Email updates

Keep up to date with the latest news and content from BMC Infectious Diseases and BioMed Central.

Open Access Research article

Budget impact analysis of a pneumococcal vaccination programme in the 65-year-old Spanish cohort using a dynamic model

Roberto Pradas1*, Angel Gil de Miguel2, Alejandro Álvaro2, Ruth Gil-Prieto2, Reyes Lorente1, Cristina Méndez3, Pablo Guijarro3 and Fernando Antoñanzas1

Author affiliations

1 Universidad de la Rioja, Logroño, La Rioja, Spain

2 Universidad Rey Juan Carlos, Alcorcón, Madrid, Spain

3 Pfizer Spain, Alcobendas, , Madrid, Spain

For all author emails, please log on.

Citation and License

BMC Infectious Diseases 2013, 13:175  doi:10.1186/1471-2334-13-175


The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-2334/13/175


Received:19 October 2012
Accepted:1 April 2013
Published:11 April 2013

© 2013 Pradas et al.; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

This study aimed to assess the costs and clinical benefits of the 13-valent pneumococcal conjugate vaccine (PCV13) administered annually to the 65-year-old cohort in Spain versus the alternative of not vaccinating patients and treating them only when infected.

Methods

Cases of pneumococcal disease avoided were calculated through a dynamic model based on the work of Anderson and May (1999). Sixty-six percent of the 65-year-old cohort was assumed to have been vaccinated with one PCV13 dose (304,492 subjects). Base-case estimated vaccine effectiveness and serotype coverage were 58% and 60%, respectively. Disease-related costs were calculated based on published data.

Results

Over the 5-year period, a total of 125,906 cases of pneumococcal disease would be avoided. Net savings of €102 million would be obtained. The cost-saving distribution was not homogeneous, starting in the 2nd year and increasing through the 5th. To demonstrate model robustness, an additional scenario analysis was performed using extreme values of model parameters (vaccination programme coverage, vaccine effectiveness, discount rate and disease costs). Under those scenarios, net savings were always achieved.

Conclusions

Based on the assumptions of the model, the 65-year-cohort pneumococcal vaccination campaign appears to be a cost-saving intervention in the Spanish population under different scenarios.

Background

Streptococcus pneumoniae is a major cause of disease and death in the adult population [1]. Pneumococcus accounts for a range of medical conditions including invasive pneumococcal diseases (IPD) and non-invasive mucosal infections (non-IPD). The clinical and economic burden of pneumococcal disease in the adult population remains high [2,3].

The process of preventing pneumococcal infections with vaccines has a long history, dating back to the beginning of 20th century. In Spain, a 23-valent pneumococcal polysaccharide vaccine (PPV23) is recommended for adults with certain underlying risk factors as well as all individuals 65 years of age and older [4,5].

PPV23 has had but limited impact on preventing IPD, while its effectiveness on mucosal disease (including community acquired pneumonia - CAP) is at the least controversial [6].

The routine use of pneumococcal conjugate vaccines, which induce a T-cell dependent immune response, has led to a significant reduction in vaccine-preventable cases of both IPD and non-IPD in young children [7,8]. Conjugate vaccines not only prevent individual cases of disease directly but also indirectly by reducing disease transmission. Both effects benefit the health economic profile of these vaccines.

In 2010, a new 13-valent conjugate vaccine (PCV13) that widened the spectrum of the former 7-valent conjugate was licensed to reduce the incidence of pneumococcal disease in children. An adult indication for the prevention of pneumococcal disease caused by the serotypes included in the vaccine has recently been approved.

At present, there is no evidence available regarding the cost-effectiveness of adult pneumococcal immunization in the Spanish population. This efficiency, which is illustrated by the pharmacoeconomic data, is becoming increasingly important in Public Health decision making.

Several cost-effectiveness studies have recently been published analysing the economic implications of implementing an adult pneumococcal immunization programme with PCV13 [9,10]. Comparisons between studies are difficult due to differences in methodology used and assumptions made.

In this context, the work by Rozenbaum et al. [9], adapted a former model developed by the authors to target PCV13 use in adults >65 years of age in the Netherlands. The authors concluded that, with a wide variety of assumptions, including an effectiveness of 60% against IPD and non-IPD and compared to a no-vaccination strategy, there were incremental cost-effectiveness ratios (ICERs) varying from cost-savings to 50,676€/life year gained.

Additionally, Smith et al. [10] compared different PCV13 vaccination strategies in the adult population versus no vaccination or PPV23. After varying PCV13 effectiveness by age and patient risk, the authors concluded that, in the base case scenario (vaccinating at 65 years of age and in younger high-risk individuals) the cost per quality-adjusted life year (QALY) was USD 28,900 versus no vaccination, and that PCV13 was more efficient than PPV23.

Both publications took into account indirect effects (herd immunity) using a static approach due to the Markovian structure of the models used.

The aim of our study was to estimate the cost-effectiveness of pneumococcal vaccination targeting a 65-year-old cohort versus a no-vaccination strategy using a transmission-dynamic model. To address this, we analysed pneumococcal epidemiology in the adult Spanish population over 50 years of age (15,448,561 inhabitants) [11] and measured the clinical and economic consequences during the first 5 years.

Methods

Model design

Most of the published pharmacoeconomic models for infectious diseases use decision trees or Markovian chains [12]. As mentioned, these type of models assume a constant force of infection (per-susceptible rate of infection) during the analysed period and therefore they do not fully compute the effects of a vaccination programme [13]. However, the dynamic models used by epidemiologists [14] capture both direct effects from the reduction in the number of susceptible individuals and the indirect effect associated with the reduction of the number of contacts between susceptible and infected individuals. The implementation of a pneumococcal vaccination programme causes both types of effect because it directly protects vaccinated individuals and, at the same time, indirectly protects unvaccinated individuals by limiting the carriage and therefore the transmission of pneumococcus between individuals [15].

A deterministic Susceptible → Infected → Susceptible (SIS) model was used, in which individuals who are susceptible can become infected, after which they return to the susceptible group once they have recovered. The SIS model was calibrated to the epidemic behaviour of the pneumococcal bacterium. If a preventive campaign is implemented, the susceptible group will be reduced every year according to the number of individuals effectively vaccinated (Figure 1); thus, the number of infections between the susceptible and infected groups is also reduced.

thumbnailFigure 1. Epidemic model.

Differential equation models can be used to model this epidemic behaviour dynamically [16-18]. Contacts between infected and susceptible individuals are taken into account by multiplying their values at each point in time as [I(t)·S(t)] according to the following non-linear system of ordinary differential equations:

<a onClick="popup('http://www.biomedcentral.com/1471-2334/13/175/mathml/M1','MathML',630,470);return false;" target="_blank" href="http://www.biomedcentral.com/1471-2334/13/175/mathml/M1">View MathML</a>

where t = time measured in months; I(t) and S(t) = the number of infected and susceptible individuals, respectively, at each point in time t; β = the transmission coefficient; and γ = the coefficient of natural recovery. First order derivatives with respect to t, dI(t)/dt and dS(t)/dt, represent the instant rate of variation in time of the functions associated with the different population classes (infected and susceptible); V(t), shows the number of individuals who are vaccinated at each point in time t.

The coefficient of natural recovery (γ) is one indicator of the rate at which infected individuals again become susceptible; it depends on how long an individual remains infected, which is 30 days (τ = 1 month) according to some authors [19,20]. Our model uses the month as the unit of time comprising each year; thus γ = 1/τ = 1. By applying a process of stepwise approximations, we estimated the transmission coefficient (β=0.000010009257) associated with the mean annual incidence rate of 563 pneumococcal infections per 100,000 individuals > 50 years of age (Table 1).

Table 1. Mean annual incidence (cases per 100,000)[21-24]

Adult pneumococcal disease incidence (IPD and non-IPD)

The pneumococcal diseases entered in this model were primary bacteremia, empyema, meningitis and bacteremic pneumonia (IPD), and hospitalized and out-patient pneumococcal pneumonia (non-IPD).

The pneumococcal disease incidence rate was calculated using the published number of hospitalized CAP cases in the Spanish population >50 years of age over a 5-year period (447,670 CAP discharges from 2003 to 2007) [21]. For this model, it was estimated that 50% of CAP cases were caused by Streptococcus pneumoniae[22].

In addition, according to several authors, 40% of CAP cases in adults do not require hospitalization, and those were considered out-patient pneumococcal pneumonia [23]. Finally, based on published data, an incidence rate of 30 IPD cases per 100,000 individuals was used [24].

Pneumococcal force of infection

The model associated the force of infection with the number of individuals infected at each point in time λ(t)= β·I(t). The transmission coefficient (β) represents the probability of a contact between a susceptible and an infected individual leading to transmission of the infection. Due to its high precision, a 4th order Runge–Kutta method was used to solve the differential equation system [25,26]. Figure 2 shows the proper adjustment between the historical series of infections and the series of values generated by the model.

thumbnailFigure 2. Annual rate of pneumococcal infections [[21]-[26]].

The system deals with vaccination progressively according to the following functions:

<a onClick="popup('http://www.biomedcentral.com/1471-2334/13/175/mathml/M2','MathML',630,470);return false;" target="_blank" href="http://www.biomedcentral.com/1471-2334/13/175/mathml/M2">View MathML</a>

where V is the hypothetical number of individuals actually vaccinated in each annual campaign. The pneumococcal vaccine is co-administered together with the influenza vaccine, as recommended, for specific groups [27]. The time is measured in months, one year being the epidemiologic period to run the model.

According to the recommendations of the Spanish National Centre for Epidemiology, the epidemiologic year for influenza starts in August (month 1) and it concludes in August of the following year. The interval in which V(t) is not zero is the same as the interval associated with the vaccination campaign (October and November).

Population, vaccine effectiveness, serotype and vaccine coverage

The target population for the vaccination programme is the 65-year-old cohort, but consequences were measured in the population >50 years of age. Although people enter the population >50 years of age through aging or migration and people leave it because of death or migration, we assumed that the population >50 years of age would not significantly change during the study period. Therefore the composition of the population >50 years of age was not changed in the model. In the base case scenario, as in previous published studies [9], a weighted mean vaccine effectiveness of 58% for both IPD and non-IPD (mainly non-bacteremic pneumococcal pneumonia) was assumed. It was assumed that the vaccination programme would reach an annual coverage of 66%, which is similar to the 2009–10 influenza programme [28]. The proportion of IPD and non-IPD cases covered by the serotypes included in the PCV13 vaccine was assumed to be 60%, which is a little lower than the 66% serotype coverage rate reported for 2009 in the Madrid region for persons over 59 years of age [29].

Costs

The costs associated with pneumococcal disease, in euros for the year 2010, were determined according to published data in the Spanish population [23,24]. The cost of the vaccination programme was calculated using the official price of PCV13 [30] (Table 2).

Table 2. Unit costs (€ 2010) [[23,24,30]]

Sensitivity analysis

In order to minimize model uncertainty, a sensitivity analysis was performed with two alternative scenarios. In those scenarios, vaccination coverage and vaccine effectiveness varied from 60% to 80% and from 40% to 75%, respectively, but serotype coverage remained unchanged.

Additionally, pneumococcal disease-related costs and discounts rates were also modified to broaden the sensitivity analysis spectrum, and those are described in Table 3.

Table 3. Sensitivity analysis parameters

Programme effectiveness

All patients would receive a single dose of PCV13. The annual number of effectively vaccinated individuals was calculated based on vaccine effectiveness and serotype and vaccination coverage. So it varies within model scenarios as depicted in Table 4[11]. PCV13 is considered safe and rarely causes any severe adverse event. Neither adverse events nor their related costs were considered in this model.

Table 4. Coverage of the pneumococcal vaccination programme[11]

Time horizon, perspective and estimated benefits

Analyses were undertaken from the Spanish Public Healthcare System perspective. Only direct costs were estimated, and results were expressed as the number of pneumococcal infections avoided, as this is the primary outcome generated by the differential equation system of the epidemiological dynamic model. Both clinical and economic consequences were measured during the first 5 years. According to the published Spanish recommendations [31], the discount rate applied for costs was 3%.

Results

Number of avoided infections

Implementation of a pneumococcal vaccination programme with PCV13 in a 65-year-old cohort would help to significantly reduce both the clinical and the economic burden caused by Streptococcus pneumoniae.

In the base case analysis, there would be a reduction of more than 125,000 pneumococcal cases compared to no vaccination (Table 5).

Table 5. Epidemiologic effect of the vaccination programme

The number of cases averted grows over time due to the progressive accumulation of vaccinated individuals. As the number of vaccinated individuals increases, the number of susceptible individuals decreases, and therefore there is a reduction in contacts between infected and susceptible individuals. Averted cases of pneumococcal disease were mainly cases of hospitalized pneumococcal pneumonia, followed by out-patient pneumococcal pneumonia (Table 6).

Table 6. Clinical and economic effects of the vaccination programme

Introduction of a pneumococcal vaccination programme with PCV13 in a 65-year-old cohort would be a cost-saving measure. Vaccination costs would be offset by cost saving for avoided cases of pneumococcal disease. Programme savings would be mainly generated by averted cases of hospitalized pneumonia followed by averted cases of bacteremic pneumonia (Table 6).

Sensitivity analysis

In the sensitivity analysis, although many parameters were modified in favourable and unfavourable ways, results were minimally affected. Even in the worst case scenario, we found that globally 88,366 pneumococcal cases would be averted (divided into 83,848 non-IPD and 4,518 IPD cases). In this conservative scenario, PCV13 resulted in cost savings as of the third year after the start of the programme and continues going forward (Table 7).

Table 7. Sensitivity analysis results

Discussion

The three scenarios analyzed in our dynamic model suggest that, after three years, the 65-year-old cohort pneumococcal vaccination campaign appears to be a cost-saving measure in Spain. The avoided cases of hospitalized pneumococcal pneumonia (bacteremic and non-bacteremic) are responsible for the majority of the cost savings.

Since the vaccination programme generates savings under all 3 scenarios studied and prevents cases of pneumococcal disease, calculating the cost-effectiveness and cost-utility ratio in terms of life years gained would have not provided additional information. Therefore estimation efforts concerning number of deaths prevented and impact on population quality of life, although interesting from a public health point of view, would have unnecessarily complicated the modelling without adding information to assist decision makers.

Strengths and weaknesses

This is the first evaluation of a national adult pneumococcal immunization programme with PCV13 using a dynamic model. Compared to other techniques, the use of differential equations captures the indirect effect of the vaccination programme for estimating health outcomes. This model adjusts fairly well to the pattern of the infective agent in the study population. The sensitivity analysis also showed that the model results were robust to changes in the parameters analyzed. The model economic outcomes were minimally sensitive to changes in vaccination coverage and PCV13 effectiveness.

Modelling the epidemiological impact of pneumococcal vaccination in adults is challenging due to several elements that have an impact on intervention outcomes and required some assumptions. Cohort and population models highlight different aspects of the infectious disease process and, therefore, we have only answered part of the questions raised about pneumococcal vaccination implementation [32]. We estimated the unknown effectiveness of PCV13 in adults and tried to minimize its uncertainty by using a sensitivity analysis. Additionally, pneumococcal nasopharyngeal carriage and adult-to-adult transmission patterns are not yet well understood.

In Spain, PCV13 is only included in the National Immunization Programmes for infants in Madrid [33] (2+1, since June 2010 with 96.3% uptake) and Galicia (2+1, since January 2012); these regions account for 19% of the Spanish population of all ages. So the childhood vaccination coverage within the country is uneven. For this reason, the potential herd effect from vaccinating the paediatric population has not been taken into account in the present model.

On the other hand, a potential additional effect of PPV23 on IPD cases in adults older than 65 years of age was not taken into account because we introduce the remaining burden of disease into the model after its long-term use.

Another limitation is that we did not take into account the potential increase in pneumococcal disease caused by serotypes not included in the PCV13. As there is currently no data available on the emergence of non-PCV13 serotypes, such a scenario was impossible to model.

This analysis did not include mortality rates and disease sequelae from pneumococcal disease. Having not incorporated mortality in our study should be considered as a model limitation. On the other hand, the implementation of an immunization programme in adults would increase population life expectancy and patient quality of life, which would further increase the benefit associated with this intervention. Additionally, we did not include indirect costs as this study has adopted a healthcare system perspective, so the vaccine value could have been underestimated. Although our model did not take into account the impact of the vaccine on patient quality of life, it would be interesting to measure how invasive and non-invasive pneumococcal disease influences quality of life. An appropriate instrument would be the EQ-5D, already used for other diseases such as the influenza, in the Spanish context [34].

Conclusions

In conclusion, despite the inherent limitations of this model, the analysis suggests that a 65-year-old cohort vaccination programme with PCV13 in Spain would avoid a large number of cases of pneumococcal disease over a 5-year period and would be a cost-saving measure from a healthcare system perspective.

Competing interest

This study was sponsored by Pfizer S.L.U., Madrid, Spain. Cristina Méndez and Pablo Guijarro are employees of Pfizer Spain. The rest of the authors don’t have any conflict of interest. All authors had complete access to the data, participated in the analysis and/or interpretation of results, and drafted the manuscript.

Authors’ contributions

RP, RL and FA developed the pneumococcal dynamic model, performed the sensitivity analysis and drafted the manuscript. AGdM, AA and RGP provided pneumococcal clinical and epidemiological data and gave advice regarding model assumptions. PG and CM conceived of the study, coordinated study group and helped to draft the manuscript. All authors participated in the study design and read and approved the final manuscript.

Acknowledgements

This study was supported by an unrestricted grant from Pfizer S.L.U., Madrid, Spain. We are indebted to Rogier Klok (Pfizer Inc., Collegeville, PA USA) and Reiko Sato (Pfizer Inc., Collegeville, PA USA) for their critical review of the manuscript.

References

  1. WHO:

    World Health Organization. Acute Respiratory Infections. (Update September 2009). 2009a.

    Available at: http://www.who.int/vaccine_research/diseases/ari/en/print.html webcite. Last accessed July 2011

    OpenURL

  2. Janssens JP, Krause KH: Pneumonia in the very old.

    Lancet Infect Dis 2004 Feb, 4(2):112-124. Publisher Full Text OpenURL

  3. Muñoz-Almagro , Ciruela P, Esteva C, Marco F, Navarro M, Bartolome R, Sauca G, Gallés C, Morta M, Ballester F, Raga X, Selva L: Serotypes and clones causing invasive pneumococcal disease before the use of new conjugate vaccines in Catalonia, Spain.

    J Infect 2011, 63:151e162. OpenURL

  4. Centers for Disease Control and Prevention: Prevention of pneumococcal disease: recommendations of the Advisory Committee on Immunization Practice (ACIP).

    MMWR Morb Mortal Wkly Rep 1997, 46(RR-8):1-24. PubMed Abstract | Publisher Full Text OpenURL

  5. Grupo de trabajo de vacunación de adultos de la ponencia de programas y registro de vacunaciones.

    Available at: http://www.msc.es/ciudadanos/proteccionSalud/vacunaciones/docs/recoVacunasAdultos.pdf webcite. Last accessed July 2011

    PubMed Abstract OpenURL

  6. Moberly SA, Holden J, Tatham DP, Andrews RM: Vaccines for preventing pneumococcal infection in adults.

    Cochrane Database Syst Rev 2008, 1:CD000422. PubMed Abstract | Publisher Full Text OpenURL

  7. Pilishvili T, Lexau C, Farley MM, Hadler J, Harrison LH, Bennett NM, Reingold A, Thomas A, Schaffner W, Craig AS, Smith PJ, Beall BW, Whitney CG, Moore MR: Sustained reductions in invasive pneumococcal disease in the era of conjugate vaccine.

    J Infect Dis 2010 Jan 1, 201(1):32-41. Publisher Full Text OpenURL

  8. Hansen J, Black S, Shinefield H, Cherian T, Benson J, Fireman B, Lewis E, Ray P, Lee J: Effectiveness of heptavalent pneumococcal conjugate vaccine in children younger than 5 years of age for prevention of pneumonia: updated analysis using World Health Organization standardized interpretation of chest radiographs.

    Pediatr Infect Dis J 2006 Sep, 25(9):779-781. Publisher Full Text OpenURL

  9. Rozenbaum MH, Hak E, van der Werf TS, Postma MJ: Results of a cohort model analysis of the cost-effectiveness of routine immunization with 13-valent pneumococcal conjugate vaccine of those aged =>65 years in the Netherlands.

    Clin Ther 2010, 32(8):1517-1531. PubMed Abstract | Publisher Full Text OpenURL

  10. Smith KJ, Raymund M, Nowalk MP, Roberts MS, Zimmerman RK: Cost-effectiveness of pneumococcal polysaccharide vaccine among healthcare workers during and influenza pandemic.

    Am J Manag Care 2010, 16(3):200-206. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  11. Instituto Nacional de Estadística:

    Cifras Oficiales de Población.

    Available at: http://www.ine.es webcite. Last accessed: July 2011

    OpenURL

  12. Drummond M, O´Brien BJ, Stoddart GL, Torrance GW: Métodos para la evaluación económica de los programas de asistencia sanitaria. Madrid: Ediciones Díaz de Santos; 2001. PubMed Abstract OpenURL

  13. Edmund WJ, Medley GF, Nokes DJ: Evaluating the cost-effectiveness of vaccination programmes: a dynamic perspective.

    Stat Med 1999, 18(23):3263-3282. PubMed Abstract | Publisher Full Text OpenURL

  14. Anderson RM, May RM: Infectious Diseases of Humans: Dynamics and Control. New York (USA): Oxford University Press; 1999. OpenURL

  15. Salleras L, Domínguez A, Borrás E, Soldevila N: Eficacia protectora de las vacunas y efectividad de las vacunaciones: introducción a la medición de la protección directa e indirecta.

    Vacunas 2011, 12(4):136-146. Publisher Full Text OpenURL

  16. Zill DG, Cullen MR: Ecuaciones diferenciales con problemas de valores en la frontera, 5ª edición. México, DF (México): Thomson Learning; 2002. OpenURL

  17. Blanchard P, Devaney RL, Hall GR: Ecuaciones diferenciales. Internacional Thomson Editores, SA: México; 1999. OpenURL

  18. Klein M: Mathematical methods for economics. Massachusetts (USA): Addison-Wesley; 1998. OpenURL

  19. Snedecor SJ, Strutton DR, Ciuryla V, Schwartz EJ, Botteman MF: Transmission-dynamic model to capture the indirect effects of infant vaccination with Prevenar (7-valent pneumococcal conjugate vaccine (PCV7)) in older populations.

    Vaccine 2009, 27(34):4694-4703. PubMed Abstract | Publisher Full Text OpenURL

  20. Trotter CL, Waight P, Andrews NJ, Slack M, Efstratiou A, George R, Miller E: Epidemiology of invasive pneumococcal disease in the pre-conjugate vaccine era: England and Wales, 1996–2006.

    J Infect 2010, 60(3):200-208. PubMed Abstract | Publisher Full Text OpenURL

  21. Gil-Prieto R, García-García L, Álvaro-Meca A, Méndez C, García A, Gil de Miguel Á: The burden of hospitalizations for community-acquired pneumonia (CAP) and pneumococcal pneumonia in adults in Spain (2003–2007).

    Vaccine 2011, 29(3):412-416. PubMed Abstract | Publisher Full Text OpenURL

  22. Vallès X, Marcos A, Pinart A, Marco J, Mensa M, Torres A: Hospitalized Community-Acquired Pneumonia Due to Streptococcus pneumoniae.

    Chest 2006, 130:800-806. PubMed Abstract | Publisher Full Text OpenURL

  23. Bartolomé M, Almirall J, Morera J, Pêra G, Ortún V, Bassa J, Bolívar I, Balanzó X, Verdaguer A, and the Maresme Community-Acquired Pneumonia Study Group (GEMPAC): A population-based study of the costs of care for community-acquired pneumonia.

    Eur Respir J 2004, 23:610-616. PubMed Abstract | Publisher Full Text OpenURL

  24. Picazo J, Méndez C, Oyagüez Q, Casado MA, Guijarro P: Coste-utilidad de la incorporación de las nuevas vacunas antineumocócicas conjugadas al programa de vacunación de la comunidad de Madrid Impacto sobre la enfermedad neumocócica invasora.

    Vacunas 2010, 11(3):96-104. Publisher Full Text OpenURL

  25. Braun M: Ecuaciones diferenciales y sus aplicaciones. Grupo Editorial Iberoamérica, SA: México; 1990. OpenURL

  26. Kincaid D, Cheney W: Análisis numérico. Las matemáticas del cálculo científico. Addison. Wesley Iberoamericana SA: Wilmington (Estados Unidos); 1994. PubMed Abstract OpenURL

  27. Farjas MP, Zubizarreta R, Louro A, Suárez B: Manual de vacunaciones del adulto. Barcelona: Laboratorios Esteve SA; 2003. OpenURL

  28. Ministerio de Sanidad, Política Social e Igualdad:

    Profesionales. Coberturas de Vacunación.

    Available at: http://www.msps.es/profesionales/saludPublica/prevPromocion/vacunaciones/coberturas.htm webcite. Last accessed July 2011

    OpenURL

  29. Servicio de Epidemiología de de la Comunidad Autónoma de Madrid: Informe sobre la enfermedad neumocócica invasora.

    Boletín Epidemiológico de la Comunidad de Madrid 2010, 16((7):23-57.

    Available at: http://www.madrid.org webcite. Last accessed: July 2011

    PubMed Abstract | Publisher Full Text OpenURL

  30. Comisión Interministerial de Precios de Medicamentos. 25 mayo 2010.

    Available at: http://www.msc.es/profeisonales/farmacia/financiacion/documentos/acuerdosCIPM25Mayo2010.pdf webcite. Last accessed: July 2011

    PubMed Abstract | Publisher Full Text OpenURL

  31. López Bastida J, Oliva J, Antoñanzas F, García-Altés A, Gisbert R, Mar J, Puig-Junoy J: Propuesta de guía para la evaluación económica aplicada a las tecnologías sanitarias.

    Gac Sanit 2010, 24(2):154-170. PubMed Abstract | Publisher Full Text OpenURL

  32. Standaert B, Demarteau N, Talbird S, Mauskopf J: Modelling the effect of conjugate vaccines in pneumococcal disease: Cohort or population models?

    Vaccine 2010, 28S:G30-G38. OpenURL

  33. Gutiérrez Rodríguez MA, Rosales Statkus ME, Córdoba Deorador E, Taveira Jiménez JA, Arce Arnáez A, Sanz Moreno JC, Barranco Ordóñez D, Ordobás Gavín M, Madrid ES: Invasive pneumococcal disease in adults older than 59 years in the autonomous region of Madrid Spain, 2008–2010.

    Clin Microbiol Infect 2012, 18(Issue Supplement s3):149. OpenURL

  34. Pradas-Velasco R, Antoñanzas-Villar F, Martínez-Zárate MP: Utilización del cuestionario `European Quality of Life-5 dimensions´ (EQ-5D) para valorar la variación de la calidad de vida relacionada con la salud debida a la gripe.

    Gac Sanit 2009, 23(2):104-108. PubMed Abstract | Publisher Full Text OpenURL

Pre-publication history

The pre-publication history for this paper can be accessed here:

http://www.biomedcentral.com/1471-2334/13/175/prepub