Early Rehabilitation Versus Conventional Approaches in Post-Traumatic Hand Injuries with Multiple Lesions: Clinical Outcomes and Future Directions
Abstract
1. Introduction
2. Materials and Methods
2.1. Study Design and Population
2.2. Therapeutic Protocol
- Immediate postoperative phase (0–14 days): This phase was only applicable to patients who underwent early rehabilitation, initiated shortly after surgical intervention. The priority during the acute phase was to control inflammation, limit edema, protect sutured tissues and prevent complications such as infection, secondary tissue damage or adhesions. Functional goals also included pain reduction and maintenance of mobility in uninvolved joints (elbow, shoulder, cervical spine) to avoid secondary stiffness. Interventions included lymphatic drainage massage (to promote venous and lymphatic return), cryotherapy for edema and pain control, passive and passive-assisted mobilization to maintain joint congruency and early tendon-gliding movements aimed at minimizing adhesions. Customized protective orthoses were used: dorsal blocking splints for flexor tendon repairs, volar blocking splints for extensor injuries and individualized “intrinsic plus” positioning to maintain optimal joint alignment and ligament tension.
- Early rehabilitation phase (2–6 weeks): This phase aimed at preventing stiffness and contractures while allowing controlled mobilization of healing tissues. Techniques focused on maintaining the flexibility of periarticular structures, promoting safe tendon excursion and gradually initiating functional use of the hand. Scar massage and desensitization techniques were introduced as healing permitted, alongside thermotherapy to improve local circulation and tissue pliability. Controlled passive and active-assisted mobilization, tendon-gliding exercises and soft tissue stretching were emphasized to restore motion safely. Complementary modalities such as mirror therapy supported cortical reorganization and pain modulation, while bandaging and physical agents (laser, ultrasound, electrotherapy) enhanced edema reduction and tissue repair. Patient education was an essential component, ensuring adherence to prescribed home exercises and recognition of warning signs (e.g., tendon rupture, excessive inflammation).
- Intermediate phase (6–12 weeks): The objectives in this stage were to consolidate early gains, progressively strengthen the hand and improve dexterity and proprioception. Active free mobilization and isometric strengthening exercises were intensified, while neuroproprioceptive facilitation techniques addressed motor control and coordination. Progressive resistance training and stretching helped restore muscle endurance and joint flexibility. Ergotherapy was introduced to retrain fine and gross motor grips in functional contexts, preparing patients for daily activities. Continued use of customized orthoses was recommended when needed, particularly to maintain joint mobility and alignment or to counteract early stiffness. Mirror therapy and desensitization could be maintained for patients with persistent sensory disturbances.
- Advanced functional reintegration phase (≥12 weeks): The final phase was oriented toward restoring complete functional independence and preventing chronic complications such as pain or stiffness. Rehabilitation progressed to complex, task-oriented exercises requiring force, dexterity and coordination. Activities included advanced strengthening, fine motor training and functional tasks such as gripping, throwing and manipulation, adapted to each patient’s professional and personal needs. Functional reintegration also involved targeted programs for athletes or manual workers, ensuring readiness for high-demand activities. Physical modalities (laser, ultrasound, electrotherapy) and thermoformable orthoses were used selectively in cases of persistent pain, deformity, or instability under stress. The ultimate objective was to reestablish maximal function, allowing safe return to occupational and sports performance while preserving quality of life.

2.3. Evaluation Protocol
2.4. Data Analysis
3. Results
4. Discussion
4.1. Principles of Postoperative Rehabilitation
4.2. Overall Outcomes in the Study Group
4.3. Classic Approach Group (CAG) Analysis
4.4. Early Rehabilitation Group (ERG) Analysis
4.5. Early Versus Classic Rehabilitation: Comparative Findings
4.6. Subgroup Analysis: Flexor Tendon vs. Complex Injuries
4.7. Clinical Implications and Innovative Contributions
4.8. Study Limitations
4.9. Future Perspectives
5. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
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| Parameter Evaluated | Assessment Tool/Method | Details |
|---|---|---|
| 1. Active Range of Motion (AROM) | Total Active Motion (TAM) Score | Sum of MCP, PIP, and DIP flexion minus total extension deficit; bilateral measurement with digital goniometer. |
| 2. Grip Strength (GS) | Jamar Hydraulic Hand Dynamometer | Standard ASHT protocol; three maximal 5 s contractions per hand; highest value recorded. |
| 3. Pain Intensity | Visual Analogue Scale (VAS) | 10 cm horizontal line from “no pain” to “worst imaginable pain”; patient marked pain level from last 24 h. |
| 4. Edema (EDM) | Figure-of-Eight Measurement | Standardized tape measurement route around hand joints; reliable for hand swelling assessment. |
| 5. Hand Function | QuickDASH Questionnaire (QD) | 11 items rated 0–5; assesses difficulty in daily activities and functional limitations. |
| 6. Anxiety Level | Generalized Anxiety Disorder Questionnaire (GAD-7) | 7 items evaluating anxiety symptoms in the past 2 weeks; facilitates early detection of psychological impact. |
| Total | ERG | CAG | |
|---|---|---|---|
| Mean Age (years) ± SD | 47.7 ± 14.9 | 50.2 ± 15.6 | 41.7 ± 11.2 |
| Male | 86.70% | 89.10% | 80.80% |
| Female | 13.30% | 10.90% | 19.20% |
| Sharp injury | 20.00% | 21.90% | 15.40% |
| Crush injury | 7.80% | 4.70% | 15.40% |
| Avulsion | 4.40% | 1.60% | 11.50% |
| Combined mechanism | 67.80% | 71.90% | 57.70% |
| Vascular injury | 54.40% | 50.00% | 65.40% |
| Nerve injury | 55.60% | 51.60% | 65.40% |
| Fracture | 68.90% | 68.80% | 69.20% |
| Flexor tendon injury | 71.10% | 65.60% | 84.60% |
| Extensor tendon injury | 64.40% | 64.10% | 65.40% |
| Parameter | Group | Baseline (Mean ± SD) | 4 Weeks (Mean ± SD) | 12 Weeks (Mean ± SD) | p-Value |
|---|---|---|---|---|---|
| VAS | Total | 8.91 ± 1.85 | 5.24 ± 1.98 | 2.13 ± 1.76 | <0.001 |
| CAG | 7.46 ± 2.64 | 5.15 ± 2.47 | 3.08 ± 2.10 | ||
| ERG | 9.50 ± 0.94 | 5.28 ± 1.76 | 1.75 ± 1.45 | ||
| EDM | Total | 61.48 ± 7.18 | 60.23 ± 6.98 | 59.09 ± 6.76 | <0.001 |
| CAG | 61.31 ± 8.05 | 59.58 ± 7.58 | 58.23 ± 7.24 | ||
| ERG | 61.55 ± 6.87 | 60.50 ± 6.76 | 59.44 ± 6.59 | ||
| GS | Total | 1.06 ± 3.15 | 3.77 ± 5.23 | 13.14 ± 8.69 | <0.001 |
| CAG | 2.52 ± 5.43 | 6.57 ± 7.94 | 14.69 ± 13.28 | ||
| ERG | 0.47 ± 1.05 | 2.64 ± 3.01 | 12.51 ± 5.95 | ||
| QD | Total | 85.08 ± 10.88 | 71.65 ± 18.18 | 35.54 ± 24.60 | <0.001 |
| CAG | 82.10 ± 13.28 | 67.82 ± 23.92 | 47.98 ± 28.84 | ||
| ERG | 86.24 ± 9.66 | 73.14 ± 15.36 | 30.68 ± 21.03 | ||
| GAD-7 | Total | 18.31 ± 4.05 | 14.32 ± 5.64 | 7.92 ± 6.59 | <0.001 |
| CAG | 17.31 ± 5.75 | 14.65 ± 6.02 | 10.04 ± 6.00 | ||
| ERG | 18.72 ± 3.07 | 14.19 ± 5.53 | 7.06 ± 6.67 | ||
| TAM | Total | 35.92 ± 26.63 | 49.08 ± 26.55 | 70.51 ± 24.22 | <0.001 |
| CAG | 21.70 ± 24.58 | 39.22 ± 28.80 | 58.13 ± 29.18 | ||
| ERG | 41.70 ± 25.39 | 53.08 ± 24.70 | 75.53 ± 20.05 |
| Group/Dif VAS I-II | Mean ± SD | p |
|---|---|---|
| CAG (p = 0.151) | 2.3 ± 1.43 | <0.001 |
| ETG (p = 0.001) | 4.21 ± 1.71 | |
| Group/Dif VAS I-III | Mean ± SD | p |
| CAG (p = 0.090) | 4.38 ± 2.11 | <0.001 |
| ERG (p = 0.003) | 7.75 ± 1.35 | |
| Group/Dif EDM I-II | Mean ± SD | p |
| Classic (p = 0.010) | 1.73 ± 1.18 | 0.004 |
| Early (p < 0.001) | 1.05 ± 0.51 | |
| Group/Dif EDM I-III | Mean ± SD | p |
| CAG (p = 0.166) | 3.08 ± 1.81 | 0.007 |
| ERG (p < 0.001) | 2.11 ± 1 | |
| Group/Dif GS I-II | Mean ± SD | p |
| CAG (p = 0.001) | −4.06 ± 4.3 | 0.061 |
| ERG (p < 0.001) | −2.17 ± 2.5 | |
| Group/Dif GS I-III | Mean ± SD | p |
| CAG (p = 0.025) | −12.17 ± 10.9 | 0.487 |
| ERG (p = 0.436) | −12 ± 5.55 | |
| Group/Dif QD I-II | Mean ± SD | p |
| CAG (p = 0.001) | 14.38 ± 13.4 | 0.456 |
| ERG (p < 0.001) | 13.1 ± 10 | |
| Group/Dif QD I-III | Mean ± SD | p |
| CAG (p = 0.001) | 34.11 ± 22.2 | <0.001 |
| ERG (p = 0.001) | 55.56 ± 17 | |
| Group/Dif GAD-7 I-II | Mean ± SD | p |
| CAG (p = 0.001) | 2.65 ± 2.92 | 0.011 |
| ERG (p = 0.003) | 4.53 ± 3.18 | |
| Group/Dif GAD-7 I-III | Mean ± SD | p |
| CAG (p = 0.367) | 7.27 ± 4.73 | <0.001 |
| ERG (p < 0.001) | 11.66 ± 5.21 | |
| Group/Dif TAM I-II | Mean ± SD | p |
| CAG (p = 0.174) | −17.53 ± 11.98 | 0.016 |
| ERG (p < 0.001) | −11.38 ± 8.66 | |
| Group/Dif TAM I-III | Mean ± SD | p |
| CAG (p = 0.048) | −36.43 ± 22.19 | 0.862 |
| ERG (p = 0.002) | −33.84 ± 16.16 |
| Parameter | Time Point | Flexor Tendon Injuries (Mean ± SD) | Other Complex Hand Injuries (Mean ± SD) | p-Value |
|---|---|---|---|---|
| VAS | Baseline | 9.05 ± 1.2 | 9.72 ± 0.7 | <0.001 |
| 4 weeks | 5.38 ± 1.62 | 5.23 ± 1.85 | ||
| 12 weeks | 2 ± 1.58 | 1.63 ± 1.39 | ||
| EDM | Baseline | 58.48 ± 7 | 63.05 ± 6.36 | <0.001 |
| 4 weeks | 57.43 ± 6.87 | 62 ± 6.25 | ||
| 12 weeks | 56.43 ± 6.78 | 60.91 ± 6.04 | ||
| GS | Baseline | 0.33 ± 0.79 | 0.53 ± 1.16 | <0.001 |
| 4 weeks | 3.14 ± 2.74 | 2.39 ± 3.14 | ||
| 12 weeks | 12.33 ± 5.52 | 12.6 ± 6.21 | ||
| QD | Baseline | 81.65 ± 11.75 | 88.48 ± 7.65 | <0.001 |
| 4 weeks | 67.6 ± 14.52 | 75.85 ± 15.18 | ||
| 12 weeks | 27.69 ± 19.8 | 32.15 ± 21.68 | ||
| GAD-7 | Baseline | 16.71 ± 3.6 | 19.7 ± 2.24 | <0.001 |
| 4 weeks | 10.57 ± 5.46 | 15.95 ± 4.68 | ||
| 12 weeks | 4.38 ± 5.39 | 8.37 ± 6.89 | ||
| TAM | Baseline | 35.81 ± 26 | 44.57 ± 24.85 | <0.001 |
| 4 weeks | 52.13 ± 24.9 | 53.54 ± 24.88 | ||
| 12 weeks | 77.6 ± 20 | 74.51 ± 20.2 |
| Injury/Dif VAS I-II | Mean ± SD | p |
|---|---|---|
| Flexor (p = 0.029) | 3.67 ± 1.19 | 0.136 |
| Other (p = 0.012) | 4.49 ± 1.87 | |
| Injury/Dif VAS I-III | Mean ± SD | p |
| Flexor (p = 0.053) | 7.05 ± 1.07 | 0.004 |
| Other (p = 0.006) | 8.09 ± 1.36 | |
| Injury/Dif EDM I-II | Mean ± SD | p |
| Flexor (p < 0.001) | 1.05 ± 0.49 | 1.000 |
| Other (p < 0.001) | 1.05 ± 0.53 | |
| Injury/Dif EDM I-III | Mean ± SD | p |
| Flexor (p = 0.064) | 2.05 ± 1.2 | 0.668 |
| Other (p < 0.001) | 2.14 ± 0.89 | |
| Injury/Dif GS I-II | Mean ± SD | p |
| Flexor (p = 0.020) | −2.81 ± 2.4 | 0.039 |
| Other (p < 0.001) | −1.86 ± 2.51 | |
| Injury/Dif GS I-III | Mean ± SD | p |
| Flexor (p = 0.458) | −12 ± 5.45 | 0.070 |
| Other (p = 0.438) | −12.07 ± 5.65 | |
| Injury/Dif QD I-II | Mean ± SD | p |
| Flexor (p = 0.015) | 14.07 ± 8.14 | 0.246 |
| Other (p < 0.001) | 12.63 ± 10.95 | |
| Injury/Dif QD I-III | Mean ± SD | p |
| Flexor (p = 0.985) | 53.96 ± 13.65 | 0.232 |
| Other (p < 0.001) | 56.33 ± 18.52 | |
| Injury/Dif GAD-7 I-II | Mean ± SD | p |
| Flexor (p = 0.460) | 6.14 ± 2.79 | 0.006 |
| Other (p = 0.003) | 3.74 ± 3.08 | |
| Injury/Dif GAD-7 I-III | Mean ± SD | p |
| Flexor (p = 0.005) | 12.33 ± 3.83 | 0.874 |
| Other (p < 0.001) | 11.33 ± 5.78 | |
| Injury/Dif TAM I-II | Mean ± SD | p |
| Flexor (p = 0.020) | −16.32 ± 10.8 | 0.003 |
| Other (p = 0.016) | −8.97 ± 6.23 | |
| Injury/Dif TAM I-III | Mean ± SD | p |
| Flexor (p = 0.143) | −41.82 ± 16.28 | 0.004 |
| Other (p = 0.002) | −29.94 ± 14.77 |
| Technology Type | Working Mode/Functionality Addressed | Advantages | Limitations/Challenges |
|---|---|---|---|
| Virtual/Augmented Reality (VR/AR) | Immersive, task-specific environments; real-time visual and kinematic feedback; gamified training. | Enhances engagement and motivation; enables high-repetition practice; supports pain modulation (phantom pain, CRPS). | Requires equipment and technical support; risk of cybersickness; transfer to daily activities still variable. |
| Robotics | End-effector systems guiding hand/arm movement; repetitive assist-as-needed training. | Increases therapy volume; ensures consistent dosing; provides objective data on performance. | High cost; bulky devices; limited availability in smaller centers; ADL transfer not always demonstrated. |
| Exoskeletons (Soft/Hard) | Wearable devices assisting or resisting finger/wrist motion. | Portable (especially soft devices); adaptable assistance; potential for home-based use. | Comfort, durability, and cost remain barriers; clinical evidence still limited. |
| Surface EMG (sEMG) Biofeedback | Records muscle activity; provides visual/game feedback; trains selective recruitment and control. | Improves voluntary activation; supports cortical reorganization; feasible for home-based training. | Requires patient understanding and calibration; may be less effective in cases with very weak or absent signals. |
| Brief Therapeutic Electrical Stimulation (TES) | Short intra-/post-operative nerve stimulation to accelerate regeneration. | Enhances axonal regrowth; improves motor/sensory recovery after nerve repair; only one session needed. | Currently experimental in many centers; requires surgical integration; long-term clinical data still emerging. |
| Orthoses (3D-printed, dynamic) | Custom immobilization or guided motion; scan-to-fit printing. | Lightweight, ventilated, higher comfort/compliance; customizable with hinges/sensors. | Access to 3D printing technology; reprinting needed for swelling changes; not yet universally available. |
| Telerehabilitation/Remote rehabilitation | Remote supervision via video, digital exercise platforms, and sensors. | Expands access; maintains adherence; outcomes comparable to in-person in selected conditions. Exercise program can be performed on a touchscreen tablet-based app in combination with face-to-face physiotherapy | Limited for complex cases needing hands-on therapy; digital literacy and internet access required. |
| Sensory-Motor Re-education | Tactile discrimination, mirror therapy, graded motor imagery. | Improves sensory recovery after nerve trauma; addresses cortical remapping; helpful for phantom pain. | Time-intensive; variable efficacy across studies; requires high patient engagement. |
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© 2025 by the authors. Published by MDPI on behalf of the Lithuanian University of Health Sciences. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
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Serban, A.; Grosu-Bularda, A.; Bordeanu-Diaconescu, E.-M.; Tache, G.-O.; Stoica, M. Early Rehabilitation Versus Conventional Approaches in Post-Traumatic Hand Injuries with Multiple Lesions: Clinical Outcomes and Future Directions. Medicina 2025, 61, 2063. https://doi.org/10.3390/medicina61112063
Serban A, Grosu-Bularda A, Bordeanu-Diaconescu E-M, Tache G-O, Stoica M. Early Rehabilitation Versus Conventional Approaches in Post-Traumatic Hand Injuries with Multiple Lesions: Clinical Outcomes and Future Directions. Medicina. 2025; 61(11):2063. https://doi.org/10.3390/medicina61112063
Chicago/Turabian StyleSerban, Adriana, Andreea Grosu-Bularda, Eliza-Maria Bordeanu-Diaconescu, Georgiana-Ozana Tache, and Marius Stoica. 2025. "Early Rehabilitation Versus Conventional Approaches in Post-Traumatic Hand Injuries with Multiple Lesions: Clinical Outcomes and Future Directions" Medicina 61, no. 11: 2063. https://doi.org/10.3390/medicina61112063
APA StyleSerban, A., Grosu-Bularda, A., Bordeanu-Diaconescu, E.-M., Tache, G.-O., & Stoica, M. (2025). Early Rehabilitation Versus Conventional Approaches in Post-Traumatic Hand Injuries with Multiple Lesions: Clinical Outcomes and Future Directions. Medicina, 61(11), 2063. https://doi.org/10.3390/medicina61112063

