Tag Archives: tendinopathy

Fluoroquinolone-induced Achilles tendinopathy – A case report and management recommendations

by Kaylem M. Feeney1,2 BSc (Hons), MSc, MChSI

The Foot and Ankle Online Journal 13 (4): 12

Fluoroquinolone antibiotics are frequently used in the management of infection despite being associated with several side effects including the potential to cause tendon injury. While numerous case reports of Achilles tendon injury related to fluoroquinolone exposure exist in the literature, there is a paucity of research evaluating the effectiveness of treatment interventions for the condition. The author presents a case of chronic bilateral Achilles tendinopathy associated with two separate exposures to ciprofloxacin and its subsequent management with eccentric loading exercises and extracorporeal shockwave therapy (ESWT).

Keywords: Fluoroquinolone, complication, Achilles, tendinopathy, ESWT

ISSN 1941-6806
doi: 10.3827/faoj.2020.1304.0012

1 – Bon Secours Hospital, Galway, Ireland
2 – School of Medicine, University of Limerick, Ireland
* – Corresponding author: kaylemfeeney1995@gmail.com


Fluoroquinolone antibiotics have long been used in the management of infection due to their broad spectrum of activity [1]. While the fluoroquinolone class of antibiotics are generally well-tolerated, they have been associated with complications including tendon injury [2]. There have been several case reports in the literature of fluoroquinolone-induced Achilles tendinopathy though few have reported on the effectiveness of interventions in this population.

Case Report

A 69-year-old male presented to the outpatient clinic with a 7-year history of pain in both Achilles tendons. The patient was generally fit and healthy and was taking no medication at the time of appointment. The patient gave a background history of a sudden onset of bilateral Achilles tendon pain during hospitalization for sepsis. The patient had been prescribed ciprofloxacin as an inpatient and within 24 hours had extreme pain in both Achilles tendons. Treatment with ciprofloxacin was ceased immediately and the patient commenced on an alternative treatment. Pain in the Achilles tendon decreased significantly over the following 6 months though the patient had a persistent low level pain in both Achilles tendons.

Eight months following the initial onset of Achilles tendon pain, the patient suffered a chest infection. The patient was prescribed ciprofloxacin and approximately 72 hours later had extreme debilitating pain in both Achilles tendons, worse than the initial occasion up to the point where he was unable to walk. Antibiotic therapy with ciprofloxacin was ceased and the patient treated with an alternative antibiotic and the chest infection cleared uneventfully. However, on this occasion, the pain in the Achilles tendons did not improve. The patient was unable to do any significant exercise and had made no significant progress in terms of pain or function over the following 6 years despite rest, stretching, strengthening and physical therapy.

Physical examination showed thickening of the midportion of the Achilles tendon bilaterally with pain on palpation and during a single leg heel raise.

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Figure 1 Sagittal view MRI showing Achilles tendon thickness of 11.8mm.

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Figure 2 Axial view MRI showing Achilles tendon thickness of 11.8mm.

MRI examination showed gross thickening of the Achilles tendon measuring 11.8mm on the sagittal view (Figure 1) consistent with chronic Achilles tendinosis. Axial view MRI also demonstrated significant thickening of the Achilles tendon in keeping with chronic Achilles tendinosis (Figure 2).

On the day of presentation the patient had a VAS score of 7/10 on a daily basis and a Roles and Maudsley score of 4.

The patient was commenced on Alfredson’s protocol [3] for Achilles tendinopathy and treated with three sessions of extracorporeal shockwave therapy (ESWT), which has shown to be effective in the management of non-insertional Achilles tendinopathy [4]. ESWT in this case consisted of treatment with 2,500 impulses at a frequency of 10Hz on three occasions spaced one week apart. At the 3-month follow up the patient reported a reduction in pain levels with a VAS score of 3/10. His Roles and Maudsley score had also improved from a score of 4 to a score of 2. At the 6-month follow up, the patient had a VAS score of 2/10 and a Roles and Maudsley score of 2. While the patient still had pain, this pain had improved significantly suggesting that treatment with eccentric loading exercises following Alfredson’s protocol [3] combined with a course of ESWT may be beneficial in reducing pain and improving function in patients with chronic, recalcitrant fluoroquinolone-induced Achilles tendinopathy.

Discussion

Fluoroquinolone antibiotics are becoming increasingly utilized because of their broad antibacterial spectrum and extensive tissue penetration [5]. The most frequently seen adverse effects include headache, skin reaction and gastrointestinal upset [6]. However, fluoroquinolone use has also been linked to tendon injury and tendon rupture including tendinopathy of the biceps brachii, supraspinatus, extensor pollicis longus and Achilles tendons [7]. The first reported case of fluoroquinolone-associated Achilles tendinopathy was in 1983 [5] and since then more than 100 cases have been reported in the literature [8]. The mechanisms of tenotoxic effects of fluoroquinolone antibiotics are unclear, though three main mechanisms have been proposed in the literature and include tendon ischaemia, degradation of tendon matrix and alteration of tenocyte activity [9]. The cause of Achilles tendinopathy not related to fluoroquinolone use is not fully understood but in the absence of acute rupture in trauma it is generally considered an overuse syndrome due to excessive loading of the tendon during activity [6,8,10,11,12]. Management is primarily conservative with rest, non-steroidal anti-inflammatory medication, steroid injection therapy, stretching, strengthening, prolotherapy, ESWT and platelet-rich plasma injection all being proposed as treatment options in the literature [13,14,15]. Fluoroquinolone-induced Achilles tendinopathy normally resolves within 2 months [15] though prolonged symptoms have been reported in one case lasting two years [15]. The effective management of fluoroquinolone-induced Achilles tendinopathy is not well documented in the literature with the majority of case reports failing to report method of treatment and success rates of treatment [14,15]. Treatment in the literature has focussed on cessation of fluoroquinolone therapy immediately followed by a period of rest and/or immobilisation [15-20]. In this present case, cessation of therapy and subsequent rest was unsuccessful in the improvement of the patient’s symptoms and as such further treatment was required. Alfredson’s protocol [3] has been shown to be effective in the management of non-insertional Achilles tendinopathy [21,22]. The patient also received three sessions of ESWT, spaced one week apart, with 2,500 impulses at a frequency of 10Hz per treatment. The mechanism of action of ESWT and its effect on tendon tissue is not fully understood though there is research to suggest that ESWT promotes neovascularization and has an inhibitory effect on nociceptors in animal models [23,24]. Furthermore, a review of biological studies has suggested that the mechanical stimulation of tenocytes during ESWT stimulates an increase in the production and release of various growth factors and the proliferation in fibroblasts [25]. However, further biological studies are necessary to fully understand the effects of ESWT on human tendon.

In this case, treatment with Alfredson’s protocol [3] combined with a course of ESWT was effective in significantly reducing the patients symptoms over a 3-month period and these improvements were maintained at 6 months. Despite the limitations of a single case study, treatment with a combination of ESWT and eccentric loading following Alfredson’s protocol [3] may be considered in cases where cessation of fluoroquinolone therapy and rest/immobilisation fail to resolve a patient’s symptoms.

Conclusion

Clinicians should be aware of the risk of fluoroquinolone treatment in the development of Achilles tendinopathy. If Achilles tendinopathy is suspected during therapy, cessation of treatment and rest is important in order to prevent progression of tendon damage and worsening of symptoms. If the condition fails to improve, eccentric loading following Alfredson’s protocol combined with a course of ESWT may improve patient symptoms and allow a return to exercise. Further research with a large sample size and longer follow-up is necessary to confirm these promising results.

References

  1. King DE, Malone R, Lilley SH. New Classification and Update on the Quinolone Antibiotic. Am Fam Physician 2000;61(9):2741-2748.
  2. Stahlmann R, Lode H. Toxicity of Quinolones. Drugs 1999; 58(2):37-42.
  3. Alfredson H, Pietilä T, Jonsson P, Lorentzon R. Heavy-Load Eccentric Calf Muscle Training For the Treatment of Chronic Achilles Tendinosis. Am J Sports Med. 1998;26(3):360-366.
  4. Rasmussen S, Christensen M, Mathiesen I, Simonson O. Shockwave Therapy for Chronic Achilles Tendinopathy: A Double-Blind, Randomized Clinical Trial of Efficacy. Acta Orthop 2008;79(2):249-256.
  5. Bailey RR, Kirk JA, Peddie BA. Norfloxacin Induced Rheumatoid Disease. N Z Med J 1983;96(736):590.
  6. Yu C, Giuffre BM. Achilles Tendinopathy After Treatment With Fluoroquinolone. Australasian Radiology 2005;49(5):407-410.
  7. Van Der Linden PD, Van Puijenbroek EP, Feenstra J. Tendon Disorders Attributed to Fluoroquinolones: A Study on 42 Spontaneous Reports in the Period 1988-1998. Arthritis Care Res 2001;45(3):235-239.
  8. Tam PK, Ho CTK. Fluoroquinolone-Induced Achilles Tendinitis. Hong Kong Med J 2014; 20(6):545-547.
  9. Childs SG. Pathogenesis of Tendon Rupture Secondary to Fluoroquinolone Therapy. Orthop Nurs 2007;26(3):175-182.
  10. Kim GK, Del Rosson JQ. The Risk of Fluroquinolone-Induced Tendinopathy and Tendon Rupture: What Does the Clinician Need to Know? J Clin Aesthet Dermatol 2010;3(4):49-54.
  11. Mafulli N, Sharma P, Luscombe KL. Achilles tendinopathy: Aetiology and Management. J R Soc Med 2004;97(10):472-476.
  12. Horn A, McCollum G. Achilles Tendinopathy – Part 1: Aetiology, Diagnosis and Non-Surgical Management. SA Orthop J 2015;14(3):24-31.
  13. Roche AJ, Calder JDF. Achilles Tendinopathy: A Review of the Current Concepts of Treatment. J Bone Joint Surg 2013;95(10):1299-1307.
  14. Lewis T, Cook J. Fluoroquinolones and Tendinopathy: A Guide for Athletes and Sports Clinicians and a Systematic Review of the Literature. J Athl Train 2014; 49(3):422-427.
  15. Khaliq Y, Zhanel GG. Fluroquinolone-Associated Tendinopathy: A Critical Review of the Literature. Clin Infect Dis 2003;36(11):1404-1410.
  16. Zabraniecki L, Negrier I, Vergne P, Arnaud M, Bonnet C, Bertin P, Treves R. Fluoroquinolone Induced Tendinopathy: Report of 6 Cases. J Rheumatol, 1996;23(3):516-520.
  17. Ribard P, Audisio F, Kahn MF, De Bandt M, Jorgensen C, Hayem G, Meyer O, Palazzo E. Seven Achilles Tendinitis Including 3 Complicated by Rupture During Fluroquinolone Therapy. J Rheumatol 1992;19(9):1479-1481.
  18. Meyboom RHB, Olsson S, Knol A, Dekens-Konter JAM, De Koning GHP. Achilles Tendinitis Induced by Pefloxacin and other Fluoroquinolone Derivatives. Pharmacoepidemiol Drug Saf 1994;3:185-189.
  19. Carrasco JM, Garcia B, Andujar C, Garrote F, de Juana P, Bermejo T. Tendonitis Associated with Ciprofloxacin. Ann Pharmacother 1997;31(1):120.
  20. Lewis JR, Gums JG, Dickensheets DL. Levofloxacin-Induced Bilateral Achilles Tendonitis. Ann Pharmacother 1999;33(7):792-795.
  21. Stevens M, Tan CW. Effectiveness of the Alfredson Protocol Compared with Lower Repetition-Volume Protocol for Midportion Achilles Tendinopathy: A Randomized Controlled Trial. J Orthop Sports Phys Ther 2014;44(2):59-67.
  22. Van der Plas A, de Jonge S, de Vos RJ, van der Heide HJL, Verhaar JAN, Weir A, Tol JL. A 5-year Follow-Up Study of Alfredson’s Heel-Drop Exercise Programme in Chronic Midportion Achilles Tendinopathy. Br J Sports Med 2012;46(3):214-218.
  23. Wang CJ, Huang HY, Pai CH. Shock Wave Enhances Neovascularization at the Tendon-Bone Junction. J Foot Ankle Surg 2002;41(1):16-22.
  24. Wang CJ, Wang FS, Yang KD, Huang CS, Hsu CC, Yang LC. Shock Wave Therapy Induced Neovascularization at the tendon-Bone Junction: A Study in Rabbits. J Orthop Res 2003;21(6):984-989.
  25. Notarnicola A, Moretti B. The Biological Effects of Extracorporeal Shock Wave Therapy (ESWT) on Tendon Tissue. Muscles Ligaments Tendons J 2012;2(1):33-37.

 

Peroneal tendinopathy in resolved Charcot foot – management with foot orthoses: A case report

by Joshua Young BSc.(Hons), MBAPO Orthotist1*

The Foot and Ankle Online Journal 12 (3): 3

This case report presents an occurrence of painful peroneal tendinopathy in a high risk diabetic foot following Charcot neuroarthropathy, managed using foot orthoses. Self-reported pain intensity was assessed using the 11-point numeric pain rating scale (NRS-11). Peak plantar pressures were assessed using the Pressure Guardian system for three conditions: 3.2mm poron inlay (control), custom foot orthosis, and custom foot orthosis with lateral wedge. Following addition of lateral wedging to the existing foot orthoses, pain reduced to a satisfactory level for the subject. Plantar pressure measurement showed that the addition of lateral wedging did not increase peak plantar pressures above 200kPa, a proposed dangerous level of pressure. Additionally, the foot orthoses still successfully reduced peak plantar pressures to below 200kPa, compared to walking without them. Peroneal tendinopathy should be considered as a possible cause of lateral ankle pain in neuropathic diabetic feet. Lateral wedging can be considered as one option to reduce pain in peroneal tendinopathy, and may not compromise the protective effect of foot orthoses in high risk feet.

Keywords: Charcot, foot, peroneal, tendinopathy, orthoses, insoles

ISSN 1941-6806
doi: 10.3827/faoj.2018.1203.0003

1 – Roehampton Rehabilitation Centre, Queen Mary’s Hospital. St George’s University Hospitals NHS Foundation Trust, London, UK.
* – Corresponding author: Joshua.Young1@nhs.net


Pain can be present even in a diabetic foot with neuropathy. Causes of pain in this group could include painful diabetic neuropathy [1–3]⁠ and Charcot neuroarthropathy (CN) or ‘Charcot foot’ [4]⁠. The cause of the pain should be determined to inform appropriate management.

Tendinopathy may also occur and cause pain in the neuropathic diabetic foot. There is a higher risk of tendinopathy in diabetes [5–7]⁠. Chronic ankle instability or ‘hind foot varus’ have been suggested as predisposing factors to developing peroneal tendinopathy [8]⁠. In theory the ground reaction force on an inverted heel deviates medially, causing an increased ankle inversion moment which must be opposed by the peroneal muscles. A more supinated foot may develop as a result of CN [9,10]⁠.

It has been proposed that the conservative management of peroneal tendinopathy may include protection, relative rest, ice, compression, elevation, medications, and rehabilitative exercise modalities (PRICEMM) in addition to foot orthoses and strengthening of ankle evertors [11]⁠. There is limited evidence on the role of foot orthoses in peroneal tendinopathy. Some work has shown that foot orthoses alter peroneal muscle activity in runners with overuse injury symptoms [12] and in adults with chronic ankle instability [13]. A foot orthosis with a 10 degree lateral wedge has been shown to increase pronation at the rearfoot and reduce the ground reaction force magnitude, suggesting increased shock attenuation by the foot and ankle[14]⁠. This case study presents a case of painful peroneal tendinopathy, which developed in a foot following CN and was subsequently managed using foot orthoses (FOs). The CARE guidelines for reporting of case studies was followed [15]. Written informed consent was obtained for the publication of the materials in this article.

Methods

The subject was a 60 year-old male with type 2 diabetes with a history of CN affecting both feet. The CN resolved 8 months previously. There was a history of superficial ulceration (Texas grade A1) [16]⁠ to the left plantar 1st metatarsal-phalangeal joint and 1st tarso-metatarsal joint, both resolved for 8 months with the use of custom foot orthoses at the time of presentation with a primary concern of right foot pain.

Clinical Findings

There was sensory neuropathy, with only 1 out of 10 sites tested with a 10g monofilament being detected (Plantar 1st and 3rd toes, plantar 1st, 3rd and 5th metatarsal-phalangeal joints bilaterally). Circulation was good with triphasic posterior tibial pulses. Passive joint ranges of motion at the foot and ankle was generally good bilaterally except reduction in midtarsal movement on the left, and reduced extension at the left 1st metatarsal-phalangeal joint (45 degrees) compared to the right (60 degrees). Foot posture was rated using the foot posture index (FPI-6)[17]⁠ as +9 on the left and +3 on the right, indicating a highly pronated foot on the left and a relatively less pronated foot on the right (Figures 1 and 2). The FPI-6 differential of 6 points exceeds both normal values for foot asymmetry and mean asymmetry reported in a CN group [10,18]. The patient presented reporting a 6 week history of right foot pain, indicating the lateral ankle. This developed despite an existing 6mm lateral flare/float addition to the right heel, intended to resist ankle inversion. Pain intensity was reported as 7/10 on the numeric rating scale (NRS-11). 

Diagnostic Assessment

Palpation of the peroneal tendons posteriorly to the lateral malleolus reproduced the pain experienced during walking. A portable ultrasound system was used by the author at this stage, indicating some fluid in the peroneal tendon sheath. 

Figure 1 Left and right feet (anterior and posterior view).

Figure 2 Lateral radiographs of left and right feet.

Figure 3 Cross sectional ultrasound image of peroneus longus showing fluid within the tendon sheath.

Figure 4 Cross sectional ultrasound image of peroneus longus and brevis using power Doppler to show hyper vascularity in the tendons.

Figure 5 Left and right foot orthoses, plantar view.

Figure 6 Right foot orthosis, posterior view.

Referral to radiology for a definitive evaluation was made, which confirmed the diagnosis of peroneal tendinopathy (Figures 3 and 4). The report identified fluid in the common peroneal tendon sheath, in keeping with tenosynovitis, and marked thickening of the peroneus brevis tendon at the insertion, in keeping with tendinosis.

Therapeutic Intervention – Orthotic Prescription

The existing FOs consisted of a 3mm thick base with 50 shore A Ethylene-vinyl acetate (EVA) at the proximal half and 30 shore A EVA at the distal half. There are ‘plugs’ under the right cuboid region, left 1st metatarsal-phalangeal joint and 1st tarso-metatarsal joint where the base material has been replaced with grey poron (Poron 4000, Algeos, Liverpool). 6mm grey poron is used as a top cover, giving a total 9mm base thickness (Figure 5).

Lateral heel wedging (3 degrees) was added to the existing foot orthoses, however the patient reported no immediate change. A further 5 degrees (8 degrees total) was added on the same day – the patient reported that the pain reduced to 1/10 immediately.

Outcome 

At review 8 weeks later, the patient reported that the pain had reduced to 0/10 24 hours following the addition of the lateral wedge. However, 72 hours after the addition of the lateral wedge the pain returned to 4/10. At this stage, the lateral heel wedge was increased to 12 degrees (Figure 6) and extended to the midfoot. The patient again reported an immediate reduction from 4/10 to 0/10.

To ensure that the aggressive wedging added was not causing high pressures in other areas of the foot, in-shoe pressure measurement was used. Comparisons were made with a 3mm poron inlay only, the custom foot orthosis only, and the custom foot orthosis with 12 degree wedge (Table 1). 

Sensor location Peak pressure (kPa) – 3mm poron inlay  Peak pressure (kPa) – custom foot orthosis Peak pressure (kPa) – custom foot orthosis with 12 degree lateral wedge
Lateral plantar heel 71 28 32
Medial plantar heel 69 18 8
Lateral plantar midfoot (Charcot deformity) 244* 94 133
Plantar 1st metatarsal-phalangeal joint 28 33 31

Table 1 Peak plantar pressures (*Indicates a peak pressure value exceeding the proposed dangerous level of 200kPa).

Considering 200kPa as a dangerous level of pressure [19], the custom FO reduced the lateral plantar midfoot (Charcot deformity) pressure to below this level. Following the addition of the lateral wedge, all plantar pressures tested remained below the 200kPa level. Some increase in pressure at the lateral midfoot was measured, reflecting the extension of the wedge to the midfoot. Slight increase in pressure was seen at the lateral heel, which seems to indicate that the centre of pressure was moved laterally by the lateral heel wedge.

At a second review appointment 6 weeks later, the pain had returned back to 4/10. The patient declined any other management and was happy to continue using the laterally wedged foot orthoses. At a third review 8 weeks later, the pain was slowly reducing and now rated as varying between 2/10 and 4/10.

Discussion

This case study illustrates a relatively successful outcome in reducing pain associated with peroneal tendinopathy, using FOs only. The initial pain level of 7/10 was reduced by at least 3 points, which exceeds reported minimal clinically important difference (MCID) values [20]. Of interest is the fact that the patient reported marked immediate effects following the addition of lateral wedging to the existing FOs. This initial effectiveness tended to reduce over time, with pain levels increasing again. One possible explanation for this reduction in initial success may be some compression of the orthoses, which were not made with rigid plastic. The outcome may have been more successful if accompanied by other approaches such as physical therapy, however in this case due to patient preference only one approach was used.

Following initial use of a lateral wedge at the heel only, longer term reductions in pain were achieved by extending the wedge to the midfoot. The extension of the wedge to the midfoot has a logical anatomical basis, as the insertion of the peroneus brevis is distal to the heel, at the base of the 5th metatarsal. It is therefore logical to apply the opposing force in this area. The angle of the lateral wedge also needed to be increased to maintain pain reduction. A systematic effect of altering heel wedge geometry on external forces acting on the foot has been shown by Sweeney [21]⁠ although this relates to medially positioned wedging. The need for these small adjustments highlights the importance in this case not just of selecting an appropriate modification, but also the size and location of the modification. 

Applying relatively aggressive wedging to orthoses for feet at risk of ulceration may be controversial, as traditional approaches to designing FOs for high risk feet often focus on accommodation, rather than altering function of the foot. In this case, use of pressure measurement enabled verification that pressure levels were brought below 200kPa by the FOs, and that this reduction persisted despite the addition of a large lateral wedge. This indicates that aggressive FO designs may be safely used in high risk diabetic feet. However pressure measurement should ideally be used to assess the effectiveness and safety of any orthotic prescription in the context of a high risk foot.

The cause of the tendinopathy in this case is uncertain. The right foot and ankle may have become more prone to inversion as a result of changes to the bony architecture following CN. This may have in turn caused increased inversion moments at the rearfoot, and hence more stress on the peroneal tendons. Neuromuscular control may also be a factor, as the timing of muscle activation has been shown to be altered in diabetic patients [22]⁠⁠. 

This case report has illustrated that lateral wedging up to 12 degrees may be safe and not compromise the protective function of a FO in a high risk diabetic foot. Clinicians should consider peroneal tendinopathy as a possible cause of lateral ankle pain in neuropathic diabetic feet. Clinicians may consider orthosis wedging as one option to reduce pain in peroneal tendinopathy, in addition to other approaches.

References

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