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1.
Artif Organs ; 44(6): 620-627, 2020 Jun.
Article in English | MEDLINE | ID: mdl-31876312

ABSTRACT

This study aims to investigate the outcomes of venoarterial extracorporeal life support (VA-ECLS) in a large single-center patient cohort regarding survival and adverse events. Between June 2009 and March 2019, 462 consecutive patients received VA-ECLS. The mean age was 66.2 ± 11.9 years. Two patient groups were identified: Group 1-patients with ECLS due to postcardiotomy shock (PCS) after cardiac surgery (PCS, n = 357); Group 2-patients with ECLS due to cardiogenic shock (CS) without previous surgery (nonPCS, n = 105). The primary end point was overall in-hospital survival, while secondary end points were adverse events during the study period. Overall, the in-hospital survival rate was 26%. There was no statistically significant difference between the groups: 26.3% for PCS and 24.8% for nonPCS, respectively (P > .05). Weaning from VA-ECLS was possible in 44.3% for PCS and in 29.5% for nonPCS (P = .004). The strong predictors of overall mortality were postoperative hepatic dysfunction (OR = 14.362, 95%CI = 1.948-105.858), cardiopulmonary resuscitation > 30 minutes (OR = 6.301, 95%CI = 1.488-26.673), bleeding with a need for revision (OR = 2.123, 95%CI = 1.343-3.355), and previous sternotomy (OR = 2.077, 95%CI = 1.021-4.223). Despite its low survival rates, VA-ECLS therapy is the last resort and the only lifesaving option for patients in refractory CS. In contrast, there is still a lack of evidence for VA-ECLS in PCS patients. Future studies are warranted to evaluate the outcomes of VA-ECLS therapy after cardiac surgery.


Subject(s)
Cardiac Surgical Procedures/adverse effects , Extracorporeal Membrane Oxygenation/adverse effects , Postoperative Complications/epidemiology , Shock, Cardiogenic/therapy , Shock, Surgical/therapy , Aged , Cardiopulmonary Resuscitation/statistics & numerical data , Extracorporeal Membrane Oxygenation/methods , Female , Hospital Mortality , Humans , Male , Middle Aged , Postoperative Complications/etiology , Shock, Cardiogenic/mortality , Shock, Surgical/etiology , Shock, Surgical/mortality , Sternotomy/adverse effects , Survival Rate , Treatment Outcome
2.
J Surg Res ; 244: 257-264, 2019 12.
Article in English | MEDLINE | ID: mdl-31302323

ABSTRACT

BACKGROUND: Despite the 6000 patients treated with extracorporeal membrane oxygenation (ECMO) annually, there is a paucity of data regarding the nutritional management of these patients. MATERIALS AND METHODS: We performed a prospective, observational study of nutrition in postcardiotomy shock patients at our institution. Over a 3.5-year study period, we identified 50 ECMO patients and 225 non-ECMO patients. We identified type, amount, duration, and disruption of nutritional delivery by cohort. The primary outcome was percent of caloric goal met, and secondary outcome was gastrointestinal complications. RESULTS: ECMO patients met less of their caloric (29% versus 40%, P = 0.017) and protein goals (34% versus 55%, P < 0.001) compared with non-ECMO patients. Tube feeds were administered more slowly (26 versus 37 mL/h, P < 0.001) and held for longer (8.3 versus 4.5 h/d, P < 0.001) in ECMO patients because of procedures (60%) and high-dose pressors (20% versus 7%, P < 0.001). Multivariate analysis demonstrated that ECMO decreased caloric intake by 14%, with no detected increased risk of gastrointestinal complications. CONCLUSIONS: -ECMO patients received significantly less nutrition support compared with a non-ECMO population. Tube feed hold deficits could potentially be avoided by utilizing postpyloric tubes to feed through procedures, by eliminating holds for vasopressors/inotropes in hemodynamically stable patients, or by establishing volume-based feeding protocols. Further clinical studies are needed to establish efficacy of these interventions and to understand the impact of nutrition on outcomes in ECMO patients.


Subject(s)
Cardiac Surgical Procedures/adverse effects , Extracorporeal Membrane Oxygenation/statistics & numerical data , Nutritional Support/statistics & numerical data , Shock, Surgical/therapy , Adult , Aged , Female , Humans , Male , Middle Aged , Prospective Studies , Shock, Surgical/etiology
3.
Eur J Cardiovasc Nurs ; 17(6): 477-485, 2018 08.
Article in English | MEDLINE | ID: mdl-29772911

ABSTRACT

BACKGROUND: Although the implantable cardioverter defibrillator is successful in terminating life threatening arrhythmias, it might give unwanted shocks in the last phase of life if not deactivated in a timely manner. AIMS: This integrated review aimed to provide an overview of studies reporting on implantable cardioverter defibrillator shock incidence and impact in the last phase of life. METHODS AND RESULTS: We systematically searched five electronic databases. Studies reporting on the incidence and/or impact of implantable cardioverter defibrillator shocks in the last month of life were included. Fifteen studies were included. Two American studies published in 1996 and 1998 reported on the incidence of shocks in patients who died non-suddenly: incidences were 24% and 33%, respectively, in the last 24 hours, and 7% and 14%, respectively, in the last hour of life. Six American studies and one Danish study published between 1991-1999 reported on patients dying suddenly: incidences were 41% and 68% in the last 24 hours and 22-66% in the last hour. Four American studies and two Swedish studies published between 2004-2015 did not distinguish the cause of death: incidences were 17-32% in the last month, 3-32% in the last 24 hours, and 8% and 31% in the last hour of life. Three American studies published between 2004-2011 reported that shocks in dying patients are painful and distressing for patients, and distressing for relatives and professional caregivers. CONCLUSION: If the implantable cardioverter defibrillator is not deactivated in a timely manner, a potentially significant proportion of implantable cardioverter defibrillator patients experience painful and distressing shocks in their last phase of life.


Subject(s)
Arrhythmias, Cardiac/surgery , Defibrillators, Implantable/adverse effects , Defibrillators, Implantable/statistics & numerical data , Shock, Surgical/etiology , Terminal Care/statistics & numerical data , Adult , Aged , Aged, 80 and over , Female , Humans , Incidence , Male , Middle Aged , Shock, Surgical/epidemiology
5.
J Craniofac Surg ; 24(3): e228-9, 2013 May.
Article in English | MEDLINE | ID: mdl-23714971

ABSTRACT

Venous air embolism is a serious complication during a neurosurgical procedure. Here is a case of a massive venous air embolism causing cardiac arrest in the supine position surgery. Identifying the alternative inflation and collapse of the sinus and taking emergency measures to avoid catastrophic result are important.


Subject(s)
Blood Loss, Surgical , Craniotomy/adverse effects , Embolism, Air/etiology , Postoperative Complications , Supine Position , Aged , Catastrophic Illness , Fatal Outcome , Heart Arrest/etiology , Humans , Hypotension/etiology , Male , Neurosurgical Procedures/adverse effects , Patient Positioning , Postoperative Hemorrhage/etiology , Reoperation , Sagittal Sinus Thrombosis/etiology , Shock, Surgical/etiology
6.
Intern Med ; 51(10): 1215-9, 2012.
Article in English | MEDLINE | ID: mdl-22687793

ABSTRACT

Shock patients with restrictive cardiomyopathy due to cardiac amyloidosis are refractory to medical treatment. Here, we report a case of early initiation of intra-aortic balloon pumping (IABP) in a patient with cardiac amyloidosis who developed postoperative shock. Continuous hemodiafiltration was also applied to control circulating fluid volume. The mechanical treatments allowed reduction of the doses of catecholamine and diuretics and resulted in full recovery. It is reasonable to initiate IABP and hemofiltration dialysis during the early stages for the appropriate control of hemodynamics and fluid in shock patients with cardiac amyloidosis.


Subject(s)
Amyloidosis/complications , Heart Diseases/complications , Hemodiafiltration , Intra-Aortic Balloon Pumping , Shock, Surgical/therapy , Aged , Blood Volume , Combined Modality Therapy , Hemodynamics , Humans , Kidney Neoplasms/complications , Kidney Neoplasms/surgery , Laparoscopy/adverse effects , Male , Nephrectomy/adverse effects , Shock, Surgical/etiology , Shock, Surgical/physiopathology
7.
Int J Surg ; 9(1): 5-12, 2011.
Article in English | MEDLINE | ID: mdl-20833279

ABSTRACT

Shock, regardless of etiology is characterized by decreased delivery of oxygen and nutrients to the tissues and our interventions are directed towards reversing the cellular ischemia and preventing its consequences. The treatment strategies that are most effective in achieving this goal obviously depend upon the different types of shock (hemorrhagic, septic, neurogenic and cardiogenic). This brief review focuses on the two leading etiologies of shock in the surgical patients: bleeding and sepsis, and addresses a number of new developments that have profoundly altered the treatment paradigms. The emphasis here is on new research that has dramatically altered our treatment strategies rather than the basic pathophysiology of shock.


Subject(s)
Resuscitation/methods , Shock, Surgical/therapy , Humans , Shock, Surgical/diagnosis , Shock, Surgical/etiology
11.
Eur J Cardiothorac Surg ; 34(4): 820-5, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18715792

ABSTRACT

OBJECTIVE: Postoperative vasoplegic syndrome (PVS) is a potentially lethal condition with increased mortality and other postoperative morbidities. Many previous studies have examined the outcomes associated with on-pump coronary artery bypass grafting (CABG) surgery, little is known about the incidence of PVS after off-pump CABG. METHODS: From November 21, 2005 to June 9, 2006, 334 patients underwent isolated on-pump CABG and 362 had off-pump CABG surgery. Perioperative variables were retrospectively compared between on-pump and off-pump CABG surgery using univariate analysis. Significant variables were included into a stepwise regression model to ascertain their independent impact on the incidence of PVS. RESULTS: The incidence of PVS in isolated on-pump CABG was 6.9%; in off-pump CABG was 2.8% (p=0.01). However, in multivariable models adjusted for confounders, on-pump CABG did not reach statistical significance as a risk factor of PVS (OR=2.3, 95% CI 0.94-5.78; p=0.07). In on-pump CABG, preoperative left ventricular EF less than 35% (OR=3.6; p=0.02) and increased body mass index (OR=1.1; p=0.04) were identified as risk predictors of PVS; whereas elective surgery (OR=0.2; p=0.02) and preoperative use of beta-blockers (OR=0.21; p=0.02) were associated with a decreased rate of PVS. PVS was associated with longer ICU stay (OR=6.0; p<0.01), postoperative ventilation (OR=4.6; p<0.01), and hospital stay (OR=2.62; p=0.03). There was a stronger association between preoperative ACE inhibitors therapy and increased risk of PVS in off-pump CABG surgery (OR=4.52, 95% CI 0.95-21.67; p=0.06) than in on-pump CABG surgery (OR=1.06, 95% CI 0.35-3.19; p=0.91), but neither of them reaches statistical significance. CONCLUSIONS: The incidence of PVS after off-pump CABG surgery was significantly lower than after on-pump CABG surgery.


Subject(s)
Coronary Artery Bypass, Off-Pump/adverse effects , Shock, Surgical/etiology , Aged , Cardiopulmonary Bypass , Coronary Artery Bypass/adverse effects , Female , Humans , Male , Middle Aged , Retrospective Studies , Risk Factors , Stroke Volume , Syndrome , Vascular Resistance
14.
Anaesthesia ; 62(8): 846-9, 2007 Aug.
Article in English | MEDLINE | ID: mdl-17635438

ABSTRACT

A 63-year-old female with known empty sella syndrome underwent coronary artery bypass grafting surgery. She became hypotensive immediately postoperatively and this did not respond to fluid resuscitation and inotropic therapy. Surgical re-exploration was undertaken and did not reveal any surgical cause. Pulmonary artery catheterisation confirmed a profound vasodilatory component to her shock. We believe this was due to unmasking of posterior pituitary hypofunction, in particular vasopressin insufficiency, due to metabolic stress. This rapidly corrected with an exogenous vasopressin infusion.


Subject(s)
Coronary Artery Bypass , Empty Sella Syndrome/complications , Hypotension/etiology , Shock, Surgical/etiology , Female , Humans , Middle Aged , Vasopressins/deficiency
15.
Eur J Pediatr ; 166(12): 1221-7, 2007 Dec.
Article in English | MEDLINE | ID: mdl-17225160

ABSTRACT

UNLABELLED: Successful therapy of vasodilatory shock in adults and children with arginine-vasopressin (AVP) has been reported previously. Data on the use of vasopressin in neonates is limited. This retrospective study reports the effects of AVP-treatment in neonates with catecholamine-resistant systemic vasodilatation after cardiopulmonary bypass. From March 2003 through December 2005, 172 neonates underwent open-heart surgery, 17 developed vasopressor-resistant hypotension and were treated with AVP. Thirteen patients had a stage I palliation of single ventricle, two had a Ross-operation and two had an arterial switch operation. All patients received multiple traditional inotropes and vasopressors prior to administration of AVP. AVP was started at median 0.0001 U x kg(-1) x min(-1) (range 0.00005-0.0002) and titrated up to a maximum of median 0.0003 U x kg(-1) x min(-1) (range 0.0001-0.001). AVP led to a significant increase in blood pressure (from 49+/-8 mmHg to 69+/-7 mmHg) and the requirement of traditional vasopressors decreased significantly. No peripheral vasoconstriction or ischemia was observed. Four of 13 patients, all with single ventricle palliation, died. In two patients death occurred due to additional complications 6 days after AVP was discontinued. One patient, who was still on AVP, died 42 hours postoperatively after prolonged hypoxemia not responding to inhaled nitric oxide. One patient arrested on the third postoperative day when AVP was almost weaned. CONCLUSION: In neonates with vasodilatory shock after cardiopulmonary bypass AVP is a potent agent to increase blood pressure when traditional vasopressors are failing.


Subject(s)
Arginine Vasopressin/therapeutic use , Cardiopulmonary Bypass/adverse effects , Shock, Surgical/drug therapy , Shock, Surgical/etiology , Vasoconstrictor Agents/therapeutic use , Arginine Vasopressin/pharmacology , Female , Heart Defects, Congenital/complications , Heart Defects, Congenital/surgery , Humans , Hypotension/drug therapy , Infant, Newborn , Male , Retrospective Studies , Treatment Outcome , Vasoconstrictor Agents/pharmacology , Vasodilation/drug effects
16.
Scand J Surg ; 96(4): 314-8, 2007.
Article in English | MEDLINE | ID: mdl-18265860

ABSTRACT

BACKGROUND AND AIMS: Arginin vasopressin (AVP) is a potent vasoconstrictor which has been used in vasodilatory shock when therapy with catecholamines and fluids has failed. In this study we evaluated the association of AVP with organ failure and mortality in cardiac surgical patients suffering from vasodilatory shock refractory to norepinephrine (NE) treatment. MATERIAL AND METHODS: Cardiac surgical patients who received AVP in addition to NE (N=33, AVP-group) and 33 control patients (NE group) who were treated with an equal dose of NE compared with AVP patients when AVP infusion started. Data on preoperative risk factors according to EuroSCORE and predicted mortality calculated by logistic EuroSCORE were collected preoperatively. Data on hemodynamics, organ dysfunctions, length of intensive care unit stay and mortality were collected. RESULTS: EuroSCORE did not differ between the groups, AVP:10.4 +/- 3.9 vs. NE 8.9 +/- 4.0. Observed 30 day mortality was lower than predicted in both groups, AVP: 7 (21.7%) vs. predicted mortality 25.9% and NE: 2 (6.1%) vs. 16.0%, respectively. There were more renal complications (36.4% vs. 9.1%, p = 0.008) and infections (30.3% vs. 3.0%, p = 0.003) in patients receiving AVP. Cardiovascular complications did not differ between the groups. CONCLUSIONS: In this prospectively observed cohort of cardiac surgical patients, AVP did not increase mortality predicted by Euroscore. Anyhow renal and infection complications were common.


Subject(s)
Arginine Vasopressin/therapeutic use , Cardiopulmonary Bypass/adverse effects , Heart Diseases/surgery , Norepinephrine/therapeutic use , Shock, Surgical/mortality , Vasoconstrictor Agents/therapeutic use , Aged , Drug Therapy, Combination , Female , Finland/epidemiology , Follow-Up Studies , Humans , Male , Middle Aged , Prognosis , Retrospective Studies , Shock, Surgical/etiology , Shock, Surgical/prevention & control , Survival Rate/trends
17.
Can J Anaesth ; 51(9): 875-9, 2004 Nov.
Article in English | MEDLINE | ID: mdl-15525611

ABSTRACT

PURPOSE: To describe cardiovascular collapse during a cemented hip hemiarthroplasty in a patient who, despite a successful cardiopulmonary resuscitation, remained in a persistent vegetative state due to cerebral fat embolism diagnosed by magnetic resonance imaging (MRI). CLINICAL FEATURES: A 75-yr-old woman with no medical history underwent cemented hip hemiarthroplasty under spinal anesthesia for a right femoral neck fracture. Shortly after insertion of the prosthesis, a sudden oxygen desaturation, hypotension, bradycardia, and cardiac arrest occurred. The patient was successfully resuscitated, but did not regain consciousness. The patient developed high-grade fever, thrombocytopenia, anemia, and oliguria. MRI scans of the brain revealed multiple high intensity signals throughout the white matter, the basal ganglia, the cerebellum, and the brain stem. The diagnosis of fat embolism was made on the basis of clinical findings and MRI images. Although her cardiorespiratory status improved over the next week, the patient remained in a persistent vegetative state. CONCLUSION: When fat embolism is suspected, serial MRI scans of the brain should be performed to diagnose the etiology of cerebral embolism as well as to evaluate the severity of brain damage.


Subject(s)
Arthroplasty, Replacement, Hip/adverse effects , Embolism, Fat/diagnosis , Intracranial Embolism/diagnosis , Magnetic Resonance Imaging , Aged , Embolism, Fat/etiology , Female , Femoral Neck Fractures/surgery , Follow-Up Studies , Humans , Intracranial Embolism/etiology , Intraoperative Complications , Persistent Vegetative State/etiology , Shock, Surgical/etiology
18.
Dent Update ; 30(1): 45-7, 2003.
Article in English | MEDLINE | ID: mdl-12619311

ABSTRACT

This article reports a project that was undertaken to determine current UK dental hospital policy with regard to the management of patients taking therapeutic doses of corticosteroids receiving dental treatment under local anaesthesia. There is variation in the medical management of this patient group, and whether practice should be standardized by means of a national policy document warrants consideration.


Subject(s)
Adrenal Cortex Hormones/administration & dosage , Adrenal Insufficiency/drug therapy , Dental Care for Chronically Ill , Shock, Surgical/prevention & control , Acute Disease , Consensus , Dental Care for Chronically Ill/adverse effects , Humans , Hypotension/etiology , Organizational Policy , Practice Guidelines as Topic , Schools, Dental , Shock, Surgical/etiology , Stress, Physiological/complications , Stress, Physiological/etiology , United Kingdom
20.
Med Hypotheses ; 59(3): 337-40, 2002 Sep.
Article in English | MEDLINE | ID: mdl-12208165

ABSTRACT

Vasodilatory shock is a syndrome with high mortality. It is becoming evident that depletion of antidiuretic hormone (ADH) after cardiac surgery or during sepsis plays an important role in the pathogenesis of this condition. Established vasodilatory shock responds well to exogenous ADH infusion. It is possible that preventing ADH depletion at an earlier stage may abrogate the onset of vasodilatory shock, or at least reduce its severity. This paper examines the evidence supporting this concept, and the potential areas of concern in considering this particular type of hormone replacement therapy.


Subject(s)
Shock, Surgical/prevention & control , Vasopressins/therapeutic use , Animals , Cardiopulmonary Bypass/adverse effects , Drug Administration Schedule , Heart-Lung Machine , Humans , Hypotension/etiology , Hypotension/prevention & control , Infusions, Intravenous , Models, Animal , Pulsatile Flow , Randomized Controlled Trials as Topic , Retrospective Studies , Safety , Shock, Septic/blood , Shock, Septic/physiopathology , Shock, Surgical/blood , Shock, Surgical/drug therapy , Shock, Surgical/etiology , Shock, Surgical/physiopathology , Vasodilation , Vasopressins/blood , Vasopressins/deficiency
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