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be given until 57 afebrile days have elapsed, unless the patient is unstable. If antibiotic treatment is stopped during neutropenia, the patient must be carefully monitored and antibiotics restarted immediately on the recurrence of fever or other evidence of bacterial infection.5 According to Bouadma and colleagues,1 few data are available about the 98 patients who were immunocompromised. We would like to know about mortality, the duration of antibiotic therapy, and the relapsing infection rate in these patients with neutropenia.
We declare that we have no conicts of interest.
group of up to 99% would not be inferior. This equates to a number needed to harm of ten. They conclude that the signicant reduction (p<00001) of 27 days in mean exposure to antibiotics is worth a possible extra death for every ten patients treated by the procalcitonin strategy. If a true excess mortality as great as 2% (one extra death for every 50 patients treated with the procalcitonin strategy) were considered acceptable for a few days fewer antibiotics, this would require a non-inferiority trial with 16 500 patients. A true excess mortality of 4%, similar to that seen in the trial, would require about 4220 patients. The PRORATA trial, which recruited 621 patients, was grossly underpowered to provide reliable evidence for policy, but could be valuable in a synthesis of similar studies. Few patients would accept up to a 99% extra risk of death for 3 days fewer antibiotics. Why should your readers?
We declare that we have no conicts of interest.
We believe that the PRORATA trial1 is of major concern, and potentially misleading, in suggesting that a strategy guided by procalcitonin could reduce antibiotic exposure and selective pressure with no apparent adverse outcomes. Lila Bouadma and colleagues assumed that a true excess mortality, or risk dierence, in the procalcitonin
Lila Bouadma and colleagues1 nicely showed that a strategy based on the daily measurement of procalcitonin concentration allowed for a reduction of antibiotic consumption in intensive care units (ICUs). Although this held true for most infections, the PRORATA trial mainly included patients with pneumonia and showed that measuring procalcitonin concentrations allowed the clinician to better adhere to the international guidelines on
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Correspondence
antibiotherapy duration.2,3 These results remind us that patients in ICUs are frequently overtreated, or at least treated for a too long. But had the patients in the control group been managed according to current recommendations,2,3 this trial would have had negative results. Before implementing costly biological analyses that could be unduly overinterpreted, we should increase educational eorts to better diuse accepted guidelines. Another concern is that the PRORATA trial was designed to exclude a 10% dierence in mortality between procalcitonin-guided and control groups. This 10% cuto is questionable, since no study in an ICU setting has ever shown such a dramatic dierence in mortality we are happy when intensive insulin therapy is associated with a 3% reduction in mortality,4 or activated protein C with a 6% reduction.5 Should we accept a 38% increase with a procalcitoninguided strategy? Obviously, this 38% increase is not statistically signicant, but the design and the power of the trial means that the trial cannot denitely exclude such a negative impact on mortality attributable to the procalcitonin strategy. We must not hide behind procalcitonin or other sophisticated biomarkers and must always ask ourselves about the appropriateness of pursuing antibiotics in any given patient.
I declare that I have no conicts of interest.
van den Berghe G, Wouters P, Weekers F, et al. Intensive insulin therapy in the critically ill patients. N Engl J Med 2001; 345: 135967. Bernard GR, Vincent JL, Laterre PF, et al, for the Recombinant human protein C Worldwide Evaluation in Severe Sepsis (PROWESS) study group. Ecacy and safety of recombinant human activated protein C for severe sepsis. N Engl J Med 2001; 344: 699709.
Authors reply
Djamel Mokart and Marc Leone point out potential diculties for interpreting procalcitonin concentrations in immunocompromised patients. In our trial, these patients had signicantly lower antibiotic exposure in the procalcitonin group than in the control group (36 days), without signicant dierences in mortality and relapse rates. However, we agree that more trials are needed to conrm that a procalcitonin-guided strategy can reduce antibiotic use without adversely aecting outcomes in that specic subset of patients. William Tarnow-Mordi and Val Gebski, Sbastien Gibot, and Gijs Landman and Nanne Kleefstra raise concerns about the safety of a procalcitonin-guided strategy to limit antibiotic use in critically ill patients, since a slightly higher number of patients in the procalcitonin group than in the control group died between days 29 and 60. They discuss the issue of the non-inferiority margin, which was set at 10% to calculate our trials sample size. We do not share their concerns for the following reasons. First, there were some slight imbalances at intensive care unit (ICU) admission and random allocation between the procalcitonin and the usual care groups, including a higher Simplied Acute Physiology Score II and a higher Sequential Organ Failure Assessment (SOFA) score in patients randomly assigned to the procalcitonin group. After adjustment for age, sex, pre-existing comorbidities, location before ICU, reason for ICU admission, SOFA score at admission, type of infection, blood culture results, septic shock, and mechanical ventilation at inclusion, the odds ratios for death by day 28 or 60 for procalcitonin-group patients versus controls were 089 (90% CI 062128) and 109 (079151), respectively. Importantly, no patients in either group who died after day 28 had an infection relapse, suggesting that this slightly higher mortality rate at day 60 is not biologically plausible, given the late separation in mortality between the two groups.
www.thelancet.com Vol 375 May 8, 2010
Sbastien Gibot
s.gibot@chu-nancy.fr
Service de Ranimation Mdicale, Hpital Central, 54035 Nancy Cedex, France 1 Bouadma L, Luyt CE, Tubach F, et al. Use of procalcitonin to reduce patients exposure to antibiotics in intensive care units (PRORATA trial): a multicentre randomised controlled trial. Lancet 2010; 375: 46374. Mandell LA, Wunderink RG, Anzueto A, et al. Infectious Diseases Society of America/ American Thoracic Society consensus guidelines on the management of communityacquired pneumonia in adults. Clin Infect Dis 2007; 44 (suppl 2): S2772. Joseph S, Solomkin JE, Mazuski JS, et al. Diagnosis and management of complicated intra-abdominal infection in adults and children: guidelines by the Surgical Infection Society and the Infectious Diseases Society of America. Clin Infect Dis 2010; 50: 13364.
Lila Bouadma and colleagues1 succeeded in reducing antibiotic use by 27 days in the procalcitonin group. With regard to mortality, the results of the PRORATA trial looked reassuring since the results are within the non-inferiority margin. In 2007, Garattini and Bertele2 discussed some important issues of non-inferiority trials, and one of the problems they discussed pertains to the PRORATA trial. The non-inferiority margin for mortality was set at 10%. The 60-day mortality turned out to be 38% lower in the group receiving usual care (90% CI 97 to 21). First, the lower limit of the 90% CI is 97%. This could mean that it is, indeed, possible that almost one in ten more patients could die when treated with a procalcitonin-based algorithm compared with usual care. Second, the use of a 90% CI is questionable. The non-inferiority margin would have been crossed if the, perhaps more appropriate, 95% CI had been used. Bouadma and colleagues are right to conclude that a procalcitonin-guided strategy could reduce antibiotic exposure in non-surgical patients in intensive care units. But concluding that there are no apparent adverse eects, when there is a possibility of an absolute increased risk of death of around 10%, is only statistically true.
We declare that we have no conicts of interest.
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