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Erschienen in: Critical Care 3/2012

Open Access 01.06.2012 | Letter

Number needed to treat and cost-effectiveness in the prevention of ventilator-associated pneumonia

verfasst von: Duncan Wyncoll, Luigi Camporota

Erschienen in: Critical Care | Ausgabe 3/2012

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The online version of this article (doi:10.​1186/​cc11346) contains supplementary material, which is available to authorized users.

Competing interests

LC declares that he has no competing interests. DW has given paid lectures or consulted for Kimberly-Clark (Irving, TX, USA), Covidien (Mansfield, MA, USA), ConvaTec (Skillman, NJ, USA), Iskus Health (Dublin, Ireland), Sage Products (Cary, IL, USA), Eli Lilly and Company (Indianapolis, IN, USA), and Pfizer Inc (New York, NY, USA) and has a stock interest in Biovo Technologies (Tel Aviv, Israel). The authors declare that they have no personal financial interests.
Abkürzungen
ICU
intensive care unit
MV
mechanical ventilation
NNT
number needed to treat
RRR
relative risk reduction
SDD
selective digestive decontamination
VAP
ventilator-associated pneumonia.
While clinicians continue to redefine ventilator-associated pneumonia (VAP), numerous innovations that claim to reduce pulmonary microaspiration and its consequences - that is, novel endotracheal cuff shapes and cuff materials, subglottic drainage, automatic cuff pressure controllers, oral anti-septics, selective digestive decontamination (SDD), and devices to combat biofilm formation within the lumen of the tracheal tube - are coming to the market [1, 2]. There are two questions that clinicians ask when deciding whether to incorporate a new product or intervention into a VAP prevention bundle. Firstly, what are its efficacy and effectiveness? In other words, what is the relative risk reduction (RRR) and therefore the number needed to treat (NNT) to prevent one additional VAP. Secondly, is this new intervention cost-effective in my local patients?
To answer the first question, one needs data from clinical trials and the knowledge of the baseline VAP rate with the likely RRR of the local case mix. We have calculated (Table 1) the NNT required to prevent one additional VAP for patients who require intubation and mechanical ventilation (MV) for more than 72 hours and an average time of MV of 10 days. The NNTs are based on an RRR ranging from 5% to 50% and a control event rate for VAP ranging from 1% to 20%, given a uniform distribution of NNTs across the range of RRRs. For example, with a VAP rate of approximately 8% and an intervention that reduces VAP by 45%, the NNT is 28 - a scenario that is realistic given a recent meta-analysis of one particular intervention [3].
Table 1
Number needed to treat in ventilator-associated pneumonia
 
Relative risk reduction
 
5%
10%
15%
20%
25%
30%
35%
40%
45%
50%
Baseline VAP rate
          
1%
2,000
1,000
667
500
400
333
286
250
222
200
2%
1,000
500
333
250
200
167
143
125
111
100
4%
500
250
167
125
100
83
71
63
56
50
6%
333
167
111
83
67
56
48
42
37
33
8%
250
125
83
63
50
42
36
31
28
25
10%
200
100
67
50
40
33
29
25
22
20
15%
133
67
44
33
27
22
19
16.7
15
13
20%
100
50
33
25
20
17
14
12.5
11
10
Number needed to treat (NNT) was calculated as: NNT [relative risk of event] = 1/(pc × RRR), where pc is the proportion of control group subjects who suffer an event and RRR is relative risk reduction. These NNTs are based on events per 10 days of mechanical ventilation, meaning that more than one event can occur in a single patient who is ventilated for more than 10 days. VAP, ventilator-associated pneumonia.
To establish whether the intervention is cost-effective, further knowledge of the cost of the intervention and the cost to treat an episode of VAP is required. A recent US study estimated the cost of VAP to be nearly $40,000 (£25,000 or €30,000) [4]. If costs are assumed to be lower in Europe, then a conservative estimate of the cost per episode of VAP would still be around £10,000, which is equivalent to an extra 7 days of intensive care unit (ICU) stay. What should we consider when assessing the cost-effectiveness of VAP prevention?
We have calculated (Table 2) the additional money (in pounds) that can be spent to prevent an episode of VAP (per 10 days of MV) to achieve cost-neutrality. If we assume a hypothetical VAP cost of £10,000, then with a VAP rate of 8% and an RRR of 45%, it is cost-effective to spend up to £360 . Furthermore, even for an ICU with a VAP rate of only 4% and an intervention that reduces VAP by just 25%, it is still cost-effective to spend up to £100 per 10 days of MV. It should be noted that some VAP prevention interventions (for example, a modified tracheal tube cuff) require just a 'one-off' initial cost whereas other interventions (for example, SDD) require an 'ongoing' daily cost.
Table 2
Cost-effectiveness of an intervention based on baseline ventilator-associated pneumonia rate and its relative risk reduction
 
Relative risk reduction
 
5%
10%
15%
20%
25%
30%
35%
40%
45%
50%
Baseline VAP rate
          
1%
£5
£10
£15
£20
£25
£30
£35
£40
£45
£50
2%
£10
£20
£30
£40
£50
£60
£70
£80
£90
£100
4%
£20
£40
£60
£80
£100
£120
£140
£160
£180
£200
6%
£30
£60
£90
£120
£150
£180
£210
£240
£270
£300
8%
£40
£80
£120
£160
£200
£240
£280
£320
£360
£400
10%
£50
£100
£150
£200
£250
£300
£350
£400
£450
£500
15%
£75
£150
£225
£300
£375
£450
£525
£600
£675
£750
20%
£100
£200
£300
£400
£500
£600
£700
£800
£900
£1,000
Values (£) refer to the average additional expense that can be spent for an intervention, per 10 days of mechanical ventilation, for it to be cost-neutral assuming a VAP cost of £10,000. VAP, ventilator-associated pneumonia.
We think that this analysis might help clinicians in making the important economic decision of whether to adopt a new VAP prevention device or procedure. Our calculations can easily be adapted to local currencies and circumstances worldwide.

Competing interests

LC declares that he has no competing interests. DW has given paid lectures or consulted for Kimberly-Clark (Irving, TX, USA), Covidien (Mansfield, MA, USA), ConvaTec (Skillman, NJ, USA), Iskus Health (Dublin, Ireland), Sage Products (Cary, IL, USA), Eli Lilly and Company (Indianapolis, IN, USA), and Pfizer Inc (New York, NY, USA) and has a stock interest in Biovo Technologies (Tel Aviv, Israel). The authors declare that they have no personal financial interests.
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Literatur
2.
3.
Zurück zum Zitat Muscedere J, Rewa O, McKechnie K, Jiang X, Laporta D, Heyland DK: Subglottic secretion drainage for the prevention of ventilator-associated pneumonia: a systematic review and meta-analysis. Crit Care Med 2011, 39: 1985-1991. 10.1097/CCM.0b013e318218a4d9CrossRefPubMed Muscedere J, Rewa O, McKechnie K, Jiang X, Laporta D, Heyland DK: Subglottic secretion drainage for the prevention of ventilator-associated pneumonia: a systematic review and meta-analysis. Crit Care Med 2011, 39: 1985-1991. 10.1097/CCM.0b013e318218a4d9CrossRefPubMed
4.
Zurück zum Zitat Kollef MH, Hamilton CW, Ernst FR: Economic impact of ventilator-associated pneumonia in a large matched cohort. Infect Control Hosp Epidemiol 2012, 33: 250-256. 10.1086/664049CrossRefPubMed Kollef MH, Hamilton CW, Ernst FR: Economic impact of ventilator-associated pneumonia in a large matched cohort. Infect Control Hosp Epidemiol 2012, 33: 250-256. 10.1086/664049CrossRefPubMed
Metadaten
Titel
Number needed to treat and cost-effectiveness in the prevention of ventilator-associated pneumonia
verfasst von
Duncan Wyncoll
Luigi Camporota
Publikationsdatum
01.06.2012
Verlag
BioMed Central
Erschienen in
Critical Care / Ausgabe 3/2012
Elektronische ISSN: 1364-8535
DOI
https://doi.org/10.1186/cc11346

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