Eligible studies were of patients aged 16 or over and treated with an intervention for clinically diagnosed symptoms of Achilles tendinosis. Symptoms were required to have been present for at least three months in one limb. Patients diagnosed with underlying pathologies such as rheumatoid arthritis or a previously ruptured tendon were excluded. Eligible studies could report any outcome measure for Achilles tendinosis (present for at least three months in one limb and confirmed by a clinical diagnosis) if it encompassed part of the International Classification of Functioning (impairments, activity limitations and participation restrictions), quality of life and patient satisfaction. Descriptive and observational/retrospective studies were excluded.
Included studies compared eccentric exercises, surgery, medication and electrotherapy with various comparators, administered at home or in a clinical setting and lasting between two weeks and six months. Included studies used varying outcome measures (a visual analogue scale (VAS) used most frequently) and reported pain on activity, rest or palpitation, strength, functional ability and patient satisfaction. Studies were conducted mainly in Scandinavia, but also the UK, Australia, Belgium and Italy.
The principal author identified relevant papers for inclusion, validated by a liaison librarian.