2019
DOI: 10.1186/s13063-018-3103-8
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Guided meditation as an adjunct to enhance postoperative recovery after cardiac surgery: study protocol for a prospective randomized controlled feasibility trial

Abstract: BackgroundCardiac surgical procedures are associated with postoperative neurological complications such as cognitive decline and delirium, which can complicate recovery and impair quality of life. Perioperative depression and anxiety may be associated with increased mortality after cardiac surgeries. Surgical prehabilitation is an emerging concept that includes preoperative interventions to potentially reduce postoperative complications. While most current prehabilitation interventions focus on optimizing phys… Show more

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Cited by 20 publications
(13 citation statements)
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References 22 publications
(27 reference statements)
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“…Nonetheless, in addition to recognizing anxiety and depression symptoms, nurses are supposed to intervene whenever these symptoms are identified (26) . Surgical pre-rehabilitation is an emergent concept that refers to interventions implemented in the preoperative period in order to improve postsurgical results (27) . This includes preventive strategies like physical therapy, and pharmacological and non-pharmacological measures to improve results (27) .…”
Section: Discussionmentioning
confidence: 99%
“…Nonetheless, in addition to recognizing anxiety and depression symptoms, nurses are supposed to intervene whenever these symptoms are identified (26) . Surgical pre-rehabilitation is an emergent concept that refers to interventions implemented in the preoperative period in order to improve postsurgical results (27) . This includes preventive strategies like physical therapy, and pharmacological and non-pharmacological measures to improve results (27) .…”
Section: Discussionmentioning
confidence: 99%
“…Currently, the Sustained Inflation and Chest Compression Versus 3:1 Chest Compression to Ventilation Ratio During Cardiopulmonary Resuscitation of Asphyxiated Newborns: A Randomized Controlled Trial (SURV1VE-trial) is recruiting term and preterm infants born > 28 +0 weeks’ gestational age requiring chest compression in the delivery room [ 63 , 64 ]. In this cluster trial, hospitals are randomized to either CC + SI or 3:1 C:V ratio for one year each [ 63 , 64 ]. The SURV1VE-trial has been approved by a human clinical research ethical committee at all participating sites, and a Data Safety Monitoring Committee is assessing the results of the trial at regular intervals to assure safety.…”
Section: Clinical Studiesmentioning
confidence: 99%
“…For flexible and tailored management, these programmes include (separately or together) personal visits, community services, or home manuals with phone or electronic support. Nursecoordinated care, case management, telemonitoring with periodic follow-up, and community-based groups with ongoing health practitioner assistance given in a variety of locations are also other options to consider [2].…”
Section: Case Reportsmentioning
confidence: 99%