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Updated: Jan 26, 2026

Reverse Total Shoulder Arthroplasty
Published on: July 5, 2011
Effect of early pendulum exercise on shoulder function after cardiac rhythm management device implantation
Wanwarang Wongcharoen1, Warisara Petvipusit1, Narawudt Prasertwitayakij1
1Division of Cardiology, Department of Internal Medicine, Faculty of Medicine, Chiang Mai University, Muang, Chiang Mai, 50200, Thailand.
Purpose:
Patients who are post-implantation of cardiac rhythm management devices (CRMDs) are commonly instructed to restrict ipsilateral arm movement to reduce risk of lead dislodgement. This immobilization practice increases risk of shoulder-related pain leading to limited shoulder function. We aimed to assess effect of pendulum exercise on shoulder function in patients after CRMD implantation.
Methods:
This study was a prospective, randomized, open-blinded end point study conducted with 200 patients undergoing CRMD implantation. They were randomized into two groups, standard care (control) and pendulum exercise (experimental) groups. The shoulder function was assessed using QuickDASH-TH scores and measurement of the range of motion (ROM) of shoulder abduction and flexion before and 1 month after implantation.
Results:
Baseline characteristics did not differ between the two groups. The lower incidence of shoulder ROM reduction after CRMD implantation was demonstrated in the pendulum exercise group compared to the control group in both flexion (16.8% vs. 40.4%, P < 0.001) and abduction (9.9% vs. 32.3%, P < 0.001). A lower disability of shoulder function after implantation assessed by QuickDASH-TH scores was also noted in the exercise group compared to control (15.2 ± 16.4 vs. 23.4 ± 18.1, P = 0.001). Two patients in the control group and one in the exercise group had atrial lead dislodgement on the day following the procedure.
Conclusions:
Early pendulum exercise with ipsilateral arm after CRMD implantation was safe and resulted in lower incidence of limited shoulder ROM and less disability of shoulder function compared to control group.
Trial Registration:
The study was registered in clinicaltrials.in.th , and the identification number is TCTR20180612003.
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