Literature DB >> 29692314

United States Travelers' Concern about Zika Infection and Willingness to Receive a Hypothetical Zika Vaccine.

Nadja A Vielot1, Lola Stamm2, James Herrington3, Linda Squiers4, Bridget Kelly4, Lauren McCormack4, Sylvia Becker-Dreps2,1.   

Abstract

The ongoing Zika pandemic has affected many countries that are common travel destinations. We assessed the willingness to receive a prophylactic Zika virus (ZIKV) vaccine, currently under development, among travelers to areas with reported autochthonous ZIKV transmission. We surveyed United States (U.S.) residents aged 18-44 years who had ever heard of ZIKV and planned to travel to Florida and/or Texas (N = 420) or a U.S. territory or foreign country (N = 415) in 2017, using a nationally representative internet panel. Travelers to Florida and/or Texas reported less concern about ZIKV infection than travelers to other destinations (27% versus 36%, P = 0.01). Female sex, Hispanic ethnicity, discussing ZIKV with medical professionals, ZIKV risk perception, and self-efficacy for ZIKV prevention predicted concern about ZIKV infection in both groups. Travelers to Florida and/or Texas (43%) and other destinations (44%) were equally willing to receive a ZIKV vaccine. Hispanic ethnicity, discussing ZIKV with medical professionals, and concern about ZIKV infection predicted vaccine willingness in both groups. Likelihood of using existing ZIKV prevention methods, confidence in the U.S. government to prevent ZIKV spread, self-efficacy for ZIKV prevention, and knowledge about ZIKV symptoms further predicted vaccine willingness in travelers to other destinations. In multivariable analyses, only concern about ZIKV infection was associated with vaccine willingness in both groups (prevalence ratio [95% confidence interval]: Florida and/or Texas: 1.34 [1.06, 1.69]; other: 1.82 [1.44, 2.29]). Targeted communications can educate travelers, particularly travelers who are pregnant or may become pregnant, about ZIKV risk to generate ZIKV vaccine demand.

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Year:  2018        PMID: 29692314      PMCID: PMC6086173          DOI: 10.4269/ajtmh.17-0907

Source DB:  PubMed          Journal:  Am J Trop Med Hyg        ISSN: 0002-9637            Impact factor:   2.345


INTRODUCTION

Since its detection in Brazil in early 2015, Zika virus (ZIKV) has spread rapidly throughout Latin America and the Caribbean. Nearly all countries in the region and two United States (U.S.) states and three territories have reported local (i.e., autochthonous) mosquito-borne transmission.[1] Millions of Americans travel to these and other areas with autochthonous ZIKV transmission each year.[2] Although ZIKV infection is asymptomatic in up to 80% of infected persons, several characteristics make ZIKV an important concern for U.S. travelers.[3] ZIKV virus appears to be unique among flaviviruses in its ability to be transmitted from mother to fetus and to cause a constellation of severe birth defects now known as congenital Zika syndrome.[4-6] Also, ZIKV infection has been found to be associated with the Guillain–Barré syndrome, a nervous system disorder that can cause symmetric muscle weakness and paralysis of the respiratory muscles.[7] Furthermore, unlike other arboviruses, there is clear evidence that ZIKV can be transmitted sexually. Of 5,168 symptomatic cases of ZIKV reported in United States in 2016, 4,897 cases were travelers returning from ZIKV-affected areas, 224 cases were individuals presumably infected locally by mosquito bites (in Florida and Texas), and 45 cases were individuals infected by sexual transmission.[8] In response to evolving knowledge about ZIKV, the U.S. Centers for Disease Control and Prevention (CDC) provided recommendations for travelers to areas with autochthonous ZIKV transmission.[9] Travel notices for various countries in the Caribbean, Central and South America, Asia, and Africa remain in place 2 years after the first cases of microcephaly were reported in Brazil, and, until more can be done to prevent ZIKV infection and its acute and long-term sequelae, there is little hope that they will be lifted. Even as the initial epidemic wanes, ZIKV is likely to become endemic in many areas and remains a concern to local populations and travelers.[10] Current strategies to prevent ZIKV infection focus largely on control of Aedes aegypti and Aedes albopictus mosquitoes, the known vectors; protection of the blood supply; and behavioral interventions, including the promotion of condom use during sex. No commercially available vaccine exists to prevent ZIKV infection. However, preclinical studies have demonstrated that multiple vaccine platforms (e.g., nucleic acid, inactivated virus, and recombinant vector-based) generate protective immunity in animal challenge models, and some of these vaccine candidates are currently in phase I human trials.[11-16] RTI International and the University of North Carolina at Chapel Hill surveyed travelers living in U.S. states on their awareness and perceptions of ZIKV and its potential effects on their travel plans. The present study explored concern about ZIKV infection while traveling among U.S. travelers and their willingness to receive a hypothetical ZIKV vaccine.

METHODS

We accessed a web-based, nationally representative panel of 50,000 adults living in the 50 U.S. states and Washington, DC from GfK Custom Research, LLC, described elsewhere.[17,18] GfK emailed a link to a self-administered, web-based survey to 8,075 randomly selected panel members. This sample was confirmed to be representative of U.S. residents aged 18–44 years based on American Community Survey (ACS) data from 2015.[19] Of these, 3,869 completed eligibility screening. Eligible respondents were aged 18–44 years; planned to travel between March and December 2017 to locations with a history of autochthonous ZIKV transmission, according to the CDC at the time of the survey; and reported having ever seen or heard any information about ZIKV.[20] Qualifying travel destinations with ongoing autochthonous ZIKV transmission or a history of autochthonous transmission included U.S. states (Florida and Texas) and territories (American Samoa, the U.S. Virgin Islands, and Puerto Rico), the Caribbean Islands, Mexico, and various countries in Central and South America, Asia, and the Pacific Islands.[18] Eligible respondents who consented to participate received periodic e-mail reminders to complete the survey in full. The survey was open between March 17 and April 4, 2017. Respondents self-reported data on demographics, travel destinations, knowledge, attitudes, and practices around ZIKV and prevention of ZIKV, and willingness to receive a hypothetical ZIKV vaccine. We summarized the sample by demographics and travel patterns using descriptive statistics. We then conducted bivariate analyses to estimate predictors of 1) concern about being infected with ZIKV while traveling and 2) willingness to receive a ZIKV vaccine. Predictors of interest included demographic characteristics, pregnancy intentions, discussing ZIKV with a health-care professional, perceived likelihood of being bitten by a ZIKV-infected mosquito (i.e., risk perception for ZIKV infection), confidence in the U.S. federal government to prevent ZIKV spread, confidence in oneself to understand ZIKV transmission and prevention (i.e., self-efficacy for ZIKV prevention), willingness to use existing ZIKV prevention methods, and knowledge of ZIKV. Concern about ZIKV infection was additionally assessed as a predictor of ZIKV vaccine willingness. Confidence in the U.S. federal government to control ZIKV, self-efficacy for ZIKV prevention, and concern about ZIKV infection were measured using three-point Likert scales. Willingness to use existing prevention methods was measured using four-point Likert scales for nine different prevention methods (e.g., using a mosquito repellant and wearing long sleeves and long pants) and by indicating some likelihood of using at least one of these methods. Next, we summarized respondents’ knowledge about ZIKV in three categories: transmission routes, symptoms, and ZIKV transmission and prevention in pregnancy (Supplemental Appendix). Knowledge scores represent the percentage of correct responses in each category, and the score distribution was divided into three groups with equal probabilities, ranked as high, medium, or low. We used the Mantel–Haenszel χ2 test to identify bivariate predictors of concern about ZIKV infection and willingness to receive a ZIKV vaccine. Fisher’s exact test was used in the event of small cell sizes (N < 5). Finally, we used log-binomial multivariable regression to estimate prevalence ratios (PR) and 95% confidence intervals for the association between selected independent variables and an individual’s willingness to receive a ZIKV vaccine, the dependent variable. Independent variables that were significantly associated at the α = 0.05 level in bivariate analyses with willingness to receive a ZIKV vaccine were included in the multivariable model. The association of pregnancy intentions with vaccine willingness was estimated in a women-only analysis, identifying model covariates using the same methods described previously. Correlated covariates were dropped from the final models to achieve parsimony and model convergence. Given that Florida and Texas did not have ongoing autochthonous ZIKV transmission at the time of the survey, we stratified all analyses by destination (Florida and/or Texas versus other destinations) to account for differences in willingness to receive a ZIKV vaccine by incidence of ZIKV transmission in intended travel destinations. We also weighted individuals in the final sample to be more representative of the U.S. population aged 18–44 years in 2015, as described elsewhere.[18] All analyses were conducted using SAS version 9.4 (SAS Institute, Cary, NC).

RESULTS

Of 8,075 panel members screened, 13.8% (N = 1,116) planned to travel in 2017 to countries and regions with reported autochthonous ZIKV transmission. Most respondents (93%, N = 1,030) had ever heard of ZIKV, and 1,001 consented to participate in the survey. We eliminated 169 respondents who planned to travel exclusively to U.S. states with no history of reported autochthonous ZIKV transmission, yielding a final analytic sample of 832 travelers (Figure 1). The sample size after weighting was N = 835. The weighted sample was representative of the general U.S. population based on 2015 ACS data with respect to age, race/ethnicity, and urban residence.
Figure 1.

Selection of final analytic sample from United States (U.S.) residents contacted from the GfK KnowledgePanel database.[17]

Selection of final analytic sample from United States (U.S.) residents contacted from the GfK KnowledgePanel database.[17] One-half of respondents (N = 420) reported travel exclusively to Florida and/or Texas, whereas one-half (N = 415) reported travel exclusively to U.S. territories or foreign countries (Table 1). Respondents overall were predominantly female (56%), aged 25 years or older (88%), and White (73%). The median annual household income range was $60,000–$84,000 (Table 1). Thirty-eight percent of respondents had a bachelor’s degree or higher and a minority of travelers were full-time (13%) or part-time (10%) college students. Most respondents (82%) planned to travel to only one destination, which was primarily Florida and/or Texas. Overall, respondents primarily reported travel for leisure, vacation, or adventure (55%), followed by visiting friends or relatives (36%) (Table 1). Respondents planning travel to destinations outside of U.S. states tended to be older, more likely to identify as Hispanic, and more likely to plan travel for leisure, vacation, or adventure (Table 1).
Table 1

Characteristics of survey respondents traveling to ZIKV-affected areas in 2017, by travel destination

Total (weighted, N = 835)Florida and/or Texas (weighted, N = 420)Other destinations (weighted, N = 415)
n (%)n (%)n (%)
Sex
 Female471 (56.4)240 (57.1)231 (55.6)
 Male364 (43.6)180 (42.9)184 (44.4)
Age group (years)
 18–24187 (22.4)98 (23.3)89 (21.4)
 25–34328 (39.3)179 (42.6)150 (36.0)
 35–44320 (38.3)143 (34.1)177 (42.6)
Race
 White607 (72.7)320 (76.2)288 (69.3)
 Black/African American125 (15.0)65 (15.4)61 (14.6)
 American Indian or Alaskan Native, Native Hawaiian or Pacific Islander14 (1.6)2 (0.4)12 (2.8)
 Asian60 (7.2)24 (5.7)36 (8.7)
 Other29 (3.5)10 (2.4)19 (4.6)
Ethnicity
 Not Spanish, Hispanic, or Latino616 (73.8)345 (82.1)271 (65.3)
 Mexican, Mexican-American, and Chicano114 (13.7)30 (7.2)84 (20.3)
 Puerto Rican31 (3.7)14 (3.4)17 (4.1)
 Cuban, Cuban American19 (2.3)9 (2.2)10 (2.4)
 Other Spanish, Hispanic, or Latino group55 (6.6)21 (5.1)22 (8.0)
Residence in ZIKV-affected states
 Florida or Texas190 (22.8)93 (22.1)97 (23.5)
 Other state645 (77.2)327 (77.9)318 (76.5)
Household income level (Quintiles)
 $0–29,999100 (12.0)51 (12.1)48 (11.7)
 $30,000–59,999191 (22.9)95 (22.6)96 (23.2)
 $60,000–84,999158 (18.9)87 (20.6)71 (17.1)
 $85,000–124,999186 (22.2)96 (22.9)90 (21.6)
 $125,000+201 (24.1)91 (21.8)110 (26.5)
Education level
 Less than high school80 (9.6)39 (9.4)40 (9.7)
 High school155 (18.6)74 (17.6)81 (19.4)
 Some college283 (33.9)144 (34.4)139 (33.4)
 Bachelor’s degree or higher318 (38.1)162 (38.6)156 (37.5)
Current college student
 No650 (77.8)330 (78.6)320 (77.1)
 Yes, full-time105 (12.6)49 (11.7)55 (13.3)
 Yes, part-time80 (9.6)41 (9.7)40 (9.6)
Number of travel destinations*
 One destination682 (81.7)420 (100.0)262 (63.1)
 Two or more destinations153 (18.3)153 (36.9)
Purpose of trip
 Business43 (5.2)27 (6.5)16 (3.9)
 Leisure, vacation, or adventure461 (55.3)221 (52.7)240 (58.0)
 Visiting friends or relatives297 (35.6)162 (38.5)135 (32.7)
 Other32 (3.9)10 (2.3)23 (5.4)

U.S. = United States; ZIKV = Zika virus.

Travel to a U.S. state (i.e., Florida and Texas) and travel to a U.S. territory (i.e., Puerto Rico, American Samoa, or U.S. Virgin Islands) are each considered a single destination.

Other includes providing or receiving medical care, research or education, and mission or nonmedical service.

Total percent may be greater than 100% because of multiple destinations reported.

Characteristics of survey respondents traveling to ZIKV-affected areas in 2017, by travel destination U.S. = United States; ZIKV = Zika virus. Travel to a U.S. state (i.e., Florida and Texas) and travel to a U.S. territory (i.e., Puerto Rico, American Samoa, or U.S. Virgin Islands) are each considered a single destination. Other includes providing or receiving medical care, research or education, and mission or nonmedical service. Total percent may be greater than 100% because of multiple destinations reported. Among all respondents, 63% reported travel to Florida and/or Texas, 8% reported travel to a U.S. territory, 3% reported travel to the Caribbean Islands, 23% reported travel to Mexico, 6% reported travel to Central and/or South America, and 2% reported travel to Asia and/or the Pacific Islands (Table 1). Among 527 respondents traveling to U.S. states, 60.2% reported travel to Florida and 24.6% reported travel to Texas. Among 833 respondents, 262 (31%) were somewhat or very concerned about becoming infected with ZIKV while traveling: 27% of travelers to Florida and/or Texas and 36% of travelers to other destinations (P = 0.01). The following predictors of concern about ZIKV infection were common to both groups of respondents: Hispanic ethnicity (Florida and/or Texas: P < 0.0001; other destinations: P = 0.03), discussing ZIKV with a medical professional (Florida and/or Texas: P = 0.008; other destinations: P = 0.001), risk perception for ZIKV infection (Florida and/or Texas: P = 0.0006; other destinations: P < 0.0001), and self-efficacy for ZIKV prevention (Florida and/or Texas: P = 0.05; other destinations: P = 0.002) (Table 2). Female sex (P = 0.02), confidence in the U.S. government to prevent ZIKV spread (P = 0.05), and low knowledge of ZIKV transmission patterns (P = 0.04) and symptoms (P = 0.001) were significantly associated with concern about ZIKV infection among travelers to Florida and/or Texas only (Table 2). Among respondents traveling to destinations outside of U.S. states, those who were likely to use an existing ZIKV prevention method were three times as likely to be concerned about ZIKV (P = 0.03) (Table 2).
Table 2

Bivariate predictors of concern about ZIKV infection among travelers to ZIKV-affected areas in 2017, by travel destination

Florida and/or Texas (weighted, N = 420)Other destinations (weighted, N = 415)
Concerned n (%)P*Concerned n (%)P*
SexSex
 Female (N = 240)77 (31.9)0.02 Female (N = 231)91 (39.3)0.07
 Male (N = 180)39 (21.5) Male (N = 183)56 (30.6)
 Missing (N = 2)
Age groupAge group
 18–33 years (N = 259)65 (25.1)0.2 18–33 years (N = 223)86 (38.4)0.2
 34–44 years (N = 161)50 (31.2) 34–44 years (N = 190)61 (32.1)
 Missing (N = 2)
EthnicityEthnicity
 Not Hispanic (N = 345)78 (23.1)< 0.0001 Not Hispanic (N = 270)86 (31.7)0.03
 Hispanic (N = 75)36 (47.5) Hispanic (N = 143)61 (42.6)
 Missing (N = 2)
Residence in ZIKV-affected statesResidence in ZIKV-affected states
 Florida or Texas (N = 92)31 (33.7)0.1 Florida or Texas (N = 97)34 (35.3)1.0
 Other (N = 327)84 (25.7) Other (N = 316)112 (35.5)
 Missing (N = 2)
Currently pregnant (N = 240 women)Currently pregnant (N = 231 women)
 Yes (N = 11)4 (31.4)1.0 Yes (N = 0)0 (0.0)
 No (N = 227)73 (32.2) No (N = 229)90 (39.5)
 Missing (N = 2) Missing (N = 2)
Planning to become pregnant (N = 240 women)Planning to become pregnant (N = 231 women)
 Yes (N = 13)7 (53.2)0.09 Yes (N = 12)6 (51.1)0.4
 No (N = 213)66 (30.9) No (N = 214)84 (39.2)
 Missing (N = 13) Missing (N = 5)
Discussed ZIKV with a medical professionalDiscussed ZIKV with a medical professional
 Yes (N = 35)16 (47.2)0.008 Yes (N = 41)24 (58.3)0.001
 No (N = 378)98 (26.0) No (N = 372)123 (32.9)
 Missing (N = 7) Missing (N = 2)
Likelihood of being bitten by a ZIKV-infected mosquitoLikelihood of being bitten by a ZIKV-infected mosquito
 Not at all likely (N = 215)43 (20.0)0.0006 Not at all likely (N = 185)44 (23.6)< 0.0001
 Somewhat to very likely (N = 194)68 (35.1) Somewhat to very likely (N = 208)90 (43.2)
 Missing (N = 11) Missing (N = 2)
Likelihood of using existing ZIKV prevention methodsLikelihood of using existing ZIKV prevention methods
 Not at all likely (N = 13)1 (10.1)0.1 Not at all likely (N = 20)2 (12.2)0.03
 Somewhat to very likely (N = 400)113 (28.1) Somewhat to very likely (N = 389)142 (36.5)
 Missing (N = 7) Missing (N = 6)
Confidence in the U.S. government’s ability to prevent ZIKV spreadConfidence in the U.S. government’s ability to prevent ZIKV spread
 Unconfident (N = 151)34 (22.8)0.05 Unconfident (N = 139)51 (34.9)0.8
 Neither confident nor unconfident (N = 142)50 (34.9) Neither confident nor unconfident (N = 157)52 (35.8)
 Confident (N = 115)28 (24.6) Confident (N = 115)43 (29.3)
 Missing (N = 12) Missing (N = 4)
Confidence in your ability to protect yourself and your family from ZIKVConfidence in your ability to protect yourself and your family from ZIKV
 Unconfident (N = 60)16 (26.2)0.05 Unconfident (N = 61)31 (51.1)0.002
 Neither confident nor unconfident (N = 132)46 (35.2) Neither confident nor unconfident (N = 135)35 (25.7)
 Confident (N = 216)50 (23.1) Confident (N = 215)81 (37.4)
 Missing (N = 12) Missing (N = 4)
ZIKV transmission knowledge scoreZIKV transmission knowledge score
 Low (N = 104)39 (37.8)0.04 Low (N = 99)38 (38.7)0.1
 Medium (N = 191)46 (24.2) Medium (N = 173)52 (30.2)
 High (N = 93)24 (25.5) High (N = 109)45 (41.0)
 Missing (N = 32) Missing (N = 34)
ZIKV symptoms knowledge scoreZIKV symptoms knowledge score
 Low (N = 127)54 (42.7)0.001 Low (N = 105)48 (45.6)0.4
 Medium (N = 81)23 (27.9) Medium (N = 83)30 (35.8)
 High (N = 66)12 (18.0) High (N = 74)32 (43.1)
 Missing (N = 146) Missing (N = 152)
ZIKV in pregnancy knowledge scoreZIKV in pregnancy knowledge score
 Low (N = 135)43 (32.0)0.6 Low (N = 135)43 (32.0)0.4
 Medium (N = 189)72 (38.3) Medium (N = 189)72 (38.3)
 High (N = 24)7 (30.5) High (N = 24)7 (30.5)
 Missing (N = 74) Missing (N = 67)

ZIKV = Zika virus. Bold values are statistically significant at α = 0.05 level.

P value represents χ2 tests for differences in vaccine willingness vs. unwillingness by levels of dependent variables, within each stratum of travel destination. Fisher’s exact test was used for comparisons in which cell sizes were < 5.

Prevention methods including using a mosquito repellent; wearing long sleeves and long pants; staying in places with air conditioning, window screens, or door screens; treating clothing with permethrin; avoiding casual contact with others; sleeping under a bednet; staying sober to avoid casual sex with persons traveling to ZIKV-affected areas; abstaining from sex with persons traveling to ZIKV-affected areas; and using condoms when having sex with persons traveling to ZIKV-affected areas.

Low, medium, and high knowledge scores are determined based on tertiles for the percentage of correct responses in each category. Transmission: low = 0–66%, medium = 67–83%, high = 84–100%. Symptoms: low = 0–50%, medium = 63–74%, high = 75–100%. Pregnancy: low = 0–74%, medium = 75–99%, high = 100%.

Bivariate predictors of concern about ZIKV infection among travelers to ZIKV-affected areas in 2017, by travel destination ZIKV = Zika virus. Bold values are statistically significant at α = 0.05 level. P value represents χ2 tests for differences in vaccine willingness vs. unwillingness by levels of dependent variables, within each stratum of travel destination. Fisher’s exact test was used for comparisons in which cell sizes were < 5. Prevention methods including using a mosquito repellent; wearing long sleeves and long pants; staying in places with air conditioning, window screens, or door screens; treating clothing with permethrin; avoiding casual contact with others; sleeping under a bednet; staying sober to avoid casual sex with persons traveling to ZIKV-affected areas; abstaining from sex with persons traveling to ZIKV-affected areas; and using condoms when having sex with persons traveling to ZIKV-affected areas. Low, medium, and high knowledge scores are determined based on tertiles for the percentage of correct responses in each category. Transmission: low = 0–66%, medium = 67–83%, high = 84–100%. Symptoms: low = 0–50%, medium = 63–74%, high = 75–100%. Pregnancy: low = 0–74%, medium = 75–99%, high = 100%. Respondents traveling to Florida and/or Texas (43%) and other destinations (44%) were equally willing to receive a ZIKV vaccine. Hispanic ethnicity (Florida and/or Texas: P < 0.0001; other destinations: P = 0.03), discussing ZIKV with a medical professional (Florida and/or Texas: P < 0.0001; other destinations: P = 0.005), and concern about ZIKV infection while traveling (both P < 0.0001) were significant positive predictors of willingness to receive a ZIKV vaccine in both groups (Table 3). Female sex was associated with greater willingness to receive a ZIKV vaccine among travelers to Florida and/or Texas (P = 0.02), whereas likelihood of using existing ZIKV prevention methods (P = 0.001), self-efficacy for ZIKV prevention (P = 0.0006), and low knowledge of ZIKV symptoms (P = 0.02) were associated with greater willingness to receive a ZIKV vaccine among travelers to destinations outside of U.S. states (Table 3).
Table 3

Bivariate predictors of willingness to receive a ZIKV vaccine among travelers to ZIKV-affected areas in 2017, by travel destination

Florida and/or Texas (weighted, N = 420)Other destinations (weighted, N = 415)
Willing n (%)P*Willing n (%)P*
SexSex
 Female (N = 235)113 (48.3)0.02 Female (N = 230)110 (47.8)0.09
 Male (N = 179)66 (37.0) Male (N = 181)71 (39.4)
 Missing (N = 6) Missing (N = 4)
Age groupAge group
 18–33 years (N = 255)118 (46.2)0.2 18–33 years (N = 223)106 (47.7)0.1
 34–44 years (N = 158)62 (39.0) 34–44 years (N = 189)75 (39.8)
 Missing (N = 6) Missing (N = 4)
EthnicityEthnicity
 Not Hispanic (N = 340)131 (38.4)< 0.0001 Not Hispanic (N = 270)109 (40.3)0.03
 Hispanic (N = 74)49 (66.4) Hispanic (N = 141)73 (51.3)
 Missing (N = 6) Missing (N = 4)
Residence in ZIKV-affected statesResidence in ZIKV-affected states
 Florida or Texas (N = 92)41 (45.2)0.7 Florida or Texas (N = 97)41 (41.9)0.6
 Other (N = 322)138 (42.9) Other (N = 315)141 (44.8)
 Missing (N = 6) Missing (N = 4)
Currently pregnant (N = 240 women)Currently pregnant (N = 231 women)
 Yes (N = 11)7 (69.0)0.2 Yes (N = 0)0 (0.0)
 No (N = 222)104 (46.9) No (N = 229)110 (48.1)
 Missing (N = 7) Missing (N = 2)
Planning to become pregnant (N = 240 women)Planning to become pregnant (N = 231 women)
 Yes (N = 13)8 (63.6)0.2 Yes (N = 12)0 (0.0)0.08
 No (N = 209)96 (45.8) No (N = 214)110 (48.06)
 Missing (N = 18) Missing (N = 4)
Discussed ZIKV with a medical professionalDiscussed ZIKV with a medical professional
 Yes (N = 34)26 (77.1)< 0.0001 Yes (N = 41)27 (64.9)0.005
 No (N = 375)151 (40.3) No (N = 371)155 (41.8)
 Missing (N = 11) Missing (N = 4)
Likelihood of being bitten by a ZIKV-infected mosquitoLikelihood of being bitten by a ZIKV-infected mosquito
 Not at all likely (N = 214)90 (42.2)0.8 Not at all likely (N = 184)71.4 (38.8)0.08
Somewhat to very likely (N = 191)83 (43.7) Somewhat to very likely (N = 207)98.8 (47.7)
 Missing (N = 15) Missing (N = 24)
Likelihood of using existing ZIKV prevention methodsLikelihood of using existing ZIKV prevention methods
 Not at all likely (N = 13)5 (37.1)0.6 Not at all likely (N = 20)2 (8.6)0.001
 Somewhat to very likely (N = 397)173 (43.7) Somewhat to very likely (N = 388)177 (45.6)
 Missing (N = 10) Missing (N = 8)
Confidence in the U.S. government’s ability to prevent ZIKV spreadConfidence in the U.S. government’s ability to prevent ZIKV spread
 Unconfident (N = 151)62 (41.4)0.09 Unconfident (N = 138)61 (43.8)0.02
 Neither confident nor unconfident (N = 141)57 (40.1) Neither confident nor unconfident (N = 156)58 (37.0)
 Confident (N = 112)59 (52.8) Confident (N = 115)62 (53.9)
 Missing (N = 16) Missing (N = 6)
Confidence in your ability to protect yourself and your family from ZIKVConfidence in your ability to protect yourself and your family from ZIKV
 Unconfident (N = 60)29 (47.9)0.2 Unconfident (N = 61)27 (43.7)0.0006
 Neither confident nor unconfident (N = 132)49 (37.3) Neither confident nor unconfident (N = 42)42 (31.1)
 Confident (N = 213)101 (47.3) Confident (N = 112)112 (52.3)
 Missing (N = 16) Missing (N = 6)
Concern about ZIKV infection while travelingConcern about ZIKV infection while traveling
 Not at all concerned (N = 299)112 (37.4) Not at all concerned (N = 267)85 (31.8)< 0.0001
 Somewhat or very concerned (N = 114)67 (59.3)< 0.0001 Somewhat or very concerned (N = 145)97 (66.9)
 Missing (N = 7) Missing (N = 4)
ZIKV transmission knowledge scoreZIKV transmission knowledge score
 Low (N = 104)47 (45.0)0.9 Low (N = 98)45 (45.7)0.4
 Medium (N = 189)83 (44.0) Medium (N = 172)71 (41.5)
 High (N = 91)42 (46.3) High (N = 109)54 (49.8)
 Missing (N = 36) Missing (N = 36)
ZIKV symptoms knowledge scoreZIKV symptoms knowledge score
 Low (N = 125)64 (51.7)0.7 Low (N = 105)66 (63.3)0.02
 Medium (N = 80)37 (45.9) Medium (N = 36)35.9 (44.0)
 High (N = 64)31 (48.3) High (N = 74)34.9 (46.9)
 Missing (N = 151) Missing (N = 154)
ZIKV in pregnancy knowledge scoreZIKV in pregnancy knowledge score
 Low (N = 117)48 (41.0)0.4 Low (N = 135)58 (43.0)0.6
 Medium (N = 186)91 (48.8) Medium (N = 187)90 (48.4)
 High (N = 39)18 (45.7) High (N = 24)12 (50.8)
 Missing (N = 78) Missing (N = 69)

ZIKV = Zika virus. Bold values are statistically significant at α = 0.05 level.

P value represents χ2 tests for differences in vaccine willingness by levels of dependent variables. Fisher’s exact test was used for comparisons in which cell sizes were < 5.

Prevention methods including using a mosquito repellent; wearing long sleeves and long pants; staying in places with air conditioning, window screens, or door screens; treating clothing with permethrin; avoiding casual contact with others; sleeping under a bednet; staying sober to avoid casual sex with persons traveling to ZIKV-affected areas; abstaining from sex with persons traveling to ZIKV-affected areas; and using condoms when having sex with persons traveling to ZIKV-affected areas.

Low, medium, and high knowledge scores are determined based on tertiles for the percentage of correct responses in each category. Basic knowledge: low = 0–50%, medium = 51–75%, high = 76–100%. Transmission: low = 0–66%, medium = 67–83%, high = 84–100%. Symptoms: low = 0–50%, medium = 63–74%, high = 75–100%. Pregnancy: low = 0–74%, medium = 75–99%, high = 100%.

Bivariate predictors of willingness to receive a ZIKV vaccine among travelers to ZIKV-affected areas in 2017, by travel destination ZIKV = Zika virus. Bold values are statistically significant at α = 0.05 level. P value represents χ2 tests for differences in vaccine willingness by levels of dependent variables. Fisher’s exact test was used for comparisons in which cell sizes were < 5. Prevention methods including using a mosquito repellent; wearing long sleeves and long pants; staying in places with air conditioning, window screens, or door screens; treating clothing with permethrin; avoiding casual contact with others; sleeping under a bednet; staying sober to avoid casual sex with persons traveling to ZIKV-affected areas; abstaining from sex with persons traveling to ZIKV-affected areas; and using condoms when having sex with persons traveling to ZIKV-affected areas. Low, medium, and high knowledge scores are determined based on tertiles for the percentage of correct responses in each category. Basic knowledge: low = 0–50%, medium = 51–75%, high = 76–100%. Transmission: low = 0–66%, medium = 67–83%, high = 84–100%. Symptoms: low = 0–50%, medium = 63–74%, high = 75–100%. Pregnancy: low = 0–74%, medium = 75–99%, high = 100%. Table 4 displays the results of multivariable models for predictors of willingness to receive a ZIKV vaccine, including covariates from Table 3 that were significant at the 0.05 alpha level in each stratum of travel destination. Among respondents traveling to Florida and/or Texas, Hispanic ethnicity (PR: 1.38 [1.07, 1.78]), discussing ZIKV with a medical professional (PR: 1.42 [1.12, 1.81]), and concern about ZIKV infection while traveling (PR: 1.34 [1.06, 1.69]) remained significantly associated with willingness to receive a ZIKV vaccine (Table 4). Among travelers to destinations outside of U.S. states, concern about ZIKV infection (PR: 1.82 [1.44, 2.29]) was the only positive predictor of willingness to receive a ZIKV vaccine. Knowledge of ZIKV symptoms was a negative predictor of willingness to receive a ZIKV vaccine (medium versus low knowledge: PR: 0.76 [0.58, 0.98]; high versus low knowledge: PR: 0.77 [0.61, 0.98]) (Table 4).
Table 4

Multivariable predictors of willingness to receive a ZIKV vaccine among travelers to ZIKV-affected areas in 2017, by travel destination

Florida and/or Texas (weighted, N = 420)Other destinations (weighted, N = 415)
Prevalence ratio (95% Confidence interval)*Prevalence ratio (95% Confidence interval)*
Sex
 Female1.0 (ref)
 Male0.85 (0.67, 1.07)
Ethnicity
 Non-Hispanic1.0 (ref)1.0 (ref)
 Hispanic1.38 (1.07, 1.78)0.94 (0.78, 1.13)
Discussed ZIKV with a medical professional
 No1.0 (ref)1.0 (ref)
 Yes1.42 (1.12, 1.81)1.09 (0.89, 1.35)
Concern about ZIKV infection while traveling
 Not at all concerned1.0 (ref)1.0 (ref)
 Somewhat or very concerned1.34 (1.06, 1.69)1.82 (1.44, 2.29)
Confidence in your ability to protect yourself and your family from ZIKV
 Unconfident1.0 (ref)
 Neither confident nor unconfident0.84 (0.58, 1.21)
 Confident1.11 (0.85, 1.44)
ZIKV symptoms knowledge score
 Low1.0 (ref)
 Medium0.76 (0.58, 0.98)
 High0.77 (0.61, 0.98)

ZIKV = Zika virus. Bold values are statistically significant at α = 0.05 level.

Models include modifiable variables that were statistically significantly associated with willingness to receive a ZIKV vaccine at the 0.05 level. All prevalence ratios are adjusted for all other variables in the model.

Multivariable predictors of willingness to receive a ZIKV vaccine among travelers to ZIKV-affected areas in 2017, by travel destination ZIKV = Zika virus. Bold values are statistically significant at α = 0.05 level. Models include modifiable variables that were statistically significantly associated with willingness to receive a ZIKV vaccine at the 0.05 level. All prevalence ratios are adjusted for all other variables in the model. Among 231 women who were not pregnant at the time of the survey and planned to travel outside of U.S. states, planning a pregnancy was significantly associated with increased willingness to receive a ZIKV vaccine (PR: 1.60 [1.12, 2.27]). However, after adjustment for Hispanic ethnicity, discussing ZIKV with a medical professional, self-efficacy for ZIKV prevention, and concern about ZIKV infection while traveling, this association was no longer statistically significant (PR: 1.35 [0.93, 1.93]). Concern about ZIKV was the only remaining significant predictor of willingness to receive a ZIKV vaccine among women traveling outside of U.S. states (PR: 1.36 [1.03, 1.80]).

DISCUSSION

This is the first published report of willingness to receive a hypothetical ZIKV vaccine among residents of U.S. states traveling to areas with a history of reported autochthonous ZIKV transmission. Nearly one-half of respondents were willing to receive a ZIKV vaccine. Demographic factors, risk perception for ZIKV infection, and self-efficacy for preventing ZIKV infection appeared to influence concern about exposure to ZIKV infection while traveling. After controlling for significant bivariate predictors of ZIKV vaccine willingness, concern about ZIKV infection while traveling was the only positive predictor of ZIKV vaccine willingness shared by travelers to Florida and/or Texas and to destinations outside of U.S. states. Although the peak of the ZIKV epidemic in the Western Hemisphere appears to have subsided, ZIKV endemicity remains a concern as the scientific community explores potential long-term sequelae of ZIKV infections in infected individuals and infants exposed in utero, including neurological, developmental, and other manifestations.[10,21-23] A vaccine could effectively prevent ZIKV, provided there is sufficient interest to promote enrollment in vaccine trials and willingness to receive a licensed vaccine. Concern about ZIKV infection might be a key factor in motivating individuals to receive a ZIKV vaccine, regardless of their intended travel destinations.[24] Prior research has focused on concern about infection as a predictor of infection control behaviors. Similar to our findings, a study of Malaysian adults found that increased worry (concern) about ZIKV relative to dengue was positively associated with practicing mosquito control after declaring ZIKV a public health emergency.[25] A Canadian study of H1N1 influenza vaccination found that concern about H1N1, but not perceived risk of H1N1, increased the odds of planning to vaccinate.[26] Risk perception in our study, indicated by perceived likelihood of being bitten by a ZIKV-infected mosquito, was not associated with increased willingness to receive a ZIKV vaccine. However, respondents with some ZIKV risk perception were nearly twice as likely to express concern about ZIKV infection, suggesting that risk perception has an indirect effect on willingness to receive a ZIKV vaccine through concern. This finding is supported by prior studies suggesting that perceived concern and perceived risk mediate one another to influence influenza vaccination.[27,28] Among travelers to destinations outside of U.S. states, concern about ZIKV infection confounded the relationships between ethnicity, self-efficacy, and preventive behaviors and willingness to receive a ZIKV vaccine. By contrast, we found multiple independent positive predictors of willingness to receive a ZIKV vaccine among travelers to Florida and/or Texas. Hispanic travelers to Florida and/or Texas reported greater willingness to receive a ZIKV vaccine than those traveling outside of U.S. states. Post hoc analyses found that Hispanic respondents traveling outside of U.S. states were significantly more likely than non-Hispanics to be visiting family or friends (52% versus 22%, P < 0.0001), whereas this association was not found among travelers to Florida and/or Texas. We hypothesize that Hispanic respondents traveling to visit friends or relatives (possibly in their countries of origin) may be less concerned about acquiring travel-related illnesses. This finding would be consistent with prior findings of decreased adoption of preventive behaviors among travelers visiting friends and relatives in their countries of origin.[29,30] Also, among travelers to Florida and/or Texas, having discussed ZIKV with a medical professional was associated with an individual’s willingness to receive a ZIKV vaccine. Given the cross-sectional nature of our study, it is unclear whether concern about ZIKV infection led travelers to discuss it with their medical providers or the reverse. However, only 10% of respondents reported discussing ZIKV with a medical professional ahead of their travel.[18] Because only a minority of travelers discuss their travel plans with a medical provider, it may also be important to provide the vaccine outside of medical offices, such as in pharmacies and travel clinics, to increase access, similar to the availability of routine seasonal influenza immunization in the U.S. Although the number of women who were pregnant or planning pregnancy was small, pregnancy intentions did not influence ZIKV vaccine willingness. By contrast, a study on willingness to receive a ZIKV vaccine among 989 pregnant women in Malaysia found 94% willingness to be vaccinated, and greater willingness to receive a ZIKV vaccine if it were recommended by a physician, friend, or relative.[31] In a study of 408 pregnant women in Atlanta, GA, 73% of women sought ZIKV information from the CDC’s website compared with < 20% who sought information from their provider’s website, and a majority preferred an informational brochure or e-mail over information on the provider’s website.[32] Providers should take advantage of these communication tools to educate their pregnant patients about ZIKV and the need for prevention. Furthermore, should a ZIKV vaccine become available, providers will need to actively inquire about their patients’ travel plans and offer the vaccine to patients visiting at-risk areas, particularly if they are pregnant or planning pregnancy. Respondents reported similar levels of willingness to receive a ZIKV vaccine across all levels of knowledge with respect to ZIKV transmission and prevention in pregnancy, suggesting that knowledge of ZIKV is not sufficient to generate interest in ZIKV vaccination. Given that ZIKV symptoms outside of pregnancy are generally mild and self-limited, increased awareness of ZIKV symptoms, transmission, and prevention methods may actually reduce vaccine interest, as suggested by our findings among travelers outside of U.S. states. However, the cross-sectional nature of this study makes it difficult to know whether interest in preventing ZIKV fuels information-seeking and increased knowledge, or the reverse. These findings indicate that knowledge can influence vaccine willingness in various ways, and future studies should implement qualitative methods to identify specific motivations for vaccination. Study limitations include exclusion of individuals who had never before heard of ZIKV. It is unknown if travelers who had never heard of ZIKV would have had different perceptions of ZIKV vaccination compared with those who had, or if awareness of ZIKV resulted from planning travel to at-risk locations. In addition, our sample included travelers to Florida and/or Texas who had a history of autochthonous transmission but no ongoing transmission at the time of the study. However, our stratified analysis allowed us to assess differences in predictors of ZIKV vaccine willingness between travelers to low- and high-transmission areas. We retained in the sample residents of Florida and/or Texas who reported travel within those states to improve statistical power, although these travelers may have different travel motivations and behaviors from those traveling outside of their home states. Furthermore, our study sample had a small number of individuals who were pregnant or planning pregnancy. However, we included a relatively large number of individuals of reproductive age, which yields useful results given that nearly one-half of all pregnancies in the U.S. are unplanned.[33] Finally, whereas the GfK KnowledgePanel from which the analytic sample was drawn is representative of the general U.S. population, our sample of travelers had a higher representation of wealthy, college-educated, Southern, and bilingual Hispanic respondents. These demographics may represent the traveling population, rather than the general U.S. population. Strengths of this study include a nationwide sample and a stratified analysis to distinguish predictors of ZIKV vaccine willingness between travelers to areas with low and high risk of ZIKV transmission. Additional research is needed to explore predictors of willingness to receive a ZIKV vaccine that were not assessed here. It is also important to understand drivers of concern about ZIKV infection to help travelers effectively address their concern, by either improving knowledge about ZIKV or offering recommendations for effective ZIKV prevention. A recent study of psychological predictors of anxiety around ZIKV infection found that contamination cognition severity, or the tendency to overestimate the severity of contamination from everyday objects, positively predicted ZIKV anxiety.[34] Although it is important to stress the importance of ZIKV prevention, these communications must avoid creating undue anxiety and must aim to provide measured recommendations based on ZIKV transmission probabilities in travel destinations and pregnancy intentions. Targeted communication between public health officials or providers about the risks of ZIKV and its sequelae could generate interest in a prophylactic ZIKV vaccine to prevent harmful long-term effects on infected individuals and their infants. Supplemental Appendix
  26 in total

1.  Vaccine Mediated Protection Against Zika Virus-Induced Congenital Disease.

Authors:  Justin M Richner; Brett W Jagger; Chao Shan; Camila R Fontes; Kimberly A Dowd; Bin Cao; Sunny Himansu; Elizabeth A Caine; Bruno T D Nunes; Daniele B A Medeiros; Antonio E Muruato; Bryant M Foreman; Huanle Luo; Tian Wang; Alan D Barrett; Scott C Weaver; Pedro F C Vasconcelos; Shannan L Rossi; Giuseppe Ciaramella; Indira U Mysorekar; Theodore C Pierson; Pei-Yong Shi; Michael S Diamond
Journal:  Cell       Date:  2017-07-13       Impact factor: 41.582

Review 2.  Progress and Works in Progress: Update on Flavivirus Vaccine Development.

Authors:  Matthew H Collins; Stefan W Metz
Journal:  Clin Ther       Date:  2017-07-25       Impact factor: 3.393

3.  Bridging Knowledge Gaps to Understand How Zika Virus Exposure and Infection Affect Child Development.

Authors:  Bill G Kapogiannis; Nahida Chakhtoura; Rohan Hazra; Catherine Y Spong
Journal:  JAMA Pediatr       Date:  2017-05-01       Impact factor: 16.193

4.  Protective efficacy of multiple vaccine platforms against Zika virus challenge in rhesus monkeys.

Authors:  Peter Abbink; Rafael A Larocca; Rafael A De La Barrera; Christine A Bricault; Edward T Moseley; Michael Boyd; Marinela Kirilova; Zhenfeng Li; David Ng'ang'a; Ovini Nanayakkara; Ramya Nityanandam; Noe B Mercado; Erica N Borducchi; Arshi Agarwal; Amanda L Brinkman; Crystal Cabral; Abishek Chandrashekar; Patricia B Giglio; David Jetton; Jessica Jimenez; Benjamin C Lee; Shanell Mojta; Katherine Molloy; Mayuri Shetty; George H Neubauer; Kathryn E Stephenson; Jean Pierre S Peron; Paolo M de A Zanotto; Johnathan Misamore; Brad Finneyfrock; Mark G Lewis; Galit Alter; Kayvon Modjarrad; Richard G Jarman; Kenneth H Eckels; Nelson L Michael; Stephen J Thomas; Dan H Barouch
Journal:  Science       Date:  2016-08-04       Impact factor: 47.728

5.  Zika virus impairs growth in human neurospheres and brain organoids.

Authors:  Patricia P Garcez; Erick Correia Loiola; Rodrigo Madeiro da Costa; Luiza M Higa; Pablo Trindade; Rodrigo Delvecchio; Juliana Minardi Nascimento; Rodrigo Brindeiro; Amilcar Tanuri; Stevens K Rehen
Journal:  Science       Date:  2016-04-10       Impact factor: 47.728

6.  Attitudes towards Zika screening and vaccination acceptability among pregnant women in Malaysia.

Authors:  Li Ping Wong; Haridah Alias; Jamiyah Hassan; Sazaly AbuBakar
Journal:  Vaccine       Date:  2017-09-05       Impact factor: 3.641

7.  Congenital Zika virus syndrome in Brazil: a case series of the first 1501 livebirths with complete investigation.

Authors:  Giovanny V A França; Lavinia Schuler-Faccini; Wanderson K Oliveira; Claudio M P Henriques; Eduardo H Carmo; Vaneide D Pedi; Marília L Nunes; Marcia C Castro; Suzanne Serruya; Mariângela F Silveira; Fernando C Barros; Cesar G Victora
Journal:  Lancet       Date:  2016-06-29       Impact factor: 79.321

8.  A live-attenuated Zika virus vaccine candidate induces sterilizing immunity in mouse models.

Authors:  Chao Shan; Antonio E Muruato; Bruno T D Nunes; Huanle Luo; Xuping Xie; Daniele B A Medeiros; Maki Wakamiya; Robert B Tesh; Alan D Barrett; Tian Wang; Scott C Weaver; Pedro F C Vasconcelos; Shannan L Rossi; Pei-Yong Shi
Journal:  Nat Med       Date:  2017-04-10       Impact factor: 87.241

9.  Vaccine protection against Zika virus from Brazil.

Authors:  Rafael A Larocca; Peter Abbink; Jean Pierre S Peron; Paolo M de A Zanotto; M Justin Iampietro; Alexander Badamchi-Zadeh; Michael Boyd; David Ng'ang'a; Marinela Kirilova; Ramya Nityanandam; Noe B Mercado; Zhenfeng Li; Edward T Moseley; Christine A Bricault; Erica N Borducchi; Patricia B Giglio; David Jetton; George Neubauer; Joseph P Nkolola; Lori F Maxfield; Rafael A De La Barrera; Richard G Jarman; Kenneth H Eckels; Nelson L Michael; Stephen J Thomas; Dan H Barouch
Journal:  Nature       Date:  2016-06-28       Impact factor: 49.962

10.  Zika Virus Prevention: U.S. Travelers' Knowledge, Risk Perceptions, and Behavioral Intentions-A National Survey.

Authors:  Linda Squiers; James Herrington; Bridget Kelly; Carla Bann; Sylvia Becker-Dreps; Lola Stamm; Mihaela Johnson; Lauren McCormack
Journal:  Am J Trop Med Hyg       Date:  2018-05-03       Impact factor: 2.345

View more
  1 in total

1.  Physicians' willingness to be vaccinated with a smallpox vaccine to prevent monkeypox viral infection: A cross-sectional study in Indonesia.

Authors:  Harapan Harapan; Abdul M Setiawan; Amanda Yufika; Samsul Anwar; Sri Wahyuni; Febrivan W Asrizal; Muhammad R Sufri; Reza P Putra; Nanda P Wijayanti; Salwiyadi Salwiyadi; Razi Maulana; Afriyani Khusna; Ina Nusrina; Muhammad Shidiq; Devi Fitriani; Muharrir Muharrir; Cut A Husna; Fitria Yusri; Reza Maulana; Naoya Itoh; Mohd Andalas; Abram L Wagner; Mudatsir Mudatsir
Journal:  Clin Epidemiol Glob Health       Date:  2020-04-30
  1 in total

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