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Cardiac Pacemaker Infection

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1. The MicraTM Transcatheter Pacing System, a leadless pacemaker, in patients indicated for single-chamber ventricular pacemaker implantation

The MicraTM Transcatheter Pacing System, a leadless pacemaker, in patients indicated for single-chamber ventricular pacemaker implantation The MicraTM Transcatheter Pacing System, a leadless pacemaker, in patients indicated for single-chamber ventricular pacemaker implantation: A single technology assessment - NIPH Search for: Søk Menu To top level Close Infectious diseases & Vaccines Mental & Physical health Environment & Lifestyle Health in Norway Quality & Knowledge Research & Access to data (...) About NIPH Close The MicraTM Transcatheter Pacing System, a leadless pacemaker, in patients indicated for single-chamber ventricular pacemaker implantation: A single technology assessment Order Download: Summary Background Permanent cardiac pacing using pacemaker implantation is an effective and necessary treatment for patients suffering from atrial fibrillation and bradycardia. In this single technology assessment, we assessed a leadless pacemaker for patients indicated for single-chamber

2018 Norwegian Institute of Public Health

2. ODFS Pace and Pace XL functional electrical stimulation devices for treating drop foot

ODFS Pace and Pace XL functional electrical stimulation devices for treating drop foot ODFS P ODFS Pace and P ace and Pace XL functional electrical ace XL functional electrical stimulation de stimulation devices for treating drop foot vices for treating drop foot Medtech innovation briefing Published: 11 March 2016 nice.org.uk/guidance/mib56 pathways Summary Summary The Odstock Dropped Foot Stimulator (ODFS) Pace and Pace XL devices are functional electrical stimulators indicated for treating (...) . Subject to Notice of rights (https://www.nice.org.uk/terms-and- conditions#notice-of-rights). Page 1 of 51Product summary and lik Product summary and likely place in ely place in ther therap apy y The Odstock Dropped Foot Stimulator (ODFS) Pace and Pace XL are portable functional electrical stimulation (FES) devices, which are used to help people with drop foot walk. The ODFS devices are used as part of an integrated rehabilitation system as an alternative, or in addition to, a foot orthosis or other

2016 National Institute for Health and Clinical Excellence - Advice

3. Infections Associated with Resterilized Pacemakers and Defibrillators. (Abstract)

Infections Associated with Resterilized Pacemakers and Defibrillators. Access to pacemakers and defibrillators is problematic in places with limited resources. Resterilization and reuse of implantable cardiac devices obtained post mortem from patients in wealthier nations have been undertaken, but uncertainty around the risk of infection is a concern.A multinational program was initiated in 1983 to provide tested and resterilized pacemakers and defibrillators to underserved nations (...) %). Overall, 85% received pacemakers and 15% received defibrillators, with one (55.5%), two (38.8%), or three (5.7%) leads. Baseline characteristics did not differ between these patients and the 3153 matched control patients. At 2 years of follow-up, infections had occurred in 21 patients (2.0%) with reused devices and in 38 (1.2%) with new devices (hazard ratio, 1.66; 95% confidence interval, 0.97 to 2.83; P = 0.06); there were no device-related deaths. The most common implicated pathogens were

2020 NEJM

4. The Effect of "Cerclage Pacing" for the Heart Failure Patients Who Need Cardiac Resynchronization Therapy (CRT)

The Effect of "Cerclage Pacing" for the Heart Failure Patients Who Need Cardiac Resynchronization Therapy (CRT) The Effect of "Cerclage Pacing" for the Heart Failure Patients Who Need Cardiac Resynchronization Therapy (CRT) - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved (...) studies (100). Please remove one or more studies before adding more. The Effect of "Cerclage Pacing" for the Heart Failure Patients Who Need Cardiac Resynchronization Therapy (CRT) (Cerclage-CRT) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details

2018 Clinical Trials

5. In vivo biocompatibility and pacing function study of silver ion-based antimicrobial surface technology applied to cardiac pacemakers Full Text available with Trip Pro

In vivo biocompatibility and pacing function study of silver ion-based antimicrobial surface technology applied to cardiac pacemakers Evidence suggests that the rate of cardiovascular implantable electronic device (CIED) infections is increasing more rapidly than the rates of CIED implantation and is associated with considerable mortality, morbidity and health economic impact. Antimicrobial surface treatments are being developed for CIEDs to reduce the risk of postimplantation infection within (...) the subcutaneous implant pocket.The feasibility of processing cardiac pacemakers with the Agluna antimicrobial silver ion surface technology and in vivo biocompatibility were evaluated. Antimicrobially processed (n=6) and control pacemakers (n=6) were implanted into subcutaneous pockets and connected to a part of the sacrospinalis muscle using an ovine model for 12 weeks. Pacemaker function was monitored preimplantation and postimplantation.Neither local infection nor systemic toxicity were detected

2017 Open heart

6. Leadless pacemaker implantation after explantation of infected conventional pacemaker systems: A viable solution? (Abstract)

diagnosed with device infection.Patients receiving an LP at our center after conventional PM lead extraction due to infection between December 1, 2013 and November 30, 2017 were included.A total of 17 patients (mean age 77.4 ± 7.77 years) underwent LP implantation (ie, 11 with Nanostim leadless cardiac pacemaker [Abbott, Chicago, IL] and 6 with Micra transcatheter pacing system [Medtronic, Minneapolis, MN]) after successful PM system explantation. In 9 PM-dependent patients, a temporary transvenous (...) Leadless pacemaker implantation after explantation of infected conventional pacemaker systems: A viable solution? Conventional cardiac device infections are increasing in incidence, causing significant morbidity and mortality. Leadless pacemaker (LP) therapy may provide new opportunities for the management of pacemaker (PM) infections as it does not require implantation of transvenous leads and a pectoral pocket.We sought to evaluate the effect of early and late LP implantation in patients

2018 Heart Rhythm

7. Neuromuscular Electrical Stimulation in Chronic Heart Failure Patient

. Soetomo General Hospital Study Details Study Description Go to Brief Summary: The purpose of the study is investigate the effects of NMES in regulation of serum IL-6 and IL-15 in chronic heart failure patients who received standard inpatient cardiac rehabilitation protocol Condition or disease Intervention/treatment Phase Chronic Heart Failure Device: Neuromuscular electrical stimulation (NMES) Not Applicable Detailed Description: Majority of chronic heart failure patients became intolerance (...) Neuromuscular Electrical Stimulation in Chronic Heart Failure Patient Neuromuscular Electrical Stimulation in Chronic Heart Failure Patient - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Neuromuscular

2018 Clinical Trials

8. Cardiac Resynchronisation Therapy Versus Rate-responsive Pacing in Heart Failure With Preserved Ejection Fraction

Cardiac Resynchronisation Therapy Versus Rate-responsive Pacing in Heart Failure With Preserved Ejection Fraction Cardiac Resynchronisation Therapy Versus Rate-responsive Pacing in Heart Failure With Preserved Ejection Fraction - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved (...) studies (100). Please remove one or more studies before adding more. Cardiac Resynchronisation Therapy Versus Rate-responsive Pacing in Heart Failure With Preserved Ejection Fraction (PREFECTUS) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details

2017 Clinical Trials

9. Cardiac rehabilitation for a skydiver after aortic valve replacement for pure aortic regurgitation and resection of the ascending aorta complicated by active infective endocarditis and heart block requiring a pacemaker Full Text available with Trip Pro

Cardiac rehabilitation for a skydiver after aortic valve replacement for pure aortic regurgitation and resection of the ascending aorta complicated by active infective endocarditis and heart block requiring a pacemaker A professional skydiver underwent aortic valve and ascending aorta replacement complicated by infective endocarditis with root abscess and pacemaker implantation. He then enrolled in the Baylor Heart and Vascular Hospital cardiac rehabilitation (CR) program as part of its (...) specificity of testing and exercise training facility. He performed specific skydiving cardiovascular and muscular strength tests at the beginning and the end of the CR program. His pacemaker was interrogated to ascertain any arrhythmias or lead displacement over the course of the CR program. Daily exercise training was customized to match the physical demands of skydiving, including two sessions at iFLY Dallas. Upon completion of the daily exercise sessions, the patient performed a simulated free-fall

2017 Proceedings (Baylor University. Medical Center)

10. Electrical Stimulation for the Treatment of Back Pain Using Peripheral Nerve Stimulation (PNS)

Electrical Stimulation for the Treatment of Back Pain Using Peripheral Nerve Stimulation (PNS) Electrical Stimulation for the Treatment of Back Pain Using Peripheral Nerve Stimulation (PNS) - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one (...) or more studies before adding more. Electrical Stimulation for the Treatment of Back Pain Using Peripheral Nerve Stimulation (PNS) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03179202 Recruitment Status : Recruiting

2017 Clinical Trials

11. Intrapocket Antibiotics to Prevent Infections from Implantable Cardioverter- Defibrillator and Pacemaker for Adult Patients Undergoing Device Insertion: A Review of Clinical Evidence and Comparative Clinical Effectiveness

. Circulation. 2007 Sep 18;116(12):1349-55. PubMed: PM17724263 5. Sohail MR, Uslan DZ, Khan AH, Friedman PA, Hayes DL, Wilson WR, et al. Risk factor analysis of permanent pacemaker infection. Clin Infect Dis. 2007 Jul 15;45(2):166-73. PubMed: PM17578774 Review Articles 6. Margey R. Cardiac implantable electronic device infections: the enemy that lurks beneath the skin. J Long Term Eff Med Implants. 2010;20(3):203-17. PubMed: PM21395519 7. Borek PP, Wilkoff BL. Pacemaker and ICD leads: strategies for long (...) Intrapocket Antibiotics to Prevent Infections from Implantable Cardioverter- Defibrillator and Pacemaker for Adult Patients Undergoing Device Insertion: A Review of Clinical Evidence and Comparative Clinical Effectiveness Disclaimer: The Rapid Response Service is an information service for those involved in planning and providing health care in Canada. Rapid responses are based on a limited literature search and are not comprehensive, systematic reviews. The intent is to provide a list

2012 Canadian Agency for Drugs and Technologies in Health - Rapid Review

12. Viewing Surface Electrical Stimulation on Pelvic Floor With Ultrasound

Viewing Surface Electrical Stimulation on Pelvic Floor With Ultrasound Viewing Surface Electrical Stimulation on Pelvic Floor With Ultrasound - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Viewing Surface (...) Electrical Stimulation on Pelvic Floor With Ultrasound The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT03528928 Recruitment Status : Active, not recruiting First Posted : May 18, 2018 Last Update Posted : May 18, 2018 Sponsor: Elidah, Inc. Information provided by (Responsible Party): Elidah, Inc. Study

2018 Clinical Trials

13. Neuromuscular Electrical Stimulation and Physical Function in Older Adults

Criteria: 1) they have participated in regular resistance training exercise or physical rehabilitation of the lower extremity within 2 months of the study 2) contraindicating conditions for electrical stimulation are present (i.e., swollen, infected or inflamed areas including open wounds, or painful areas on the lower limbs, implanted electronics including cardiac pacemakers, electronic infusion pumps, implanted stimulators, or surgical hardware in the lower limbs) 3) they have current knee injury (...) Neuromuscular Electrical Stimulation and Physical Function in Older Adults Neuromuscular Electrical Stimulation and Physical Function in Older Adults - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more

2018 Clinical Trials

14. Use of Neural Functional Electrical Stimulation for the Recovery of Grasping Movements for Patient With Quadriplegia.

. Nerve stimulation would activate more muscles through a reduced number of electrodes, limiting the number of internal components, reduces the risk of spreading infections and require less electrical energy for its operation. Condition or disease Intervention/treatment Phase Spinal Cord Injuries Device: Intra-operative neural cuff stimulation Not Applicable Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Estimated Enrollment : 9 participants (...) epilepsy. 3. Unstable cardiovascular pathology (coronary heart disease, major hypertension, heart failure etc.). 4. wearing a pacemaker. 5. Dermatological problems contraindicate the application of surface electrodes. 6. body weight> 100kg Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor. Please refer to this study by its

2018 Clinical Trials

15. Electrical Stimulation of Human Myocytes in Microgravity

is acceptable), or hepatic enzyme tests are ≥2.5 times normal limit. Participant has a chronic, contagious, infectious disease, such as active tuberculosis, Hepatitis B or C, or HIV, per self-report. Participant is an amputee and/or has presence of partial or full artificial limb. Participant has had a significant cardiovascular event (e.g. myocardial infarction, stroke) ≤ 6 months prior to screening visit; or stated history of congestive heart failure; or participant has evidence of cardiovascular disease (...) Electrical Stimulation of Human Myocytes in Microgravity Electrical Stimulation of Human Myocytes in Microgravity - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Electrical Stimulation of Human Myocytes

2018 Clinical Trials

16. Clinical Effect Observation for Electrical Pudendal Nerve Stimulation in Treating Urethral Pain Syndrome

Clinical Effect Observation for Electrical Pudendal Nerve Stimulation in Treating Urethral Pain Syndrome Clinical Effect Observation for Electrical Pudendal Nerve Stimulation in Treating Urethral Pain Syndrome - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100 (...) ). Please remove one or more studies before adding more. Clinical Effect Observation for Electrical Pudendal Nerve Stimulation in Treating Urethral Pain Syndrome The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03671993

2018 Clinical Trials

17. Percutaneous Electrical Nerve Stimulation (PENS) of the Auricle for Post Operative Pain Solution(POPS)

, renal dysfunction, sternal wound infections. These make alternative therapies, including non pharmacological modalities, attractive options for optimal analgesic therapy during the post operative period. Alternative methods like topical application of COX -2 inhibitors, intravenous magnesium, Transcutaneous Electrical Nerve Stimulation (TENS) have been tried with varied results in cardiac surgery. A somatotopic relationship has been described between the auricle and the other anatomical regions (...) Percutaneous Electrical Nerve Stimulation (PENS) of the Auricle for Post Operative Pain Solution(POPS) Percutaneous Electrical Nerve Stimulation (PENS) of the Auricle for Post Operative Pain Solution(POPS) - Cardiac Surgery - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved

2018 Clinical Trials

18. Peripherical Neuromuscular Electrical Stimulation in Systemic Autoimmune Myopathies

Peripherical Neuromuscular Electrical Stimulation in Systemic Autoimmune Myopathies Peripherical Neuromuscular Electrical Stimulation in Systemic Autoimmune Myopathies - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before (...) adding more. Peripherical Neuromuscular Electrical Stimulation in Systemic Autoimmune Myopathies The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03751644 Recruitment Status : Recruiting First Posted : November 22, 2018

2018 Clinical Trials

19. Effects of High-frequency Electrical Stimulation for Preventing Loss of Muscle Mass in Patients With Sepsis

with a diagnosis of sepsis or septic shock, aged ≥ 18 years, body mass index (BMI) ≤ 35 kg / m2, without diabetic polyneuropathy, without cardiac pacemaker, without diagnosis of neuromuscular diseases, absence of skin lesions. Exclusion Criteria: heart attack, death. Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor. Please refer (...) Sirio-Libanes: sepsis septic shock electrical stimulation Additional relevant MeSH terms: Layout table for MeSH terms Sepsis Toxemia Shock Shock, Septic Infection Systemic Inflammatory Response Syndrome Inflammation Pathologic Processes

2018 Clinical Trials

20. Efficacy and Safety of Electric Stimulation-guided Epidural Anesthesia for Cesarean Section

Efficacy and Safety of Electric Stimulation-guided Epidural Anesthesia for Cesarean Section Efficacy and Safety of Electric Stimulation-guided Epidural Anesthesia for Cesarean Section - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more (...) studies before adding more. Efficacy and Safety of Electric Stimulation-guided Epidural Anesthesia for Cesarean Section The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03443466 Recruitment Status : Recruiting First Posted

2018 Clinical Trials

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