Abstract

All transplant recipients receive tacrolimus, mycophenolate and glucocorticoids and these drugs have many side-effects and drug-drug interactions. Common complications include surgical complications, infections, rejection and acute kidney injury. Infections as CMV and PJP can be prevented with prophylactic treatment. Given the complexity of organ transplant recipients a multi-disciplinary team of intensivists, surgeons, pharmacists and transplant specialists is essential. After heart transplantation a temporary pacemaker is required until the conduction system recovers. Stiffening of the heart and increased cardiac markers indicate rejection. An endomyocardial biopsy is performed via the right jugular vein, necessitating its preservation. For lung transplant patients, early intervention for aspiration is warranted to prevent chronic rejection. Risk of any infection is high, requiring active surveillance and intensive treatment, mainly of fungal infections. The liver is immunotolerant requiring lower immunosuppression. Transplantation surgery is often accompanied by massive blood loss and coagulopathy. Other complications include portal vein or hepatic artery thrombosis and biliary leakage or stenosis. Kidney transplant recipients have a high risk of cardiovascular disease and posttransplant anemia should be treated liberally. After postmortal transplantation, delayed graft function is common and dialysis is continued. Ureteral anastomosis complications can be diagnosed with ultrasound.

Highlights

  • Worldwide, music is commonly played in the operation room

  • Motion analysis and mental workload assessment using the Surgery Task Load Index (SURGTLX) was performed of all 97 participants who completed the study

  • Heart rate and heart rate variability (HRV) analysis was performed of 93 participants (Fig. 2)

Read more

Summary

Materials and methods

This study was approved in September 2019 by the Medical Ethics Committee Erasmus MC (MEC-2019-0537) and prospectively registered with the Netherlands Trial Register (Trial NL7961). The study was performed in accordance with the ethical standards of the Helsinki Declaration of 1975. Reporting adhered to the 2010 Consolidated Standard of Reporting Trials (CONSORT) extension for randomized crossover trials [27]

Study design
Results
Participants included for data analysis:
Discussion
Conclusion
Compliance with ethical standards

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.