| Literature DB >> 31323868 |
Louise C Burgess1, Thomas W Wainwright2,3.
Abstract
Early mobilisation is a cornerstone of Enhanced Recovery after Surgery (ERAS) and is encouraged following spinal procedures. However, evidence of its implementation is limited and there are no formal guidelines on optimal prescription. This narrative review aimed to evaluate the evidence for the effect of early mobilisation following elective spinal surgery on length of stay, postoperative complications, performance-based function and patient-reported outcomes. Four trials (five articles) that compared a specific protocol of early in-hospital mobilisation to no structured mobilisation or bed rest were selected for inclusion. Nine studies that investigated the implementation of a multimodal intervention that was inclusive of an early mobilisation protocol were also included. Results suggest that goal-directed early mobilisation, delivered using an evidence-based algorithm with a clear, procedure-specific inclusion and exclusion criteria, may reduce length of stay and complication rate. In addition, there is evidence to suggest improved performance-based and patient-reported outcomes when compared to bed rest following elective spinal surgery. Whilst this review reveals a lack of evidence to determine the exact details of which early mobilisation protocols are most effective, mobilisation on the day of surgery and ambulation from the first postoperative day is possible and should be the goal. Future work should aim to establish consensus-based, best practice guidelines on the optimal type and timing of mobilisation, and how this should be modified for different spinal procedures.Entities:
Keywords: early mobilisation; enhanced recovery after surgery (ERAS); physiotherapy; rehabilitation; spine surgery
Year: 2019 PMID: 31323868 PMCID: PMC6787602 DOI: 10.3390/healthcare7030092
Source DB: PubMed Journal: Healthcare (Basel) ISSN: 2227-9032
PICOS (Population, Intervention, Comparison, Outcome measures, Study design) criteria.
| PICOS Item | Inclusion Criteria | Exclusion Criteria |
|---|---|---|
| Population |
Adults (over 18 years old) receiving elective spinal surgery Revision spinal surgery Surgery for scoliosis, kyphosis or lordosis Lumbar, cervical, thoracic or sacrum surgery |
Children (under 18 years) receiving elective spinal surgery Non-elective surgery Coccyx surgery Surgery for spinal cord injury |
| Intervention |
Early mobilisation (with out of bed activities starting no later than postoperative day one) Enhanced recovery (also termed “rapid recovery” or “fast-track”) programme inclusive of an early mobilisation intervention |
Enhanced recovery programme without mobilisation protocol described Physical therapy intervention initiated later than postoperative day one Ambulatory surgery Neural mobilisation |
| Comparison |
No early mobilisation (standard care) Best rest Pre/post comparison of early mobilisation intervention implementation. |
No control group or comparison data |
| Outcome measures |
Postoperative complication rate Length of hospital stay Patient disposition Readmission rate Performance-based function Patient-reported outcome measures Intervention adherence |
Cost (economic evaluations) |
| Study design |
Randomised clinical trials Non-randomised clinical trials Retrospective analyses Pilot randomised trials |
Case studies Review articles Abstracts Editorials |
| Publication |
Published in English Access to full text |
Unpublished studies Study protocols |
Summary of studies (early mobilisation intervention only).
| Study | Type of Surgery | Study Design | Patients | Early Mobilisation Protocol | Outcome Measures of Interest | Results |
|---|---|---|---|---|---|---|
| Adogwa et al. 2017 [ | Elective spinal surgery (multilevel lumbar decompression and fusion for the correction of adult degenerative scoliosis) | Ambispective (early ambulation vs. late ambulation) | Early ambulators: | Early ambulators were mobilised within 24 h following surgery and late ambulators were at a minimum of 48 h after surgery | Postoperative complications, 30-day hospital readmission rate, postoperative functional status (duration to first ambulation, distance ambulated on the first day of ambulation, the distance of ambulation at discharge), LOS and discharge disposition. | There was a significantly lower incidence of pneumonia in the early ambulators (1.51% vs. 8.47%, |
| Nielsen et al. 2008, 2010 [ | Lumbar fusion or decompression for degenerative lumbar disease with low back pain and radiating pain | RCT (prehabilitation and early rehabilitation vs. standard care) | IG: | The physiotherapist mobilised the patient of the day of the operation and 30 min twice daily in the following days. Exercises with a focus on improved muscle strength for the back and abdomen and cardiovascular conditioning were given. Milestones for patients post-surgery were: (1) Assisted positional change in bed; (2) Independent positional change in bed; (3) Assisted mobilisation to bedside; (4) Independent mobilisation to bedside; (5) Assisted mobilisation in walking frame; (6) Independent mobilisation to walking frame; (7) Independent personal hygiene; (8) Independent daily function on ward; (9) Walking without aids; (10) Complete training programme; (11) Independent stair climb; and (12) Discharge to home. | HRQOL, pain (BPI), function (Roland Morris Questionnaire, sit to stand, TUG, milestone achieved under hospitalisation), postoperative complications, and LOS. | At operation, the IG had improved function and postoperatively reached recovery milestones faster than the CG (1–6 days versus 3–13 days |
| Rupich et al. 2018 [ | Anterior cervical discectomy and fusion, lumbar laminectomy, cervical nonfusion, and posterior laminectomy/foraminoteomy | Retrospective analysis (pre/post early mobility protocol implementation) | IG: | Cervical laminectomies and foraminotomies, anterior cervical discectomy and fusion and lumbar laminectomies, foraminotomies and discectomies: PO day 1: mobilise within 6 h of admission to floor, light activity in the room, bed to chair/bed to bathroom, out of bed to bathroom, no urinal/commode, out of bed for dinner. PO day 2: PCA/IVF discontinued at 6:00 am, foley removed at 6:00 am for lumbar fusions, increase mobility as tolerated, out of bed to bathroom, no urinal/commode, out of bed to chair for all meals starting with breakfast, may mobilise with patient care technician, do not have to wait for physiotherapist. | LOS, intervention adherence | Average compliance to protocol rates was 87.3% per month. Fall rates were monitored quarterly, and over one year the unit’s fall rates remained stable. Over a one-year period, implementation of the protocol resulted in a nine-hour reduction in LOS per hospitalisation in neurosurgical spine patients who underwent lumbar laminectomies. The protocol also allowed nurses more autonomy in patient care and was a catalyst for patient involvement in their postoperative mobility. There were no other statistically significant changes in LOS. The overall adjusted LOS reduction of 2.9 h for the IG was non-significant. |
| Qvarfordh et al. 2014 [ | Lumbar discectomy | Pilot RCT | IG: | In the PACU, patients were mobilised to sit, stand and visit the toilet at least one hour after surgery. The patients rested in bed before they walked the 50 m to the general ward. They used a walking frame and were accompanied by a porter and a nurse with a wheelchair in case the patient feltuncomfortable. In the CG, patients were not mobilised in the PACU. They were driven to the general ward. Once in the general ward, both groups (IG and CG) were mobilised with assistance of a nurse or physiotherapist | Postoperative complications, pain, patient experience, time to mobilisation in the general ward and LOS | During the first 24 h postoperatively, IG had lower consumption of opioid compared with the CG, although there were no differences in pain between groups before and after mobilisation. In both groups, the level of nausea was low, and mobilisation did not worsen the level and incidence of nausea in either group. No vomiting was recorded, and only a few mild dizziness cases were registered in each group. Time to first mobilisation in the IG was 35 min (20–270) min and 180 (10–245) min in the CG. During the first 24 h in the general ward, patients in the IG left their bed an average of 9 times (3–16) and in the CG 7 times (4–11) and were out of bed for 171 min (50–670) and 210 (90–420) min, respectively. Patients in the IG were hospitalised for an average of 27 (21–32) h and in the CG for 25 (21–49) h. |
DVT—deep vein thrombosis; PE—pulmonary embolism; MI—myocardial infarction; RCT—randomised controlled trial; IG—intervention group; CG—control group; BPI—brief pain inventory; TUG—timed up and go; HRQOL—health-related quality of life; IVF—intravenous fluid; PCA—patient-controlled analgesia; PO—postoperative; LOS—length of stay; PACU—post-anaesthesia care unit.
Summary of studies (multimodal interventions).
| Study | Type of Surgery | Study Design | Patients | Early Mobilisation Protocol | Outcome Measures of Interest | Results |
|---|---|---|---|---|---|---|
| Blackburn et al. 2016 [ | Elective spinal surgery (discectomy, decompression, fusion and realignment operations to the cervical, thoracic and lumbar spine) | Retrospective analysis (pre/post ERAS implementation) | This study does not report the number of patients included in the analysis. The mean age of all patients at the institute is 55 years | The “Bums off Beds” initiative implemented as part of a Spinal Enhanced Recovery after Surgery programme in Musgrove Park Hospital, Taunton, recommended consultants to visit all patients postoperatively on the day of surgery to get them out of bed, either standing or marching on the spot to show them that mobilisation was safe | LOS, patient satisfaction, readmission rate | The pathway improved reliability of care, patient satisfaction and LOS (5.7 days at the start of the intervention to 2.7 days). A total of 100% of patients rated their care as “good” or “excellent”. The 52% reduction in length of stay was calculated to save the trust a theoretical £7800 per year (bed cost £174 per day) |
| Bradywood et al. 2017 [ | Non-complex lumbar fusion (less than six levels) | Retrospective analysis (pre/post evidence based clinical care pathway implementation) adaption of “Lean” | 244 (ERAS) vs. 214 (non-ERAS) | Right after surgery: log roll with help and walk to the doorway. Fitted for a corset brace but it is not required for movement. Recovery after surgery: sit on edge of the bed, stand at the bedside, and sit in a chair. Ready to leave: can walk with supervision multiple times each day, use brace when walking | LOS, patient disposition, pain and falls | LOS decreased from 3.9–3.4 days, a difference of 0.5 days (CI: 0.3, 0.8, |
| Chakravarthy et al. 2019 [ | Multilevel lumbar or thoracolumbar spinal fusion | Retrospective analysis (pre/post ERAS implementation) | 799 (ERAS) vs. 971 (non-ERAS) | All patients without contraindication were mobilised by the nursing staff within 8 h of arriving to the regular nursing floor. If the patient was unable to be mobilised by the nursing staff or was considered high risk, an order for physical therapy was automatically generated. Removal of the urinary catheter on POD 1 was encouraged to allow for easier mobilisation and to reduce the risk of urinary tract infection. | Infection prevention, blood management | Forty surgical site infections were seen in the pre-intervention cohort and 16 in the post-intervention group (4.12% vs. 2.00%; RR 0.48, 95% CI: 0.27–0.86; |
| Grasu et al. 2018 [ | Spine surgery for metastatic tumours | Retrospective analysis (pre/post ERSS implementation) | 41 (ERSS) vs. 56 (non-ERSS) | Out of bed POD 1: movement 3 times daily, bed to chair, chair to bed at minimum assist level. By discharge: ambulate at minimum assist level for 50 ft with or without an assistive device; if non-ambulatory (i.e., wheelchair bound), bed to chair, chair to bed transfers at minimum assist level. Non-ERAS protocol = not consistently mobilised with frequency | Pain (NRS), LOS, readmission rate and postoperative complications | The ERSS group showed a trend toward better pain scores when compared to the with the pre-ERSS group. There were no significant differences in LOS, 30-day readmission rate, or 30-day complication rate observed between the two groups |
| Tarikci Kilic et al. 2019 [ | Single-level lumbar microdiscetomy | Retrospective analysis (pre/post ERAS implementation) | 60 (ERAS) vs. 60 (non-ERAS) | When the patients returned to the regular ward, they were encouraged to sit out of the bed for mobilisation within 2 h and oral intake was resumed as soon as possible | Time to first mobilisation, PONV, preoperative-postoperative VAS pain scores, postoperative analgesic requirement and LOS | LOS was shorter for the ERAS group (30.10 ± 7.80 h pre-ERAS and 26.52 ± 5.16 h ERAS). First oral intake and first mobilisation were earlier in the ERAS group. The incidence of PONV was less in the ERAS group. Postoperative analgesic requirements and postoperative VAS scores were significantly less in the ERAS group |
| Li et al. 2018 [ | Laminoplasty | Retrospective analysis (pre/post ERAS programme implementation) | 114 (ERAS) vs. 110 (non-ERAS) | Early mobilisation included on-bed movement on the day of surgery, as well as sitting and assisted walking on the postoperative day 1. Pre-ERAS, there was no requirement for postoperative mobilisation | Physiological function (early eating, mobilise), postoperative pain (VAS), LOS, postoperative complications, adverse reactions and protocol compliance | LOS was shorter for the ERAS group compared to the traditional care cohort (5.75 ± 2.46 vs. 7.67 ± 3.45 days, |
| Shields et al. 2017 [ | Spine fusion (except cervical) with and without major comorbidities | Retrospective analysis (2011–2014, multidisciplinary meetings initiated in 2011) | 1978 (total) | Night of surgery: Patient sits on edge of bed. POD 1: Physical therapy on two occasions. | LOS and readmission rate | LOS improved over the three years of intervention implementation. Average LOS for lumbar fusion (without major comorbidity) was statistically different for 2011–2012 vs. 2013–2014 ( |
| Staartjes et al. 2019 [ | Elective tubular microdiscectomy, mini-open decompression and minimally invasive anterior or posterior lumbar fusion | Retrospective analysis (ERAS implemented in 2013, data from 2013–2018 compared) | 2595 (total) | Whenever feasible, early mobilisation was 2 h after operation under guidance of a physiotherapist | LOS, readmission rate, adverse events, reoperations, PROMs, function (ODI), health-related QOL (EQ-5D), pain (EQ-VAS), leg pain and back pain | Over the 5-year period, a trend toward a higher proportion of patients discharged home after a 1-night stay was observed ( |
| Sivaganesan et al. 2018 [ | Elective lumbar or cervical surgery for the treatment of stenosis, disc herniation, spondylolisthesis, adjacent segment disease or pseudarthrosis | Retrospective analysis (pre/post implementation of perioperative protocol) | Preprotocol: | Bed rest after durotomy: Immediate mobilisation if water-tight primary closure achieved | 90-day complication rate, EQ-5D, ODI, neck disability index, back and leg pain (NRS), patient satisfaction, LOS and discharge disposition | After protocol implementation, patients undergoing lumbar surgery had a significantly shorter LOS (2.5 ± 1.7 days versus 2.9 ± 2.2 days, |
ERAS—Enhanced Recovery after Surgery; ERSS—Enhanced Recovery after Spine Surgery; POD—postoperative day; PROMS—patient-reported outcome measures; ODI—Oswestry Disability Index; QOL—quality of life; VAS—visual analogue scale; PONV—postoperative nausea and vomiting; NRS—numeric rating scale; LOS—length of stay; EQ-5D—EuroQol five-dimension scale; CI—confidence interval; CG—control group; RR—relative risk.
Figure 1Study identification flow chart (adapted from the Preferred Reporting Items for Systematic Reviews and Meta-Analysis flowchart) [49].
Modified Downs and Black Checklist, UTD—Unable to determine.
| Item | Description | Nielsen et al. [ | Rupich et al. [ | Qvarfordh et al. [ | Adogwa et al. [ |
|---|---|---|---|---|---|
| 1 | Is the hypothesis/aim/objective of the study clearly described? | Yes (1) | Yes (1) | Yes (1) | Yes (1) |
| 2 | Are the main outcomes to be measured clearly described in the Introduction or Methods section? | Yes (1) | Yes (1) | Yes (1) | Yes (1) |
| 3 | Are the characteristics of the patients included in the study clearly described? | Yes (1) | Yes (1) | Yes (1) | Yes (1) |
| 4 | Are the interventions of interest clearly described? | Yes (1) | Yes (1) | Yes (1) | Yes (1) |
| 6 | Are the main findings of the study clearly described? | Yes (1) | Yes (1) | Yes (1) | Yes (1) |
| 7 | Does the study provide estimates of the random variability in the data for the main outcomes? | Yes (1) | Yes (1) | Yes (1) | Yes (1) |
| 8 | Have all important adverse events that may be a consequence of the intervention been reported? | Yes (1) | Yes (1) | Yes (1) | Yes (1) |
| 10 | Have actual probability values been reported? | Yes (1) | Yes (1) | No (0) | Yes (1) |
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| 11 | Were the subjects asked to participate in the study representative of the entire population from which they were recruited? | Yes (1) | Yes (1) | Yes (1) | UTD (0) |
| 12 | Were those subjects who were prepared to participate representative of the entire population from which they were recruited? | Yes (1) | Yes (1) | Yes (1) | UTD (0) |
| 13 | Were the staff, places, and facilities where the patients were treated, representative of the treatment the majority of patients receive? | Yes (1) | Yes (1) | Yes (1) | Yes (1) |
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| 17 | In trials and cohort studies, do the analyses adjust for different lengths of follow-up of patients, or in case-control studies, is the time period between the intervention and outcome the same for cases and controls? | Yes (1) | Yes (1) | Yes (1) | Yes (1) |
| 18 | Were the statistical tests used to assess the main outcomes appropriate? | Yes (1) | Yes (1) | UTD (0) | Yes (1) |
| 19 | Was compliance with the intervention/s reliable? | No (0) | No (0) | Yes (1) | Yes (1) |
| 20 | Were the main outcome measures used accurate (valid and reliable)? | Yes (1) | Yes (1) | Yes (1) | Yes (1) |
| 21 | Were the patients in different intervention groups (trials and cohort studies) or were the cases and controls (case-control studies) recruited from the same population? | Yes (1) | Yes (1) | Yes (1) | Yes (1) |
| 22 | Were study subjects in different intervention groups (trials and cohort studies) or were case and controls (case control studies) recruited over the same period of time? | Yes (1) | No (0) | Yes (1) | Yes (1) |
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