“…Outcomes included the impact of PD on caregivers' sleep (Bartolomei et al, 2018), burden (Bartolomei et al, 2018; Kudlicka et al, 2013), daily routines (Hurt et al, 2018; Padovani et al, 2018), and QoL (Bartolomei et al, 2018; Shin & Tan, 2019). The amount and quality of support caregivers received (Dekawaty et al, 2019; Shin & Tan, 2019), cultural and spiritual meaning gained (Dekawaty et al, 2019), caregivers' compassion (Walga, 2019), and self-care efforts (Hurt et al, 2018) were reported. Financial implications for caregivers (Martinez-Martin et al, 2018) and the shortage of and cost of PD medications were described (Walga, 2019).…”