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Population effectiveness of the pentavalent and monovalent rotavirus vaccines: a systematic review and meta-analysis of observational studies

BMC Infectious DiseasesBMC series – open, inclusive and trusted201717:569

https://doi.org/10.1186/s12879-017-2613-4

Received: 4 July 2016

Accepted: 18 July 2017

Published: 15 August 2017

Abstract

Background

Rotavirus was the leading cause of acute gastroenteritis (AGE) in infants and young children prior to the introduction of routine vaccination. Since 2006 there have been two licensed vaccines available; with successful clinical trials leading the World Health Organization to recommend rotavirus vaccination for all children worldwide. In order to inform immunisation policy we have conducted a systematic review and meta-analysis of observation studies to assess population effectiveness against acute gastroenteritis.

Methods

We systematically searched PubMed, Medline, Web of Science, Cinhal and Academic Search Premier and grey literature sources for studies published between January 2006 and April 2014. Studies were eligible for inclusion if they were observational measuring population effectiveness of rotavirus vaccination against health care attendances for rotavirus gastroenteritis or AGE. To evaluate study quality we use used the Newcastle-Ottawa Scale for non-randomised studies, categorising studies by risk of bias. Publication bias was assessed using funnel plots. If two or more studies reported a measure of vaccine effectiveness (VE), we conducted a random effects meta-analysis. We stratified analyses by World Bank country income level and used study quality in sensitivity analyses.

Results

We identified 30 studies, 19 were from high-income countries and 11 from middle-income countries. Vaccine effectiveness against hospitalization for laboratory confirmed rotavirus gastroenteritis was highest in high-income countries (89% VE; 95% CI 84-92%) compared to middle-income countries (74% VE; 95% CI 67-80%). Vaccine effectiveness was higher for those receiving the complete vaccine schedule (81% VE; 95% CI 75-86%) compared to partial schedule (62% VE; 95% CI 55-69%). Two studies from high-income countries measured VE against community consultations for AGE with a pooled estimate of 40% (95% CI 13-58%; 2 studies).

Conclusions

We found strong evidence to further support the continued use of rotavirus vaccines. Vaccine effectiveness was similar to that reported in clinical trials for both high and middle-income countries. There is limited data from Low income settings at present. There was lower effectiveness against milder disease. Further studies, should continue to report effectiveness against AGE and less-severe rotavirus disease because as evidenced by pre-vaccine introduction studies this is likely to contribute the greatest burden on healthcare resources, particularly in high-income countries.

Keyword

Rotavirus Vaccine effectiveness Gastroenteritis Meta-Analysis Systematic review

Background

Prior to the introduction of rotavirus vaccine into childhood immunisation schedules, rotavirus was the most common cause of severe gastroenteritis in infants and young children. Thus, rotavirus gastroenteritis (RVGE) was estimated to be responsible for 453,000 deaths worldwide in children under 5 years of age in 2008, with over 90% of deaths occurring in low-income countries [1]. The global morbidity from rotavirus infection was also substantial with pre-vaccine introduction studies indicating that approximately 40% of diarrhoeal hospitalisations in children were caused by rotavirus [2]. In middle and high income countries without vaccination the burden of RVGE remains substantial in infants and young children with high rates of disease and RV the major contributor to diarrhoea hospitalisation. In the UK prior to vaccine introduction RVGE was estimated to be responsible for 45% of acute gastroenteritis hospital admissions, 80,000 primary care consultations and 750,000 annual diarrhoeal episodes in children under 5 years of age [3, 4]. In middle income countries such as, Mexico and Peru, prior to vaccine introduction the average incidence of RVGE was 0.3 episodes per child per year in children <2 years, resulting in significant healthcare use and mortality [5]. Although the large majority of severe RVGE occurs among young children, older children and adults can be affected, however rotavirus infection often causes milder symptoms or is asymptomatic in these ages, meaning the true burden and rate of disease incidence is poorly understood.

Since improvements in sanitation and hygiene are not expected to reduce the incidence of rotavirus infection, and treatment of RVGE is limited to rehydration therapy, immunisation of infants is considered the best option for control of the global burden of rotavirus disease. Since 2006 there have been two live-attenuated oral rotavirus vaccines that are licensed for use globally. A two dose monovalent vaccine (Rotarix®, GlaxoSmithKline Biologicals, Belgium), with the first dose typically administered at between 6-8 weeks and a second dose at least 4 weeks later and a three dose pentavalent vaccine (RotaTeq®, Merck), administered at 6-12 weeks of age with subsequent doses at 4-10 week intervals. Randomised controlled trials (RCTs) demonstrated both vaccines to be efficacious against severe RVGE; vaccine efficacy of over 80% has been shown in middle and high-income countries, whilst trials in low-income settings have reported efficacy against severe RVGE of 40-60% [6]. These trials led to a World Health Organisation recommendation for universal vaccination of all children [1, 7]. More than 90 countries have since adopted rotavirus vaccination and the global mortality from RVGE estimated to have fallen to 215 000 in 2013 with almost 50% of deaths occurring in four lower-income countries [8, 9]. Currently within the European Union only nine countries include rotavirus vaccination in their childhood immunisation programme [10, 11].

It is now a decade since the licensing and first introduction of rotavirus vaccination into childhood vaccination schedule. In order to inform immunisation policy, we have conducted a systematic review and meta-analysis of the literature on observational studies in order to assess the population effectiveness of the Rotarix® and RotaTeq® against rotavirus gastroenteritis. Effectiveness was examined by severity and by region.

Methods

Inclusion/exclusion criteria

We included prospective or retrospective observational studies (cohort and case-control studies) reporting the population effectiveness of the monovalent Rotarix® (RV1) or pentavalent RotaTeq® (RV5) against healthcare attendance for RVGE or other acute gastroenteritis (AGE), in countries where the vaccines are included in the national immunisation programme or privately offered through medical insurance. Studies published between January 2006 and 28th April 2014 were eligible for inclusion. Review articles, editorials and conference abstracts were included in citation checking but excluded from final analysis. Randomised controlled trials were also excluded.

Search strategy

We followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. We systematically searched PubMed, Medline, Web of Science, Cinhal and Academic Search Premier, OpenGrey and the Cochrane Library databases using a well-defined search strategy following a protocol registered on the University of York database for Prospectively Registered Systematic Reviews (PROSPERO: 2014:CRD42014012974). A number of relevant organisations websites were also systematically searched, and included the World Health Organisation, Public Health England, and Centers for Disease Control and Prevention. We systematically searched the literature by, pairing the terms [vacc*] and [rotavirus] with the following key words: [immuni*], [effect*], [ evaluation], and [efficacy].

Authors (DH and CM) replicated the search strategy and independently screened titles and abstracts to identify full studies that were eligible for full publication review. Subsequently these two authors independently assessed the full text publications and their final inclusion was based on a consensus between the reviewers (DH, CM, KS, AT).

Data extraction

Data extraction was autonomously carried out by three authors (DH, AT, KS) and a collaborator (MSC) using a pre-designed internally piloted extraction tool. For each study the following information was extracted: Author, Year of publication, country and region of study, funding source, study period, country vaccine coverage, study type, sample size, age of subjects, type of vaccine (RV1 and / or RV5) in case and controls groups, case definition, control definition, number of vaccine doses, relative risks / risk ratios (RR) or odds ratio (OR) or vaccine effectiveness (VE) and 95% confidence intervals (95% CI) and, if applicable, a measure of intussusception.

Grading of selected studies

The Newcastle-Ottawa Scale (NOS) for assessing the quality of non-randomised studies was identified as an appropriate tool to assess study quality [12]. Case-control and cohort-studies were assessed using the tool by the same three researchers that carried out data extraction. To quality assess case-control studies the scale used: 1) adequate definition of a case and the representativeness of cases; 2) controls selection and case definition; 3) matching of controls or adjustment for confounders in analysis; 4) ascertainment of method of cases and controls in terms of exposure (rotavirus vaccination) and non-response rate. To quality assess cohort-studies the factors assessed were: 1) representativeness of the vaccinated cohort and selection of unvaccinated cohort in relation to the vaccinated; 2) ascertainment of vaccination record, confirmation of rotavirus negative at start of study; 3) matching of exposed and non-exposed in design or adjustment for confounders in analysis; 4) ascertainment of outcome (rotavirus infection); 5) follow-up duration in relation to outcome appearance (e.g. 1 year from vaccination date) and was follow-up adequate (we defined adequate as ascertainment of outcomes for >80% of participants). The scale is categorised into three groups, selection, comparability and outcome/exposure; a maximum of nine stars can be awarded to each study. Studies scoring 0 in any of the categories were classified as having a high risk of bias, studies scoring 1 in any categories (moderate risk of bias) and 2 or above in all categories (low risk of bias).

Statistical analysis

We used Stata, version 14, statistical software (Stata Corp., College Station, TX, USA) to perform all statistical calculations for this meta-analysis. Meta-analyses were conducted separately for cohort and case-control studies. We used the study published RR for cohort studies and OR for case-control studies and calculated standard errors (SE) using study reported confidence intervals in the formula:
$$ SE=\frac{\mathit{\ln}\left( Upper confidence interval\right)-\mathit{\ln}\left( Lower Confidence interval\right)}{3.92} $$

Where studies did not report OR or RR, authors calculated crude OR or RR and SE using reported numbers of cases and controls. When a study reported both unadjusted and adjusted RRs/ORs, adjusted RRs/ORs were included in meta-analysis and unadjusted estimates excluded. Vaccine effectiveness was defined as 100 × (1 − RR) or 100 × (1 − OR). A random effects model was used to provide pooled estimates of VE. Because of differences in reported vaccine efficacy a decision was taken during data extraction, for analyses to be stratified by country income category, as defined by the World Bank and measured using gross national income per capita [6, 13]. Where a study had reported VE for multiple years the estimate for mid or most recent year (if only two years) were included in the meta-analysis. Heterogeneity was measured using chi-squared (χ2) heterogeneity p-values and I 2 statistics. A p-value<0.1 was considered to identify statistically significant heterogeneity rather than 0.05 due to the small number of studies included. The percentage of variance across studies due to heterogeneity rather than chance was categorised as low, moderate and high using I 2 values of 25-49%, 50-74% and >=75%, respectively [14].

Sensitivity analysis was conducted based on the NOS score, excluding studies with a high or moderate risk of bias and assessing whether a study was conducted in a country with routine vaccination (part of recommended health policy) or in countries where vaccination provision is private or only available in some states. Subgroup analysis was conducted on: number of doses (1 dose, and full doses), age group, and vaccine type. Both number of doses and vaccine type were identified as important analyses post-hoc. Where studies reported had more than one type of control group the following hierarchy was used to select estimates for use in meta-analyses: 1) community/neighbourhood; 2) hospital non AGE controls; hospital RV negative AGE controls.

Publication bias was checked by funnel plot asymmetry and use of Begg’s test [15].

Results

Study characteristics

The initial search strategy identified 2,097 studies as potentially relevant; of these, 30 were eligible for inclusion in the review (Fig. 1) [1645]. Two summary tables of study characteristics are available in Additional file 1. Seven studies were cohort studies and 23 were case-control studies (Tables 1 and 2.) Nineteen were from high-income countries and eleven were from middle income countries. Seven studies declared some funding from industry related to the rotavirus vaccines under study. Over a third of studies were conducted in the USA (n=12). The majority of studies (27/30) reported on RVGE hospitalisations and/or emergency department (ED) attendances for AGE with a positive laboratory test for rotavirus. A study by Mast et al., [16] measuring vaccine effectiveness against RVGE hospitalisation and ED attendances included only cases with severe disease defined by a Vesikari score of greater than 11 in their VE estimate [16, 46, 47]. Two studies reported RVGE ED attendances and hospitalisations combined. Five studies included community consultations for either RVGE or AGE [1721], which included a range of definitions including outpatient attendance, physician consultation and telephone consultation. The study by Fontes Vieira et al. 2011 conducted in Brazil on a community cohort examined effectiveness of vaccination against laboratory confirmed RVGE but did not report an estimate of VE; a crude estimate was therefore calculated by the authors [17]. In the majority of studies, laboratory confirmation of RVGE followed hospitalisation, an ED attendance or GP consultation for gastroenteritis symptoms such as diarrhoea. Study selection identified five studies from countries (Spain and Israel) where routine childhood vaccination is not available but either the monovalent or pentavalent vaccine is available privately and / or only in some states [18, 22, 24, 31, 42].
Fig. 1

Flow chart of publications included and excluded for this review

Table 1

Cohort study vaccine effectiveness against hospitalisations, emergency department attendances and community consultations for RVGE or AGE

Study

Country

Vaccine

Age-group (months)

Cohort year

Vaccinated (N)

Incidence among unvaccinated (N)

Vaccine effectiveness (95% CI)

Dose

Incidence

Unadjusted

Adjusted

Hospitalisation for RVGE

Eberly et al. 2011 [23]

USA

RV1 and RV5

<60

All

1

NR

581/237660

86 (78-91)

NR

1 or more

42/140213

88 (83-91)

NR

2 RV1 / 3 RV5

11/NR

90 (82-95)

NR

Panozzo et al. 2014* [30]

USA

RV1 and RV5

8-20

1

1 or more

3/68380

60/64929

NR

87 (58-96)

2

23/175890

91/91051

NR

87 (80-92)

3

22/250035

74/61218

NR

92 (87-95)

4

8/254377

13/41946

NR

90 (75-96)

Hospitalisation and ED attendance for RVGE

Wang et al. 2010 [20]

USA

RV5

<36

All

3

0/7700

23/5831

100 (87-100)

NR

Wang, 2013 [21]

USA

RV5

<36

All

1

2/5019

11/3343

88 (45-99)

NR

All

2

1/5886

13/4432

94 (61-100)

NR

Hospitalisation and ED attendance for AGE

Wang et al. 2010 [20]

USA

RV5

<36

All

3

87/7700

160/5831

59 (46-69)

59 (47-68)

Wang, 2013 [21]

USA

RV5

<36

All

1

53/5019-

63/3343

44 (18-62)

46 (22-63)

All

2

78/5886

98/4432

40 (18-56)

39 (16-55)

Hospitalisation for AGE

Panozzo et al. 2014* [30]

USA

RV1 and RV5

8-20

1

1 or more

142/68378

271/64928

NR

22 (3-37)

2

413/175765

317/90882

NR

40 (30-48)

3

512/249838

300/61136

NR

56 (49-62)

4

398/254232

109/41888

NR

41 (27-53)

Community consultations for RVGE

Wang et al. 2010 [20]

USA

RV5

<36

All

3

1/7700

20/5831

96 (76-100)

NR

Wang et al. 2013 [21]

USA

RV5

<36

All

1

0/5019 -

7/3343

100 (54-100)

NR

All

2

4/5886

5/4432

40 (<0-88)

NR

Community consultations for AGE

Fontes-Vieira et al. 2011 [17]**

Brazil

RV1

<12

1

2

87/100

84/100

-4 (-16 to 8)

NR

2

52/100

42/100

-24 (-67 to 8)

NR

Muhsen et al. 2011 [18]

Israel

RV1

<12

All

1

153/716

8801/18591

54 (47-60)

NR

All

2

1605/6870

50 (47-52)

NR

Nolan et al. 2012 [19]†

USA

RV5

<24

1

1 or more

NR

NR

NR

28 (-21 to58)

1

NR

NR

NR

22 (-13 to 46)

2

NR

NR

NR

37 (-37 to 71)

Wang et al. 2010 [20]

USA

RV5

<36

All

3

1321/7700

1377/5831

27 (22-33)

28 (22-33)

Wang et al. 2013 [21]

USA

RV5

<36

All

1

651/5019

521/3343

17 (6-26)

17 (7-26)

All

2

774/5886

847/4432

31 (24-38)

28 (21-35)

* Direct effect estimates, ** Crude VE calculated by authors, NR not reported, ED emergency department, d days, AGE acute gastroenteritis, RVGE rotavirus gastroenteritis, †GP consultations reported, paper also reported telephone triage and episodes (calls and visits within ten days), two cohorts were followed, the 1st for two seasons and 2nd for one season

Table 2

Case-control study vaccine effectiveness against hospitalisations, emergency department attendances for RVGE or AGE (partial is for 1 dose of RV1 or RV5 if reported)

Study

Country

Vaccine

Age in months (m) and / or days (d)

Control group

Cases vaccinated (N/Total)

Controls vaccinated (N/Total)

Vaccine effectiveness (95% CI)

Partial

Full

Partial

Full

Partial

Full

Hospitalisations for RVGE

Braeckman et al. 2012 [32]

Belgium

RV1

<36

Hospital - RV (-) AGE

81/179*

70/160

208/228

179/198

91 (82-95)

90 (81-95)

3-11

36/77*

30/66

99/104

79/84

93 (80-97)

91 (75-97)

12-31

45/102*

40/94

109/124

100/114

89 (75-95)

90 (76-96)

Carvalho-Costa et al. 2009 [25]

Brazil

RV1

<60

Hospital - RV (-) AGE

NR

4/14

NR

35/60

NR

71 (-15-93)

Castilla et al. 2012 [31]

Spain

RV1 & RV5

3-59

Hospital - RV (-) AGE

NR

9/262

NR

80/518

NR

83 (65-93)

<24

NR

8/215

NR

69/371

NR

82 (60-93)

24-59

NR

1/43

NR

11/99

NR

89 (17-99.8)

Correia et al. 2010 [35]

Brazil

RV1

6-11

Hospital - RV (-) AGE

NR

NR

NR

NR

NR

77 (42-91)

Cortese et al. 2011 [36]

USA

RV5

>7

Hospital - RV (-) AGE

NR

20/140

NR

163/280

NR

92 (86-96)

>7

Communitya

NR

17/221

NR

672/1953

NR

90 (84-94)

Cortese et al. 2013 [37]

USA

RV1

>7

Hospital - RV (-) AGE

NR

2/30

NR

101/140

NR

98 (90-100)

>7

Communitya

NR

2/28

NR

206/440

NR

94 (71-99)

Cotes-Cantillo et al. 2014 [29]

Colombia

RV1

<60

Hospital - RV (-) AGE

NR

6/84

NR

670/711

NR

-2 (-182 to 63)

6-11

NR

12/15

NR

628/655

NR

84 (23-97)

≥12

NR

64/67

NR

628/655R

NR

-80 (-559 to 51)

de Palma et al. 2010 [38]

El Salvador

RV1

<25

Community

72/171

152/251

199/352

617/770

51 (26-67)

76 (64-84)

6-11

NR

49/63

NR

205/222

NR

83 (68-91)

12-24

NR

79/108

NR

284/335

NR

59 (27-77)

Desai et al. 2010 [39]

USA

RV1 & RV5

2-35

Hospital - RV (-) AGE

5/42*

NR

24/80

NR

94 (55-99)

NR

Community

5/42*

NR

21/73

NR

96 (59-99.8)

NR

Guh et al. 2011 [40]

USA

RV5

<36

Community

2/54

0/54

34/270

25/270

84 (25-96)

92 (48-100)

Ichihara et al. 2014 [41]

Brazil

RV1

4-24

Hospital – RV (-) and non-vaccine preventable

33/215

115/215

279/1961

1481/1961

60(37-75)

72(44-85)

Justino et al. 2011 [33]*

Brazil

RV1

3-11

Hospital - non AGE or vaccine preventable

NR/120

NR/77

NR/120

NR/77

61 (28-78)

56 (12-78)

12-35

NR/324

NR/235

NR/324

NR/235

35 (4-56)

32 (-4 to 46)

3-35

NR/444

NR/312

NR/444

NR/312

44 (23-60)

40 (14-58)

3-11

Community no AGE symptoms

NR/91

NR/64

NR/91

NR/64

89 (63-97)

96 (68-99)

12-35

NR/240

NR/185

NR/240

NR/185

48 (17-68)

65 (37-81)

3-35

NR/331

NR/249

NR/331

NR/249

62 (42-75)

76 (58-86)

Muhsen et al. 2010 [42]*

Israel

RV1 & RV5

<28 (approx.)

Hospital - RV (-) AGE

2/111

NR

36/216

NR

89 (52-98)

NR

Martinon-Torres et al. 2011 [24]

Spain

RV1 & RV5

<24

Hospital - RV (-) AGE

2/75

1/74

22/186

130/294

80 (11-95)

98 (87-99.8)

Patel et al. 2009 [26]

Nicaragua

RV5

<24

Community

31/80

143/192

116/213

442/539

52 (14-73)

43 (9-64)

Hospital - RV (-) AGE

31/80

143/192

106/181

350/425

60 (24-78)

49 (17-68)

Community and Hospital - RV (-) AGE

31/80

143/192

222/394

792/964

55 (22-74)

44 (15-63)

Patel et al. 2013 [43])

Bolivia

RV1

6-11

Hospital - RV (-) non AGE

NR

NR

NR

NR

NR

77 (51-89)

12-35

NR

NR

NR

NR

NR

76 (59-86)

<36

100/192

208/300

226/343

857/974

56 (32-72)

77 (65-84)

6-11

Hospital - RV (-) AGE

NR

NR

NR

NR

NR

64 (34-80)

12-35

NR

NR

NR

NR

NR

72 (52-86)

<36

100/192

208/300

131/208

510/587

36 (0-59)

69 (54-79)

Patel et al. 2012 [27]

Nicaragua

RV5

6-44

Hospital - RV (-) Non AGE or vaccine preventable and Community

NR

773/849

NR

3914/4062

NR

70 (59-78)

6-11

NR

NR

NR

NR

NR

73 (54-84)

12-44

NR

NR

NR

NR

NR

68 (51-79)

6-44

Hospital - RV (-) AGE

NR

773/849

NR

3097/3247

NR

45 (25-59)

6-11

NR

NR

NR

NR

NR

64 (43-78)

12-44

NR

NR

NR

NR

NR

30 (-5 – 53)

Payne et al. 2013 [28]

USA

RV1

<60

Hospital - RV (-) AGE

NR/22

NR

NR/34

NR

32 (-156-82)

NR

RV5

NR/130

NR

NR/372

NR

86 (74-91)

NR

Snelling et al. 2009 [44]

Australia

RV1

<60

Community

10/21

3/21

58/83

32/83

57 (<0-83)

85 (23-97)

Staat et al. 2011 [34]

USA

RV5

1-37

Hospital - RV (-) AGE

1/38

3/40

12/44

17/49

89 (16-99)

95 (48-99)

1-37

Hospital - RV (-) ARI

1/60

29/102

5/64

40/113

94 (55-99)

82 (50-93)

Hospital admissions for AGE

Snelling et al. 2009 [44]

Australia

RV1

<60

Community

21/42

11/42

120/166

72/166

67 (29-84)

78 (40-92)

ED attendances for RVGE

Cotes-Cantillo et al. 2014 [29]

Colombia

RV1

<60

ED - RV (-) AGE

NR

143/156

NR

670/711

NR

16 (79-61)

6-11

NR

27/31

NR

27/655

NR

79 (24-94)

≥12

NR

112/119

NR

628/655

NR

-40 (-271 to 47)

Cortese et al. 2011 [36]

USA

RV5

>7

Hospital- RV (-) AGE

NR

8/41

NR

163/280

NR

81 (53-92)

>7

Community

NR

6/62

NR

138/567

NR

84 (58-94)

Cortese et al. 2013 [37]

USA

RV1

>7

Hospital- RV (-) AGE

NR

20/65

NR

101/140

NR

86 (67-94)

>7

Community

NR

17/61

NR

438/862

NR

65 (35-81)

Payne et al. 2013 [28]

USA

RV1

<60

ED- RV (-) AGE

38

NR

121

NR

78 (46-91)

NR

RV5

<60

ED- RV (-) AGE

229

NR

1439

NR

81 (70-84)

NR

Staat et al. 2011 [34]

USA

RV5

15 d-47m

ED- RV (-) AGE

5/56

8/59

12/66

22/76

75 (-64 -96)

74 (16-92)

15 d-47m

ED - ARI

7/76

8/77

16/101

54/139

45 (-80 -83)

88 (64-96)

Hospitalisations and ED attendances for RVGE

Cortese et al. 2011 [36]

USA

RV5

>7

Hospital RV (-) AGE

10/163

23/283

20/137

141/341

69 (27-87)

89 (81-94)

8-11

NR

4/24

NR

63/92

NR

93 (75-99)

12-23

NR

21/102

NR

86/147

NR

89 (77-94)

>23

NR

3/55

NR

14/41

NR

91 (62-99)

56d-5m

11/69

NA

97/248

NA

71 (40-87)

NA

56d-5m

Communitya

11/69

NA

184/633

NA

62 (20-82)

NA

>7

NR

23/283

NR

850/2520

NR

89 (83-93)

8-11

NR

3/109

NR

194/1009

NR

94 (78-99)

12-23

NR

17/116

NR

517/988

NR

88 (80-93)

>23

NR

3/58

NR

139/523

NR

87 (56-96)

Cortese et al. 2013 [37]

USA

RV1

>7

Hospital RV (-) AGE

NR

22/95

NR

101/140

NR

91 (80-95)

8-11

NR

5/14

NR

45/61

NR

85 (35-97)

12-23

NR

14/66

NR

46/68

NR

91 (75-96)

>7

Communitya

NR

19/89

NR

644/1302

NR

76 (58-86)

8-11

NR

4/14

NR

114/196

NR

70 (24-91)

12-23

NR

13/65

NR

462/967

NR

76 (53-87)

Donauer et al. 2013 [45]

USA

RV5

<36

Community

8/76

2/76

165/743

329/743

77 (14-94)

92(60-99)

Hospital - RV (-) AGE

8/76

2/76

47/179

15/179

68 (-18 to 91)

92(21-99)

Hospital - RV (-) ARI

8/76

2/76

71/288

27/288

58 (-38 to 87)

92(33-99)

Mast et al. 2011 [16]

Nicaragua

RV5

Overall

Community

NR

241/300

NR

812/851

NR

87(74-93)

<12

NR

62/84

NR

219/225

NR

93(62-99)

≥ 12

NR

179/216

NR

593/626

NR

85(69-93)

Overall

Hospital – RV(-) AGE

NR

241/300

NR

711/792

NR

64(44-78)

<12

NR

62/84

NR

215/233

NR

78(49-91)

≥ 12

NR

179/216

NR

496/559

NR

55(22-74)

Overall

Combined

NR

241/300

NR

1523/1643

NR

76(63-84)

<12

NR

62/84

NR

434/458

NR

85(66-93)

≥ 12

NR

179/216

NR

1089/1185

NR

71(51-82)

Payne et al. 2013 [28]

USA

RV1

<60

Hospital - RV (-) AGE

46

56

83

140

57 (-45-87)

70 (39-86)

<60 (2011 season only)

53

NR

96

-

64 (23-83)

NR

12-23

7

NR

54

-

56 (-59-100)

NR

24-35

46

NR

79

NR

86 (60-95)

NR

RV5

<60

Hospital - RV (-) AGE

233

537

307

1445

70 (50-82)

84 (78-88)

<60 (2010 season only)

111

NR

924

NR

82 (69-89)

NR

<60 (2011 season only)

248

NR

887

NR

84 (77-89)

NR

12-23

34

NR

402

NR

85 (63-94)

NR

24-35

121

NR

681

NR

89 (82-93)

NR

36-47

91

NR

414

NR

83 (69-90)

NR

Staat et al. 2011 [34]

USA

RV5

15d -37m

Hospital - RV (-) AGE

9/136

16/143

40/191

87/238

74 (37-90)

87 (71-94)

1-11

6/65

3/62

30/109

19/98

63 (7-87)

86 (31-97)

12-23

3/38

8/43

6/45

48/87

81 (22-97)

90 (65-97)

15d -37m

Hospital - RV (-) ARI

10/159

17/166

79/391

195/507

73% (43-88)

85 (72-91)

1-11

6/76

3/73

60/230

43/213

74 (31-90)

84 (41-96)

12-23

4/41

9/46

15/87

104/176

70 (16-92)

87 (68-95)

Any episode of RVGE

Bellido-Blasco et al. 2012 [22]

Spain

RV1 & RV5

<36

RV (-) AGE

2/71

NR

57/261

NR

88 (46–99.7)

NR

Castilla et al. 2012 [31]

Spain

RV1 & RV5

3-59

RV (-) AGE

45/756*

34/756

1094/6036*

849/6036

78 (70-84)

78 (68-85)

3-11

NR

12/309

NR

248/1365

NR

78 (58-88)

12-23

NR

16/318

NR

481/2678

NR

82 (69-89)

24-59

NR

6/118

NR

120/1748

NR

61 (0-84)

Martinon-Torres et al. 2011 [24]

Spain

RV1 & RV5

<24

RV (-) AGE

3/143

8/148

22/186

130/294

84(46-95)

93 (85-97)

AGE, all cause gastroenteritis symptoms; ARI, acute respiratory infection; RV (-), rotavirus test negative; ED, emergency department; d, days

*One or more doses reported for partial

Controls for case-control studies were primarily hospital controls that were admitted for AGE symptoms but with a rotavirus negative laboratory test result. A few studies also used community asymptomatic controls or non-AGE hospital controls, such as children admitted with acute respiratory infection (Additional file 1: Table S2). VE was measured for a range of age groups across studies.

Quality of included observational studies

The quality of studies varied considerably (Table 3). It was difficult to ascertain for most studies whether history of disease in control subjects was considered. The majority of studies used a combination of vaccination cards and medical records to ascertain vaccination status. The majority of studies either matched controls or adjusted for age in the analysis as a minimum and those with community controls often used an indicator of residence such as GP location as a covariate. A high risk of bias was identified in two out of seven cohort studies [17, 23] and two out of 23 case-control studies had a high risk of bias [24, 25].
Table 3

Quality of observational studies included in the review of rotavirus vaccine effectiveness. Using the Newcastle-Ottawa Scale

Study No.

Study

Country

Study design

Selection

Comparability

Outcome / exposure

Overall

Bias

1

Bellido-Blasco et al. 2012 [22]

Spain

Case-control

3

2

3

8

Low

2

Braeckman et al. 2012 [32]

Belgium

Case-control

3

2

3

8

Low

3

Carvalho-Costa et al. 2009 [25]

Brazil

Case-control

2

0

1

3

High

4

Castilla et al. 2012 [31]

Spain

Case-control

3

2

3

8

Low

5

Correia et al. 2010 [35]

Brazil

Case-control

3

1

3

8

Moderate

6

Cortese et al., 2011 [36]

USA

Case-control

3

2

3

8

Low

7

Cortese et al. 2013 [37]

USA

Case-control

3

2

3

8

Low

8

Cotes-Cantillo et al. 2014 [29]

Colombia

Case-control

3

2

3

8

Low

9

de Palma et al. 2010 [38]

El Salvador

Case-control

3

2

3

8

Low

10

Desai et al. 2010 [39]

USA

Case-control

3

2

2

7

Low

11

Donauer et al. 2013 [45]

USA

Case-control

2

2

2

6

Low

12

Guh et al. 2011 [40]

USA

Case-control

4

1

3

9

Moderate

13

Ichihara et al. 2014 [41]

Brazil

Case-control

3

2

2

7

Moderate

14

Justino et al. 2011 [33]

Brazil

Case-control

4

2

3

9

Low

15

Martinon-Torres et al. 2011 [24]

Spain

Case-control

4

0

2

6

High

16

Mast et al. 2011 [16]

Nicaragua

Case-control

3

2

1

7

Moderate

17

Muhsen et al. 2010 [42]

Israel

Case-control

3

2

1

6

Moderate

18

Patel et al. 2009 [26]

Nicaragua

Case-control

4

2

3

9

Low

19

Patel et al. 2012 [27]

Nicaragua

Case-control

4

2

2

8

Low

20

Patel et al. 2013 [43]

Bolivia

Case-control

3

2

3

8

Low

21

Payne et al. 2013 [28]

USA

Case-control

3

2

2

7

Low

22

Snelling et al. 2009 [44]

Australia

Case-control

3

2

3

8

Low

23

Staat et al. 2011 [34]

USA

Case-control

3

2

2

7

Low

24

Eberly et al. 2011 [23]

USA

Cohort

3

0

3

6

High

25

Fontes-Vieira et al. 2011 [17]

Brazil

Cohort

3

0

2

5

High

26

Muhsen et al. 2011 [18]

Israel

Cohort

3

1

3

7

Moderate

27

Nolan et al. 2012 [19]

USA

Cohort

4

2

3

9

Low

28

Panozzo et al. 2014 [30]

USA

Cohort

4

2

3

9

Low

29

Wang et al. 2010 [20]

USA

Cohort

4

1

3

8

Moderate

30

Wang et al. 2013 [21]

USA

Cohort

4

1

3

8

Moderate

Meta-analysis of vaccine effectiveness against hospitalisation or combined hospitalisation and emergency department attendance for laboratory confirmed RVGE

For this outcome measure cohort studies were too few to conduct a meta-analysis (Table 1). We therefore, included 21 out of the 22 case control studies that measured vaccine effectiveness against hospitalisation or hospitalisation and ED attendance for laboratory confirmed RVGE in the meta-analysis. Patel et al. 2009 was excluded because a more recent publication Patel et al., 2012 provided more recent estimates of effectiveness for the same cohort [26, 27]. If studies reported more than one age group the overall estimate for the broadest age group was included in the meta-analysis. Studies which reported on 0 doses vs full dose or 0 dose vs 1+ dose were included. Some 22 estimates from 21 studies were included, as Payne et al, 2013 had separate results for RV1 and RV5 [28]. The funnel plot shows some asymmetry, however this is not significant for Begg’s (p=0.06) tests (Fig. 2). Therefore, we included all 21 studies in the meta-analysis.
Fig. 2

Funnel plot of vaccine effectiveness against hospitalisation or hospitalisation and emergency department attendance for laboratory confirmed RVGE (only adjusted effect estimates included)

There was statistically significant heterogeneity (I 2= 60.6, p < 0.001) across all studies (Fig. 3). Therefore pooled estimates of OR (0.18, 95% CI 0.14–0.23, 21 studies [22 estimates], p<0.001) were calculated using a random effects model. The pooled VE was therefore 82% (95% CI 80–88%; 21 studies [22 estimates], p<0.001). A stratified analysis by World Bank Country Classifications calculated pooled estimated ORs. Pooled VE was lower in middle-income countries (74% VE; 95% CI 67-80%; 9 studies, p<0.001) compared with high income countries (89% VE; 95% CI 84-92%; 12 studies [13 estimates], p<0.001). There was low to moderate heterogeneity for middle (I 2= 37.4%, p=0.120) and high income countries (I 2 = 40.8%, p=0.06). The study by Cotes-Cantillo et al., 2014 was the only study to report a negative vaccine effectiveness (-2 VE; 95% CI -182 to 63%) [29].
Fig. 3

Vaccine effectiveness against hospitalisation or hospitalisation and emergency department attendance for laboratory confirmed RVGE (only adjusted effect estimates included)

Pooled estimates for case-control studies in high income settings (89% VE; 95% CI 84-92%; 12 studies [13 estimates]) were comparable to the three unpooled cohort study estimates. All cohort studies were conducted in high income settings. One study reported an adjusted VE estimate of 87% (95% CI 80-92%) and other two studies stated unadjusted estimates of 100% (95% CI 87-100%), and 90% (95% CI 82-95%) [20, 23, 30].

Sensitivity analysis

We identified the possibility of study bias using the Newcastle-Ottawa Scale. The pooled OR for studies with a low risk of bias was 0.18 (95% CI 0.13-0.25; 13 studies [14 estimates], p<0.001), suggesting that any bias in these studies may have been minimal. The corresponding pooled estimates by World Bank classification did not change substantially. When studies from countries with state-based or private rotavirus vaccine provision (Castilla et al 2012, Martinon-Torres, 2011 and Muhsen et al., 2010) were dropped from the meta-analysis the pooled OR remained similar (0.19 OR; 95% CI 0.14-0.25; 18 studies [19 estimates], p<0.001) [24, 31, 42].

To further investigate the potential for publication bias, specifically that the effect of industry funding, we excluded 4 studies which had measured RVGE hospitalisations but were funded by industry [16, 3234]. Overall pooled ORs remained comparable (0.19 OR; 95% CI 0.14-0.26 ; 17 studies [18 estimates], p<0.001). We also established that including an estimate from a study which measured vaccine effectiveness against severe disease (Vesikari score ≥11), did not cause an overestimation of the pooled estimate [16].

Subgroup analyses

Age

Because the age groups included in studies were varied we grouped ages in to the following groups to assess VE by crude age groups: <1 year, <2 years, >1 year and 1-2 years of age. In middle-income countries there was some variation in pooled estimates by age group but confidence intervals overlapped between estimates (Fig. 4a). Here estimates should be interpreted with caution as there was only 1 study in each of the 1-2 year and <2 year groups. Additionally, the VE estimate for children aged >12 months from the 2014 study by Cotes-Cantillo stood out as being heterogeneous. As the authors note this is likely to be due to the low sample size in this group and potentially due to a variation in strain dominance by age [29]. Estimates were very similar across age ranges in high-income countries (Fig. 4b).
Fig. 4

Vaccine effectiveness against hospitalisation or hospitalisation and emergency department attendance for laboratory confirmed RVGE comparing partial age groups a middle income countries, b high income countries. (only adjusted effect estimates included)

Full v partial vaccine dose

To determine the impact of the number of vaccine doses on vaccine effectiveness we compared studies which reported full dose vaccination with first dose vaccination for RV1 and RV5 vaccine effectiveness estimates. There were 21 studies which either reported full or partial vaccination giving 32 estimates (13 partial schedule; 19 full vaccine schedule). Pooled vaccine effectiveness for full dose (81% VE; 95% CI 75-86%, p<0.001) was higher than for partial dose (62% VE; 95% CI 55-69%, p<0.001). However, there was moderate to high heterogeneity for studies reporting estimates for full dose (I2= 60.2%, p<0.001). When stratified by World Bank classification, this difference was most pronounced in middle income countries, where pooled vaccine effectiveness for full dose was 74% (95% CI 67-80%, p<0.001) and 57% (95% CI 47-66%, p<0.001) for partial dose (Fig. 5a). Wider confidence intervals were reported in studies reporting full vaccination, likely due to smaller available sample sizes. In high income countries VE for partial vaccine dose was 72% (95% CI 60-80%, p<0.001) compared to 87% (95% CI 81-91%, p<0.001) for full dose (Fig. 5b).
Fig. 5

Vaccine effectiveness against hospitalisation or hospitalisation and emergency department attendance for laboratory confirmed RVGE comparing partial dose to full dose a middle income countries, b high income countries (only adjusted effect estimates included)

RV1 and RV5 vaccine effectiveness

Pooled VE for RV1 and RV5 stratified by World Bank country classification showed that RV5 has slightly higher VE point estimates in both high and middle income countries but this difference was not significant. RV1 is the predominant vaccine used in studies from middle income countries included in the meta-analysis (7/10). In high income countries three studies reported VE for RV1, six for RV5 and four RV1 and RV5 combined.

Meta-analysis of vaccine effectiveness against emergency department attendances for RVGE

There were 4 estimates from three studies that included measure of VE for ED attendances for RVGE [28, 29, 34]. Three estimates were from high income countries and one from middle-income. Publication bias was not assessed as there were inadequate numbers of studies to properly assess via a Begg’s. Heterogeneity was high for these studies (I2=78.7%, p<0.001). Random effects meta-analysis gave a pooled OR of 0.26 (95% CI 0.12-0.57, p=0.001), indicating a significant effect of vaccination against ED attendances for RVGE (Fig. 6). Analysis stratified by World Bank country classifications showed significant VE of 81% (95% CI 75-86%, p<0.001) for studies from high income countries. There was only one study from middle income countries with a VE of 16% (95% CI -79% to 61%, p=0.651).
Fig. 6

Vaccine effectiveness against emergency department attendances for RVGE (only adjusted effect estimates included)

Meta-analysis of vaccine effectiveness against community consultations for AGE

A single study reported full dose vaccine effectiveness against community consultations for laboratory confirmed RVGE, reporting a high unadjusted VE estimate of 96% (95% CI 76-100%) [20, 21]. However, four cohort studies included estimates of vaccine effectiveness for community consultations for AGE [1721]. Three studies were from high income countries and one from middle-income. Only two out of the four studies reported adjusted estimates. The study by Nolan et al., 2012 only reported an adjusted VE for 1 or more doses [19]. We therefore could only include three cohort studies which report unadjusted VE in the meta-analysis. Publication bias was not assessed as there were inadequate numbers of studies to properly assess via a Begg’s test. Heterogeneity was very high for these studies (I2=97.9%, p<0.001). Random effects meta-analysis gave a pooled RR of 0.74 (95% CI 0.52-1.06, p=0.10), indicating a non-significant effect of vaccination against community consultations for AGE (Fig. 7). However, analysis stratified by World Bank country classifications showed significant VE of 40% (95% CI 13-58%, p=0.008) for studies from high income countries. There was only one study from middle income countries with a VE of -24% (95% -67% to 8%, p=0.157), this study was assessed as having a high risk of bias as crude VE was calculated by the authors and children in the vaccinated cohort were significantly younger than the unvaccinated cohort.
Fig. 7

Vaccine effectiveness against community consultations for AGE (only unadjusted effect estimates included)

Discussion

The pooled data from case-control studies indicates that RV vaccination is highly effective for preventing hospitalisations and / or ED attendances for laboratory confirmed rotavirus, as VE was 89% (95% CI 84-92) for high income countries and 74% (95% CI 67-80) for middle income countries. This finding is further supported by comparable estimates from the unpooled cohort studies. Most studies reporting VE for community consultations could not identify the causative organism and therefore reported a much lower effectiveness against community consultations for AGE (26% VE; 95% CI -6 to 48%). However, like VE against RVGE hospitalisations and ED attendances, the pooled VE for community consultations for AGE was significant in high income countries (40% VE; 95% CI 13-58%). This study was also able to show that studies from countries with similar economic classification demonstrate similar effectiveness and that effectiveness was lower in middle income countries compared with high income countries. Vaccine effectiveness against RVGE hospitalisations in high income countries (89% VE; 95% CI 84-92%) was consistent with but at the upper limit of that reported in reported in a Cochrane Review of RCTs; 85% (95% CI 80-88%) for RV1 and 82% (95% CI 50-93%) for RV5 for preventing severe rotavirus diarrhoea in children up to two years of age [6]. Differing study definitions of severity and age maybe responsible for the slight difference between pooled estimates. Additionally, pooled VE estimates from meta-analysis for RVGE hospitalisations in middle income countries (Brazil, Colombia, Nicaragua and Bolivia) were significantly lower than high-income countries, again consistent with estimates from efficacy studies [6, 48].

Our systematic review found substantial differences in the quality and design of studies and considerable heterogeneity. However, there was no evidence of publication bias. Heterogeneity was dealt with by stratifying the analysis by World Bank income classification when heterogeneity was low to moderate and by using sensitivity analysis to identify factors which may have caused bias in the overall estimate. We conclude that the best pooled estimates are provided by stratifying by World Bank country classification. Sensitivity analyses for RVGE hospitalisations and or ED attendances did not identify any substantial effects resulting from differences in study quality. Exclusion of studies from countries with only state based or private provision of RV vaccination made little difference to the overall effect estimates.

Sub-analyses by vaccine dose identified that 1 dose of RV vaccine conferred a lower overall VE estimate than full course dose, particularly in middle income countries, indicating that there is a clear benefit for children completing the full schedule. Wider confidence intervals were seen for partial dose estimates due to smaller available sample sizes which are likely a result of the majority of children completing recommended schedules.

It was difficult to assess VE by age as the different studies reported VE for different age groups and therefore finding standard categorisations for age was problematic. Pooled VE estimates in children aged >1 year of age in middle income countries were lower than for that for infants <1 year of age. This could be due to the higher relative disease burden in infants, a consequence of acquiring natural immunity with age, independent of vaccination [49]. Nonetheless, classifications used here showed no significant differences between age groups in both high and middle income countries, suggesting that the RV vaccination is highly effective against RVGE hospitalisation regardless of age. Interestingly, one study from Colombia reported high VE in the <1 year olds (84.4% VE; 95% CI 23-97%) but negative VE in >1 year olds (-79% VE; 95% CI -556 to 51%), the authors indicated that this could be because of a low sample size in the older group and a change in the predominant rotavirus strains circulating in Colombia during the study to heterotypic non-vaccine strains [29].

Additionally, whilst prior to vaccination the predominant strain type in many high income countries was G1P [8, 50] in lower and middle income countries there is often greater strain diversity and concurrent circulation of several strains simultaneously [1, 50]. It is possible that the frequency of more strains that heteroptypic to vaccine types may contribute to the lower effectiveness of the vaccine in middle income countries. However, there are likely to be inherent immununological and epidemiological factors at play [51].

Using meta-analysis to review VE against community consultations for AGE is particularly important in high income countries where the majority of the healthcare burden from rotavirus infection is in community healthcare settings. For instance in the UK rotavirus was deemed to be responsible for approximately 800 000 general practice consultations per year prior to vaccine introduction [4]. Pooled estimates presented here show a considerably lower vaccine effectiveness against AGE community consultations compared with RVGE hospitalisations in high income countries. Since only one study is available for middle income countries, evaluation of the effectiveness of vaccination against AGE community consultations in this setting is difficult, particularly because this study had high risk of bias predominantly due to significant differences in age of the vaccinated and unvaccinated cohorts.

Whereas clinical trials have suggested lower efficacy against milder disease [48, 52], a single study here reported VE against laboratory confirmed RVGE community consultations on par with VE against RVGE hospitalisations [20, 21]. Whilst there was no-indicator of disease severity in the study, the healthcare setting suggests milder disease. Therefore there is a need for more robustly designed studies in middle income settings and high income countries in order to properly assess RV vaccine effectiveness against milder disease resulting in community consultations for RVGE.

Studies reviewed here represent countries with a World Bank country classification of high or middle income, and clearly show lower VE in middle income countries. However, the burden of disease is likely to be greater in middle income countries representing a superior population greater potential benefit of vaccination in these settings. At time of review no studies could be included from low income settings However, findings from a recent study in Malawi suggest a VE of 64% (95% CI 24–83), similar to that reported in middle income countries [53]. Future reviews will be required to capture studies from these settings.

As these studies were conducted in the “real world” with population level vaccine introduction the VE estimates are likely to include both the direct effect and any herd protective effect of population vaccination. This could be particularly significant in cohort studies with high population vaccine uptake. Indeed only one study attempted to separate the herd protection and direct effect from the overall effect of vaccination, estimating a substantial increase in indirect effect of vaccination as cohort vaccine uptake increased over time [30]. More evidence of the indirect effect of vaccination is therefore required through subsequent cohort studies.

We searched three widely used databases—PubMed, Web of Science, and Academic Search Premier —as well as grey literature using a pre-specified, systematic search protocol. We were able to quality assess the studies included using an established critically appraised tool specifically for use with non-randomised studies in meta-analysis, allowing a good understanding of a studies validity importantly with reference to RCT as a gold standard. The majority of studies were assessed as being at low or moderate risk of bias strengthening the meta-analysis for RVGE hospitalisation. However, our assessment of study bias used one specific tool, the Newcastle-Ottawa Scale, with some author defined criteria, therefore it is possible that another bias assessment tool and criteria would identify different risk of bias. Furthermore, variations in study outcome definitions and statistical methods could have introduced error into some of our meta-analyses. For instance, heterogeneity was moderate to high in some of the meta-analyses, particularly those that examined community consultations; this could be related to varying definitions of a community consultation.

Conclusions

This review and meta-analysis has enabled the systematic production of pooled VE estimates for rotavirus vaccination globally from the literature. We conclude that RV vaccines represent a highly effective preventive measure against severe rotavirus disease, with “real world” vaccine effectiveness estimates as high as efficacy measures from RCTs. There is sufficient evidence to promote the continued roll out of both RV vaccines in both high and middle income settings. The modest benefits from vaccination against community consultations for RVGE represent information which can be used in appropriate cost-effectiveness studies, which may provide better understanding of the value of reducing mild to moderate disease through vaccination.

Notes

Abbreviations

ARI: 

Acute respiratory infection

CI: 

Confidence interval

ED: 

Emergency department

ICD: 

International Classification of Diseases

NOS: 

Newcastle-Ottawa Scale

OR: 

Odds ratio

PRISMA: 

Preferred Reporting Items for Systematic Reviews and Meta-Analyses

RCT: 

Randomised controlled trials

RR: 

Relative risks / risk ratios

RV1: 

Rotarix® vaccine

RV5: 

RotaTeq® vaccine

RVGE: 

Rotavirus gastroenteritis; acute gastroenteritis

VE: 

Vaccine effectiveness

WHO: 

World Health Organisation

Declarations

Acknowledgements

The study team would like to acknowledge the contributions of: Maria Saavedra-Campos from Public Health England, Professor Paul Garner at the Liverpool School of Tropical Medicine, Daniel Pope and David Taylor-Robinson from the Department of Public Health and Policy, University of Liverpool for their advice.

Funding

The authors received no financial support or other form of compensation related to the development of the manuscript. RV receives a salary contribution from NIHR Health Protection Research Unit in Emerging and Zoonotic Infections; RV and MIG also receive salary contributions from the NIHR Health Protection Research Unit in Gastrointestinal Infections.

Availability of data and materials

The dataset that is supporting the conclusions reached in this manuscript is available in Tables 1 and 2.

Authors’ contributions

DH conceived of the study, performed the searches, led data extraction and data analysis and produced the manuscript. NF conceived of the study and contributed to the design, analyses and the interpretation. KS performed data extraction, contributed to analyses and the interpretation. AT performed data extraction, contributed to analyses and interpretation. MIG conceived of the study and contributed to the interpretation. CM performed the searches and assisted with data extraction. NC conceived of the study and contributed to the interpretation. All authors contributed to the drafted manuscript. All authors read, contributed and approved the final manuscript.

Ethics approval and consent to participate

Not applicable for this study

Consent for publication

Not applicable.

Competing interests

NC, NF, MIG, RV and DH are in receipt of research grant support from GlaxoSmithKline (GSK) Biologicals (EPI Rota-048); MIG is in receipt of research grant support from Sanofi Pasteur–MSD (SPMSD); NC has received honoraria for participation in GSK Rotavirus Vaccine Advisory Board Meetings.

Publisher’s Note

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Authors’ Affiliations

(1)
Institute of Infection and Global Health, University of Liverpool
(2)
Field Epidemiology Service, National Infection Service, Public Health England
(3)
The Centre for Global Vaccine Research, University of Liverpool
(4)
Health Education North West
(5)
NIHR Health Protection Research Unit in Gastrointestinal Infections
(6)
NIHR Health Protection Research Unit in Emerging and Zoonotic Infections
(7)
Department of Medical Microbiology, Alder Hey Children’s NHS Foundation Trust
(8)
Royal Liverpool and Broadgreen University Hospitals NHS Trust

References

  1. World Health Organization. Rotavirus vaccines. WHO position paper – January 2013. Relevé Épidémiologique Hebd. Wkly. Epidemiol. Rec. 2013;88:49–64.Google Scholar
  2. World Health Organization. Global networks of rotavirus gastroenteritis, 2001-2008. Wkly. Epidemiol. Rec. 2008;83:421–8.Google Scholar
  3. Harris JP, Jit M, Cooper D, Edmunds WJ. Evaluating rotavirus vaccination in England and Wales: Part I. Estimating the burden of disease. Vaccine. 2007;25:3962–70.View ArticlePubMedGoogle Scholar
  4. Tam CC, Rodrigues LC, Viviani L, Dodds JP, Evans MR, Hunter PR, et al. Longitudinal study of infectious intestinal disease in the UK (IID2 study): incidence in the community and presenting to general practice. Gut. 2012;61:69–77.View ArticlePubMedGoogle Scholar
  5. Granados-García V, Velázquez FR, Salmerón J, Homedes N, Salinas-Escudero G, Morales-Cisneros G. Burden of disease and costs of treating rotavirus diarrhea in Mexican children for the period 2001–2006. Vaccine. 2011;29:6712–9.View ArticlePubMedGoogle Scholar
  6. Soares-Weiser K, Maclehose H, Bergman H, Ben-Aharon I, Nagpal S, Goldberg E, et al. Vaccines for preventing rotavirus diarrhoea: vaccines in use. Cochrane Database Syst. Rev. 2012;11:CD008521.PubMedGoogle Scholar
  7. World Health Organization. Rotavirus vaccines WHO position paper: January 2013 - Recommendations. Vaccine. 2013;31:6170–1.Google Scholar
  8. Tate JE, Burton AH, Boschi-Pinto C, Parashar UD, World Health Organization–Coordinated Global Rotavirus Surveillance Network. Global, Regional, and National Estimates of Rotavirus Mortality in Children <5 Years of Age, 2000-2013. Clin. Infect. Dis. Off. Publ. Infect. Dis. Soc. Am. 2016;62 Suppl 2:S96–105.Google Scholar
  9. ROTA Council. Global Introduction Status [Internet]. ROTA Council. [cited 2017 Jul 21]. Available from: http://rotacouncil.org/vaccine-introduction/global-introduction-status/.
  10. Parez N, Giaquinto C, Du Roure C, Martinon-Torres F, Spoulou V, Van Damme P, et al. Rotavirus vaccination in Europe: drivers and barriers. Lancet Infect. Dis. 2014;14:416–25.View ArticlePubMedGoogle Scholar
  11. European Centre for Disease Prevention and Control. Vaccine schedule: Recommended immunisations for rotavirus infection [Internet]. ECDC. [cited 2015 Mar 2]. Available from: http://vaccine-schedule.ecdc.europa.eu/Pages/Scheduler.aspx
  12. Wells G, Shea B, O’Connell D, Peterson J, Welch V, Losos M, et al. The Newcastle-Ottawa Scale (NOS) for assessing the quality of nonrandomised studies in meta-analyses [Internet]. Ott. Hosp. Res. Inst. Available from: http://www.ohri.ca/programs/clinical_epidemiology/oxford.asp
  13. World Bank. Country and Lending Groups | Data [Internet]. 2013 [cited 2015 Oct 20]. Available from: http://data.worldbank.org/about/country-and-lending-groups
  14. Higgins JPT, Thompson SG, Deeks JJ, Altman DG. Measuring inconsistency in meta-analyses. BMJ. 2003;327:557–60.View ArticlePubMedPubMed CentralGoogle Scholar
  15. Begg CB, Mazumdar M. Operating characteristics of a rank correlation test for publication bias. Biometrics. 1994;50:1088–101.View ArticlePubMedGoogle Scholar
  16. Mast TC, Khawaja S, Espinoza F, Paniagua M, Del Carmen LP, Cardellino A, et al. Case-control study of the effectiveness of vaccination with pentavalent rotavirus vaccine in Nicaragua. Pediatr. Infect. Dis. J. 2011;30:e209–15.View ArticlePubMedGoogle Scholar
  17. Fontes Vieira SC, Gurgel RQ, Kirby A, Barreto IP, de Souza LD, Oliveira OC, et al. Acute diarrhoea in a community cohort of children who received an oral rotavirus vaccine in Northeast Brazil. Mem. Inst. Oswaldo Cruz. 2011;106:330–4.View ArticleGoogle Scholar
  18. Muhsen K, Chodick G, Goren S, Shalev V, Cohen D. The uptake of rotavirus vaccine and its effectiveness in preventing acute gastroenteritis in the community. Vaccine. 2011;29:91–4.View ArticleGoogle Scholar
  19. Nolan SM, Prasad P, Fiks AG, Zaoutis T, Tenhave TR, Coffin SE. Effect of rotavirus vaccine on reducing acute gastroenteritis in a large outpatient pediatric network. Arch. Pediatr. Adolesc. Med. 2012;166:232–9.View ArticlePubMedGoogle Scholar
  20. Wang FT, Mast TC, Glass RJ, Loughlin J, Seeger JD. Effectiveness of the pentavalent rotavirus vaccine in preventing gastroenteritis in the United States. Pediatrics. 2010;125:e208–13.View ArticlePubMedGoogle Scholar
  21. Wang FT, Mast TC, Glass RJ, Loughlin J, Seeger JD. Effectiveness of an incomplete RotaTeq (RV5) vaccination regimen in preventing rotavirus gastroenteritis in the United States. Pediatr. Infect. Dis. J. 2013;32:278–83.PubMedGoogle Scholar
  22. Bellido-Blasco JB, Sabater-Vidal S, Salvador-Ribera Mdel M, Arnedo-Pena A, Tirado-Balaguer MD, Meseguer-Ferrer N, et al. Rotavirus vaccination effectiveness: A case–case study in the EDICS project, Castellón (Spain). Vaccine. 2012;30:7536–40.View ArticlePubMedGoogle Scholar
  23. Eberly MD, Gorman GH, Eide MB, Olsen CH, Rajnik M. The effect of rotavirus immunization on rotavirus gastroenteritis hospitalization rates in military dependents. Vaccine. 2011;29:650–9.View ArticlePubMedGoogle Scholar
  24. Martinon-Torres F, Bouzon Alejandro M, Redondo Collazo L, Sanchez Lastres JM, Pertega Diaz S, Seoane Pillado MT, et al. Effectiveness of rotavirus vaccination in Spain. Hum. Vaccin. 2011;7:757–61.View ArticlePubMedGoogle Scholar
  25. Carvalho-Costa FA, Araujo IT, Santos de Assis RM, Fialho AM, Miranda de Assis Martins CM, Boia MN, et al. Rotavirus genotype distribution after vaccine introduction, Rio de Janeiro, Brazil. Emerg. Infect. Dis. 2009;15:95–7.View ArticlePubMedPubMed CentralGoogle Scholar
  26. Patel M, Pedreira C, De Oliveira LH, Tate J, Orozco M, Mercado J, et al. Association between pentavalent rotavirus vaccine and severe rotavirus diarrhea among children in Nicaragua. Jama-J. Am. Med. Assoc. 2009;301:2243–51.View ArticleGoogle Scholar
  27. Patel M, Pedreira C, De Oliveira LH, Umaña J, Tate J, Lopman B, et al. Duration of protection of pentavalent rotavirus vaccination in Nicaragua. Pediatrics. 2012;130:e365–72.View ArticlePubMedGoogle Scholar
  28. Payne DC, Boom JA, Staat MA, Edwards KM, Szilagyi PG, Klein EJ, et al. Effectiveness of pentavalent and monovalent rotavirus vaccines in concurrent use among US children <5 years of age, 2009–2011. Clin. Infect. Dis. 2013;57:13–20.View ArticlePubMedPubMed CentralGoogle Scholar
  29. Cotes-Cantillo K, Paternina-Caicedo A, Coronell-Rodríguez W, Alvis-Guzmán N, Parashar UD, Patel M, et al. Effectiveness of the monovalent rotavirus vaccine in Colombia: A case-control study. Vaccine. 2014;32(25):3035–40.View ArticlePubMedGoogle Scholar
  30. Panozzo CA, Becker-Dreps S, Pate V, Weber DJ, Jonsson Funk M, Stürmer T, et al. Direct, indirect, total, and overall effectiveness of the rotavirus vaccines for the prevention of gastroenteritis hospitalizations in privately insured US children, 2007–2010. Am. J. Epidemiol. 2014;179:895–909.View ArticlePubMedPubMed CentralGoogle Scholar
  31. Castilla J, Beristain X, Martinez-Artola V, Navascues A, Garcia Cenoz M, Alvarez N, et al. Effectiveness of rotavirus vaccines in preventing cases and hospitalizations due to rotavirus gastroenteritis in Navarre. Spain. Vaccine. 2012;30:539–43.View ArticlePubMedGoogle Scholar
  32. Braeckman T, Van Herck K, Meyer N, Pircon J-Y, Soriano-Gabarro M, Heylen E, et al. Effectiveness of rotavirus vaccination in prevention of hospital admissions for rotavirus gastroenteritis among young children in Belgium: case-control study. BMJ. 2012;345:e4752.View ArticlePubMedPubMed CentralGoogle Scholar
  33. Justino MCA, Linhares AC, Lanzieri TM, Miranda Y, Mascarenhas JDP, Abreu E, et al. Effectiveness of the monovalent G1P[8] human rotavirus vaccine against hospitalization for severe G2P[4] rotavirus gastroenteritis in Belem, Brazil. Pediatr. Infect. Dis. J. 2011;30(5):396–401.View ArticlePubMedGoogle Scholar
  34. Staat MA, Payne DC, Donauer S, Weinberg GA, Edwards KM, Szilagyi PG, et al. Effectiveness of pentavalent rotavirus vaccine against severe disease. Pediatrics. 2011;128:e267–75.View ArticlePubMedGoogle Scholar
  35. Correia JB, Patel MM, Nakagomi O, Montenegro FMU, Germano EM, Correia NB, et al. Effectiveness of Monovalent Rotavirus Vaccine (Rotarix) against Severe Diarrhea Caused by Serotypically Unrelated G2P[4] Strains in Brazil. J. Infect. Dis. 2010;201:363–9.View ArticlePubMedGoogle Scholar
  36. Cortese MM, Leblanc J, White KE, Jerris RC, Stinchfield P, Preston KL, et al. Leveraging state immunization information systems to measure the effectiveness of rotavirus vaccine. Pediatrics. 2011;128:e1474–81.View ArticlePubMedGoogle Scholar
  37. Cortese MM, Immergluck LC, Held M, Jain S, Chan T, Grizas AP, et al. Effectiveness of monovalent and pentavalent rotavirus vaccine. Pediatrics. 2013;132:e25–33.View ArticlePubMedPubMed CentralGoogle Scholar
  38. de Palma O, Cruz L, Ramos H, de Baires A, Villatoro N, Pastor D, et al. Effectiveness of rotavirus vaccination against childhood diarrhoea in El Salvador: case-control study. BMJ. 2010;340:c2825.View ArticlePubMedPubMed CentralGoogle Scholar
  39. Desai SN, Esposito DB, Shapiro ED, Dennehy PH, Vazquez M. Effectiveness of rotavirus vaccine in preventing hospitalization due to rotavirus gastroenteritis in young children in Connecticut. USA. Vaccine. 2010;28:7501–6.View ArticlePubMedGoogle Scholar
  40. Guh AY, Hadler JL. Use of the state immunization information system to assess rotavirus vaccine effectiveness in Connecticut, 2006-2008. Vaccine. 2011;29:6155–8.View ArticlePubMedGoogle Scholar
  41. Ichihara MYT, Rodrigues LC, Teles Santos CAS, Teixeira Mda G, De Jesus SR, Alvim De Matos SM, et al. Effectiveness of rotavirus vaccine against hospitalized rotavirus diarrhea: A case-control study. Vaccine. 2014;32:2740–7.View ArticlePubMedGoogle Scholar
  42. Muhsen K, Shulman L, Kasem E, Rubinstein U, Shachter J, Kremer A, et al. Effectiveness of rotavirus vaccines for prevention of rotavirus gastroenteritis-associated hospitalizations in Israel: a case-control study. Hum. Vaccin. 2010;6:450–4.View ArticlePubMedGoogle Scholar
  43. Patel MM, Patzi M, Pastor D, Nina A, Roca Y, Alvarez L, et al. Effectiveness of monovalent rotavirus vaccine in Bolivia: case-control study. BMJ. 2013;346:f3726.View ArticlePubMedPubMed CentralGoogle Scholar
  44. Snelling TL, Schultz R, Graham J, Roseby R, Barnes GL, Andrews RM, Carapetis JR. Rotavirus and the indigenous children of the Australian outback: monovalent vaccine effective in a high-burden setting. Clin. Infect. Dis. 2009;43:428–31.View ArticleGoogle Scholar
  45. Donauer S, Payne DC, Edwards KM, Szilagyi PG, Hornung RW, Weinberg GA, et al. Determining the effectiveness of the pentavalent rotavirus vaccine against rotavirus hospitalizations and emergency department visits using two study designs. Vaccine. 2013;31:2692–7.View ArticlePubMedPubMed CentralGoogle Scholar
  46. Ruuska T, Vesikari T. Rotavirus disease in Finnish children: use of numerical scores for clinical severity of diarrhoeal episodes. Scand. J. Infect. Dis. 1990;22:259–67.View ArticlePubMedGoogle Scholar
  47. Ruuska T, Vesikari T. A prospective study of acute diarrhoea in Finnish children from birth to 2 1/2 years of age. Acta Paediatr. Scand. 1991;80:500–7.View ArticlePubMedGoogle Scholar
  48. Jiang V, Jiang B, Tate J, Parashar UD, Patel MM. Performance of rotavirus vaccines in developed and developing countries. Hum. Vaccin. 2010;6:532–42.View ArticlePubMedPubMed CentralGoogle Scholar
  49. Richardson V, Hernandez-Pichardo J, Quintanar-Solares M, Esparza-Aguilar M, Johnson B, Gomez-Altamirano CM, et al. Effect of rotavirus vaccination on death from childhood diarrhea in Mexico. N. Engl. J. Med. 2010;362:299–305.View ArticlePubMedGoogle Scholar
  50. Hungerford D, Vivancos R, EuroRotaNet network members, Read JM, Pitzer VE, Cunliffe N, et al. In-season and out-of-season variation of rotavirus genotype distribution and age of infection across 12 European countries before the introduction of routine vaccination, 2007/08 to 2012/13. Euro Surveill. Bull. Eur. Sur Mal. Transm. Eur. Commun. Dis. Bull. 2016;21 doi:10.2807/1560-7917.
  51. Lopman BA, Pitzer VE, Sarkar R, Gladstone B, Patel M, Glasser J, et al. Understanding reduced rotavirus vaccine efficacy in low socio-economic settings. Plos One. 2012;7:e41720.View ArticlePubMedPubMed CentralGoogle Scholar
  52. Bresee JS, Parashar UD, Widdowson M-A, Gentsch JR, Steele AD, Glass RI. Update on rotavirus vaccines. Pediatr. Infect. Dis. J. 2005;24:947–52.View ArticlePubMedGoogle Scholar
  53. Bar-Zeev N, Kapanda L, Tate JE, Jere KC, Iturriza-Gomara M, Nakagomi O, et al. Effectiveness of a monovalent rotavirus vaccine in infants in Malawi after programmatic roll-out: an observational and case-control study. Lancet Infect. Dis. 2015;15:422–8.View ArticlePubMedPubMed CentralGoogle Scholar

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