Percutaneous tracheostomy is safe in patients with severe thrombocytopenia.

Standard

Percutaneous tracheostomy is safe in patients with severe thrombocytopenia. / Kluge, Stefan; Meyer, Andreas; Kühnelt, Peter; Baumann, Hans Jörg; Kreymann, Georg.

in: CHEST, Jahrgang 126, Nr. 2, 2, 2004, S. 547-551.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Kluge, S, Meyer, A, Kühnelt, P, Baumann, HJ & Kreymann, G 2004, 'Percutaneous tracheostomy is safe in patients with severe thrombocytopenia.', CHEST, Jg. 126, Nr. 2, 2, S. 547-551. <http://www.ncbi.nlm.nih.gov/pubmed/15302743?dopt=Citation>

APA

Kluge, S., Meyer, A., Kühnelt, P., Baumann, H. J., & Kreymann, G. (2004). Percutaneous tracheostomy is safe in patients with severe thrombocytopenia. CHEST, 126(2), 547-551. [2]. http://www.ncbi.nlm.nih.gov/pubmed/15302743?dopt=Citation

Vancouver

Kluge S, Meyer A, Kühnelt P, Baumann HJ, Kreymann G. Percutaneous tracheostomy is safe in patients with severe thrombocytopenia. CHEST. 2004;126(2):547-551. 2.

Bibtex

@article{e226b7a36957491cb96b40d7e62f7db3,
title = "Percutaneous tracheostomy is safe in patients with severe thrombocytopenia.",
abstract = "STUDY OBJECTIVES: Severe thrombocytopenia has been described as a contraindication for percutaneous tracheostomy (PT). The objective of this study was to assess the safety of PT in mechanically ventilated patients with severe thrombocytopenia (defined by a platelet count of <50 x 10(9) cells/L). DESIGN: Retrospective, single-center cohort study. SETTING: Medical ICU of the University Hospital Hamburg-Eppendorf, Germany. PATIENTS: Forty-two medical patients with acute respiratory failure and severe thrombocytopenia. INTERVENTIONS: Bedside PT under bronchoscopic guidance using the Griggs guidewire forceps technique.Measurements and main results: The mean (+/- SD) intubation time prior to undergoing PT was 6.7 +/- 3.9 days (range, 1 to 20 days). The mean platelet count was 26.4 +/- 11.6 x 10(9) cells/L (range, 1 x 10(9) to 47 x 10(9) cells/L). The median transfusion of platelets before the procedure in 40 of the 42 patients was 6 +/- 2.5 U (range, 3 to 12 U). Twenty-two patients (52%) had an additional coagulopathy (activated partial thromboplastin time [APTT], > 40 s; international normalized ratio, > 1.5). PT was safely performed in all 42 patients. Only two (5%) patients developed major postprocedural bleeding complications that required suturing. Both of these patients had an elevated APTT due to heparin therapy. CONCLUSIONS: When performed by experienced personnel, PT with bronchoscopic guidance has a low complication rate in patients with severe thrombocytopenia, provided that platelets are administered beforehand. However, in order to minimize bleeding complications heparin infusions should be temporarily interrupted during the procedure.",
author = "Stefan Kluge and Andreas Meyer and Peter K{\"u}hnelt and Baumann, {Hans J{\"o}rg} and Georg Kreymann",
year = "2004",
language = "Deutsch",
volume = "126",
pages = "547--551",
journal = "CHEST",
issn = "0012-3692",
publisher = "American College of Chest Physicians",
number = "2",

}

RIS

TY - JOUR

T1 - Percutaneous tracheostomy is safe in patients with severe thrombocytopenia.

AU - Kluge, Stefan

AU - Meyer, Andreas

AU - Kühnelt, Peter

AU - Baumann, Hans Jörg

AU - Kreymann, Georg

PY - 2004

Y1 - 2004

N2 - STUDY OBJECTIVES: Severe thrombocytopenia has been described as a contraindication for percutaneous tracheostomy (PT). The objective of this study was to assess the safety of PT in mechanically ventilated patients with severe thrombocytopenia (defined by a platelet count of <50 x 10(9) cells/L). DESIGN: Retrospective, single-center cohort study. SETTING: Medical ICU of the University Hospital Hamburg-Eppendorf, Germany. PATIENTS: Forty-two medical patients with acute respiratory failure and severe thrombocytopenia. INTERVENTIONS: Bedside PT under bronchoscopic guidance using the Griggs guidewire forceps technique.Measurements and main results: The mean (+/- SD) intubation time prior to undergoing PT was 6.7 +/- 3.9 days (range, 1 to 20 days). The mean platelet count was 26.4 +/- 11.6 x 10(9) cells/L (range, 1 x 10(9) to 47 x 10(9) cells/L). The median transfusion of platelets before the procedure in 40 of the 42 patients was 6 +/- 2.5 U (range, 3 to 12 U). Twenty-two patients (52%) had an additional coagulopathy (activated partial thromboplastin time [APTT], > 40 s; international normalized ratio, > 1.5). PT was safely performed in all 42 patients. Only two (5%) patients developed major postprocedural bleeding complications that required suturing. Both of these patients had an elevated APTT due to heparin therapy. CONCLUSIONS: When performed by experienced personnel, PT with bronchoscopic guidance has a low complication rate in patients with severe thrombocytopenia, provided that platelets are administered beforehand. However, in order to minimize bleeding complications heparin infusions should be temporarily interrupted during the procedure.

AB - STUDY OBJECTIVES: Severe thrombocytopenia has been described as a contraindication for percutaneous tracheostomy (PT). The objective of this study was to assess the safety of PT in mechanically ventilated patients with severe thrombocytopenia (defined by a platelet count of <50 x 10(9) cells/L). DESIGN: Retrospective, single-center cohort study. SETTING: Medical ICU of the University Hospital Hamburg-Eppendorf, Germany. PATIENTS: Forty-two medical patients with acute respiratory failure and severe thrombocytopenia. INTERVENTIONS: Bedside PT under bronchoscopic guidance using the Griggs guidewire forceps technique.Measurements and main results: The mean (+/- SD) intubation time prior to undergoing PT was 6.7 +/- 3.9 days (range, 1 to 20 days). The mean platelet count was 26.4 +/- 11.6 x 10(9) cells/L (range, 1 x 10(9) to 47 x 10(9) cells/L). The median transfusion of platelets before the procedure in 40 of the 42 patients was 6 +/- 2.5 U (range, 3 to 12 U). Twenty-two patients (52%) had an additional coagulopathy (activated partial thromboplastin time [APTT], > 40 s; international normalized ratio, > 1.5). PT was safely performed in all 42 patients. Only two (5%) patients developed major postprocedural bleeding complications that required suturing. Both of these patients had an elevated APTT due to heparin therapy. CONCLUSIONS: When performed by experienced personnel, PT with bronchoscopic guidance has a low complication rate in patients with severe thrombocytopenia, provided that platelets are administered beforehand. However, in order to minimize bleeding complications heparin infusions should be temporarily interrupted during the procedure.

M3 - SCORING: Zeitschriftenaufsatz

VL - 126

SP - 547

EP - 551

JO - CHEST

JF - CHEST

SN - 0012-3692

IS - 2

M1 - 2

ER -