Division of Pulmonary, Allergy, and Critical Care Medicine, Department of Internal Medicine, Pusan National University School of Medicine, Transplantation Research Center, Research Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan, Korea
© 2026 The Korean Society of Critical Care Medicine
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
CONFLICT OF INTEREST
Woo Hyun Cho is an editorial board member of the journal but was not involved in the peer reviewer selection, evaluation, or decision process of this article. No other potential conflicts of interest relevant to this article were reported.
FUNDING
This study was supported by a 2025 research grant from Pusan National University Yangsan Hospital.
ACKNOWLEDGMENTS
The authors would like to thank the intensive care unit nursing and rehabilitation teams for their support in patient mobilization and care during the study.
AUTHOR CONTRIBUTIONS
Conceptualization: JHJ. Data curation: EC, ES. Visualization: JHJ, SHY, HYS. Project administration: HJY, WHC, DJ, YSK. Writing-original draft: JHJ, HJY. Writing-review and editing: JHJ, SEL, HJY. All authors read and agreed to the published version of the manuscript.
| Study | Study design | ECMO configuration | Patient | Frequency and duration | Rehabilitation modality | Outcome | Adverse event |
|---|---|---|---|---|---|---|---|
| Abrams et al. (2014) [13] | Retrospective cohort study | VV (n=31) | n=35 (out of 100 total ECMO patients who received active PT) | 1. Median time from ECMO initiation to first PT session: 2 days (IQR, 1–4.5) | Active-assisted range of motion (32%), sitting in bed or at EOB (9%), standing (9%), ambulation (51%), cycle ergometer | 1. Liberation from MV during ECMO: 66% (23/35) | No patient-related complications reported |
| VA (n=4) | - Patients receiving active PT: 35 | 2. PT sessions per week per patient: median, 2.8 (IQR, 0.5–7.8) | 2. Survival | ||||
| (BTT: 19; BTR: 16) | - BTT: 10/19 (53%) underwent transplant | ||||||
| - BTR: 14/16 (88%) survived to discharge | |||||||
| Hermens et al. (2015) [77] | Retrospective case series | VV (n=9) | n=9 (all patients were awake and non-intubated as a bridge to lung transplantation | Unknown | 1. Extensive sputum mobilization | 1. Survivors (n=4): mean MRC score increased from 3.75 to 4.25 before transplant. | Observed only in bifemoral cannulation cases: one large rectus hematoma and one obstructing thrombus in the return cannula |
| 2. Lower body muscle training | 2. Non-survivors (n=5): only 1 patient could perform muscle training, with no improvement in strength. | ||||||
| 3. Bed-to-chair mobilization | |||||||
| Ko et al. (2015) [14] | Retrospective case series | VV (n=7) | n=8 | Total PT sessions: 62 | 1. 31 sessions (50%): passive ROM + NMES | Study focused on feasibility and safety. No clinically significant adverse events were reported. | 3 sessions (5%) were interrupted due to: 1 case of tachycardia (HR, 132/min) and 2 cases of tachypnea (RR, 46–47/min) |
| VA (n=1) | - BTT (lung): 4 | 2. 17 sessions (27%): sitting | |||||
| - BTT (heart): 1 | 3. 2 sessions (3%): elastic band | ||||||
| - BTR: 3 | 4. 11 sessions (18%): standing or marching in place | ||||||
| 5. 1 session (2%): walking | |||||||
| Bain et al. (2016) [76] | Retrospective cohort study | VV (n=9) | n=9 (all BTT on MV prior to ECMO) | Unknown | Progressive rehabilitation followed by ambulation | 1. Post-transplant ICU stay was significantly shorter in the ambulatory group (median, 8 days vs. 45 days). | No specific adverse events during rehabilitation |
| - Usual care: 4 | 2. Total hospital stay was also shorter (median, 50 days vs. 94 days). | ||||||
| - Active rehabilitation including ambulation: 5 | 3. Post-transplant MV was shorter (median, 2 days vs. 29.5 days). | ||||||
| Munshi et al. (2017) [50] | Retrospective cohort study | VV (n=57) | n=61 (all ARDS, bridge to recovery) | Number of PT days on ECMO: median, 3 days (IQR, 1–5). | 1. Passive ROM | 1. ICU mortality | No specific adverse events during rehabilitation |
| VA (n=4) | - Usual care: 11 | 2. Active ROM | - 30% overall (18/61) | ||||
| - Active rehabilitation: 50 | 3. Sitting (in bed or EOB) | - 22% among those who received physiotherapy vs. 64% without physiotherapy (P=0.006) | |||||
| 4. Standing | |||||||
| Activity levels: | |||||||
| - Passive ROM: 28 (61%) | |||||||
| - IMS ≥2 (active exercises in bed): 18 (39%) | |||||||
| - IMS ≥4 (actively sitting at bedside): 8 (17%) | |||||||
| Wells et al. (2018) [53] | Retrospective cohort study | VV (n=98) | Total ECMO: 254 | Total PT sessions: 607 | 1. Therapeutic exercises (268 sessions) | 1. Overall survival to discharge: 109/167 (65.3%). | 1. Minor events: 2 episodes of NSVT and 1 episode of hypotension |
| VA (n=69) | - PT while on ECMO: 167 (intervention group) | 2. Bed mobility (170 sessions) | 2. Mode-specific survival | 2. Major events: none | |||
| - PT after decannulation: 48 | 3. EOB activities (100 sessions) | - VA: 41/69 (59.4%) | |||||
| - No PT: 39 | 4. Sit-to-stand transfers (106 sessions) | - VV: 68/98 (69.4%) | |||||
| 5. Stand pivot transfers (39 sessions) | |||||||
| 6. Standing (98 sessions) | |||||||
| 7. Ambulation (37 sessions) | |||||||
| Pasrija et al. (2019) [61] | Retrospective case series | VA (n=15) | Total n=104 | 1. Median time from cannulation to first out-of-bed mobilization: 3 days (range, 0–26). | 1. Bed-to-chair transfer. | 1. In-hospital survival: 100% | 1. No major adverse events (decannulation, limb ischemia, or major bleeding). |
| - Ambulated with femoral cannulas: 15 | 2. Median time from cannulation to ambulation: 4 days (range, 1–42). | 2. Marching in place. | 2. 1-year survival: 100% | 2. Minor bleeding events: 3 patients (20%) had oozing around cannula site, managed by adding sutures. | |||
| (7 with decompensated heart failure, 8 with massive PE) | 3. Median ambulation distance (first walk): 300 ft (IQR, 160–300). | 3. Walking (goal: ≥300 ft) | |||||
| Braune et al. (2020) [62] | Prospective observational study | VV (n=12) | Total n=115 on ECLS | 1. Total active mobilizations (IMS ≥3): 332 during 1,242 ECLS day (26.7%). | 1. Functional strengthening | Active mobilization (IMS ≥3) of ECLS patients undertaken by an experienced multi-professional team was feasible | 1. Major events in mobilized group: |
| VA (n=17) | - Mobilized patients (IMS ≥3): 43 (37.4%) | 2. Median duration per mobilization session: 130 min (IQR, 44–215). | 2. Breathing exercises | - 3: major bleedings from femoral cannulation sites (6.9%) | |||
| VV-ECCO2R (n=7) | - Non-mobilized (IMS <3): 72 (62.6%) | 3. Active upper and lower limb training | - 1: accidental venous cannula displacement (2.3%) | ||||
| AV-ECCO2R (n=3) | 4. Endurance exercises | 2. Minor events not detailed | |||||
| RVAD (n=4) | 5. Standing, chair transfer, walking | ||||||
| Hayes et al. (2021) [73] | Pilot RCT (phase II) | VV (n=5) | Total = 15 | Mean exercise time: 28.7 min/session (intensive PT) vs. 4.2 min/session (standard PT) | 1. Intensive PT group | 1. In-hospital mortality | No specific adverse events during rehabilitation |
| VA (n=10) | - Intensive PT: 7 | - Passive/active ROM | - 3/7 (42.9%, intensive) vs. 1/8 (12.5%, standard) | ||||
| - Standard PT: 8 | - Resistance training | 2. Time to first stand: 5.5 days (intensive) vs. 20.8 days (standard), P=0.03. | |||||
| - Sitting, standing, and ambulation | |||||||
| 2. Standard PT group | |||||||
| - Passive ROM | |||||||
| Abrams et al. (2022) [17] | Retrospective cohort study | VV (1,076 sessions) | Total = 511 | Total PT sessions: 2,706 (median, 8 sessions per patient; IQR, 2–21). | 1. Bed exercise | 1. 108 (61%) patients ambulated at least once (95 BTT, 13 BTR). | 1. Total events: 59 across 2,706 sessions (2%). |
| VA (1,630 sessions) | - Active PT cohort: 177 (BTT 124, BTR 53) | 2. Sitting, standing | 2. Out-of-bed activity (IMS ≥4): 138 patients (78%), 2,298 sessions (85%). | 2. Major events | |||
| 3. Transfer to chair | 3. Survival to hospital discharge: 107/177 (60%). | - 2: cerebrovascular accidents | |||||
| 4. Marching in place and walking | - 1: cardiac arrest during PT | ||||||
| 5. Cycle ergometer | |||||||
| Mayer et al. (2022) [74] | Retrospective study | VV (n=142) | Total n=315 | PT during ECMO: | 1. In-bed passive/active exercises | Survival was significantly higher in patients achieving mobility milestones: sitting at EOB (47% vs. 13%) and walking >45 m (26% vs. 3.5%). | No specific adverse events during rehabilitation |
| VA (n=153) | - PT during ECMO: 218 | - Mean sessions: 7.4 (SD, 12.7) | 2. Sitting, standing, walking | ||||
| Hybrid (n=20) | - PT after ECMO: 70 | - Frequency: 0.41 sessions/day | 3. Mobility milestones (median days from ECMO start): | ||||
| - No PT: 27 | - Time to first PT session: 4.5 day after ECMO start | - Sitting at edge of bed (IMS, 3): 13.2 days | |||||
| - Standing (IMS, 4): 16.9 days | |||||||
| - Walking >1.5 m (IMS, 7): 19.7 days | |||||||
| - Walking >45 m: 18.7 days | |||||||
| Sheasby et al. (2022) [78] | Retrospective cohort study | VV (n=42) | Total n=42 | Unknown | 1. Bed side PT, upper/lower limb ROM | Mobilized group had improved survival (73.1% vs. 43.8%; P=0.004) | Occurrences of cannula repositioning: 16 events (mobilized) vs. 1 event (non-mobilized), P=0.03 |
| - Non-mobilized: 16 | 2. Sitting, standing, and marching in place | ||||||
| - Mobilized: 26 | 3. Ambulation | ||||||
| Cerier et al. (2023) [18] | Retrospective study | VV (n=67) | Total n=67 | Unknown | 1. Verticalization | Functional outcome (ambulation, day of discharge): | No specific adverse events during rehabilitation |
| - Early PT/OT(<7 days form cannulation): 30 | 2. Dangling at the EOB | 163.5 ft (early PT/OR) vs. 59.5 ft (delayed PT/OT), P<0.001 | |||||
| - Delayed PT/OT: 37 | 3. Standing | ||||||
| 4. Ambulation | |||||||
| 5. Strength and aerobic exercises | |||||||
| Rottmann et al. (2023) [79] | Retrospective cohort study | VV (n=343) | Total n=343 | Unknown | 1. In-bed activities | 1. 30-day survival: IMS ≥ 2: 71% vs. 48% in IMS <2 (P=0.0012) | No specific adverse events during rehabilitation |
| - IMS ≥2 (active mobilization): 62 (18%) | 2. EOB sitting | 2. Ventilator weaning: 61.3% (IMS ≥2) vs. 46.6% (IMS <2), P=0.0489 | |||||
| - IMS <2 (passive or no mobilization): 281 (82%) | 3. Transfer to chair | ||||||
| 4. Standing | |||||||
| Liu et al. (2024) [80] | Prospective cohort study | VV (n=45) | Total n=45 | 1. Conventional rehabilitation | 1. Passive exercises | 1. Early rehabilitation group showed less variation in the breathing-related muscles and motor muscles than the control group | No specific adverse events during rehabilitation |
| - Early rehabilitation: 23 | - Head elevation, turning every 2 hours, daily ~30 min session | 2. Physical factor therapy: NMES, electrotherapy, phototherapy | 2. ECMO duration: Shorter in the early rehabilitation group (8.0 vs. 12.0 days, P=0.002) | ||||
| - Conventional rehabilitation: 22 | 2. Early rehabilitation | 3. Respiratory training: inspiratory muscle training, abdominal breathing, deep breathing | |||||
| - Passive exercises: 1–2 sessions/day, 10–30 min each, ≥20 min/day, ≥ 5 day/wk | 4. Progressive resistance training: upper and lower limb exercises, bed cycling, bedside sitting | ||||||
| - Physical factor therapy: 2 sessions/day, 10–30 min each | 5. Out-of-bed activities: standing with assistance, wheelchair pedaling, step training, and walking | ||||||
| - Respiratory training: 1–2 sessions/day, 5–7 day/wk | |||||||
| - Progressive resistance training: 1–2 sessions/day, 10–30 min each, ≥30 min/day, ≥ 5 day/wk | |||||||
| - Out-of-bed activities: 1–2 sessions/day, 10–30 min each, ≥30 min/day, ≥ 5 day/wk |
ECMO: extracorporeal membrane oxygenation; VV: venovenous; VA: venoarterial; PT: physical therapy; BTT: bridge to transplantation; BTR: bridge to recovery; IQR: interquartile range; EOB: edge of bed; MV: mechanical ventilation; MRC: medical research council; ROM: range of motion; NMES: neuromuscular electrical stimulation; HR: heart rate; RR: respiratory rate; ICU: intensive care unit; ARDS: acute respiratory distress syndrome; IMS: intensive care unit mobility scale; NSVT: non-sustained ventricular tachycardia; PE: pulmonary embolism; ECCO2R: extracorporeal carbon dioxide removal; RVAD: right ventricular assist device; ECLS: extracorporeal life support; RCT: randomized controlled trial; OT: occupational therapy.
| Category | Inclusion criteria | Exclusion criteria (relative or absolute) |
|---|---|---|
| Hemodynamic stability | 1. Stable ECMO flow and sweep gas | 1. Escalating vasopressor needs in the last 12 hr |
| 2. Heart rate: 40–150 bpm | 2. High doses of inotropes and vasopressors | |
| 3. SBP: 80–180 mm Hg | 3. MAP persistently <65 mm Hg | |
| 4. MAP ≥65 mm Hg with low to moderate vasopressor support | ||
| Respiratory status | Acceptable oxygenation and ventilation | Severe hypoxemia or hypercapnia unresponsive to ECMO adjustments |
| 1. FiO2 <0.6, PEEP <10 cm H2O | ||
| 2. SpO2 >90% | ||
| 3. pO2 >60 mm Hg | ||
| 4. pCO2 <80 mm Hg (pH >7.25) | ||
| 5. RR <30/min | ||
| Neurological status | Arousable or awake for active rehabilitation; adequate response on sedation scales (e.g., RASS –1 to +1) | Deep sedation or coma preventing purposeful interaction; uncontrolled delirium |
| Cannulation status | Securely fixed cannulas; no signs of dislodgement or local complications | Cannula instability, recent cannulation without secure fixation, local infection, or active bleeding |
| Bleeding risk | No major active bleeding; stable anticoagulation profile | Active bleeding, recent high-risk procedures, or severe coagulopathy |
| Cardiopulmonary reserve | Adequate cardiac and pulmonary reserve to tolerate mild to moderate exercise demand | Uncontrolled arrhythmias, acute myocardial ischemia, severe pulmonary hypertension |
| Device compatibility | Compatible ventilator and ECMO equipment for mobilization; manageable number of infusion lines and devices | Multiple critical or unstable device making safe mobilization technically infeasible |
| Team and resources | Available multidisciplinary team including intensivists, nurses, physiotherapists, perfusionists; access to necessary equipment and monitoring resources | Lack of adequately trained staff, monitoring limitations, or absence of emergency preparedness protocol |
| Stage | Rehabilitation target | Key intervention | Entry criteria | Stop criteria |
|---|---|---|---|---|
| Phase 1: Passive | Sedated or unconscious patients | Passive ROM, NMES, limb positioning, contracture prevention | · Hemodynamically stable (MAP ≥65 mm Hg with low-moderate vasopressor) | · MAP <60 mm Hg or ≥ 20% drop |
| · Ventilator FiO2 ≤0.6 with SpO2 ≥88% | · New arrhythmia | |||
| · RASS –5 to –2 | · SpO2 <85% or RR >40/min | |||
| · ECMO flow fluctuation >0.5 L/min | ||||
| Phase 2: Active-assisted | Patients emerging from sedation with preserved motor function and minimal cognitive responsiveness | In-bed cycle ergometry (passive/active), assisted sitting on edge of bed | · Able to follow simple commands | · Increased work of breathing |
| · RASS –1 to +1 | · Tachycardia >130/min | |||
| · Maintain MAP ≥65 mm Hg with stable vasopressor dose | · Patient distress or agitation | |||
| Phase 3: Early upright mobilization | Patients with sitting balance | Independent sitting on edge of bed, tilt-table, weight shifting, bed-to-chair transfers, assisted standing | · Able to maintain sitting balance ≥5 sec | · Orthostatic hypotension symptoms |
| · No cannulation restriction | · Cannula tension or oozing | |||
| Phase 4: Advanced upright mobilization | Fully awake, cooperative, hemodynamically stable patients | Standing, marching in place, ambulation with assistive devices | · Secure cannula (preferable non-femoral or single femoral) | · Any sign of cannula traction |
| · Able to stand with minimal assistance | · Chest pain, neurologic change |
| Study | Study design | ECMO configuration | Patient | Frequency and duration | Rehabilitation modality | Outcome | Adverse event |
|---|---|---|---|---|---|---|---|
| Abrams et al. (2014) [13] | Retrospective cohort study | VV (n=31) | n=35 (out of 100 total ECMO patients who received active PT) | 1. Median time from ECMO initiation to first PT session: 2 days (IQR, 1–4.5) | Active-assisted range of motion (32%), sitting in bed or at EOB (9%), standing (9%), ambulation (51%), cycle ergometer | 1. Liberation from MV during ECMO: 66% (23/35) | No patient-related complications reported |
| VA (n=4) | - Patients receiving active PT: 35 | 2. PT sessions per week per patient: median, 2.8 (IQR, 0.5–7.8) | 2. Survival | ||||
| (BTT: 19; BTR: 16) | - BTT: 10/19 (53%) underwent transplant | ||||||
| - BTR: 14/16 (88%) survived to discharge | |||||||
| Hermens et al. (2015) [77] | Retrospective case series | VV (n=9) | n=9 (all patients were awake and non-intubated as a bridge to lung transplantation | Unknown | 1. Extensive sputum mobilization | 1. Survivors (n=4): mean MRC score increased from 3.75 to 4.25 before transplant. | Observed only in bifemoral cannulation cases: one large rectus hematoma and one obstructing thrombus in the return cannula |
| 2. Lower body muscle training | 2. Non-survivors (n=5): only 1 patient could perform muscle training, with no improvement in strength. | ||||||
| 3. Bed-to-chair mobilization | |||||||
| Ko et al. (2015) [14] | Retrospective case series | VV (n=7) | n=8 | Total PT sessions: 62 | 1. 31 sessions (50%): passive ROM + NMES | Study focused on feasibility and safety. No clinically significant adverse events were reported. | 3 sessions (5%) were interrupted due to: 1 case of tachycardia (HR, 132/min) and 2 cases of tachypnea (RR, 46–47/min) |
| VA (n=1) | - BTT (lung): 4 | 2. 17 sessions (27%): sitting | |||||
| - BTT (heart): 1 | 3. 2 sessions (3%): elastic band | ||||||
| - BTR: 3 | 4. 11 sessions (18%): standing or marching in place | ||||||
| 5. 1 session (2%): walking | |||||||
| Bain et al. (2016) [76] | Retrospective cohort study | VV (n=9) | n=9 (all BTT on MV prior to ECMO) | Unknown | Progressive rehabilitation followed by ambulation | 1. Post-transplant ICU stay was significantly shorter in the ambulatory group (median, 8 days vs. 45 days). | No specific adverse events during rehabilitation |
| - Usual care: 4 | 2. Total hospital stay was also shorter (median, 50 days vs. 94 days). | ||||||
| - Active rehabilitation including ambulation: 5 | 3. Post-transplant MV was shorter (median, 2 days vs. 29.5 days). | ||||||
| Munshi et al. (2017) [50] | Retrospective cohort study | VV (n=57) | n=61 (all ARDS, bridge to recovery) | Number of PT days on ECMO: median, 3 days (IQR, 1–5). | 1. Passive ROM | 1. ICU mortality | No specific adverse events during rehabilitation |
| VA (n=4) | - Usual care: 11 | 2. Active ROM | - 30% overall (18/61) | ||||
| - Active rehabilitation: 50 | 3. Sitting (in bed or EOB) | - 22% among those who received physiotherapy vs. 64% without physiotherapy (P=0.006) | |||||
| 4. Standing | |||||||
| Activity levels: | |||||||
| - Passive ROM: 28 (61%) | |||||||
| - IMS ≥2 (active exercises in bed): 18 (39%) | |||||||
| - IMS ≥4 (actively sitting at bedside): 8 (17%) | |||||||
| Wells et al. (2018) [53] | Retrospective cohort study | VV (n=98) | Total ECMO: 254 | Total PT sessions: 607 | 1. Therapeutic exercises (268 sessions) | 1. Overall survival to discharge: 109/167 (65.3%). | 1. Minor events: 2 episodes of NSVT and 1 episode of hypotension |
| VA (n=69) | - PT while on ECMO: 167 (intervention group) | 2. Bed mobility (170 sessions) | 2. Mode-specific survival | 2. Major events: none | |||
| - PT after decannulation: 48 | 3. EOB activities (100 sessions) | - VA: 41/69 (59.4%) | |||||
| - No PT: 39 | 4. Sit-to-stand transfers (106 sessions) | - VV: 68/98 (69.4%) | |||||
| 5. Stand pivot transfers (39 sessions) | |||||||
| 6. Standing (98 sessions) | |||||||
| 7. Ambulation (37 sessions) | |||||||
| Pasrija et al. (2019) [61] | Retrospective case series | VA (n=15) | Total n=104 | 1. Median time from cannulation to first out-of-bed mobilization: 3 days (range, 0–26). | 1. Bed-to-chair transfer. | 1. In-hospital survival: 100% | 1. No major adverse events (decannulation, limb ischemia, or major bleeding). |
| - Ambulated with femoral cannulas: 15 | 2. Median time from cannulation to ambulation: 4 days (range, 1–42). | 2. Marching in place. | 2. 1-year survival: 100% | 2. Minor bleeding events: 3 patients (20%) had oozing around cannula site, managed by adding sutures. | |||
| (7 with decompensated heart failure, 8 with massive PE) | 3. Median ambulation distance (first walk): 300 ft (IQR, 160–300). | 3. Walking (goal: ≥300 ft) | |||||
| Braune et al. (2020) [62] | Prospective observational study | VV (n=12) | Total n=115 on ECLS | 1. Total active mobilizations (IMS ≥3): 332 during 1,242 ECLS day (26.7%). | 1. Functional strengthening | Active mobilization (IMS ≥3) of ECLS patients undertaken by an experienced multi-professional team was feasible | 1. Major events in mobilized group: |
| VA (n=17) | - Mobilized patients (IMS ≥3): 43 (37.4%) | 2. Median duration per mobilization session: 130 min (IQR, 44–215). | 2. Breathing exercises | - 3: major bleedings from femoral cannulation sites (6.9%) | |||
| VV-ECCO2R (n=7) | - Non-mobilized (IMS <3): 72 (62.6%) | 3. Active upper and lower limb training | - 1: accidental venous cannula displacement (2.3%) | ||||
| AV-ECCO2R (n=3) | 4. Endurance exercises | 2. Minor events not detailed | |||||
| RVAD (n=4) | 5. Standing, chair transfer, walking | ||||||
| Hayes et al. (2021) [73] | Pilot RCT (phase II) | VV (n=5) | Total = 15 | Mean exercise time: 28.7 min/session (intensive PT) vs. 4.2 min/session (standard PT) | 1. Intensive PT group | 1. In-hospital mortality | No specific adverse events during rehabilitation |
| VA (n=10) | - Intensive PT: 7 | - Passive/active ROM | - 3/7 (42.9%, intensive) vs. 1/8 (12.5%, standard) | ||||
| - Standard PT: 8 | - Resistance training | 2. Time to first stand: 5.5 days (intensive) vs. 20.8 days (standard), P=0.03. | |||||
| - Sitting, standing, and ambulation | |||||||
| 2. Standard PT group | |||||||
| - Passive ROM | |||||||
| Abrams et al. (2022) [17] | Retrospective cohort study | VV (1,076 sessions) | Total = 511 | Total PT sessions: 2,706 (median, 8 sessions per patient; IQR, 2–21). | 1. Bed exercise | 1. 108 (61%) patients ambulated at least once (95 BTT, 13 BTR). | 1. Total events: 59 across 2,706 sessions (2%). |
| VA (1,630 sessions) | - Active PT cohort: 177 (BTT 124, BTR 53) | 2. Sitting, standing | 2. Out-of-bed activity (IMS ≥4): 138 patients (78%), 2,298 sessions (85%). | 2. Major events | |||
| 3. Transfer to chair | 3. Survival to hospital discharge: 107/177 (60%). | - 2: cerebrovascular accidents | |||||
| 4. Marching in place and walking | - 1: cardiac arrest during PT | ||||||
| 5. Cycle ergometer | |||||||
| Mayer et al. (2022) [74] | Retrospective study | VV (n=142) | Total n=315 | PT during ECMO: | 1. In-bed passive/active exercises | Survival was significantly higher in patients achieving mobility milestones: sitting at EOB (47% vs. 13%) and walking >45 m (26% vs. 3.5%). | No specific adverse events during rehabilitation |
| VA (n=153) | - PT during ECMO: 218 | - Mean sessions: 7.4 (SD, 12.7) | 2. Sitting, standing, walking | ||||
| Hybrid (n=20) | - PT after ECMO: 70 | - Frequency: 0.41 sessions/day | 3. Mobility milestones (median days from ECMO start): | ||||
| - No PT: 27 | - Time to first PT session: 4.5 day after ECMO start | - Sitting at edge of bed (IMS, 3): 13.2 days | |||||
| - Standing (IMS, 4): 16.9 days | |||||||
| - Walking >1.5 m (IMS, 7): 19.7 days | |||||||
| - Walking >45 m: 18.7 days | |||||||
| Sheasby et al. (2022) [78] | Retrospective cohort study | VV (n=42) | Total n=42 | Unknown | 1. Bed side PT, upper/lower limb ROM | Mobilized group had improved survival (73.1% vs. 43.8%; P=0.004) | Occurrences of cannula repositioning: 16 events (mobilized) vs. 1 event (non-mobilized), P=0.03 |
| - Non-mobilized: 16 | 2. Sitting, standing, and marching in place | ||||||
| - Mobilized: 26 | 3. Ambulation | ||||||
| Cerier et al. (2023) [18] | Retrospective study | VV (n=67) | Total n=67 | Unknown | 1. Verticalization | Functional outcome (ambulation, day of discharge): | No specific adverse events during rehabilitation |
| - Early PT/OT(<7 days form cannulation): 30 | 2. Dangling at the EOB | 163.5 ft (early PT/OR) vs. 59.5 ft (delayed PT/OT), P<0.001 | |||||
| - Delayed PT/OT: 37 | 3. Standing | ||||||
| 4. Ambulation | |||||||
| 5. Strength and aerobic exercises | |||||||
| Rottmann et al. (2023) [79] | Retrospective cohort study | VV (n=343) | Total n=343 | Unknown | 1. In-bed activities | 1. 30-day survival: IMS ≥ 2: 71% vs. 48% in IMS <2 (P=0.0012) | No specific adverse events during rehabilitation |
| - IMS ≥2 (active mobilization): 62 (18%) | 2. EOB sitting | 2. Ventilator weaning: 61.3% (IMS ≥2) vs. 46.6% (IMS <2), P=0.0489 | |||||
| - IMS <2 (passive or no mobilization): 281 (82%) | 3. Transfer to chair | ||||||
| 4. Standing | |||||||
| Liu et al. (2024) [80] | Prospective cohort study | VV (n=45) | Total n=45 | 1. Conventional rehabilitation | 1. Passive exercises | 1. Early rehabilitation group showed less variation in the breathing-related muscles and motor muscles than the control group | No specific adverse events during rehabilitation |
| - Early rehabilitation: 23 | - Head elevation, turning every 2 hours, daily ~30 min session | 2. Physical factor therapy: NMES, electrotherapy, phototherapy | 2. ECMO duration: Shorter in the early rehabilitation group (8.0 vs. 12.0 days, P=0.002) | ||||
| - Conventional rehabilitation: 22 | 2. Early rehabilitation | 3. Respiratory training: inspiratory muscle training, abdominal breathing, deep breathing | |||||
| - Passive exercises: 1–2 sessions/day, 10–30 min each, ≥20 min/day, ≥ 5 day/wk | 4. Progressive resistance training: upper and lower limb exercises, bed cycling, bedside sitting | ||||||
| - Physical factor therapy: 2 sessions/day, 10–30 min each | 5. Out-of-bed activities: standing with assistance, wheelchair pedaling, step training, and walking | ||||||
| - Respiratory training: 1–2 sessions/day, 5–7 day/wk | |||||||
| - Progressive resistance training: 1–2 sessions/day, 10–30 min each, ≥30 min/day, ≥ 5 day/wk | |||||||
| - Out-of-bed activities: 1–2 sessions/day, 10–30 min each, ≥30 min/day, ≥ 5 day/wk |
ECMO: extracorporeal membrane oxygenation; SBP: systolic blood pressure; MAP: mean arterial pressure; PEEP: positive end-expiratory pressure; RR: respiratory rate; RASS: Richmond Agitation-Sedation Scale.
ECMO: extracorporeal membrane oxygenation; ROM: range of motion; NMES: neuromuscular electrical stimulation; MAP: mean arterial pressure; RASS: Richmond Agitation-Sedation Scale; RR: respiratory rate.
ECMO: extracorporeal membrane oxygenation; VV: venovenous; VA: venoarterial; PT: physical therapy; BTT: bridge to transplantation; BTR: bridge to recovery; IQR: interquartile range; EOB: edge of bed; MV: mechanical ventilation; MRC: medical research council; ROM: range of motion; NMES: neuromuscular electrical stimulation; HR: heart rate; RR: respiratory rate; ICU: intensive care unit; ARDS: acute respiratory distress syndrome; IMS: intensive care unit mobility scale; NSVT: non-sustained ventricular tachycardia; PE: pulmonary embolism; ECCO2R: extracorporeal carbon dioxide removal; RVAD: right ventricular assist device; ECLS: extracorporeal life support; RCT: randomized controlled trial; OT: occupational therapy.