Axillary Web Syndrome
Conditions
Keywords
Breast Neoplasm, Physiotherapy, Rehabilitation
Brief summary
The aim of this study is verify the effectiveness of manual maneuver associated with stretching exercises in the treatment of Axillary Web Syndrome.
Detailed description
Axillary Web Syndrome (AWS) is one of the short / medium-term sequela of surgical treatment for breast cancer with axillary dissection (AD) or sentinel lymph node biopsy (SLNB), with incidence reported in literature between 28% and 72%. AWS could be described as a thrombophlebitis of veno-lymph vessels due to a trauma of the region subjected to surgery, with the same characteristics of Mondor's disease diagnosed in post-traumatic and surgical areas where is a large presence of veno-lymphatic capillaries. The syndrome onset occur in approximately 2-4 weeks after the surgery and its complete regression happen in 3-6 months after the onset. The clinical signs frequently described are pain and tension during movement in the axillary region, elbow, forearm and wrist, following the arm lymphatic pathway. Moreover, patients report difficulties in moving the arm into activities that require a moderate range of motion and could feel and see in the affected arm cords similar to a tendon. Even if the impairment can cause disability for a limited period of time, rehabilitation is usually advice to prevent further complications such as frozen shoulder, articular impeachment syndrome and long-term chronic pain, complications that could worsen patient's quality of life with a significant increase in costs and time to recovery. Nowadays there are no studies in the literature that demonstrate the effectiveness of physiotherapy in AWS, with just case reports describing different treatments techniques, without a scientifically defined experimented rehabilitation protocol. This experimental, monocentric, randomized clinical trial wants verify the effectiveness of a manual maneuver associated with stretching exercises in the treatment of AWS.
Interventions
OTHERManual manoeuver + stretching
Patients in experimental group will receive, after AWS diagnose, a manual manoeuver to snap the cord, follow by a demonstration and education of the exercise to be made at home.
OTHERstretching exercise
Patients in control group will receive, after AWS diagnose, just a demonstration and education of the exercise to be made at home.
Sponsors
Fondazione Umberto Veronesi
European Institute of Oncology
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 70 Years
Healthy volunteers
No
Inclusion criteria
* Female patients with age between 18 and 70 years old * Axillary dissection with or without plastic reconstruction with prothesis * Positive diagnose of axillary web syndrome. * Patients without mental or psychological problems which could affect the proposed treatment execution. * Signed informed consensus form.
Exclusion criteria
* Chronic or acute upper limb pathology which could affect the proposed treatment execution. * Patients with mental or psychological problems which could affect the proposed treatment execution. * Plastic reconstruction with abdominal (DIEP or TRAM) and dorsal grafts or with expander. * Previous head and neck, sentinel lymph node biopsy or axillary dissection surgery. * Previous breast, axillary or head and neck radiotherapy. * Halsted mastectomy. * Previous lymphedema. * Bilateral axillary dissection surgery * Physiotherapy treatment execute outside hospital during the study.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Range of motion change overtime | Baseline, 7 days and 30 days after baseline measure | Range of motion measured with a handheld goniometer, in degrees. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Lymphedema assessment | 3 years after baseline measure | Lymphedema measured with centimetric and constant dielectric method |
Other
| Measure | Time frame | Description |
|---|---|---|
| Pain change overtime | Baseline, 7 days and 30 days after baseline measure | Pain measured with 0-10 numeric rate scale |
Countries
Italy
Outcome results
None listed