Abstract
Introduction
Plantar heel pain causes soreness or tenderness of the sole of the foot under the heel, which sometimes extends into the medial arch. The prevalence and prognosis are unclear, but the symptoms seem to resolve over time in most people.
Methods and outcomes
We conducted a systematic review and aimed to answer the following clinical question: What are the effects of treatments for plantar heel pain? We searched: Medline, Embase, The Cochrane Library and other important databases up to January 2007 (BMJ Clinical Evidence reviews are updated periodically, please check our website for the most up-to-date version of this review). We included harms alerts from relevant organisations such as the US Food and Drug Administration (FDA) and the UK Medicines and Healthcare products Regulatory Agency (MHRA).
Results
We found 15 systematic reviews, RCTs, or observational studies that met our inclusion criteria. We performed a GRADE evaluation of the quality of evidence for interventions.
Conclusions
In this systematic review we present information relating to the effectiveness and safety of the following interventions: casted orthoses (custom-made insoles), corticosteroid injection (alone, or plus non-steroidal anti-inflammatory drugs), extracorporeal shock wave therapy, heel cups, heel pads (alone or with corticosteroid injection), lasers, local anaesthetic injection (alone or with corticosteroid injection), night splints plus non-steroidal anti-inflammatory drugs, stretching exercises, surgery, taping, and ultrasound.
Key Points
Plantar heel pain causes soreness or tenderness of the sole of the foot under the heel, which sometimes extends into the medial arch.
The prevalence and prognosis are unclear, but in most people the symptoms seem to resolve over time.
Casted orthoses (custom-made insoles) may improve function (but not pain) at 3 months in people with plantar heel pain compared with a sham orthosis, but they may be no better than appropriate prefabricated orthoses.
Supportivetaping may improve pain in the short term at 1 week, but we found no evidence on its effectiveness beyond 1 week.
We don't know whether heel pads, heel cups, or night splints reduce pain.
Corticosteroid injections are commonly used to treat plantar heel pain, but we don't know whether they reduce pain compared with placebo or other treatments.
Corticosteroid injections have been associated with long-term complications.
We don't know whether local anaesthetic injections, alone or added to corticosteroids, improve pain relief compared with corticosteroids alone.
Extracorporeal shock wave therapy may reduce pain, but we don't know for sure that it is beneficial.
We don't know whether laser treatment, ultrasound, or surgery reduce symptoms compared with sham treatment or no treatment.
We don't know whether stretching exercises reduce pain compared with no treatment or other treatments.
About this condition
Definition
Plantar heel pain is soreness or tenderness of the heel that is restricted to the sole of the foot. It often radiates from the central part of the heel pad or the medial tubercle of the calcaneum, but may extend along the plantar fascia into the medial longitudinal arch of the foot. Severity may range from an irritation at the origin of the plantar fascia, which is noticeable on rising after rest, to an incapacitating pain. This review excludes clinically evident underlying disorders; for example, calcaneal fracture, and calcaneal nerve entrapment, which may be distinguished clinically — a calcaneal fracture may present after trauma, and calcaneal nerve entrapment gives rise to shooting pains and feelings of "pins and needles" on the medial aspect of the heel.
Incidence/ Prevalence
The incidence and prevalence of plantar heel pain are uncertain. However, it has been estimated that 7% of people aged over 65 years report tenderness in the region of the heel, that plantar heel pain accounts for a quarter of all foot injuries relating to running, and that the diagnosis and treatment of plantar heel pain accounts for over 1 million visits a year to physicians in the USA. The condition affects both athletic and sedentary people, and does not seem to be influenced by gender.
Aetiology/ Risk factors
Unknown. Suggested risk factors include overweight, prolonged standing, and having a reduced range of motion in the ankle and 1st metatarsophalangeal joint.
Prognosis
One systematic review found that almost all of the included trials reported an improvement in discomfort regardless of the intervention received (including placebo), suggesting that the condition is at least partially self-limiting. A telephone survey of 100 people treated conservatively (average follow-up 47 months) found that 82 people had resolution of symptoms, 15 had continued symptoms but no limitations of activity or work, and three had persistent bilateral symptoms that limited activity or changed work status. Thirty-one people said that they would have seriously considered surgical treatment at the time that medical attention was sought. In addition, one recent RCT has observed marked improvement in pain and function over time in 45 people randomised to a sham intervention.
Aims of intervention
To reduce pain and immobility, with minimal adverse effects.
Outcomes
Pain reduction (often measured using visual analogue scales); improvement in function or walking distance; quality of life; adverse effects.
Methods
BMJ Clinical Evidence search and appraisal January 2007. The following databases were used to identify studies for this systematic review: Medline 1966 to January 2007, Embase 1980 to January 2007, and The Cochrane Database of Systematic Reviews and Cochrane Central Register of Controlled Clinical Trials 2006, Issue 4. Additional searches were carried out using these websites: NHS Centre for Reviews and Dissemination (CRD) — for Database of Abstracts of Reviews of Effects (DARE) and Health Technology Assessment (HTA), Turning Research into Practice (TRIP), and NICE. Abstracts of the studies retrieved from the initial search were assessed by an information specialist. Selected studies were then sent to the author for additional assessment, using pre-determined criteria to identify relevant studies. Study design criteria for evaluation in this review were: published systematic reviews and RCTs in any language, and containing more than 20 individuals of whom more than 80% were followed up. There was no minimum length of follow-up required to include stu dies. We excluded all studies described as "open", "open label", or not blinded unless blinding was impossible. We use a regular surveillance protocol to capture harms alerts from organisations such as the FDA and the UK Medicines and Healthcare products Regulatory Agency (MHRA), which are added to the reviews as required. We have performed a GRADE evaluation of the quality of evidence for interventions included in this review (see table ).
Table.
Important outcomes | Pain relief, functional improvement, quality of life, adverse effects | ||||||||
Number of studies (participants) | Outcome | Comparison | Type of evidence | Quality | Consistency | Directness | Effect size | GRADE | Comment |
What are the effects of treatments for plantar heel pain? | |||||||||
1 (91) | Functional improvement | Casted orthoses v placebo/no treatment | 4 | –1 | 0 | 0 | 0 | Moderate | Quality point deducted for sparse data |
1 (91) | Pain relief | Casted orthoses v placebo/no treatment | 4 | –1 | 0 | 0 | 0 | Moderate | Quality point deducted for sparse data |
1 (89) | Pain relief | Casted orthoses v prefabricated orthoses | 4 | –1 | 0 | 0 | 0 | Moderate | Quality point deducted for sparse data |
1 (89) | Functional improvement | Casted orthoses v prefabricated orthoses | 4 | –1 | 0 | 0 | 0 | Moderate | Quality point deducted for sparse data |
1 (103) | Pain relief | Casted orthoses plus pad plus taping v heel pad plus pain medication | 4 | –2 | 0 | 0 | 0 | Low | Quality points deducted for sparse data and no intention-to-treat analysis |
1 (236) | Pain relief | Casted orthoses plus stretching exercises v heel pad plus stretching exercises | 4 | –1 | 0 | 0 | 0 | Moderate | Quality point deducted for incomplete reporting of results |
1(222) | Pain relief | Casted orthoses v night splints | 4 | –2 | 0 | –1 | 0 | Very low | Quality points deducted for incomplete reporting of results and uncertainty about intention-to-treat analysis. Directness points deducted for differences in withdrawal rates between groups |
1 (43) | Pain relief | Casted orthoses v orthosis plus night splints | 4 | –3 | 0 | 0 | 0 | Very low | Quality points deducted for sparse data, incomplete reporting of results and lack of blinding |
1 (91) | Pain relief | Corticosteroid injection plus local anaesthesia v local anaesthetic (short term) | 4 | –3 | 0 | –2 | 0 | Very low | Quality points deducted for sparse data, lack of placebo controls, no intention-to-treat analysis and poor follow-up. Directness points deducted for uncertainty of clinical relevance and heterogeneity between interventions |
2 (97) | Pain relief | Corticosteroid injection plus local anaesthesia v heel pad alone | 4 | –3 | –1 | –1 | 0 | Very low | Quality points deducted for sparse data, lack of placebo controls, no intention-to-treat analysis and poor follow-up. Consistency point deducted for different results at different endpoints. Directness point deducted for heterogeneity between interventions |
1 (80) | Pain relief | Corticosteroid injection plus local anaesthesia v corticosteroid plus local anaesthetic plus heel pad | 4 | –3 | 0 | –2 | 0 | Very low | Quality points deducted for sparse data, lack of placebo controls, no intention-to-treat analysis and poor follow-up. Directness points deducted for uncertainty of clinical relevance and heterogeneity between interventions |
1 (80) | Pain relief | Corticosteroid injection plus local anaesthesia plus heel pad v heel pad | 4 | –3 | 0 | –1 | 0 | Very low | Quality points deducted for sparse data, lack of placebo controls, no intention-to-treat analysis and poor follow-up. Directness point deducted for heterogeneity between interventions |
1 (91) | Pain relief | Corticosteroid injection plus local anaesthesia v local anaesthetic (medium term) | 4 | –3 | 0 | –2 | 0 | Very low | Quality points deducted for sparse data, lack of placebo controls, no intention-to-treat analysis and poor follow-up. Directness points deducted for uncertainty of clinical relevance and heterogeneity between interventions |
1 (80) | Pain relief | Corticosteroid injection plus local anaesthesia v heel pad alone | 4 | –3 | 0 | –1 | 0 | Very low | Quality points deducted for sparse data, lack of placebo controls, no intention-to-treat analysis and poor follow-up. Directness point deducted for heterogeneity between interventions |
1 (80) | Pain relief | Corticosteroid injection plus local anaesthesia v corticosteroid plus local anaesthetic plus heel pad | 4 | –3 | –1 | –2 | 0 | Very low | Quality points deducted for sparse data, lack of placebo controls, no intention-to-treat analysis and poor follow-up. Consistency point deducted for different results at different endpoints. Directness points deducted for uncertainty of clinical relevance and heterogeneity between interventions |
1 (103) | Pain relief | Corticosteroid injection plus local anaesthesia plus NSAIDs v heel pad plus paracetamol | 4 | –3 | 0 | –2 | 0 | Very low | Quality points deducted for sparse data, lack of placebo controls, no intention-to-treat analysis and poor follow-up. Directness point deducted for heterogeneity between interventions |
1 (103) | Pain relief | Corticosteroid injection plus local anaesthesia plus NSAIDs v pad plus taping plus orthoses | 4 | –3 | 0 | –2 | 0 | Very low | Quality points deducted for sparse data, lack of placebo controls, no intention-to-treat analysis and poor follow-up. Directness point deducted for heterogeneity between interventions |
8 (1183) | Pain relief | Extracorporeal shock wave therapy v placebo | 4 | –1 | –1 | –1 | 0 | Very low | Quality point deducted for incomplete reporting of results. Consistency point deducted for conflicting results. Directness point deducted for uncertainty of clinical relevance of effect |
1 (32) | Pain relief | Lasers v placebo | 4 | –2 | 0 | –1 | 0 | Very low | Quality points deducted for sparse data and incomplete reporting of results. Directness point deducted for uncertainty about outcome measured |
2 (133) | Pain relief | Taping v placebo/no treatment | 4 | –1 | 0 | 0 | 0 | Moderate | Quality point deducted for sparse data |
1 (92) | Functional improvement | Taping v placebo/no treatment | 4 | –1 | 0 | 0 | 0 | Moderate | Quality point deducted for sparse data |
1 (116) | Pain relief | Night splints plus NSAIDs v NSAIDs | 4 | –2 | 0 | 0 | 0 | Low | Quality points deducted for sparse data and incomplete reporting of results |
1 (236) | Pain relief | Stretching exercises v orthoses plus stretching exercises | 4 | –1 | 0 | 0 | 0 | Moderate | Quality point deducted for incomplete reporting of results |
1 (166) | Pain relief | Stretching exercises v heel pad plus stretching exercises | 4 | –1 | 0 | 0 | 0 | Moderate | Quality point deducted for sparse data |
1 (101) | Pain relief | Plantar fascia stretching plus heel pad v Achilles tendon stretching plus heel pad | 4 | –2 | 0 | 0 | 0 | Low | Quality points deducted for sparse data and for not reporting treatment adherence rates |
1 (19) | Pain relief | Ultrasound v sham ultrasound | 4 | –1 | 0 | 0 | 0 | Moderate | Quality point deducted for sparse data |
Type of evidence: 4 = RCT; 2 = Observational; 1 = Non-analytical/expert opinion. Consistency: similarity of results across studies Directness: generaliseability of population or outcomes Effect size: based on relative risk or odds ratio
Glossary
- Accommodative orthoses
Full-length orthoses made of foam or rubber that offload high pressure areas under the foot.
- Achilles tendon stretching
A stretch achieved by either hanging the heel from a step while keeping the knee straight, or by leaning into the wall from a standing position with the affected leg placed behind the other leg.
- Casted orthoses
Orthoses fabricated by moulding a thermoplastic or thermomouldable foam material over an impression (or negative cast) of a person’s foot.
- Extracorporeal shock wave therapy (ESWT)
Shock waves are pulsed acoustic waves that dissipate mechanical energy at the interface of two substances with different acoustic impedance.
- Heel cups
Prefabricated rubber or silicone heel pads that contour the heel, thus surrounding and supporting the fibro fatty heel pad.
- Heel pads
Padding underneath the heel that may be constructed from semicompressed felt, sponge foam, rubber, or silicone.
- High-quality evidence
Further research is very unlikely to change our confidence in the estimate of effect
- Low-quality evidence
Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
- Moderate-quality evidence
Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
- Plantar fascia stretching
A stretch achieved by crossing the affected leg over the other leg from a seated position, placing the fingers of the affected side across the base of the toes (distal to the metatarsal phalangeal joints), and pulling the toes back until a stretch in the arch of the foot can be felt.
- Prefabricated orthoses
Orthoses which are already made to a pre-determined size and shape, and which can be used immediately as there is no lengthy fabrication process.
- Very low-quality evidence
Any estimate of effect is very uncertain.
Disclaimer
The information contained in this publication is intended for medical professionals. Categories presented in Clinical Evidence indicate a judgement about the strength of the evidence available to our contributors prior to publication and the relevant importance of benefit and harms. We rely on our contributors to confirm the accuracy of the information presented and to adhere to describe accepted practices. Readers should be aware that professionals in the field may have different opinions. Because of this and regular advances in medical research we strongly recommend that readers' independently verify specified treatments and drugs including manufacturers' guidance. Also, the categories do not indicate whether a particular treatment is generally appropriate or whether it is suitable for a particular individual. Ultimately it is the readers' responsibility to make their own professional judgements, so to appropriately advise and treat their patients.To the fullest extent permitted by law, BMJ Publishing Group Limited and its editors are not responsible for any losses, injury or damage caused to any person or property (including under contract, by negligence, products liability or otherwise) whether they be direct or indirect, special, incidental or consequential, resulting from the application of the information in this publication.
Contributor Information
Please enter your position here Karl B Landorf, Podiatry Department and Muscoluskeletal Research Centre, Faculty of Health Sciences, La Trobe University, Victoria, Australia.
Please enter your position here Hylton B Menz, Musculoskeletal Research Centre, Faculty of Health Sciences, La Trobe University, Victoria, Australia.
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