Tendering process for pneumococcal conjugate vaccine: Difference between revisions
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[[op_fi:Pneumokokkirokotteen_hankinta_kansalliseen_rokotusohjelmaan]] | [[op_fi:Pneumokokkirokotteen_hankinta_kansalliseen_rokotusohjelmaan]] | ||
{{summary box | {{summary box | ||
|question = | |question = How should vaccine products be compared in the national procurement of the pneumococcal conjugate vaccine in Finland? | ||
|answer = To answer this question, [[THL]] | |answer = In brief, the suggestion is to use vaccine price only, because the two products in the market are very similar in respect to their efficacy and (minimal) side effects. | ||
To answer this question, [[THL]] organised an open discussion during summer and early autumn 2014. The outcome of this process was presented to the National Immunization Technical Advisory Group (NITAG) and the Ministry of Social Affairs and Health in September. The discussion focussed on three topics: | |||
* [[Comparison criteria|What criteria should be used when comparing pneumococcal vaccine products?]] | * [[Comparison criteria|What criteria should be used when comparing pneumococcal vaccine products?]] | ||
* [[Epidemiological modelling|How should the health effects of pneumococcal vaccination be assessed?]] | * [[Epidemiological modelling|How should the health effects of pneumococcal vaccination be assessed?]] | ||
* [[Economical assessment|How should the | * [[Economical assessment|How should the cost-effectiveness of pneumococcal vaccination be evaluated?]] | ||
Participation happened in two ways with these instructions: | |||
# Write your comments into the comment box at the end of each substance page. Moderator will include it into the text of the page. | # Write your comments into the comment box at the end of each substance page. Moderator will include it into the text of the page. | ||
# Sign in Opasnet and participate by editing the talk pages of any substance page. See instructions for [[discussion]] and [[Help:Quick reference for wiki editing|wiki editing]]. | # Sign in Opasnet and participate by editing the talk pages of any substance page. See instructions for [[discussion]] and [[Help:Quick reference for wiki editing|wiki editing]]. | ||
You should first browse the pneumococcus assessment pages so that you can give your comments on a right page and check whether your comment has actually been raised already. Comments are not repeated, and irrelevant comments will be removed. All relevant content will stay on the pages. Please note, however, that other participants may try to prove your comments false; if proven false, your comments as such will not be reflected in the final recommendation that is given to NITAG and the Ministry of Social Affairs and Health. | You should first browse the pneumococcus assessment pages so that you can give your comments on a right page and check whether your comment has actually been raised already. Comments are not repeated, and irrelevant comments will be removed. All relevant content will stay on the pages. Please note, however, that other participants may try to prove your comments false; if proven false, your comments as such will not be reflected in the final recommendation that is given to NITAG and the Ministry of Social Affairs and Health. | ||
}} | }} | ||
{{progression class|progression=Checked|curator=THL|date=2016-03-21}} | |||
== Question == | == Question == | ||
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* We discuss assumptions underlying the epidemiological model and the cost-effectiveness analysis. | * We discuss assumptions underlying the epidemiological model and the cost-effectiveness analysis. | ||
* The preparation of the criteria is based on current knowledge of the impact of pneumococcal conjugate vaccination. | * The preparation of the criteria is based on current knowledge of the impact of pneumococcal conjugate vaccination. | ||
* The procurement can only involve a product that has marketing authorisation in EU/Finland (see Section 20a of the Medicines Act | * The procurement can only involve a product that has marketing authorisation in EU/Finland (see Section 20a of the Medicines Act [http://www.fimea.fi/download/18580_Laakelaki_englanniksi_paivitetty_5_2011.pdf](pdf)). | ||
* The procurement must follow [http://www.finlex.fi/en/laki/kaannokset/2007/en20070348?search%5Btype%5D=pika&search%5Bpika%5D=public%20procurement the Act on Public Contracts]. | * The procurement must follow [http://www.finlex.fi/en/laki/kaannokset/2007/en20070348?search%5Btype%5D=pika&search%5Bpika%5D=public%20procurement the Act on Public Contracts]. | ||
* The discussion on these pages is not binding the preparation of the procurement. | * The discussion on these pages is not binding the preparation of the procurement. | ||
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== Answer == | == Answer == | ||
A preliminary answer | A preliminary answer was to base the selection criteria on the vaccine price and the predicted impact of vaccination on invasive pneumococcal disease in the entire Finnish population. Safety will not be used as one of the criteria because there is no indication about any differences in the safety of the currently licensed pneumococcal vaccine products. | ||
An epidemiological model was applied to assess the differences between the 10- and 13-valent vaccines in quality-adjusted life-years gained and in medical costs saved. If serotype 3 included in the 13-valent vaccine does not induce population level (indirect) effects, then the differences between the two vaccines in quality-adjusted life-years gained and in medical costs saved are small in comparison to differences in predictions due to intrinsic uncertainties in the model. Therefore, the vaccines can be regarded as equally effective and vaccine price should be the predominant selection criterion. | |||
== Rationale == | == Rationale == | ||
The rationale has been summarised in the following three pages: | The rationale has been summarised in the following three pages: | ||
[[Comparison_criteria|Comparison criteria for pneumococcal vaccines]], [[Epidemiological_modelling|Epidemiological modelling]] and [[Economical_assessment| | [[Comparison_criteria|Comparison criteria for pneumococcal vaccines]], [[Epidemiological_modelling|Epidemiological modelling]] and [[Economical_assessment|Economic evaluation]]. | ||
Comparison of vaccine products will be based on their price and expected health benefits ([[Comparison_criteria|Comparison criteria for pneumococcal vaccines]]). | Comparison of vaccine products will be based on their price and expected health benefits ([[Comparison_criteria|Comparison criteria for pneumococcal vaccines]]). | ||
The health benefits mean the expected reduction in the annual number of invasive pneumococcal disease in the Finnish population, if the vaccine would be used in the national infant immunisation programme. The assessment of the benefits is realised by using an [[Epidemiological_modelling|epidemiological model]]. The effectiveness of the vaccination programme will be quantified as the | The health benefits mean the expected reduction in the annual number of invasive pneumococcal disease in the Finnish population, if the vaccine would be used in the national infant immunisation programme. The assessment of the benefits is realised by using an [[Epidemiological_modelling|epidemiological model]]. The effectiveness of the vaccination programme will be quantified as the | ||
expected improvement in health-associated quality of life. The selection criterion is formulated so that the | expected improvement in health-associated quality of life. The selection criterion is formulated so that the most cost-effective | ||
will be identified ([[Economical_assessment|Economic evaluation]]). | |||
== See also == | == See also == | ||
{{assessment|moderator=Mnud}} | |||
{{pneumococcal vaccine}} | {{pneumococcal vaccine}} | ||
Latest revision as of 16:25, 11 December 2019
| Main message: |
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| Question:
How should vaccine products be compared in the national procurement of the pneumococcal conjugate vaccine in Finland? In brief, the suggestion is to use vaccine price only, because the two products in the market are very similar in respect to their efficacy and (minimal) side effects. To answer this question, THL organised an open discussion during summer and early autumn 2014. The outcome of this process was presented to the National Immunization Technical Advisory Group (NITAG) and the Ministry of Social Affairs and Health in September. The discussion focussed on three topics:
Participation happened in two ways with these instructions:
You should first browse the pneumococcus assessment pages so that you can give your comments on a right page and check whether your comment has actually been raised already. Comments are not repeated, and irrelevant comments will be removed. All relevant content will stay on the pages. Please note, however, that other participants may try to prove your comments false; if proven false, your comments as such will not be reflected in the final recommendation that is given to NITAG and the Ministry of Social Affairs and Health. |
In Opasnet many pages being worked on and are in different classes of progression. Thus the information on those pages should be regarded with consideration. The progression class of this page has been assessed:
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The content and quality of this page is/was being curated by the project that produced the page.
The quality was last checked: 2016-03-21. |
Question
How should vaccine products be compared in the national procurement of the pneumococcal conjugate vaccine?
Scope
- We restrict the analysis to vaccination within the infant immunisation programme.
- We specify criteria for comparing pneumococcal conjugate vaccine products.
- The aim is to prepare selection criteria that enable the choice of the economically most advantageous tender.
- We discuss assumptions underlying the epidemiological model and the cost-effectiveness analysis.
- The preparation of the criteria is based on current knowledge of the impact of pneumococcal conjugate vaccination.
- The procurement can only involve a product that has marketing authorisation in EU/Finland (see Section 20a of the Medicines Act [1](pdf)).
- The procurement must follow the Act on Public Contracts.
- The discussion on these pages is not binding the preparation of the procurement.
Answer
A preliminary answer was to base the selection criteria on the vaccine price and the predicted impact of vaccination on invasive pneumococcal disease in the entire Finnish population. Safety will not be used as one of the criteria because there is no indication about any differences in the safety of the currently licensed pneumococcal vaccine products.
An epidemiological model was applied to assess the differences between the 10- and 13-valent vaccines in quality-adjusted life-years gained and in medical costs saved. If serotype 3 included in the 13-valent vaccine does not induce population level (indirect) effects, then the differences between the two vaccines in quality-adjusted life-years gained and in medical costs saved are small in comparison to differences in predictions due to intrinsic uncertainties in the model. Therefore, the vaccines can be regarded as equally effective and vaccine price should be the predominant selection criterion.
Rationale
The rationale has been summarised in the following three pages: Comparison criteria for pneumococcal vaccines, Epidemiological modelling and Economic evaluation.
Comparison of vaccine products will be based on their price and expected health benefits (Comparison criteria for pneumococcal vaccines). The health benefits mean the expected reduction in the annual number of invasive pneumococcal disease in the Finnish population, if the vaccine would be used in the national infant immunisation programme. The assessment of the benefits is realised by using an epidemiological model. The effectiveness of the vaccination programme will be quantified as the expected improvement in health-associated quality of life. The selection criterion is formulated so that the most cost-effective will be identified (Economic evaluation).
See also
| Moderator:Mnud (see all) |
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