| Literature DB >> 31050337 |
Kentaro Iwakiri1, Akio Kobayashi1, Yuichi Takeuchi1, Yusuke Kimura1, Yoichi Ohta2, Hiroaki Nakamura2.
Abstract
BACKGROUND: Cryotherapy is rarely reported on the usefulness of cryotherapy applied after total hip arthroplasty (THA), and there are no reports about patient satisfaction against the cryotherapy following THA. The aim of this study was whether cryotherapy can be useful for relieving pain, reducing blood loss, and swelling, and improving patient satisfaction after THA.Entities:
Year: 2019 PMID: 31050337 PMCID: PMC6498864 DOI: 10.1051/sicotj/2019010
Source DB: PubMed Journal: SICOT J ISSN: 2426-8887
Demographic data of patients in two groups.
| Control | Cryotherapy |
| |
|---|---|---|---|
|
| 30 | 30 | |
| Female/male | 29/1 | 29/1 | – |
| Age (years) | 67.6 ± 8.9 | 68.1 + 9.6 | 0.824 |
| BMI (kg/m2) | 23.9 ± 3.1 | 24.1± 3.1 | 0.787 |
| OA/ION | 29/1 | 29/1 | – |
| Blood loss during surgery(mL) | 391.2 ± 173.5 | 451.1 ± 240.6 | 0.274 |
| Duration of surgery (min.) | 96.6 ± 15.6 | 100.4 ± 16.7 | 0.367 |
| Hospital stay (day) | 24.7 ± 7.0 | 25.7 ± 5.6 | 0.558 |
Data are shown as mean ± standard deviation or numbers.
OA, osteoarthritis; ION, idiopathic osteonecrosis of the femoral head.
Mann–Whitney U test.
Figure 1(a) A cooling pad (28 × 29 cm) wrapped in a waterproof cover for the surgical wound and the thigh (Sigmax, Tokyo, Japan). (b) A computer-controlled cooling device (Icing System CF3000, Sigmax, Tokyo, Japan).
Primary outcomes.
| Control | Cryotherapy |
| |
|---|---|---|---|
| Laboratory data | |||
| CK (IU/L) | |||
| Pre-op. | 96.6 ± 63.7 | 107.0 ± 79.4 | 0.578 |
| Day 1 | 439.1 ± 201.4 | 467.1 ± 234.8 | 0.622 |
| Day 4 | 447.1 ± 233.6 | 525.7 ± 266.8 | 0.230 |
| Day 7 | 183.2 ± 106.8 | 181.9 ± 144.5 | 0.054 |
| Day 14 | 53.3 ± 13.6 | 67.5 ± 38.9 | 0.067 |
| Day 21 | 57.3 ± 15.4 | 60.5 ± 31.7 | 0.668 |
| CRP (mg/dL) | |||
| Pre-op. | 0.21 ± 0.24 | 0.13 ± 0.15 | 0.145 |
| Day 1 | 1.93 ± 0.93 | 1.50 ± 0.69 | 0.056 |
| Day 4 | 4.59 ± 3.05 | 4.57 ± 2.74 | 0.971 |
| Day 7 | 1.27 ± 1.06 | 1.42 ± 1.02 | 0.574 |
| Day 14 | 0.38 ± 0.37 | 0.44 ± 0.68 | 0.701 |
| Day 21 | 0.28 ± 0.27 | 0.32 ± 0.48 | 0.719 |
| Estimated blood loss (mL) | 784.7 ± 293.3 | 699.6 ± 296.2 | 0.268 |
| Pain VAS | |||
| Pre-op. | 29.3 ± 33.9 | 24.1 ± 28.5 | 0.536 |
| Day 4 | 9.3 ± 13.6 | 11.5 ± 19.3 | 0.624 |
| Day 7 | 7.1 ± 9.7 | 11.5 ± 17.3 | 0.243 |
| Day 14 | 5.4 ± 9.4 | 9.4 ± 17.8 | 0.294 |
| Day 28 | 1.2 ± 2.2 | 3.3 ± 7.1 | 0.342 |
| Thigh girth (the ratio of Post/Pre) | |||
| Pre-op. | 1 | 1 | |
| Day 4 | 1.067 ± 0.055 | 1.041 ± 0.038 | 0.045 |
| Day 7 | 1.047 ± 0.057 | 1.062 ± 0.045 | 0.267 |
| Day 14 | 1.006 ± 0.030 | 1.021 ± 0.048 | 0.156 |
| Day 28 | 1.007 ± 0.026 | 0.946 ± 0.270 | 0.246 |
| Total amount of dicrofenac sodium suppository (mg) | |||
| 72.2 ± 79.5 | 31.7 ± 60.9 | 0.070 |
Data are shown as mean ± standard deviation.
Secondary outcomes.
| Control | Cryotherapy |
| |
|---|---|---|---|
| WOMAC | |||
| Pre-op | 37.0 ± 17.0 | 38.9 ± 20.5 | 0.698 |
| Post-op 3 months | 15.0 ± 11.8 | 13.9 ± 10.6 | 0.408 |
| Patient-satisfaction of walking ability | |||
| Day 4 | 38 ± 25 | 62 ± 16 | 0.030 |
| Day 7 | 48 ± 33 | 67 ± 17 | 0.040 |
| Day 14 | 51 ± 31 | 67 ± 20 | 0.080 |
| Day 28 | 61 ± 31 | 75 ± 20 | 0.120 |
| Adverse events | |||
| Wound complications | 0 | 0 | – |
| Surgical site infections | 0 | 0 | – |
| Nerve palsy | 0 | 0 | – |
| Deep venous thrombosis | 0 | 0 | – |
Data are shown as mean ± standard deviation or numbers.