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Dive into the research topics where Oliver Hahn is active.

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Featured researches published by Oliver Hahn.


Critical Care Medicine | 2014

Mechanical Ventilation During Cardiopulmonary Resuscitation With Intermittent Positive-pressure Ventilation, Bilevel Ventilation, or Chest Compression Synchronized Ventilation in a Pig Model*

Clemens Kill; Oliver Hahn; Florian Dietz; Christian Neuhaus; Stefan Schwarz; Robert Mahling; Pascal Wallot; Andreas Jerrentrup; Thorsten Steinfeldt; Hinnerk Wulf; Wolfgang Dersch

Objective:Mechanical ventilation with an automated ventilator is recommended during cardiopulmonary resuscitation with a secured airway. We investigated the influence of intermittent positive-pressure ventilation, bilevel ventilation, and the novel ventilator mode chest compression synchronized ventilation, a pressure-controlled ventilation triggered by each chest compression, on gas exchange, hemodynamics, and return of spontaneous circulation in a pig model. Design:Animal study. Setting:University laboratory. Subjects:Twenty-four three-month-old female domestic pigs. Interventions:The study was performed on pigs under general anesthesia with endotracheal intubation. Arterial and central venous catheters were inserted and IV rocuronium (1 mg/kg) was injected. After 3 minutes of cardiac arrest (ventricular fibrillation at t = 0 min), animals were randomized into intermittent positive-pressure ventilation (control group), bilevel, or chest compression synchronized ventilation group. Following 10 minute uninterrupted chest compressions and mechanical ventilation, advanced life support was performed (100% O2, up to six defibrillations, vasopressors). Measurements and Main Results:Blood gas samples were drawn at 0, 4 and 13 minutes. At 13 minutes, hemodynamics was analyzed beat-to-beat in the end-inspiratory and end-expiratory cycle comparing the IPPV with the bilevel group and the CCSV group. Data were analyzed with the Mann-Whitney U test. Return of spontaneous circulation was achieved in five of eight (intermittent positive-pressure ventilation), six of eight (bilevel), and four of seven (chest compression synchronized ventilation) pigs. The results of arterial blood gas analyses at t = 4 minutes and t = 13 minutes (torr) were as follows: PaO2 intermittent positive-pressure ventilation, 143 (76/256) and 262 (81/340); bilevel, 261 (109/386) (p = 0.195 vs intermittent positive-pressure ventilation) and 236 (86/364) (p = 0.878 vs intermittent positive-pressure ventilation); and chest compression synchronized ventilation, 598 (471/650) (p < 0.001 vs intermittent positive-pressure ventilation) and 634 (115/693) (p = 0.054 vs intermittent positive-pressure ventilation); PaCO2 intermittent positive-pressure ventilation, 40 (38/43) and 45 (36/52); bilevel, 39 (35/41) (p = 0.574 vs intermittent positive-pressure ventilation) and 46 (42/49) (p = 0.798); and chest compression synchronized ventilation, 28 (27/32) (p = 0.001 vs intermittent positive-pressure ventilation) and 26 (18/29) (p = 0.004); mixed venous pH intermittent positive-pressure ventilation, 7.34 (7.31/7.35) and 7.26 (7.25/7.31); bilevel, 7.35 (7.29/7.37) (p = 0.645 vs intermittent positive-pressure ventilation) and 7.27 (7.17/7.31) (p = 0.645 vs intermittent positive-pressure ventilation); and chest compression synchronized ventilation, 7.34 (7.33/7.39) (p = 0.189 vs intermittent positive-pressure ventilation) and 7.35 (7.34/7.36) (p = 0.006 vs intermittent positive-pressure ventilation). Mean end-inspiratory and end-expiratory arterial pressures at t = 13 minutes (mm Hg) were as follows: intermittent positive-pressure ventilation, 28.0 (25.0/29.6) and 27.9 (24.4/30.0); bilevel, 29.1 (25.6/37.1) (p = 0.574 vs intermittent positive-pressure ventilation) and 28.7 (24.2/36.5) (p = 0.721 vs intermittent positive-pressure ventilation); and chest compression synchronized ventilation, 32.7 (30.4/33.4) (p = 0.021 vs intermittent positive-pressure ventilation) and 27.0 (24.5/27.7) (p = 0.779 vs intermittent positive-pressure ventilation). Conclusions:Both intermittent positive-pressure ventilation and bilevel provided similar oxygenation and ventilation during cardiopulmonary resuscitation. Chest compression synchronized ventilation elicited the highest mean arterial pressure, best oxygenation, and a normal mixed venous pH during cardiopulmonary resuscitation.


PLOS ONE | 2015

Chest Compression Synchronized Ventilation versus Intermitted Positive Pressure Ventilation during Cardiopulmonary Resuscitation in a Pig Model

Clemens Kill; Monika Galbas; Christian Neuhaus; Oliver Hahn; Pascal Wallot; Karl Kesper; Hinnerk Wulf; Wolfgang Dersch

Background Guidelines recommend mechanical ventilation with Intermitted Positive Pressure Ventilation (IPPV) during resuscitation. The influence of the novel ventilator mode Chest Compression Synchronized Ventilation (CCSV) on gas exchange and arterial blood pressure compared with IPPV was investigated in a pig model. Methods In 12 pigs (general anaesthesia/intubation) ventricular fibrillation was induced and continuous chest compressions were started after 3min. Pigs were mechanically ventilated in a cross-over setting with 5 ventilation periods of 4min each: Ventilation modes were during the first and last period IPPV (100% O2, tidalvolumes = 7ml/kgKG, respiratoryrate = 10/min), during the 2nd, 3rd and 4th period CCSV (100% O2), a pressure-controlled and with each chest compression synchronized breathing pattern with three different presets in randomized order. Presets: CCSVA: Pinsp = 60mbar, inspiratorytime = 205ms; CCSVB: Pinsp = 60mbar, inspiratorytime = 265ms; CCSVC: Pinsp = 45mbar, inspiratorytime = 265ms. Blood gas samples were drawn for each period, mean arterial (MAP) and centralvenous (CVP) blood pressures were continuously recorded. Results as median (25%/75%percentiles). Results Ventilation with each CCSV mode resulted in higher PaO2 than IPPV: PaO2: IPPVfirst: 19.6(13.9/36.2)kPa, IPPVlast: 22.7(5.4/36.9)kPa (p = 0.77 vs IPPVfirst), CCSVA: 48.9(29.0/58.2)kPa (p = 0.028 vs IPPVfirst, p = 0.0001 vs IPPVlast), CCSVB: 54.0 (43.8/64.1) (p = 0.001 vs IPPVfirst, p = 0.0001 vs IPPVlast), CCSVC: 46.0 (20.2/58.4) (p = 0.006 vs IPPVfirst, p = 0.0001 vs IPPVlast). Both the MAP and the difference MAP-CVP did not decrease during twelve minutes CPR with all three presets of CCSV and were higher than the pressures of the last IPPV period. Conclusions All patterns of CCSV lead to a higher PaO2 and avoid an arterial blood pressure drop during resuscitation compared to IPPV in this pig model of cardiac arrest.


Resuscitation | 2011

AP015 Chest compression synchronized ventilation during CPR: Technical solution and flow-volume curves of a novel ventilator mode

Florian Dietz; Christian Neuhaus; Wolfgang Dersch; Pascal Wallot; Oliver Hahn; Stefan Schwarz; Robert Mahling; Hinnerk Wulf; Clemens Kill

Mechanical ventilation with an automated ventilator is recommended during CPR with secured airway 1 . We developed and investigated the novel ventilator mode Chest Compression Synchronized Ventilation (CCSV), a pressure controlled ventilation triggered by each chest compression. The new ventilator mode and trigger technology are described and the resulting flow-volume curves were investigated in a pig model.


Resuscitation | 2010

Mechanical ventilation during CPR: Influence of intermitted positive pressure ventilation and BILEVEL ventilation on tidal volumes in a pig model

Christian Neuhaus; Florian Dietz; Oliver Hahn; Stefan Schwarz; Robert Mahling; H. Wulf; Clemens Kill


Resuscitation | 2015

Cerebral oxygenation during resuscitation: Influence of the ventilation modes Chest Compression Synchronized Ventilation (CCSV) or Intermitted Positive Pressure Ventilation (IPPV) and of vasopressors on cerebral tissue oxygen saturation

Clemens Kill; Rebecca Thonke; Oliver Hahn; Pascal Wallot; Karl Kesper; Hinnerk Wulf; Wolfgang Dersch


Resuscitation | 2011

AP025 CHEST COMPRESSION SYNCHRONIZED VENTILATION DURING CPR: INFLUENCE ON HAEMODYNAMICS IN A PIG MODEL

Clemens Kill; Pascal Wallot; Oliver Hahn; Christian Neuhaus; Florian Dietz; Stefan Schwarz; Robert Mahling; Hinnerk Wulf; Wolfgang Dersch


Resuscitation | 2014

Influence of mechanical ventilation with Chest Compression Synchronized ventilation (CCSV) or Intermitted Positive Pressure Ventilation (IPPV) on haemodynamics in a pig model

Clemens Kill; Oliver Hahn; Christian Neuhaus; Monika Galbas; Pascal Wallot; Elisabeth Boesl; Hinnerk Wulf; Wolfgang Dersch


Resuscitation | 2013

Resuscitation with mechanical ventilation: The effects of Chest Compression Synchronized Ventilation (CCSV) or Intermitted Positive Pressure Ventilation (IPPV) on lung injury in a pig model

Wolfgang Dersch; Philipp Hoselmann; Christian Neuhaus; Ulrich Palm; Elisabeth Bösl; Pascal Wallot; Oliver Hahn; Wilhelm Nimphius; Hinnerk Wulf; Clemens Kill


Resuscitation | 2012

Resuscitation and mechanical ventilation with Chest Compression Synchronized Ventilation (CCSV) or Intermitted Positive Pressure Ventilation (IPPV): Influence on gas exchange and return of spontaneous circulation in a pig modelCategory: CPR Systems

Wolfgang Dersch; Pascal Wallot; Oliver Hahn; Christopher Sauerbrei; Andreas Jerrentrup; Christian Neuhaus; Ulrich Palm; H. Wulf; Clemens Kill


Resuscitation | 2011

AP024 Chest compression synchronized ventilation during CPR: Influence of a novel ventilator mode on gas exchange in a pig model

Clemens Kill; Wolfgang Dersch; Oliver Hahn; Christian Neuhaus; Florian Dietz; Robert Mahling; Stefan Schwarz; Hinnerk Wulf; Pascal Wallot

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H. Wulf

University of Marburg

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