Detail
Článek
Článek online
FT
Medvik - BMČ
  • Je něco špatně v tomto záznamu ?

Landiolol for heart rate control in patients with septic shock and persistent tachycardia. A multicenter randomized clinical trial (Landi-SEP)

S. Rehberg, S. Frank, V. Černý, R. Cihlář, R. Borgstedt, G. Biancofiore, F. Guarracino, A. Schober, H. Trimmel, T. Pernerstorfer, C. Siebers, P. Dostál, A. Morelli, M. Joannidis, I. Pretsch, C. Fuchs, T. Rahmel, M. Podbregar, É. Duliczki, K....

. 2024 ; 50 (10) : 1622-1634. [pub] 20240919

Jazyk angličtina Země Spojené státy americké

Typ dokumentu časopisecké články, randomizované kontrolované studie, multicentrická studie

Perzistentní odkaz   https://www.medvik.cz/link/bmc25003999
E-zdroje Online Plný text

NLK ProQuest Central od 1997-01-01 do Před 1 rokem
Medline Complete (EBSCOhost) od 2000-01-01 do Před 1 rokem
Nursing & Allied Health Database (ProQuest) od 1997-01-01 do Před 1 rokem
Health & Medicine (ProQuest) od 1997-01-01 do Před 1 rokem

PURPOSE: Excessive tachycardia in resuscitated septic shock patients can impair hemodynamics and worsen patient outcome. We investigated whether heart rate (HR) control can be achieved without increased vasopressor requirements using the titratable highly selective, ultra-short-acting β1-blocker landiolol. METHODS: This randomized, open-label, controlled trial was conducted at 20 sites in 7 European countries from 2018 to 2022 and investigated the efficacy and safety of landiolol in adult patients with septic shock and persistent tachycardia. Patients were randomly assigned to receive either landiolol along with standard treatment (n = 99) or standard treatment alone (n = 101). The combined primary endpoint was HR response (i.e., HR within the range of 80-94 beats per minute) and its maintenance without increasing vasopressor requirements during the first 24 h after treatment start. Key secondary endpoints were 28-day mortality and adverse events. RESULTS: Out of 196 included septic shock patients, 98 received standard treatment combined with landiolol and 98 standard treatment alone. A significantly larger proportion of patients met the combined primary endpoint in the landiolol group than in the control group (39.8% [39/98] vs. 23.5% [23/98]), with a between-group difference of 16.5% (95% confidence interval [CI]: 3.4-28.8%; p = 0.013). There were no statistically significant differences between study groups in tested secondary outcomes and adverse events. CONCLUSION: The ultra-short-acting beta-blocker landiolol was effective in reducing and maintaining HR without increasing vasopressor requirements after 24 h in patients with septic shock and persistent tachycardia. There were no differences in adverse events and clinical outcomes such as 28-day mortality vs. standard of care. The results of this study, in the context of previous trials, do not support a treatment strategy of stringent HR reduction (< 95 bpm) in an unselected septic shock population with persistent tachycardia. Further investigations are needed to identify septic shock patient phenotypes that benefit clinically from HR control.

Anaesthesiology and Intensive Care Unit Szabolcs Szatmár Bereg County Hospitals and University Teaching Hospital Jósa András Teaching Hospital Nyíregyháza Hungary

AOP Health International Management AG Ruggell Liechtenstein

AOP Orphan Pharmaceuticals GmbH Vienna Austria

Clinic of Anaesthesiology and Intensive Care 1St Intensive Care Unit Tartu University Hospital Tartu Estonia

Department of Anaesthesia and Critical Care Medicine Cardiothoracic and Vascular Anaesthesiology and Intensive Care Azienda Ospedaliero Universitaria Pisana Pisa Italy

Department of Anaesthesia and Intensive Care Charles University 3rd Medical Faculty and University Hospital Královské Vinohrady Prague Czech Republic

Department of Anaesthesiology and Intensive Care Hospital of Garmisch Partenkirchen Garmisch Partenkirchen Germany

Department of Anaesthesiology and Intensive Care Medicine Charles University Faculty of Medicine in Hradec Kralove Hradec Králové Czech Republic

Department of Anaesthesiology and Intensive Care Medicine University Hospital Hradec Králové Hradec Králové Czech Republic

Department of Anaesthesiology and Intensive Care Ordensklinikum Linz GmbH Barmherzige Schwestern Linz Austria

Department of Anaesthesiology and Transplant Intensive Care Unit University School of Medicine Pisa Pisa Italy

Department of Anaesthesiology Intensive Care Emergency and Pain Medicine University Hospital Greifswald Greifswald Germany

Department of Anaesthesiology Intensive Care Emergency Medicine Transfusion Medicine and Pain Therapy University Hospital of Bielefeld Bielefeld Germany

Department of Anaesthesiology Intensive Care Medicine and Pain Therapy University Hospital Knappschaftskrankenhaus Bochum Bochum Germany

Department of Anaesthesiology LMU University Hospital LMU Munich Munich Germany

Department of Anaesthesiology Perioperative Medicine and Intensive Care Masaryk Hospital Ústí Nad Labem Czech Republic

Department of Anesthesia Pain Management and Perioperative Medicine Dalhousie University Halifax Canada

Department of Anesthesiology and Intensive Care Hospital České Budějovice České Budějovice Czech Republic

Department of Anesthesiology Emergency Medicine and General Intensive Care State Hospital Wiener Neustadt Wiener Neustadt Austria

Department of Cardiology Klinik Floridsdorf and Karl Landsteiner Institute for Cardiovascular and Critical Care Research C O Klinik Floridsdorf Vienna Austria

Department of Clinical Internal Anesthesiological and Cardiovascular Sciences University of Rome La Sapienza Policlinico Umberto Primo Rome Italy

Department of Internal Medicine 2 Division of Cardiology and Intensive Care Paracelsus Medical University of Salzburg Salzburg Austria

Division of Emergency Medicine and Intensive Care Department Internal Medicine Medical University Innsbruck Innsbruck Austria

Internal Intensive Care Department General Hospital Celje Celje Slovenia

Medical Faculty University of Ljubljana Ljubljana Slovenia

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc25003999
003      
CZ-PrNML
005      
20250206105029.0
007      
ta
008      
250121s2024 xxu f 000 0|eng||
009      
AR
024    7_
$a 10.1007/s00134-024-07587-1 $2 doi
035    __
$a (PubMed)39297945
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxu
100    1_
$a Rehberg, Sebastian $u Department of Anaesthesiology, Intensive Care, Emergency Medicine, Transfusion Medicine and Pain Therapy, University Hospital of Bielefeld, Bielefeld, Germany. Sebastian.Rehberg@uni-bielefeld.de $1 https://orcid.org/0000000258357083
245    10
$a Landiolol for heart rate control in patients with septic shock and persistent tachycardia. A multicenter randomized clinical trial (Landi-SEP) / $c S. Rehberg, S. Frank, V. Černý, R. Cihlář, R. Borgstedt, G. Biancofiore, F. Guarracino, A. Schober, H. Trimmel, T. Pernerstorfer, C. Siebers, P. Dostál, A. Morelli, M. Joannidis, I. Pretsch, C. Fuchs, T. Rahmel, M. Podbregar, É. Duliczki, K. Tamme, M. Unger, J. Sus, C. Klade, K. Krejcy, N. Kirchbaumer-Baroian, G. Krumpl, F. Duška, LANDI-SEP Study Group
520    9_
$a PURPOSE: Excessive tachycardia in resuscitated septic shock patients can impair hemodynamics and worsen patient outcome. We investigated whether heart rate (HR) control can be achieved without increased vasopressor requirements using the titratable highly selective, ultra-short-acting β1-blocker landiolol. METHODS: This randomized, open-label, controlled trial was conducted at 20 sites in 7 European countries from 2018 to 2022 and investigated the efficacy and safety of landiolol in adult patients with septic shock and persistent tachycardia. Patients were randomly assigned to receive either landiolol along with standard treatment (n = 99) or standard treatment alone (n = 101). The combined primary endpoint was HR response (i.e., HR within the range of 80-94 beats per minute) and its maintenance without increasing vasopressor requirements during the first 24 h after treatment start. Key secondary endpoints were 28-day mortality and adverse events. RESULTS: Out of 196 included septic shock patients, 98 received standard treatment combined with landiolol and 98 standard treatment alone. A significantly larger proportion of patients met the combined primary endpoint in the landiolol group than in the control group (39.8% [39/98] vs. 23.5% [23/98]), with a between-group difference of 16.5% (95% confidence interval [CI]: 3.4-28.8%; p = 0.013). There were no statistically significant differences between study groups in tested secondary outcomes and adverse events. CONCLUSION: The ultra-short-acting beta-blocker landiolol was effective in reducing and maintaining HR without increasing vasopressor requirements after 24 h in patients with septic shock and persistent tachycardia. There were no differences in adverse events and clinical outcomes such as 28-day mortality vs. standard of care. The results of this study, in the context of previous trials, do not support a treatment strategy of stringent HR reduction (< 95 bpm) in an unselected septic shock population with persistent tachycardia. Further investigations are needed to identify septic shock patient phenotypes that benefit clinically from HR control.
650    _2
$a lidé $7 D006801
650    12
$a septický šok $x farmakoterapie $x komplikace $x patofyziologie $7 D012772
650    _2
$a mužské pohlaví $7 D008297
650    _2
$a ženské pohlaví $7 D005260
650    _2
$a lidé středního věku $7 D008875
650    12
$a močovina $x analogy a deriváty $x terapeutické užití $x farmakologie $7 D014508
650    12
$a tachykardie $x farmakoterapie $x patofyziologie $x komplikace $7 D013610
650    _2
$a senioři $7 D000368
650    12
$a srdeční frekvence $x účinky léků $7 D006339
650    12
$a morfoliny $x terapeutické užití $x farmakologie $7 D009025
651    _2
$a Evropa $7 D005060
655    _2
$a časopisecké články $7 D016428
655    _2
$a randomizované kontrolované studie $7 D016449
655    _2
$a multicentrická studie $7 D016448
700    1_
$a Frank, Sandra $u Department of Anaesthesiology, LMU University Hospital, LMU Munich, Munich, Germany
700    1_
$a Černý, Vladimír $u Department of Anaesthesia and Intensive Care, Charles University, 3rd Medical Faculty and University Hospital Královské Vinohrady, Prague, Czech Republic $u Department of Anaesthesiology, Perioperative Medicine and Intensive Care, Masaryk Hospital, Ústí Nad Labem, Czech Republic $u Department of Anaesthesiology and Intensive Care Medicine, Charles University, Faculty of Medicine in Hradec Kralove, Hradec Králové, Czech Republic $u Department of Anesthesia, Pain Management and Perioperative Medicine, Dalhousie University, Halifax, Canada $u Department of Anaesthesiology and Intensive Care Medicine, University Hospital Hradec Králové, Hradec Králové, Czech Republic
700    1_
$a Cihlář, Radek $u Department of Anesthesiology and Intensive Care, Hospital České Budějovice, České Budějovice, Czech Republic
700    1_
$a Borgstedt, Rainer $u Department of Anaesthesiology, Intensive Care, Emergency Medicine, Transfusion Medicine and Pain Therapy, University Hospital of Bielefeld, Bielefeld, Germany
700    1_
$a Biancofiore, Gianni $u Department of Anaesthesiology and Transplant Intensive Care Unit, University School of Medicine Pisa, Pisa, Italy
700    1_
$a Guarracino, Fabio $u Department of Anaesthesia and Critical Care Medicine, Cardiothoracic and Vascular Anaesthesiology and Intensive Care, Azienda Ospedaliero Universitaria Pisana, Pisa, Italy
700    1_
$a Schober, Andreas $u Department of Cardiology, Klinik Floridsdorf & Karl Landsteiner Institute for Cardiovascular and Critical Care Research C/O Klinik Floridsdorf, Vienna, Austria
700    1_
$a Trimmel, Helmut $u Department of Anesthesiology, Emergency Medicine and General Intensive Care, State Hospital Wiener Neustadt, Wiener Neustadt, Austria
700    1_
$a Pernerstorfer, Thomas $u Department of Anaesthesiology and Intensive Care, Ordensklinikum Linz GmbH, Barmherzige Schwestern, Linz, Austria
700    1_
$a Siebers, Christian $u Department of Anaesthesiology and Intensive Care, Hospital of Garmisch-Partenkirchen, Garmisch-Partenkirchen, Germany
700    1_
$a Dostál, Pavel $u Department of Anaesthesiology and Intensive Care Medicine, Charles University, Faculty of Medicine in Hradec Kralove, Hradec Králové, Czech Republic $u Department of Anaesthesiology and Intensive Care Medicine, University Hospital Hradec Králové, Hradec Králové, Czech Republic
700    1_
$a Morelli, Andrea $u Department of Clinical Internal, Anesthesiological and Cardiovascular Sciences, University of Rome, "La Sapienza", Policlinico Umberto Primo, Rome, Italy
700    1_
$a Joannidis, Michael $u Division of Emergency Medicine and Intensive Care, Department Internal Medicine, Medical University Innsbruck, Innsbruck, Austria
700    1_
$a Pretsch, Ingrid $u Department of Internal Medicine II, Division of Cardiology and Intensive Care, Paracelsus Medical University of Salzburg, Salzburg, Austria
700    1_
$a Fuchs, Christian $u Department of Anaesthesiology, Intensive Care, Emergency and Pain Medicine, University Hospital Greifswald, Greifswald, Germany
700    1_
$a Rahmel, Tim $u Department of Anaesthesiology, Intensive Care Medicine and Pain Therapy, University Hospital Knappschaftskrankenhaus Bochum, Bochum, Germany
700    1_
$a Podbregar, Matej $u Internal Intensive Care Department, General Hospital Celje, Celje, Slovenia $u Medical Faculty, University of Ljubljana, Ljubljana, Slovenia
700    1_
$a Duliczki, Éva $u Anaesthesiology and Intensive Care Unit, Szabolcs-Szatmár-Bereg County Hospitals and University Teaching Hospital Jósa András Teaching Hospital, Nyíregyháza, Hungary
700    1_
$a Tamme, Kadri $u Clinic of Anaesthesiology and Intensive Care, 1St. Intensive Care Unit, Tartu University Hospital, Tartu, Estonia
700    1_
$a Unger, Martin $u AOP Orphan Pharmaceuticals GmbH, Vienna, Austria
700    1_
$a Sus, Jan $u AOP Orphan Pharmaceuticals GmbH, Vienna, Austria
700    1_
$a Klade, Christoph $u AOP Orphan Pharmaceuticals GmbH, Vienna, Austria
700    1_
$a Krejcy, Kurt $u AOP Orphan Pharmaceuticals GmbH, Vienna, Austria
700    1_
$a Kirchbaumer-Baroian, Nairi $u AOP Orphan Pharmaceuticals GmbH, Vienna, Austria
700    1_
$a Krumpl, Günther $u AOP Health International Management AG, Ruggell, Liechtenstein
700    1_
$a Duška, František $u Department of Anaesthesia and Intensive Care, Charles University, 3rd Medical Faculty and University Hospital Královské Vinohrady, Prague, Czech Republic
710    2_
$a LANDI-SEP Study Group
773    0_
$w MED00002258 $t Intensive care medicine $x 1432-1238 $g Roč. 50, č. 10 (2024), s. 1622-1634
856    41
$u https://pubmed.ncbi.nlm.nih.gov/39297945 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y - $z 0
990    __
$a 20250121 $b ABA008
991    __
$a 20250206105024 $b ABA008
999    __
$a ok $b bmc $g 2263627 $s 1240006
BAS    __
$a 3
BAS    __
$a PreBMC-MEDLINE
BMC    __
$a 2024 $b 50 $c 10 $d 1622-1634 $e 20240919 $i 1432-1238 $m Intensive care medicine $n Intensive Care Med $x MED00002258
LZP    __
$a Pubmed-20250121

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...