.1–11.3)5.6 (3.0–10.3)5.5 (2.8–10.8)8.5 (4.0–17.2)1.8 (0.6–5.5)
016.3 (12.1–21.7)18.4 (11.5–28.2)14.6 (9.8–21.2)10.7 (6.2–17.7)15.0 (8.3–25.5)5.4 (2.0–13.7)
>15 yn = 561n = 232n = 329n = 354n = 168n = 186
255.7 (50.0–61.3)†52.5 (44.8–60.0)58.0 (50.7–65.0)70.8 (63.9–76.9)†57.9 (47.4–67.8)82.7 (75.7–88.0)
17.6 (5.3–10.9)7.9 (4.5–13.6)7.4 (4.0–13.2)8.4 (5.3–13.1)12.9 (7.6–21.1)4.3 (2.1–8.6)
036.7 (31.5–42.1)39.6 (32.4–47.2)34.6 (28.7–41.0)20.8 (15.7–27.0)29.2 (20.5–39.7)13.0 (8.6–19.2)

*Vaccination status was assessed from special cards distributed to document doses administered during the campaign, if available, or by recall; in every selected household, 1 person was randomly selected from each age group. Statistical analyses accounted for the weights and the study design. 
†Design effect (DE) and estimated intraclass correlations (ICC) = (DE−1)/(b−1), where b is the average number of responses per cluster. DE is based on accounting for clustering only (The finite population correction and weighting are ignored). Petite Anse: age group: 1–4 y, DE = 1.3 and ICC = 0.05; 5–14 y, DE = 1.4 and ICC = 0.04; >15 y, DE = 2.1 and ICC = 0.06. Cerca Carvajal: age group 1–4 y, DE = 2.4 and ICC = 0.15; 5–14 y, DE = 3.9 and ICC = 0.22; >15 y; DE = 2.3 and ICC = 0.07.

*Vaccination status was assessed from special cards distributed to document doses administered during the campaign, if available, or by recall; in every selected household, 1 person was randomly selected from each age group. Statistical analyses accounted for the weights and the study design. 
†Design effect (DE) and estimated intraclass correlations (ICC) = (DE−1)/(b−1), where b is the average number of responses per cluster. DE is based on accounting for clustering only (The finite population correction and weighting are ignored). Petite Anse: age group: 1–4 y, DE = 1.3 and ICC = 0.05; 5–14 y, DE = 1.4 and ICC = 0.04; >15 y, DE = 2.1 and ICC = 0.06. Cerca Carvajal: age group 1–4 y, DE = 2.4 and ICC = 0.15; 5–14 y, DE = 3.9 and ICC = 0.22; >15 y; DE = 2.3 and ICC = 0.07. In Petite Anse, two thirds of respondents reported having received OCV at home (66.4%, 95% CI 58.5%–73.5%) and nearly a quarter at mobile posts (23.9%, 95% CI 18.1%–30.8%). In Cerca Carvajal, almost half of respondents reported having received OCV at mobile posts (49.6%, 95% CI 41.5%–57.8%) and 19.4% (95% CI 15.3%–24.3%) at health centers. About 7% and 5% of respondents in Petite Anse and Cerca Carvajal, respectively, reported spitting out part of the first dose because of its bad taste; <5% in both areas reported spitting out part of the second OCV dose.

Knowledge about OCV

Of 1,459 respondents who had received at least 1 OCV dose, almost one third (34% in Petite Anse, 33% in Cerca Carvajal) reported that they thought OCV alone was enough to protect them from cholera. Most (73%) respondents did not know the duration of protection provided by OCV; <2% thought protection lasted 3–5 years, and 16% in Petite Anse and 10% in Cerca Carvajal thought protection lasted a lifetime.

Adverse Events following Vaccination and Reasons for Nonvaccination

Among respondents who reported having received at least 1 dose of OCV, minor adverse events following the first dose were reported by 8% and following the second dose by almost 5%. The most commonly reported adverse events were nausea, vertigo, and abdominal pain (Table 3). No major adverse events were reported. The most common reason for not receiving the first or the second dose in both regions was absence during the campaign (Table 4).
Table 3

Adverse events reported within 14 days of receipt of oral cholera vaccine, by area, Haiti, 2013*

Adverse event
Petite Anse, no. (%)
Cerca Carvajal, no. (%)
First dose
No. who received dose 768691
Total events reported68 (7.9; 95% CI 6.0–10.3)56 (8.0; 95% CI 5.4–11.7)
Common events reported†
Nausea20 (2.6)17 (2.5)
Vertigo15 (2.0)11 (1.6)
Abdominal pain13 (1.7)17 (2.5)
Weakness/fatigue11 (1.4)4 (0.6)
Diarrhea9 (1.2)9 (1.3)
Vomiting5 (0.7)5 (0.7)
Bloating3 (0.4)7 (1.0)
Fever8 (1.0)5 (0.7)
Headache2 (0.3)4 (0.6)
Rash
4 (0.5)
Not reported
Second dose
No. who received dose697637
Total events reported 35 (4.7; 95% CI 3.0–7.3)29 (4.1; 95% CI 2.4–6.8)
Common events reported‡
Vertigo6 (0.9)7 (1.1)
Nausea7 (1.0)5 (0.8)
Abdominal pain6 (0.9)9 (1.4)
Vomiting1 (0.1)2 (0.3)
Diarrhea2 (0.3)4 (0.6)
Fever4 (0.6)3 (0.5)
Weakness/fatigue4 (0.6)1 (0.2)
Headache3 (0.4)3 (0.5)
Rash6 (0.9)Not reported
Bloating2 (0.3)Not reported

*The categories for adverse events are not mutually exclusive as participants had the option to report multiple adverse events. 
†Denominator incudes persons who received the first dose. Percentages are unweighted for the purpose of description only.
‡Denominator includes persons who received the second dose. Percentages are unweighted for the purpose of description only.

Table 4

Principal reasons for not receiving oral cholera vaccine, by area, Haiti, 2013*

ReasonPetite Anse, no. ( %)Cerca Carvajal, no. ( %)
First dose
No. who did not receive dose348117
Absent during the campaign141 (40.5)63 (53.8)
Did not hear about the vaccination activities41 (11.8)15 (12.8)
Busy/no time34 (9.8)7 (6.0)
Sick during the campaign14 (4.0)4 (3.4)
Didn’t think vaccination was important/necessary20 (5.7)2 (1.7)
Don’t think vaccines are safe/vaccines can harm10 (2.9)2 (1.7)
Vaccines not available5 (1.4)4 (3.4)
Didn’t know when or where to go6 (1.7)2 (1.7)
Clinic closed/vaccinator not there/vaccinator refused to vaccinate6 (1.7)2 (1.7)
Other
71 (20.4)
16 (13.7)
Second dose†
No. who did not receive dose7354
Absent during second campaign21 (28.8)13 (24.1)
Clinic closed/vaccinator refused to vaccinate5 (6.8)1 (1.9)
Busy/no time4 (5.5)11 (20.4)
Bad experience/ adverse event after first dose6 (8.2)2 (3.7)
Did not know needed a second dose3 (4.1)1 (1.9)
Sick during the campaign2 (2.7)Not reported
Didn’t know when or where to goNot reported2 (3.7)
Forgot to go2 (2.7)1 (1.9)
Vaccines not available1 (1.4)7 (13.0)
Other29 (39.7)9 (16.7)

*Categories are mutually exclusive because respondents were allowed to give only 1 primary reason. Percentages are unweighted for the purpose of description only.
†Of those who received the first dose.

*The categories for adverse events are not mutually exclusive as participants had the option to report multiple adverse events. 
†Denominator incudes persons who received the first dose. Percentages are unweighted for the purpose of description only.
‡Denominator includes persons who received the second dose. Percentages are unweighted for the purpose of description only. *Categories are mutually exclusive because respondents were allowed to give only 1 primary reason. Percentages are unweighted for the purpose of description only.
†Of those who received the first dose.

Discussion

We report OCV coverage, barriers to vaccination, and adverse events after the first government-implemented OCV campaign in Haiti. The overall rates of 2-dose OCV coverage in rural Cerca Carvajal (77%) and urban Petite Anse (63%) were lower than the reported administrative coverage. Potential explanations could be the inaccurate population denominators used to calculate administrative coverage because the most recent census data were for 2003. In addition, several persons came from other areas to receive the vaccine, especially in Petite Anse, a crowded urban area, leading to overestimation of administrative coverage. Furthermore, the splitting and delaying of the second round of vaccination in Petite Anse created some confusion among the population regarding the vaccination dates and could have contributed to the high dropout rates. Nevertheless, the 2-dose OCV coverage achieved in Haiti is considered acceptable because herd immunity after 2-dose coverage with Shanchol as low as 28% has been reported (), and mathematical models have shown that cholera might be controlled in disease-endemic settings starting with 2-dose OCV coverage of 50% (). Our results are comparable to those reported after a pilot OCV vaccination campaign conducted in 2012 by 2 NGOs in Haiti, for which coverage was 77% in rural Bocozel () and 69% in urban slums in Port-au-Prince (). Two-dose OCV coverage rates in rural Haiti are similar to those reported in Bangladesh (72%) during the cholera off season () and rural Guinea (76%) during a cholera outbreak (). Furthermore, OCV coverage rates in Haiti are among the highest observed thus far, compared with those reported after NGO-implemented campaigns in South Sudan, India, Mozambique, and Zanzibar (,,,). This campaign is one of the few OCV campaigns implemented by a government in a cholera-endemic setting; when the governments of Vietnam and Micronesia conducted OCV vaccinations in disease-endemic or outbreak settings, coverage rates were <80% and 50%, respectively (,). OCV coverage was much lower among persons >15 years of age in both regions and lower among male than female respondents in Cerca Carvajal. Similar findings have been reported for Mozambique, Bangladesh, India, South Sudan, Guinea, and Vietnam (,,,,,). However, as in other countries (,,,,), awareness and acceptance of OCV was relatively high. The major reason for not receiving the vaccine was absence during the campaign. Unlike previous vaccination campaigns in Haiti, which primarily targeted children or women of reproductive age, OCV campaigns targeted all nonpregnant persons >1 year of age. Vaccination campaigns focused on adults need to include vaccination sessions either very early in the morning or in the evenings, when working men and women are more likely to be at home. More than two thirds of persons in Petite Anse were vaccinated at home. Vaccinators visited homes during the day, when several respondents might have been at work or at the market. In addition, adults in general and men in particular may believe that vaccines are intended for children and might not seek vaccination. Hence, additional efforts are needed to explain the need for adults to receive OCV. If vaccines are available, additional activities to reach those who were not vaccinated because of absence during the campaign might help increase coverage. Most respondents did not know the duration of protection provided by the vaccine, and almost one third thought that vaccine alone would be enough to protect them from cholera. This poor knowledge about the vaccine may result from limited messaging about the vaccine during the campaign; most of the information was spread through pamphlets, which probably were of limited usefulness because of low literacy rates in the target communities. These findings are concerning because persons who believe they are completely protected from cholera after vaccination might abandon protective behavior such as treating drinking water and practicing good hygiene. OCV campaigns should offer an opportunity to promote hygiene and safe water and food practices; an OCV campaign conducted in 2012 by an NGO in rural Haiti included a strong cholera and WASH education component and was associated with improved cholera knowledge and hygiene practices (). Future campaigns in Haiti should focus on word-of-mouth messaging to spread cholera prevention educational information. Health care workers and trained social mobilizers with megaphones could transmit these messages before, during, and after the vaccination campaign. Although the 200,000 OCV doses for the 2013 campaign were purchased directly from the manufacturer by the United Nations Children’s Fund, future OCV for use in cholera-endemic and -epidemic settings will be mainly obtained through the OCV stockpile managed by the International Coordinating Group and the Global Task Force on Cholera Control (–). Given the limited amount of vaccine available, epidemiologic, technical, and operational evidence, as well as local capacity to conduct OCV campaigns, will be assessed for optimal stockpile vaccine use. Moreover, the International Coordinating Group highlights the need to integrate OCV use with early case detection, appropriate case management, provision of adequate WASH infrastructure, and raising of awareness in the affected communities. Therefore, the cornerstones for cholera prevention and control remain safe water, improved sanitation, and adequate hygiene; WHO recommends that OCV use should complement traditional cholera control measures, including WASH interventions (7). As has been noted for other Shanchol campaigns (,,,,), no major adverse events were reported. Although the rates of minor adverse events were not higher than those reported by the manufacturer and in Bangladesh (), they were higher than adverse events reported within 48 hours of vaccination during 2 pilot NGO-run OCV campaigns in Haiti (0.5%–1.3%) (,) and a campaign in Guinea (1%) (). This survey has 2 main limitations. Only half of respondents who received both OCV doses in Petite Anse and 70% of those in Cerca Carvajal could document OCV vaccination by card. Therefore, in some instances we based vaccine status on a patient’s verbal report, which could have led to overestimation of vaccine coverage. However, the extent of this bias was probably limited because the survey was conducted shortly after the campaign, and respondents correctly identified campaign dates and route of OCV administration. Second, overestimating coverage in the sample size calculation and underestimating the design effect in Cerca Carvajal contributed to the wide confidence intervals. However, we have reported the estimated design effect caused by clustering and the estimated intraclass correlation (Table 2, footnote). Future OCV surveys in Haiti can use these intraclass correlations, along with the expected number of responses in each cluster, to estimate the design effect caused by clustering. In conclusion, coverage rates after the first government-implemented OCV campaign in Haiti were acceptable. As part of the national plan for the elimination of cholera, results from this survey would be essential for planning future OCV campaigns in Haiti to reach those who remain nonvaccinated. Given the lack of accurate data about target population estimates and high vaccine demand from nearby areas, it may be useful to overestimate required vaccine doses to improve vaccination coverage and avoid running out of vaccine during future campaigns. Printing enough vaccination cards and emphasizing the value of keeping the card and bringing it back when receiving the second vaccine dose are needed. Vaccination sessions should be tailored to reach persons who work during the day and men in general. Furthermore, OCV campaigns should be coordinated with WASH activities to ensure a comprehensive approach to cholera control and prevention and to promote the elimination of cholera from Haiti.
  29 in total

1.  Cholera, 2012.

Authors: 
Journal:  Wkly Epidemiol Rec       Date:  2013-08-02

2.  Oral cholera vaccine campaign among internally displaced persons in South Sudan.

Authors: 
Journal:  Wkly Epidemiol Rec       Date:  2014-05-16

3.  5 year efficacy of a bivalent killed whole-cell oral cholera vaccine in Kolkata, India: a cluster-randomised, double-blind, placebo-controlled trial.

Authors:  Sujit K Bhattacharya; Dipika Sur; Mohammad Ali; Suman Kanungo; Young Ae You; Byomkesh Manna; Binod Sah; Swapan K Niyogi; Jin Kyung Park; Banwarilal Sarkar; Mahesh K Puri; Deok Ryun Kim; Jacqueline L Deen; Jan Holmgren; Rodney Carbis; Mandeep Singh Dhingra; Allan Donner; G Balakrish Nair; Anna Lena Lopez; Thomas F Wierzba; John D Clemens
Journal:  Lancet Infect Dis       Date:  2013-10-18       Impact factor: 25.071

4.  Coverage and cost of a large oral cholera vaccination program in a high-risk cholera endemic urban population in Dhaka, Bangladesh.

Authors:  Iqbal Ansary Khan; Amit Saha; Fahima Chowdhury; Ashraful Islam Khan; Md Jasim Uddin; Yasmin A Begum; Baizid Khoorshid Riaz; Sanjida Islam; Mohammad Ali; Stephen P Luby; John D Clemens; Alejandro Cravioto; Firdausi Qadri
Journal:  Vaccine       Date:  2013-10-22       Impact factor: 3.641

5.  Use of Vibrio cholerae vaccine in an outbreak in Guinea.

Authors:  Francisco J Luquero; Lise Grout; Iza Ciglenecki; Keita Sakoba; Bala Traore; Melat Heile; Alpha Amadou Diallo; Christian Itama; Anne-Laure Page; Marie-Laure Quilici; Martin A Mengel; Jose Maria Eiros; Micaela Serafini; Dominique Legros; Rebecca F Grais
Journal:  N Engl J Med       Date:  2014-05-29       Impact factor: 91.245

6.  Cholera vaccination in urban Haiti.

Authors:  Vanessa Rouzier; Karine Severe; Marc Antoine Jean Juste; Mireille Peck; Christian Perodin; Patrice Severe; Marie Marcelle Deschamps; Rose Irene Verdier; Sabine Prince; Jeannot Francois; Jean Ronald Cadet; Florence D Guillaume; Peter F Wright; Jean W Pape
Journal:  Am J Trop Med Hyg       Date:  2013-10       Impact factor: 2.345

7.  First outbreak response using an oral cholera vaccine in Africa: vaccine coverage, acceptability and surveillance of adverse events, Guinea, 2012.

Authors:  Francisco J Luquero; Lise Grout; Iza Ciglenecki; Keita Sakoba; Bala Traore; Melat Heile; Alpha Amadou Dialo; Christian Itama; Micaela Serafini; Dominique Legros; Rebecca F Grais
Journal:  PLoS Negl Trop Dis       Date:  2013-10-17

8.  Use of oral cholera vaccine in Haiti: a rural demonstration project.

Authors:  Louise C Ivers; Jessica E Teng; Jonathan Lascher; Max Raymond; Jonathan Weigel; Nadia Victor; J Gregory Jerome; Isabelle J Hilaire; Charles P Almazor; Ralph Ternier; Jean Cadet; Jeannot Francois; Florence D Guillaume; Paul E Farmer
Journal:  Am J Trop Med Hyg       Date:  2013-10       Impact factor: 2.345

9.  Cholera vaccination campaign contributes to improved knowledge regarding cholera and improved practice relevant to waterborne disease in rural Haiti.

Authors:  Omowunmi Aibana; Molly F Franke; Molly Franke; Jessica E Teng; Jessica Teng; Johanne Hilaire; Max Raymond; Louise C Ivers
Journal:  PLoS Negl Trop Dis       Date:  2013-11-21

10.  Mass vaccination with a new, less expensive oral cholera vaccine using public health infrastructure in India: the Odisha model.

Authors:  Shantanu K Kar; Binod Sah; Bikash Patnaik; Yang Hee Kim; Anna S Kerketta; Sunheang Shin; Shyam Bandhu Rath; Mohammad Ali; Vittal Mogasale; Hemant K Khuntia; Anuj Bhattachan; Young Ae You; Mahesh K Puri; Anna Lena Lopez; Brian Maskery; Gopinath B Nair; John D Clemens; Thomas F Wierzba
Journal:  PLoS Negl Trop Dis       Date:  2014-02-06
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  21 in total

1.  Evaluation of Knowledge and Practices Regarding Cholera, Water Treatment, Hygiene, and Sanitation Before and After an Oral Cholera Vaccination Campaign-Haiti, 2013-2014.

Authors:  Lana Childs; Jeannot François; Alina Choudhury; Kathleen Wannemuehler; Amber Dismer; Terri B Hyde; Catherine Y Yen; Kashmira A Date; Stanley Juin; Mark A Katz; Erica Felker Kantor; Janell Routh; Melissa Etheart; Tracie Wright; Paul Adrien; Rania A Tohme
Journal:  Am J Trop Med Hyg       Date:  2016-10-31       Impact factor: 2.345

2.  Model distinguishability and inference robustness in mechanisms of cholera transmission and loss of immunity.

Authors:  Elizabeth C Lee; Michael R Kelly; Brad M Ochocki; Segun M Akinwumi; Karen E S Hamre; Joseph H Tien; Marisa C Eisenberg
Journal:  J Theor Biol       Date:  2017-01-24       Impact factor: 2.691

3.  Eliminating Cholera Transmission in Haiti.

Authors:  Louise C Ivers
Journal:  N Engl J Med       Date:  2016-12-07       Impact factor: 91.245

4.  Oral Cholera Vaccine Coverage during an Outbreak and Humanitarian Crisis, Iraq, 2015.

Authors:  Eugene Lam; Wasan Al-Tamimi; Steven Paul Russell; Muhammad Obaid-Ul Islam Butt; Curtis Blanton; Altaf Sadrudin Musani; Kashmira Date
Journal:  Emerg Infect Dis       Date:  2017-01       Impact factor: 6.883

5.  Lessons learnt from 12 oral cholera vaccine campaigns in resource-poor settings.

Authors:  Amber Hsiao; Sachin N Desai; Vittal Mogasale; Jean-Louis Excler; Laura Digilio
Journal:  Bull World Health Organ       Date:  2017-02-21       Impact factor: 9.408

6.  Neighborhood-targeted and case-triggered use of a single dose of oral cholera vaccine in an urban setting: Feasibility and vaccine coverage.

Authors:  Lucy A Parker; John Rumunu; Christine Jamet; Yona Kenyi; Richard Laku Lino; Joseph F Wamala; Allan M Mpairwe; Vincent Muller; Augusto E Llosa; Florent Uzzeni; Francisco J Luquero; Iza Ciglenecki; Andrew S Azman
Journal:  PLoS Negl Trop Dis       Date:  2017-06-08

7.  Highly targeted cholera vaccination campaigns in urban setting are feasible: The experience in Kalemie, Democratic Republic of Congo.

Authors:  Louis Albert Massing; Soumah Aboubakar; Alexandre Blake; Anne-Laure Page; Sandra Cohuet; Adalbert Ngandwe; Eric Mukomena Sompwe; Romain Ramazani; Marcela Allheimen; Philippe Levaillant; Pauline Lechevalier; Marie Kashimi; Axelle de la Motte; Arielle Calmejane; Malika Bouhenia; Ernest Dabire; Didier Bompangue; Benoit Kebela; Klaudia Porten; Francisco Luquero
Journal:  PLoS Negl Trop Dis       Date:  2018-05-07

8.  Cost Evaluation of a Government-Conducted Oral Cholera Vaccination Campaign-Haiti, 2013.

Authors:  Janell A Routh; Nandini Sreenivasan; Bishwa B Adhikari; Lesly L Andrecy; Margarette Bernateau; Taiwo Abimbola; Joseph Njau; Ernsley Jackson; Stanley Juin; Jeannot Francois; Rania A Tohme; Martin I Meltzer; Mark A Katz; Eric D Mintz
Journal:  Am J Trop Med Hyg       Date:  2017-10       Impact factor: 2.345

9.  Near real-time forecasting for cholera decision making in Haiti after Hurricane Matthew.

Authors:  Damiano Pasetto; Flavio Finger; Anton Camacho; Francesco Grandesso; Sandra Cohuet; Joseph C Lemaitre; Andrew S Azman; Francisco J Luquero; Enrico Bertuzzo; Andrea Rinaldo
Journal:  PLoS Comput Biol       Date:  2018-05-16       Impact factor: 4.475

10.  Lessons Learned from Emergency Response Vaccination Efforts for Cholera, Typhoid, Yellow Fever, and Ebola.

Authors:  Jenny A Walldorf; Kashmira A Date; Nandini Sreenivasan; Jennifer B Harris; Terri B Hyde
Journal:  Emerg Infect Dis       Date:  2017-12       Impact factor: 6.883

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