TY - JOUR
T1 - Postoperative continuous-flow cryocompression therapy in the acute recovery phase of hip fracture surgery
T2 - A randomized controlled clinical trial
AU - Leegwater, Nick C.
AU - Bloemers, Frank W.
AU - de Korte, Niels
AU - Heetveld, Martin J.
AU - Kalisvaart, Kees J.
AU - Schönhuth, Casper P.
AU - Pijnenburg, Bas A.C.M.
AU - Burger, Bart J.
AU - Ponsen, Kornelis J.
AU - Maier, Andrea B.
AU - van Royen, Barend J.
AU - Nolte, Peter A.
PY - 2017/12
Y1 - 2017/12
N2 - Background: The acute recovery phase after hip fracture surgery is often complicated by severe pain, postoperative blood loss with subsequent transfusion, and delirium. Prevalent comorbidity in hip fracture patients limit the use of opioid-based analgesic therapies, yielding a high risk for inferior pain treatment. Postoperative cryotherapy is suggested to provide an analgesic effect, and to reduce postoperative blood loss. In this prospective, open-label, parallel, multicentre, randomized controlled, clinical trial, we aimed to determine the efficacy of continuous-flow cryocompression therapy (CFCT) in the acute recovery phase after hip fracture surgery. Methods: Patients with an intra or extracapsular hip fracture scheduled for surgery were included. Subjects were allocated to receive postoperative CFCT or usual care. The primary endpoint was numeric rating scale (NRS) pain the first 72 postoperative hours. Secondly, analgesic use; postoperative haemoglobin change and transfusion incidence; functional outcome; length of stay; delirium incidence; location of rehabilitation; patient-reported health outcome; complications and feasibility were assessed. Results: Sixty-one subjects in the control group, and 64 subjects in the CFCT group were analysed. Within the CFCT group, post treatment NRS pain declined 0.31 (p = 0.07) at 24. h, 0.28 (p = 0.07) at 48. h, and 0.47 (p = 0.002) at 72. h relative to pre treatment NRS pain. Sensitivity analysis at 72. h showed that NRS pain was 0.92 lower in the CFCT group when compared to the control group (1.50 vs. 2.42; p = 0.03). Postoperative analgesic use was comparable between groups. Between postoperative day one and three haemoglobin declined 0.29. mmol/l in the CFCT group and 0.51. mmol/l in controls (p = 0.06), and transfusion incidence was comparable. The timed up and go test and length of stay were also comparable between both groups. Complications, amongst delirium and cryotherapy-related adverse events were not statistically significantly different. Discharge locations did not differ between groups. At outpatient follow-up subjects did not differ in patient-reported health outcome scores. Subjects rated CFCT satisfaction with an average of 7.1 out of 10 points. Conclusions: No evidence was recorded to suggest that CFCT has an added value in the acute recovery phase after hip fracture surgery. If patients complete the CFCT treatment schedule, a mild analgesic effect is observed at 72. h.
AB - Background: The acute recovery phase after hip fracture surgery is often complicated by severe pain, postoperative blood loss with subsequent transfusion, and delirium. Prevalent comorbidity in hip fracture patients limit the use of opioid-based analgesic therapies, yielding a high risk for inferior pain treatment. Postoperative cryotherapy is suggested to provide an analgesic effect, and to reduce postoperative blood loss. In this prospective, open-label, parallel, multicentre, randomized controlled, clinical trial, we aimed to determine the efficacy of continuous-flow cryocompression therapy (CFCT) in the acute recovery phase after hip fracture surgery. Methods: Patients with an intra or extracapsular hip fracture scheduled for surgery were included. Subjects were allocated to receive postoperative CFCT or usual care. The primary endpoint was numeric rating scale (NRS) pain the first 72 postoperative hours. Secondly, analgesic use; postoperative haemoglobin change and transfusion incidence; functional outcome; length of stay; delirium incidence; location of rehabilitation; patient-reported health outcome; complications and feasibility were assessed. Results: Sixty-one subjects in the control group, and 64 subjects in the CFCT group were analysed. Within the CFCT group, post treatment NRS pain declined 0.31 (p = 0.07) at 24. h, 0.28 (p = 0.07) at 48. h, and 0.47 (p = 0.002) at 72. h relative to pre treatment NRS pain. Sensitivity analysis at 72. h showed that NRS pain was 0.92 lower in the CFCT group when compared to the control group (1.50 vs. 2.42; p = 0.03). Postoperative analgesic use was comparable between groups. Between postoperative day one and three haemoglobin declined 0.29. mmol/l in the CFCT group and 0.51. mmol/l in controls (p = 0.06), and transfusion incidence was comparable. The timed up and go test and length of stay were also comparable between both groups. Complications, amongst delirium and cryotherapy-related adverse events were not statistically significantly different. Discharge locations did not differ between groups. At outpatient follow-up subjects did not differ in patient-reported health outcome scores. Subjects rated CFCT satisfaction with an average of 7.1 out of 10 points. Conclusions: No evidence was recorded to suggest that CFCT has an added value in the acute recovery phase after hip fracture surgery. If patients complete the CFCT treatment schedule, a mild analgesic effect is observed at 72. h.
KW - Analgesia
KW - Complications
KW - Cryotherapy
KW - Delirium
KW - Functional outcome
KW - Haemoglobin
KW - Hip fracture
KW - Induced hypothermia
KW - Journal Article
KW - Opioid analgesics
KW - Pain
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U2 - https://doi.org/10.1016/j.injury.2017.10.024
DO - https://doi.org/10.1016/j.injury.2017.10.024
M3 - Article
C2 - 29079365
SN - 0020-1383
VL - 48
SP - 2754
EP - 2761
JO - Injury
JF - Injury
IS - 12
ER -