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Comparison between surgical and percutaneous tracheostomy effects on procalcitonin kinetics in critically ill patients

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Open Access

Comparison between surgical and

percutaneous tracheostomy effects on

procalcitonin kinetics in critically ill patients

Maria Vargas

*

, Pasquale Buonanno, Lina Giorgiano, Giovanna Sorriento, Carmine Iacovazzo and Giuseppe Servillo

Abstract

Available evidence from randomized controlled trials

including adult critically ill patients tends to show

that percutaneous dilatational tracheostomy (PDT)

techniques are performed faster and reduce stoma

inflammation and infection but are associated with

increased technical difficulties compared with

surgical tracheostomy (ST). A recent meta-analysis

found that PDT was superior to reduce risk of

periprocedural stoma inflammation and infection

compared with ST. WE found no differences in

procalcitonin, C-reactive protein, SOFA, and SAPS II

between critically ill patients with ST or PDT.

Keywords: Tracheostomy, Procalcitonin, Infection,

Sepsis, C-reactive protein, Critically ill patients

In critically ill patients, tracheostomy may be

per-formed with surgical or percutaneous approaches [

1

].

Available evidence from randomized controlled trials

including adult critically ill patients tends to show

that percutaneous dilatational tracheostomy (PDT)

techniques are performed faster and reduce stoma

flammation and infection but are associated with

in-creased technical difficulties compared with surgical

tracheostomy (ST) [

2

,

3

]. Overall complication rates

are similar for PDT and ST, but with an increased

inci-dence of infection for ST [

4

]. A recent meta-analysis

found that PDT was superior to reduce risk of

periproce-dural stoma inflammation and infection compared with

ST [

4

]. In the elderly population, fever is the most

com-mon

postoperative

complication

after

ST

(42%),

followed by wound infection (4%) [

4

]. Procalcitonin

(PCT)

may

be

a

reliable

biomarker

to

predict

* Correspondence:[email protected]

Department of Neurosciences, Reproductive and Odontostomatological Sciences, University of Naples“Federico II”, via pansini, Naples, Italy

infectious or septic complications related to

tracheos-tomy performed in the ICU [

5

]. A retrospective study

reported

that

PCT

was

not

elevated

after

ST

performed in the ICU [

5

]. However, little is known

about procalcitonin kinetics after ST or PDT in

critic-ally ill patients, since ST seems to be associated with

an increased incidence of infection in this cohort of

patients.

We screened 122 critically ill patients for

tracheos-tomy, of which 12 received ST and 13 received

PDT (Table

1

). We found no difference in the

base-line characteristics of patients between the two

groups. Upper respiratory, blood, and urinary cultures

performed 3 days before the procedure were negative

for each patient. We found no difference between

PCT, C-reactive protein (CRP), Sepsis Organ Failure

Assessment

(SOFA)

score,

and

Simplified

Acute

Physiology Score (SAPS) II between the groups (all

p > 0.05; Fig.

1

). Upper respiratory, blood, and urinary

cultures performed 3 days after the procedure were

negative for each patient. The trends of PCT levels

over time did not correlate with the trend of CRP

levels in each group (ST group,

r = 0.074, p = 0.671;

r

2

= 0.139,

p = 0.425; PDT group, r = − 0.169, p = 0.297;

r

2

=

− 0.063, p = 0.697).

To our knowledge this is the first report evaluating

the kinetics of different biomarkers of infection in a

cohort of tracheostomized patients. According to the

literature, ST was associated with an increased risk of

infections [

4

,

5

]. We found that the biomarkers of

infection were not different between the ST and PDT

groups and remained stable in the first week after the

procedure. According to these data, ST may not

increase the risk of infections and sepsis in critically

ill patients.

© The Author(s). 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. Vargaset al. Critical Care (2018) 22:297

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Abbreviations

CRP:C-reactive protein; PCT: Procalcitonin; PDT: Percutaneous dilatational tracheostomy; SAPS II: Simplified Acute Physiology Score II; SOFA: Sepsis Organ Failure Assessment; ST: Surgical tracheostomy

Acknowledgements Not applicable. Funding No funding.

Availability of data and materials Not applicable.

Authors’ contributions

MV, PB, LG, GS, CI, FA, and GS analyzed and interpreted the data, wrote the paper, and approved the manuscript.

Ethics approval and consent to participate

University of Naples“Federico II” - protocol number132/17. Consent for publication

Not applicable. Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

1 day before T Tracheostomy 1 day after T 2 days after T 7 days after T

0.0 0.2 0.4 0.6 0.8 1.0 10 20 30 40 CRP ST CRP PDT PCT ST PCT PDT mg/L ng/ml

1 day before T Tracheostomy 1 day after T 2 days after T 7 days after T

4 6 8 10 30 40 50 60 Points SOFA ST SOFA PDT SAPS II ST SAPS II PDT

Fig. 1 The PCT, CRP, SOFA, and SAPS II values remained stable over time for both groups (ST group, p value for PCT = 0.530, p value for CRP = 0.588, p value for SOFA = 0.480, p value for SAPS II = 0.289; PDT group, p value for PCT = 0.176, p value for CRP = 0.419, p value for SOFA = 0.402, p value for SAPS II = 0.993. Left panel: CRP and PCT kinetics in critically ill patients who underwent surgical and percutaneous tracheostomy. Right panel: SAPS II and SOFA scores in critically ill patients who underwent surgical and percutaneous tracheostomy. CRP C-reactive protein, PCT procalcitonin, SOFA Sepsis Organ Failure Assessment, SAPS Simplified Acute Physiology Score, ST surgical tracheostomy, PDT percutaneous dilatational tracheostomy, T tracheostomy

Table 1 Characteristics of included patients

Surgical tracheostomy (n = 12) Percutaneous dilatational tracheostomy (n = 13) p Age (years) 60 ± 10 56 ± 10 0.778 Gender (M/F) 8/5 7/6 0.539 BMI 20 ± 10 20.6 ± 8 0.345

Reason for ICU admission (N) 0.678 - Medical 7 6 - Trauma 3 4 - Surgical 2 3 Duration of endotracheal intubation before T 15 ± 3 13 ± 5 0.257 Variables during procedure (N) 0.675 - Antibiotics 3 4 - Corticosteroid 4 3 - Fever (> 37°) 0 0

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Received: 24 September 2018 Accepted: 18 October 2018

References

1. Vargas M, Pelosi P, Servillo G. Percutaneous tracheostomy: it’s time for a shared approach! Crit Care. 2014;8:448.

2. Vargas M, Sutherasan Y, Antonelli M, Brunetti I, Corcione A, Laffey JG, Putensen C, Servillo G, Pelosi P. Tracheootmy procedures in the intensive care unit: an international survey. Crit Care. 2015;19:291–301.

3. Vargas M, Servillo G, Arditi E, et al. Tracheostomy in Intensive Care Unit: a national survey in Italy. Minerva Anestesiol. 2013;79:156–64.

4. Putensen C, Theuerkauf N, Guenther U, et al. Percutaneous and surgical tracheostomy in critically ill adult patients: a meta-analysis. Crit Care. 2014; 18:544.

5. Sato K, Okajima M, Noda T, et al. Impact of bedside tracheostomy on procalcitonin kinetics in critically ill patients. J Intensive Care Med. 2017. https://doi.org/10.1177/0885066617696845[Epub ahead of print].

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