The effect of robotic telerounding in the surgical intensive care units impact on medical education
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Abstract
Robotic telerounding is effective from the standpoint of patients’ satisfaction and patients’ care in teaching and community hospitals. However, the impact of robotic telerounding by the intensivist rounding remotely in the surgical intensive care unit (SICU), on patients’ outcome and on the education of medical students physician assistants and surgical residents, as well as on nurses’ satisfaction has not been studied. Prospective evaluation of robotic telerounding (RT) using a Likert Scale measuring tool to assess whether it can replace conventional rounding (CR) from the standpoint of patients’ care and outcome, nursing satisfaction, and educational effectiveness. RT did not have a negative impact on patients’ outcome during the study interval: mortality 5/42 (12 %) versus 6/37 (16 %), RT versus CR, respectively, p = 0.747. The intensivists rounding in the SICU were satisfied with their ability to deliver the same patients’ care remotely (Likert score 4.4 ± 0.2). The educational experience of medical students, physicia assistants, and surgical residents was not affected by RT (average Likert score 4.5 ± 0.2, 3.9 ± 0.4, and 4.4 ± 0.4 for surgical residents, medical students and PAs, respectively, p > 0.05). However, as shown by a Likert score of 3.5 ± 1.0, RT did not meet nurses’ expectations from several standpoints. Intensivists regard robotic telerounding as an effective alternative to conventional rounding from the standpoint of patients’ care and teaching. Medical students, physician assistants (PA’s), and surgical residents do not believe that RT compromises their education. Despite similar patients’ outcome, nurses have a less favorable opinion of RT; they believe that the physical presence of the intensivist is favorable at all times.
Keywords
Robot Telerounding SICU Medical education OutcomeNotes
Conflict of interest
Corrado P Marini, MD, has no conflicts of interest to disclose. Garry Ritter PA has no conflicts of interest to disclose. Cordelia Sharma, MD, has no conflicts of interest to disclose. John McNelis, MD, has no conflicts of interest to disclose. Mr. Michael Goldberg has no conflicts of interest to disclose. Rafael Barrera, MD, has no conflicts of interest to disclose.
Informed consent
All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1975, as revised in 2000 (5). Informed consent was obtained from all patients for being included in the study.
Supplementary material
References
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