Skip to main content
Human Vaccines & Immunotherapeutics logoLink to Human Vaccines & Immunotherapeutics
. 2018 Dec 11;15(6):1251–1259. doi: 10.1080/21645515.2018.1540827

Vaccine coverage and compliance in Mexico with the two-dose and three-dose rotavirus vaccines

Gerardo Luna-Casas a, Roberto Carreño-Manjarrez c, Andrés Castañeda-Prado a, Maria Yolanda Cervantes-Apolinar d, Ricardo Navarro-Rodriguez a, Gilberto Sánchez-González a,, Ricardo Cortés-Alcalá d, Rodrigo DeAntonio b
PMCID: PMC6783135  PMID: 30380975

ABSTRACT

Worldwide, rotavirus infection has been a leading cause of severe diarrhea morbidity and mortality. Two rotavirus vaccines have been used in the National Immunization Program (NIP) in Mexico; two-dose Rotarix from 2006 to 2011 and three-dose RotaTeq since 2011. This study assessed coverage (receiving at least one dose or full dose series) in eligible infants, compliance (% completing dose series and % completing series on schedule) in eligible infants vaccinated with Rotarix (2010) versus RotaTeq (2012), using Mexican Social Security Institute data nationwide and by regions.

In 2010, 80.7% received at least one dose of Rotarix, 75.6% received both doses and 57.0% received both doses on schedule. In 2012, 85.7% received at least one dose of RotaTeq, 61.0% received all three doses and 43.2% received all three doses on schedule. More eligible infants received all doses with Rotarix versus RotaTeq (p < 0.001). Among infants vaccinated with Rotarix versus RotaTeq, 93.7% versus 71.1% completed full series (p < 0.001), and 75.5% versus 70.9% completed full series on schedule (p = 0.105), respectively. The full series coverage and compliance decreased in all regions with RotaTeq compared with Rotarix. In conclusion, rotavirus vaccination has successfully reduced morbidity and mortality in children under 5 years in Mexico. This study found significant differences in full series coverage and compliance among infants and a higher proportion of completed scheduled at an earlier age in Mexico when comparing a two-dose vaccine in 2010 with a three-dose vaccine in 2012. Such differences might need to be taken into consideration to maximize NIP benefits, including early protection of the rotavirus vaccination program.

KEYWORDS: Rotarix, RotaTeq, rotavirus, Mexico, dosing, coverage, compliance

Introduction

Worldwide, rotavirus infection affects almost all children by the age of five. Though many cases have mild features with prompt recovery, some cases can lead to severe forms including dehydration which is the most common cause of associated death.1 Rotavirus is the leading cause of severe diarrhea, causing around 215,000 deaths in young children globally in 2013.2 By 2014, more than 70 countries included rotavirus vaccines in their national immunization program (NIP), increasing to 95 countries offering some form of rotavirus vaccine program by 2018.3 As a result, significant reductions in hospitalizations and deaths are observed (e.g., Mexico, Brazil and Panama reported 22–50% fewer diarrhea-related deaths in young children).2

In Mexico, prior to rotavirus vaccination, diarrheal disease was responsible for around 5% of deaths in children under five years, and 3,000 deaths per year.4 Introducing two-dose rotavirus vaccine (Rotarix, GSK) in the NIP of Mexico in 2007 substantially reduced mortality and morbidity in children under five, regardless of differences by region or socioeconomic status. Mortality related to diarrhea declined by 35% the three years after introducing rotavirus in the NIP as well as an 40% reduction in hospitalizations.57

Sustained yearly decreases in mortality of 53% and morbidity of 47% were also reported after seven year post vaccine introduction in the NIP, resulting in 959 deaths and 5,831 hospitalizations averted annually post vaccine introduction among children under 5 years reported by Sánchez-Uribe et al.8

In addition to two-dose Rotarix (administered at 2 and 4 months of age), three-dose RotaTeq (Merck) is available, administered at 2, 4, and 6 months of age.911 Rotarix was available on the private market in Mexico since 2005, implemented in the NIP in some areas in 2006 and nationally in 2007.12 Since 2011, the NIP uses RotaTeq.13 Both Rotarix and RotaTeq have good efficacy and safety profiles, supported by extensive data.1,1416

Due to differences in the number of doses between the vaccines, this study assessed coverage and compliance achieved with Rotarix (in 2010) and RotaTeq (in 2012), using national public data from the Mexican Social Security Institute (Instituto Mexicano del Seguro Social, Spanish acronym: IMSS) database of eligible and vaccinated Mexican infants. Outcomes for coverage included the proportion of eligible infants who received at least one dose (i.e., one-dose coverage) and the full series (i.e., full-series coverage). Outcomes for compliance included the proportion of vaccinated infants who received the full series (i.e., series completion) and who received the full series at the age recommended by the NIP and dose intervals (i.e., series timeliness). Data by gender, vaccine schedule, age, state and region were also compared.

Results

The IMSS registry included 659,249 infants (50.7% male) eligible for Rotarix in 2010 and 780,483 infants (51.2% male) eligible for RotaTeq in 2012. Most eligible infants were located in the North and Central regions (Figure 1). The registry considered the working force population and their families associated with the IMSS in 2010, and in 2012 also included the population from the Oportunidades Program, in addition to the standard IMSS population.

Figure 1.

Figure 1.

Distribution of Rotarix and RotaTeq eligible infants (%) by region.

IMSS: Instituto Mexicano del Seguro Social; Rotarix: two-dose rotavirus vaccine; RotaTeq: three-dose rotavirus vaccine; Green: North region; Blue: Central region; Pink: South region; Yellow: Mexico City.

Vaccine coverage

The 2010 cohort vaccinated with at least one dose of Rotarix comprised 532,082 infants (51.3% male) and the 2012 cohort vaccinated with at least one dose of RotaTeq comprised 668,958 infants (51.0% male). The national coverage of infants receiving at least one dose was 80.7% with Rotarix and 85.7% with RotaTeq (p = 0.11), and was similar between male and female infants, respectively (i.e., 81.7% and 79.7% for Rotarix, and, 85.4% and 86.1% for RotaTeq) (Table 1). Regional coverage with Rotarix ranged from 68.8% in the South to 98.0% in Mexico City, and with RotaTeq from 78.9% in the North to 98.8% in Mexico City (Figure 2).

Table 1.

Rotarix and RotaTeq vaccine coverage (infants receiving at least one dose or full series out of all eligible infants) by sex and region.

Vaccine coverage among vaccine-eligible children
  Rotarix (N = 659,249)
RotaTeq
(N = 780,483)
Rotarix vs. RotaTeq
  n % n % n % p
At least one dose coverage 532,082 80.7 668,958 85.7 136,876 5 0.11
By sex:  
 Male 272,981 81.7 341,220 85.4 68,239 3.6 0.21
 Female 259,101 79.7 327,738 86.1 68,637 6.4 0.04
By region:  
 North 193,285 82.3 193,577 78.9 292 −3.5 0.39
 Center 191,668 83.3 265,165 90.7 73,497 7.3 0.02
 Mexico City 44,804 98.0 61,497 98.8 16,693 0.8 0.11
 South 102,325 68.8 148,719 82.5 46,394 13.7 0.01
Full series coverage 498,312 75.6 475,845 61.0 −22,467 −14.6 <0.001
By sex:  
 Male 256,513 76.8 242,693 60.7 −13,820 −16.1 <0.001
 Female 241,799 74.4 233,152 61.2 −8,647 −13.1 <0.001
By region:  
 North 181,382 77.3 145,714 59.4 −35,668 −17.9 <0.001
 Center 179,471 78.0 190,045 65.0 10,574 −13.1 <0.001
 Mexico City 41,902 91.6 45,018 72.3 3,116 −19.3 <0.001
 South 95,557 64.2 95,068 52.7 −489 −11.5 <0.001

Rotarix: two-dose rotavirus vaccine; RotaTeq: three-dose rotavirus vaccine; N: total number of vaccinated infants; n: number in subcategory; Chi square proportion comparison; p value. Full series coverage: Number of vaccine-eligible infants that received full series of rotavirus vaccines regardless of timeliness. At least one dose coverage: Number of vaccine-eligible infants that received at least one dose of rotavirus vaccine regardless of timeliness.

Figure 2.

Figure 2.

Rotarix and RotaTeq vaccine coverage (at least one dose and full series) by region.

IMSS: Instituto Mexicano del Seguro Social; Rotarix: two-dose rotavirus vaccine; RotaTeq: three-dose rotavirus vaccine; Green: North region; Blue: Central region; Pink: South region; Yellow: Mexico City.

The number of infants who received the full vaccination series was 498,312 for Rotarix and 475,845 for RotaTeq, which corresponds to an estimated full series coverage of 75.6% with Rotarix and 61.0% with RotaTeq (p < 0.001). The full series coverage was comparable for male and female infants (Table 1). Regional differences existed, with full series coverage ranging from 64.2% to 91.6% with Rotarix, and 52.7% to 72.3% with RotaTeq in the South versus Mexico City, respectively (Figure 2).

Vaccine compliance

The number of infants who completed the full series among those vaccinated was 498,312 (93.7%) with Rotarix and 475,845 (71.1%) with RotaTeq nationally (p < 0.001). Compliance was consistently high throughout the country with Rotarix but varied considerably across regions with RotaTeq (Figure 3, Table 2): the highest compliance was observed in the North (75.3%) and the lowest in the South (63.9%).

Figure 3.

Figure 3.

Rotarix and RotaTeq compliance (series completion, timeliness) by region.

IMSS: Instituto Mexicano del Seguro Social; Rotarix: two-dose rotavirus vaccine; RotaTeq: three-dose rotavirus vaccine; Green: North region; Blue: Central region; Pink: South region; Yellow: Mexico City.

Table 2.

Rotarix and RotaTeq compliance (infants with series completion and timeliness) among Rotarix- or RotaTeq-vaccinated infants and among all eligible infants.

Vaccine compliance among vaccinated infants
  Rotarix (N = 532,082)
RotaTeq (N = 668,958)
Rotarix versus RotaTeq
  n % n % n % p
Full series completion 498,312 93.7 475,845 71.1 −22,467 −22.5 <0.001
By sex:  
 Male 256,513 94.0 242,693 71.1 −13,820 −22.8 <0.001
 Female 241,799 93.3 233,152 71.1 −8,647 −22.2 <0.001
By region  
 North 181,382 93.4 145,714 75.3 −35,668 −18.6 <0.001
 Center 179,471 93.6 190,045 71.7 10,574 −22.0 <0.001
 Mexico City 41,902 93.5 45,018 73.2 3,116 −20.3 <0.001
 South 95,557 93.4 95,068 63.9 −489 −29.5 <0.001
Full series timeliness 375,992 75.5 337,424 70.9 −38,568 −4.5 0.105
By sex:  
 Male 195,405 76.2 174,695 72.0 −20,710 −4.2 0.36
 Female 180,587 74.7 162,729 69.8 −17,858 −4.9 0.31
By region:  
 North 136,313 75.2 103,395 71.0 −32,918 −4.2 0.52
 Center 136,231 75.9 137,126 72.2 895 −3.8 0.48
 Mexico City 30,290 72.3 32,810 72.9 2,520 0.6 0.95
 South
73,158
76.6
64,093
67.4
−9,065
−9.1
0.23
Vaccine compliance among vaccine-eligible infants
  Rotarix (N = 659,249)
RotaTeq (N = 780,483)
Rotarix versus RotaTeq
 
n
%
n
%
n
%
p
Full series coverage 498,312 75.6 475,845 61.0 −22,467 −14.6 <0.01
Full series coverage timeliness
375,992
57.0%
337,424
43.2%
−38,568
−13.8
<0.01
Vaccine timeliness characteristics among infants with full series coverage timeliness
  Rotarix RotaTeq Rotarix versus RotaTeq
 
(N = 375,992)
(N = 337,424)
 
 
n
Age at last dose (Mean weeks) 14.6 19.8 5.2    
Interval 1st to last dose (Mean weeks) 5.1 10.3 5.2    

Rotarix: two-dose rotavirus vaccine; RotaTeq: three-dose rotavirus vaccine; n: number in subcategory; Chi square proportion comparison; p value. Full series completion: Number of vaccination infants who completed all recommended doses regardless of timeliness. Full series timeliness: number of vaccinated infants who completed all doses as per the NIP guidance at recommended age and intervals, Full series coverage: Number of vaccine-eligible infants that received full series of rotavirus vaccines regardless of timeliness. At least one dose coverage: Number of vaccine-eligible infants that received at least one dose of rotavirus vaccine regardless of timeliness; Full series coverage timeliness: number of vaccine-eligible infants who completed all doses as per the NIP guidance at recommended age and intervals.

The mean age to complete the Rotarix last dose was 14.6 months while the mean age for completing RotaTeq was 19.8 months (p < 0.01) (see Supplementary file 1).

The number of infants who completed the full series at the designated age and correct dosing intervals among those vaccinated (i.e., compliance timeliness among vaccinated infants) was 375,992 (75.5%) with Rotarix and 337,424 (70.9%) with RotaTeq (p = 0.105). There was more consistency across regional rates among those that complied with the full dosing schedule on time, with a range of 72.3–76.6% with Rotarix and 67.4–72.9% with RotaTeq (Figure 3). When comparing compliance timeliness among the full eligible population (both vaccinated and unvaccinated infants), the difference in compliance between Rotarix and RotaTeq is even more pronounced: 57.0% compliance with Rotarix versus 43.2% with RotaTeq, a resulting decrease of nearly 14% (p < 0.01) (Table 2).

Early protection

Among infants who initiated rotavirus vaccination, 29.3% of infants by 16 weeks of age had already completed the full series with Rotarix compared to 14.3% with Rotateq (p < 0.01). By 16 weeks of age,29.3% of infants had completed the full series with Rotarix while14.3% with RotaTeq (p < 0.01). Additionally, 31.2% and 26.1% completed the full series by24 weeks of age for Rotarix and RotaTeq, respectively (p < 0.05) (Table 3); similar trends were observed in the vaccine eligible infant population

Table 3.

Rotarix and RotaTeq early protection in vaccine eligible and vaccinated infants.

Early protection among vaccine eligible infants
  Rotarix
RotaTeq
   
  (N = 659,249)
(N = 780,483)
Rotarix vs. RotaTeq difference
  n % n % % p
Full series coverage by age:
16 WoA 155,806 23.6% 95,340 12.2% −11.4% < 0.01
24 WoA 165,994 25.2% 174,452 22.4% −2.8% < 0.05
32 WoA
176,512
26.8%
206,052
26.4%
−0.4%
> 0.05
Early protection among vaccinated infants
  Rotarix
RotaTeq
   
  (N = 532,082)
(N = 668,958)
Rotarix vs. RotaTeq
 
n
%
n
%
%
p
Full series completion by age:
16 WoA 155,806 29.3% 95,340 14.3% −15.0% <0.01
24 WoA 165,994 31.2% 174,452 26.1% −5.1% <0.05
32 WoA 176,512 33.2% 206,052 30.8% −2.4% <0.05

WoA: weeks of age (age in weeks)

Full series coverage by age: the number of infants who received all doses by that age divided by the number of vaccine eligible infants

Full series completion by age: the number of infants who received all doses by that age divided by the number of vaccinated infants

Comparison with full series coverage of DTaP+ IPV+ Hib

The full series coverage of pentavalent DTaP+ IPV+ Hib vaccine was 78.0% in 2010 and 70.7% in 2012, giving a difference of −7.3% in 2012 versus 2010, however, this difference was not statistically significant (p = 0.06) (Table 4, Figure 4). The largest changes in coverage were observed in the North and in Mexico City with a difference in full series coverage in 2012 versus 2010 of −12.2% and −13.2%, respectively). Full series coverage also decreased within the rotavirus vaccination program between 2010 and 2012 but to a much larger degree than observed with the DTaP+ IPV+ Hib vaccine and was statistically significant (difference of −14.6%, p < 0.001) (Table 4).

Table 4.

Comparison of full series coverage with DTaP+ IPV+ Hib and rotavirus program between 2010 to and 2012.

Vaccine coverage among vaccine-eligible infants
  2010 (N = 659,249)
2012
(N = 780,483)
2010 vs. 2012
  n % n % n % p
Full series coverage DTaP+ IPV+ Hib 514,328 78.0 551,978 70.7 37,650 −7.3 0.06
By region:
 North 189,204 80.6 167,911 68.4 −21,293 −12.2 <0.001
 Center 183,556 79.8 213,973 73.2 30,417 −6.7 0.12
 Mexico City 42,867 93.8 50,166 80.6 7,299 −13.2 0.06
 South 98,701 66.3 119,928 66.5 21,227 0.2 0.97
Full series coverage Rotavirus program 498,312 75.6 475,845 61.0 −22,467 −14.6 <0.001
By region:
 North 181,382 77.3 145,714 59.4 −35,668 −17.9 <0.001
 Center 179,471 78.0 190,045 65.0 10,574 −13.1 <0.001
 Mexico City 41,902 91.6 45,018 72.3 3,116 −19.3 <0.001
 South 95,557 64.2 95,068 52.7 −489 −11.5 <0.001

IMSS: Mexican Social Security Institute (Instituto Mexicano del Seguro Social); DTaP+ IPV+ Hib: pentavalent DTaP+ IPV+ Hib vaccine against diphtheria, tetanus, pertussis, polio and Haemophilus influenzae type b; Rotarix: two-dose rotavirus vaccine; RotaTeq: three-dose rotavirus vaccine; n: number in subcategory; Chi square proportion comparison; p value. Full series coverage: Number of vaccine-eligible infants that received full series of rotavirus vaccines regardless of timeliness.

Figure 4.

Figure 4.

Full series coverage of DTaP+ IPV+ Hib and rotavirus vaccines in 2010 and 2012.

DTaP3: DTaP+ IPV+ Hib three-dose vaccine; Rotarix: two-dose rotavirus vaccine; RotaTeq: three-dose rotavirus vaccine. Full series coverage: Number of vaccine-eligible infants that received full series of rotavirus vaccines regardless of timeliness.

Discussion

Due to differences in the scheduled number of doses between Rotarix and RotaTeq, the vaccine coverage and compliance achieved with each vaccine were compared. Vaccine coverage for infants receiving at least one dose of vaccine was higher in 2012 with RotaTeq than in 2010 with Rotarix (85.7% versus 80.7%) nationally, mainly due to increases in coverage in the Center region (83.3% to 90.7%) and the South region (68.8% to 82.5%). The improvement in first-dose coverage may reflect an increased acceptance of the rotavirus vaccination program in 2012. Vaccine coverage for infants completing the full series, however, was higher with Rotarix than RotaTeq (75.6% versus 61.0%) nationally and in all regions; i.e., full series coverage decreased between 2010 and 2012 in the North (77.3% to 59.4%), Mexico City (91.6% to 72.3%), the Center (78.0% to 65.0%) and the South (64.2% to 52.7%). Despite efforts to assure vaccine coverage by the NIP, significantly more Rotarix-vaccinated infants compared with RotaTeq-vaccinated infants completed the full series (93.7% versus 71.1%) and completed the full series according to the recommended age and dose intervals (57.0% versus 43.2% among all eligible infants). Such differences were even more pronounced within the Southern region, aless developed areas, which had the lowest full series coverage (with Rotarix and RotaTeq) and compliance (with RotaTeq), highlighting the need to strengthen existing vaccination programs and implement strategies to increase vaccination particularly in these vulnerable areas. Improving coverage and timely delivery of vaccinations will result in more health benefits from the vaccination program for both vaccinated individuals and the population at large. When vaccine coverage is low or when timely compliance with the full series is not achieved, infants are left vulnerable to infectious diseases and their negative impact on their health.17

The findings of this study are in line with other studies from the US which reported suboptimal coverage of rotavirus vaccination despite the availability of two effective vaccines. Coverage and compliance with two-dose Rotarix were, however, higher than with three-dose RotaTeq. One US study found that 91% of those receiving Rotarix received all doses compared with 83% receiving RotaTeq (p < 0.001), and that 75% on Rotarix were fully compliant with the recommended dosing schedule versus 60% on RotaTeq (p < 0.001).18 Better series completion rates and schedule compliance rates were also found for Rotarix versus RotaTeq in studies of commercially-insured US populations; e.g., 85% of Rotarix versus 76% of RotaTeq vaccinated infants completed the full series at any time, and 69% Rotarix versus 54% RotaTeq completed on schedule (both comparisons statistically significant).19 Similarly, another study found significantly more commercially-insured US infants receiving Rotarix completed the full series than RotaTeq or a mix of both vaccines (87% versus 79% versus 73%).20 Among Medicaid-covered infants, significantly higher completion (65% versus 46%) and compliance (65% versus 31%) were observed with Rotarix than RotaTeq, respectively.21 The results also highlight the advantage of Rotarix two dose schedule in offering early protection by assuring most children will have the recommended schedule before 24 weeks of age, which has been associated with improving the vaccine effectiveness for rotavirus vaccination as recommended by the WHO.22

To explore possible temporal biases on vaccination coverage between Rotarix cohort in 2010 and the Rotateq cohort in 2012, we evaluated the pentavalent DTaP+ IPV+ Hib vaccine coverage. As this vaccine is one of the most homogenous and stable vaccination programs in Latin America it was considered a good reference for the assessment of change in general coverage and rates over time. In 2010, the full series vaccine coverage for the pentavalent vaccine was 78.0% decreasing to 70.7% in 2012 (p = 0.06) nationally but not statistically significant. which led to the conclusion that other driving factors besides general coverage decreases in the NIP (i.e., differences between Rotarix and RotaTeq dosing) also contributed to the decreased coverage of the rotavirus program between 2010 and 2012.

An increase in the eligible population of approximately 120,000 was observed in 2012 compared to 2010 due to the expansion of the IMSS registry to include coverage of infants from vulnerable population living in rural or marginal urban areas in 2012. Although we observed these differences in the population, when we evaluate the pentavalent DTaP+ IPV+ Hib vaccine coverage in 2010 and 2012, the vaccine coverage was similar suggesting minimal bias on vaccination coverage due to difference in eligible population in 2010 vs 2012.

Rotavirus vaccination has already dramatically reduced the burden of disease in Mexico by reducing childhood deaths and hospitalizations due to diarrhea. The challenge is now to reverse the decreasing coverage and compliance rates observed in all geographic regions, in order to maximize protection against this vaccine-preventable disease. A systematic review of vaccination compliance issues in developed countries identified a range of significant factors in families and in healthcare systems that had a negative effect on compliance. Some key factors influencing poor compliance in families were: low socioeconomic status, no health insurance, low parental education, lack of knowledge about disease and vaccination, younger maternal age, and forgetting vaccination appointments. Some healthcare system factors contributing to poor compliance were: inadequate support, lack of health structures, doubts about medical information, and accessibility issues.23 To address some of these barriers to vaccination, educational programs could be implemented to address knowledge gaps for parents as well as healthcare providers, healthcare systems can record and remind patients about vaccinations, and immunization services can be integrated into other healthcare sites to improve access.24

There are several limitations to this analysis. This was a retrospective database analysis that relied on IMSS data generated for the institution’s administrative and statistical purposes and not for the specific objectives of this study. Therefore, despite covering a large proportion of the country’s population, the data may be subject to omissions or errors of capture and record bias. The study compared data from one year only (2010 versus 2012) for each vaccine rather than longer term trends. Therefore, it was not possible to assess the impact on coverage increases over time with the two-dose versus the three-dose vaccine. Even though implementation time was shorter for Rotateq, the rotavirus vaccination program was already fully established and running in the year of this assessment. Additionally, no supplies issues were reported during the years evaluated.

Because of the upper age restriction for rotavirus vaccination linked to the risk of intussusception, there is only a limited window to vaccinate these infants and therefore, compliance and timeliness is even more important in the case with RV vaccine. As seen in the data, providers appeared to follow the strict recommendations about this window and since this is even smaller for 3rd dose, it results in many of the Rotateq children not receiving full schedule and not able to achieve the recommended protection against rotavirus disease.

Conclusion

Rotavirus vaccination has successfully reduced morbidity and mortality in children under 5 years in Mexico since the introduction of a NIP in 2007.

This study found significant differences in full series coverage and compliance and a higher proportion of completed scheduled at an earlier age among infants in Mexico when comparing a two-dose vaccine in 2010 with a three-dose vaccine in 2012. Such differences might need to be taken into consideration to maximize NIP benefits, including early protection, of the rotavirus vaccination program.

Patients and methods

Data from all infants in the IMSS registry aged 2 to 8 months and who received their first dose of Rotarix vaccine between January 1 and December 31, 2010, or their first dose of RotaTeq between January 1 and December 31, 2012 was included. Data was reviewed till February 2011 for Rotarix and March 2013 for Rotateq for infants whom received the first dose in the second half of the study year to allow enough time for infants to be age eligible to receive all doses of each vaccine. Those with incomplete data were excluded from the analysis.

The data collected were the date of birth, gender, residential state, rotavirus vaccine, total number of doses, and the date of each dose. The following databases were accessed to retrieve these data; Integral Healthcare Information System (Sistema Informático de Atención Integral a la Salud del IMSS, SIAIS), Yearbooks IMSS, National Health Information System (Sistema Nacional de Información en Salud, SINAIS), and National Transparency Platform (Plataforma Nacional de Transparencia, PNT).

The outcomes assessed were: vaccine coverage (defined as the number of infants vaccinated with one dose or the full series divided by the number of eligible infants) and vaccine compliance (defined as the number of infants who received all doses (full series completion) or received all doses at the recommended time (full series timeliness) divided by the number of vaccinated infants) (see Supplementary file 2).

Findings were presented at the national level and stratified by region (i.e., North, Central, South and Mexico City), as previously done in the 2012 National Health and Nutrition Survey (see Supplementary file 3).25 The outcomes were also analyzed by gender, rotavirus vaccine, age, and state.

For compliance and timeliness outcomes, the following recommendations were considered:

  • Rotarix is a two-dose oral vaccine; the first dose can be administered between six and 20 weeks of age (eight weeks is the practice at IMSS), with a minimum interval of four weeks before the second dose, and a schedule completion date before the age of 24 weeks.10,26

  • RotaTeq is a three-dose oral vaccine; the first dose can be administered between six and 12 weeks of age (eight weeks is the practice at IMSS), with the subsequent doses administered at 4-to-10-week intervals. The third dose should not be given after 32 weeks of age.11,26

All variables collected were analyzed descriptively using STATA version 14.1; numbers and percentages for dichotomous and polychotomous variables, means, medians and percentiles, results stratified by analytic period and bivariate comparisons of outcome measures by cohort (Rotarix vs RotaTeq), and by state and geographic region. For each analytic period, the number of eligible recipients was tabulated by age, gender and number of vaccine doses completed. Time and attrition between doses was examined by tabulating the number of infants by the number of Rotarix and RotaTeq doses completed. Compliance was assessed during each analytic period by comparing the proportion of infants who received their respective vaccination on-schedule, and the proportion completing their respective vaccination series.

Proportions of cases achieving each outcome in the Rotarix versus RotaTeq groups were compared using the Chi-squared test, as recommended by Campbell (2007)27 and Richardson (2011),28 and p values were calculated, according to the recommended method given by Altman et al. (2000).29

Temporal bias assessment

The study compared 2010 data for Rotarix to 2012 data for RotaTeq, therefore potential temporal bias needed to be assessed. As such, changes in coverage with the pentavalent DTaP+ IPV+ Hib vaccine between 2010 and 2012 (using the same data sources) were analyzed and compared to changes in coverage with the rotavirus program. If similar coverage changes are observed, then differences between Rotarix and RotaTeq are likely to be associated with operational factors of the program, rather than differences in the number of doses.

Supplementary Material

Supplemental Material

Funding Statement

GlaxoSmithKline Biologicals S.A. funded this study (GSK identifier number HO-15-16204) and all costs related to the development of the abstract, presentation, manuscript.

Declarations

Trademark statement

Rotarix is a trademark of the GSK group of companies.

RotaTeq is a trademark of Merck & Co., Inc.

Patient highlights

  • Rotavirus infection affects most young children worldwide, causing diarrhea which can sometimes lead to severe dehydration and death. Many countries, including Mexico, now protect infants with either a two-dose (Rotarix) or three-dose (RotaTeq) vaccination schedule.

  • This study looked at how many infants received the complete dose series of Rotarix (in 2010) or RotaTeq (in 2012), and whether they received them at the recommended age to have optimal protection from the vaccine.

  • Among infants who were eligible to be vaccinated, many more received the full series of doses with Rotarix than with RotaTeq: 75.6% versus 61.0%.

  • Among infants who initiated rotavirus vaccination, many more who received Rotarix got the full series of doses compared with those who received RotaTeq (93.7% versus 71.1%), and 75.5% versus 70.9% completed the full series according to the schedule recommended by the NIP.

  • A higher proportion of infants who initiated rotavirus vaccination were able to complete the full schedule at an earlier age with Rotarix compared to Rotateq: 29.3% versus 14.3% by 16 weeks of age, 31.2% versus 26.1% by 24 weeks of age and 33.2% and 30.8% by 32 weeks of age

Since Mexico switched from using Rotarix to RotaTeq in 2011, this study found that fewer eligible infants received the full series of doses, and fewer vaccinated infants completed the full series or completed it according to recommendations. This reduction was seen across all geographic regions of the country.

Acknowledgments

The authors thank Business & Decision Life Sciences platform for editorial assistance and publication coordination, on behalf of GSK. Pierre-Paul Prévot (Business & Decision Life Sciences) coordinated publication development and editorial support. Gabriela Oliveros and Ingrid Leal (both GSK) supported publication development. The authors also thank Kavi Littlewood (freelance on behalf of GSK) for providing medical writing support.

Authors’ contributions

All authors participated in the design or implementation or analysis, and interpretation of the study; and the development of this manuscript. All authors had full access to the data and gave final approval before submission.

Disclosure of potential conflicts of interest

Patricia Juliao, Roberto Carreño-Manjarrez and Maria Yolanda Cervantes-Apolinar are employees of the GSK group of companies. Patricia Juliao, Maria Yolanda Cervantes-Apolinar, and Rodrigo DeAntonio report ownership of shares/options in the GSK group of companies. Rodrigo DeAntonio and Ricardo Cortes-Alcala were employees of the GSK group of companies during the study. Ricardo Navarro, Gilberto Sanchez, Gerardo Luna and Andrés Castañeda are external consultants and received payment for this study from the GSK group of companies through their institution.

References

  • 1.World Health Organization (WHO) Rotavirus vaccines WHO position paper. 2013. January Accessed 2017 Sept 30 <http://www.who.int/wer/2013/wer8805.pdf>.
  • 2.Tate JE, Burton AH, Boschi-Pinto C, Parashar UD.. Global, regional, and national estimates of rotavirus mortality in children 5 years of age, 2000–2013. Clin Infect Dis. 2016;62(Suppl 2):S96–s105. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Rota Council Global introduction status. 2018. Accessed 2017 September 30 <http://rotacouncil.org/vaccine-introduction/global-introduction-status/>.
  • 4.Gastanaduy PA, Sanchez-Uribe E, Esparza-Aguilar M, Desai R, Parashar UD, Patel M, Richardson V. Effect of rotavirus vaccine on diarrhea mortality in different socioeconomic regions of Mexico. Pediatrics. 2013;131:e1115–20. doi: 10.1542/peds.2012-2797. [DOI] [PubMed] [Google Scholar]
  • 5.Richardson V, Parashar U, Patel M. Childhood diarrhea deaths after rotavirus vaccination in Mexico. N England J Med. 2011;365:772–773. doi: 10.1056/NEJMc1100062. [DOI] [PubMed] [Google Scholar]
  • 6.Richardson V, Hernandez-Pichardo J, Quintanar-Solares M, Esparza-Aguilar M, Johnson B, Gomez-Altamirano CM, Parashar U, Patel M. Effect of rotavirus vaccination on death from childhood diarrhea in Mexico. N England J Med. 2010;362:299–305. doi: 10.1056/NEJMoa0905211. [DOI] [PubMed] [Google Scholar]
  • 7.Quintanar-Solares M, Yen C, Richardson V, Esparza-Aguilar M, Parashar UD, Patel MM. Impact of rotavirus vaccination on diarrhea-related hospitalizations among children 5 years of age in Mexico. Pediatr Infect Dis J. 2011;30:S11–5. [DOI] [PubMed] [Google Scholar]
  • 8.Sanchez-Uribe E, Esparza-Aguilar M, Parashar UD, Richardson V. Sustained reduction of childhood diarrhea-related mortality and hospitalizations in mexico after rotavirus vaccine Universalization. Clin Infect Dis. 2016;62(Suppl 2):S133–9. doi: 10.1093/cid/civ1205. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Aguado T, Bhutta Z, De Oliveira L, Neuzil K, Parashar U, Steele D. Detailed review paper on rotavirus vaccines, 2009. Accessed 2017 September 30 <http://www.who.int/immunization/sage/3_Detailed_Review_Paper_on_Rota_Vaccines_17_3_2009.pdf>.
  • 10.US Food and Drug Administration (FDA) Rotarix Full prescribing information. Accessed 2017. September 30 <https://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/ApprovedProducts/UCM133539.pdf>.
  • 11.US Food and Drug Administration (FDA) RotaTeq Full prescribing information. Accessed 2017. September 30 <https://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/ApprovedProducts/UCM142288.pdf>.
  • 12.Gobierno Federal Mexico Manual de vacunacion 2008–2009. Accessed 2017. September 30 <https://www.gob.mx/cms/uploads/attachment/file/17243/Manual_Vacunacion2008-2009b.pdf>.
  • 13.Secretaría de Salud Mexico Manual de Eventos supuestamente atribuibles a la vacunación o inmunización. 2014. Accessed 2017 September 30 <https://www.gob.mx/cms/uploads/attachment/file/17248/ESAVI_2014.pdf>.
  • 14.Patel MM, Parashar UD, Santosham M, Richardson V. The rotavirus experience in Mexico: discovery to control. Clin Infect Dis. 2013;56:548–551. doi: 10.1093/cid/cis939. [DOI] [PubMed] [Google Scholar]
  • 15.Pindyck T, Tate JE, Parashar UD. A decade of experience with rotavirus vaccination in the United States - vaccine uptake, effectiveness, and impact. Expert Rev Vaccines. 2018. doi: 10.1080/14760584.2018.1489724. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Roczo-Farkas S, Kirkwood CD, Cowley D, Barnes GL, Bishop RF, Bogdanovic-Sakran N, Boniface K, Donato CM, Bines JE. The impact of rotavirus vaccines on genotype diversity: a comprehensive analysis of 2 decades of australian surveillance data. J Infect Dis. 2018. doi: 10.1093/infdis/jiy197. [DOI] [PubMed] [Google Scholar]
  • 17.Walton S, Cortina-Borja M, Dezateux C, Griffiths LJ, Tingay K, Akbari A, Bandyopadhyay A, Lyons RA, Bedford H. Measuring the timeliness of childhood vaccinations: using cohort data and routine health records to evaluate quality of immunisation services. Vaccine. 2017;35:7166–7173. doi: 10.1016/j.vaccine.2017.10.085. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Krishnarajah G, Davis EJ, Fan Y, Standaert BA, Buikema AR. Rotavirus vaccine series completion and adherence to vaccination schedules among infants in managed care in the United States. Vaccine. 2012;30:3717–3722. doi: 10.1016/j.vaccine.2011.12.077. [DOI] [PubMed] [Google Scholar]
  • 19.Eisenberg DF, Gu T, Krishnarajah G. Adherence to rotavirus vaccination quality measures in a commercially insured population. Hum Vaccin Immunother. 2013;9:389–397. doi: 10.4161/hv.22877. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Panozzo CA, Becker-Dreps S, Pate V, Jonsson Funk M, Sturmer T, Weber DJ, Brookhart MA. Patterns of rotavirus vaccine uptake and use in privately-insured US infants, 2006–2010. PloS one. 2013;8:e73825. doi: 10.1371/journal.pone.0073825. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Krishnarajah G, Landsman-Blumberg P, Eynullayeva E. Rotavirus vaccination compliance and completion in a Medicaid infant population. Vaccine. 2015;33:479–486. doi: 10.1016/j.vaccine.2014.06.059. [DOI] [PubMed] [Google Scholar]
  • 22.Burke RM, Tate JE, Pringle KD, Patel M, De Oliveira LH, Parashar UD. Effect of age at vaccination on rotavirus vaccine effectiveness in bolivian infants. Pediatr Infect Dis J. 2018;37:e216–e21. doi: 10.1097/INF.0000000000001907. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Falagas ME, Zarkadoulia E. Factors associated with suboptimal compliance to vaccinations in children in developed countries: a systematic review. Curr Med Res Opin. 2008;24:1719–1741. doi: 10.1185/03007990802085692. [DOI] [PubMed] [Google Scholar]
  • 24.Esposito S, Principi N, Cornaglia G. Barriers to the vaccination of children and adolescents and possible solutions. Clin Microbiol Infect. 2014;20(Suppl 5):25–31. doi: 10.1111/1469-0691.12447. [DOI] [PubMed] [Google Scholar]
  • 25.Barquera S, Campos-Nonato I, Hernandez-Barrera L, Pedroza A, Rivera-Dommarco JA. Prevalence of obesity in Mexican adults 2000–2012. Salud publica de Mexico. 2013;55(Suppl 2):S151–60. doi: 10.21149/spm.v55s2.5111. [DOI] [PubMed] [Google Scholar]
  • 26.Instituto Mexicano del Seguro Social (IMSS) IMSS vaccination basic chart (revised 2017). Accessed 2017. September 30 <http://www.imss.gob.mx/sites/all/statics/pdf/cuadros-basicos/G23-Vacunas.pdf>.
  • 27.Campbell I. Chi-squared and Fisher-Irwin tests of two-by-two tables with small sample recommendations. Stat Med. 2007;26:3661–3675. doi: 10.1002/(ISSN)1097-0258. [DOI] [PubMed] [Google Scholar]
  • 28.Richardson JT. The analysis of 2 × 2 contingency tables–yet again. Stat Med. 2011;30:890, author reply 1-2. doi: 10.1002/sim.4116. [DOI] [PubMed] [Google Scholar]
  • 29.Altman DG, Machin D, Bryant TN, Gardner MJ. Statistics with confidence. 2nd ed. BMJ Books; 2000. p. 49, Wiley. [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplemental Material

Articles from Human Vaccines & Immunotherapeutics are provided here courtesy of Taylor & Francis

RESOURCES