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Case Report

Pain and Function in the Runner a Ten (din) uous Link

1
Department of Science and Health, Institute of Technology Carlow, Carlow, Ireland
2
Musculoskeletal Health Research Group, Leeds Beckett University, Leeds LS13HE, UK
3
Centre for Pain for Research, Leeds Beckett University, Leeds LS13HE, UK
*
Author to whom correspondence should be addressed.
Medicina 2020, 56(1), 21; https://doi.org/10.3390/medicina56010021
Submission received: 28 November 2019 / Accepted: 27 December 2019 / Published: 7 January 2020
(This article belongs to the Special Issue Chronic Pain Management)

Abstract

:
A male runner (30 years old; 10-km time: 33 min, 46 s) had been running with suspected insertional Achilles tendinopathy (AT) for ~2 years when the pain reached a threshold that prevented running. Diagnostic ultrasound (US), prior to a high-volume stripping injection, confirmed right-sided medial insertional AT. The athlete failed to respond to injection therapy and ceased running for a period of 5 weeks. At the beginning of this period, the runner completed the Victoria institute of sports assessment–Achilles questionnaire (VISA-A), the foot and ankle disability index (FADI), and FADI sport prior to undergoing an assessment of bi-lateral gastrocnemius medialis (GM) muscle architecture (muscle thickness (MT) and pennation angle (PA); US), muscle contractile properties (maximal muscle displacement (Dm) and contraction time (Tc); Tensiomyography (TMG)) and calf endurance (40 raises/min). VISA-A and FADI scores were 59%/100% and 102/136 respectively. Compared to the left leg, the right GM had a lower MT (1.60 cm vs. 1.74 cm), a similar PA (22.0° vs. 21.0°), a lower Dm (1.2 mm vs. 2.0 mm) and Tc (16.5 ms vs. 17.7 ms). Calf endurance was higher in the right leg compared to the left (48 vs. 43 raises). The athlete began a metronome-guided (15 BPM), 12-week progressive eccentric training protocol using a weighted vest (1.5 kg increments per week), while receiving six sessions of shockwave therapy concurrently (within 5 weeks). On returning to running, the athlete kept daily pain (Numeric Rating Scale; NRS) and running scores (miles*rate of perceived exertion (RPE)). Foot and ankle function improved according to scores recorded on the VISA-A (59% vs. 97%) and FADI (102 vs. 127/136). Improvements in MT (1.60 cm vs. 1.76 cm) and PA (22.0° vs. 24.8°) were recorded via US. Improvements in Dm (1.15 mm vs. 1.69 mm) and Tc (16.5 ms vs. 15.4 ms) were recorded via TMG. Calf endurance was lower in both legs and the asymmetry between legs remained (L: 31, R: 34). Pain intensity (mean weekly NRS scores) decreased between week 1 and week 12 (6.6 vs. 2.9), while running scores increased (20 vs. 38) during the same period. The program was maintained up to week 16 at which point mean weekly NRS was 2.2 and running score was 47.

1. Introduction

Achilles tendinopathy (AT) is the 2nd most common running injury [1,2]. It is primarily located in the mid-portion of the tendon or at the insertion with the calcaneus (insertional tendinopathy) [3]. The stages of tendinopathy have been characterized as reactive (a non-inflammatory cellular response to acute loading that results in tendon thickening), dysrepair (failed healing that demonstrates greater matrix breakdown and the separation of collagen) and degenerative (increased cell death, matrix breakdown, neuronal and capillary in growth) [4]. Pain can be present or absent at any stage of the tendon pathology continuum. Furthermore, tendons can have discrete regions at different stages of the pathology-continuum at the same time [4,5]. Pathological findings as a result of imaging the tendon do not always correlate with patient symptoms [6].
The majority of running injuries are characterized by repetitive overuse and are usually to tissues ill-equipped for load absorption (i.e., non-contractile) [1]. The insidious onset of pain at a threshold (e.g., <5/10 on a Numeric Rating Scale; NRS) [7] below that experienced during traumatic insults often allows the runner to continue to run. In other words, there is a dissociation between pain and function in chronic injuries [8]. There are several pharmacological (e.g., NSAID’s, injection therapy) and non-pharmacological (e.g., heavy isometric loading, shock-wave therapy, cross-training) aids that produce short-term analgesic effects in tendinopathy [9,10,11,12,13]. However, chronic pain can reach a threshold whereby it is more akin to that experienced in traumatic pain (>5/10 on an NRS). This can force the athlete to stop running and seek longer-term resolutions.
The strongest evidence for the long-term resolution for Achilles tendon pain comes from exercise protocols [14]. Variations of the Alfredsson protocol (straight and bent knee eccentric exercise on the edge of a step) [15,16] appear to be most effective in patients with mid-portion tendinopathy. Excessive dorsi-flexion on the edge of a step is thought to increase the compressive load at the tendon insertion and therefore, straight leg exercises on a flat surface appear to be more effective for those with insertional tendinopathy [17]. These protocols have been further enhanced by a greater understanding of the other neuromuscular deficits that occur as a result of Achilles tendon injury. For example, externally paced eccentric exercise using a metronome standardizes the time the muscle is under tension and enhances neural plasticity [18].
The reasons pain and function respond positively to this form of training are multi-factorial [19]. To the best of the authors’ knowledge, there are no scientific reports which capture self-reported function (Victoria institute of sports assessment–Achilles questionnaire; VISA-A, the foot and ankle disability index FADI, and FADI Sport) [20,21,22], muscle architecture (Ultrasonography; US), muscle contractile properties (Tensiomyography; TMG), muscle endurance (Calf Endurance Test) and pain (Numeric Rating Scale; NRS) pre and post conservative Achilles tendon management.

2. Case Report

2.1. Case History

The patient provided written informed consent for the publication of this case report. A male runner (30 years, 10-km time: 33 min 46 s) had been running with suspected insertional AT for 110 weeks (~2 years) having had the symptoms for the previous 5 years. The average miles per week for the 2-year period was 30. The average miles per week during phases of race preparation was ~40 and the maximum miles per week was 50. During this period, pain (~≤5/10; NRS) and or stiffness was present every morning during the first steps on walking. Pain usually subsided as running progressed and returned after periods of prolonged rest. The runner used a 4-day-per-week running schedule and a 3-day-per-week cross-training schedule to manage running loads applied to the tendon and to lower the risk of other injury. Occasionally, pain increased (≥5/10; NRS) and was relieved using heavy double-legged isometric exercise (~85 kg) and reducing running from four days to three. No structured Achilles tendon rehabilitation was undertaken other than calf raise exercises on days the runner attended the gym (maximum 2*per week). The above summarises the training and pain status of the runner for much of the 2 years prior to cessation. This period included personal bests over 5 km (16:10), 10 km (33:46) and half-marathon (78:00).
Nine weeks before cessation (week 101/110), the runner began to increase the volume and sometimes intensity of one weekly run in an attempt to train for a marathon. This elevated daily pain to 7/10 and to a point where conservative self-management (as above) was no longer effective. The runner attended a sports medicine physician for an ultrasound guided high-volume stripping injection as prescribed in Humphreys et al. [10]. The diagnosis of right-sided medial insertional AT was made by a qualified medical doctor using ultrasonography. The doctor had ~20-years’ experience in the diagnosis of musculoskeletal conditions, diagnostic ultrasound and steroid injection therapy. The doctor was a member of the British Association of Sports and Exercise Medicine. Diagnosis was obtained by palpating the painful site on the medial calcaneus and using ultrasonography to image the same area (Figure 1). Over the course of 1 week (no running), the runner failed to respond to injection therapy and ceased running.

2.2. Assessment

The runner reported to the laboratory (Figure 2) at Leeds Beckett University and completed the Victoria institute of sports assessment-Achilles questionnaire (Victoria institute of sports assessment-Achilles questionnaire; VISA-A), the foot and ankle disability index (FADI and FADI Sport), prior to undergoing an assessment of bi-lateral gastrocnemius medialis (GM) muscle architecture (muscle thickness (MT) and pennation angle (PA); US), muscle contractile properties (maximal muscle displacement (Dm) and contraction time (Tc); Tensiomyography (TMG)) and calf endurance (40 raises/min).
VISA-A and FADI scores were 59%/100% and 102/136, respectively. Compared to the left leg, the right GM had a lower MT (1.60 cm vs. 1.74 cm), a similar PA (22.0° vs. 21.0°), a lower Dm (1.2 mm vs. 2.0 mm) and Tc (16.5 ms vs. 17.7 ms). Calf endurance was higher in the injured leg (right) compared to the left (48 vs. 43 raises).

2.3. Intervention

The athlete ceased running for 5 weeks and began a metronome guided (15-BPM), 12-week progressive eccentric training protocol (3 sets, 12 reps, 2*day) on a flat surface, using a weighted-vest (1.5 kg increments per week). The exercise was performed by bilaterally plantar flexing both legs and lowering unilaterally on the affected leg to a count of 4 s (15 BPM). The athlete also received six sessions of shockwave therapy (2000 shocks per session at a pressure and frequency of 1.8–2.2 bar and 10 Hz, respectively) concurrently within the first 5 weeks. The athlete recorded daily pain scores (NRS) [23] throughout the intervention (Figure 3). On return to running (after 5 weeks), the athlete also recorded a score composed of miles * rate of perceived exertion (RPE) [24]. Running miles* rate of perceived exertion (RPE) was recorded in order to provide a crude estimate of running load. Running began with a 2.5-mile jog, barefoot and on a hard grass surface (British Summer Time). This was progressed (week 6–13) until the athlete could run 8 miles, three times per week at an RPE of 11 (light). The laboratory measures were re-assessed at the 12-week point. The athlete continued to perform the eccentric training protocol and record pain and running load data up to week 16 (Figure 3). Between week 13 and 16, the three 8-mile runs were replaced with an 8-mile run over an undulating surface (shod; RPE: 13), a track session that began with 4 × 400 m and progressed to 16 × 400 m (shod; RPE 15) and a long run that progressed to 12 miles (barefoot and occasionally shod; RPE 11).

2.4. Outcomes

The athlete had a compliance of 80.4% (135/168 possible sessions) to the 12-week eccentric training protocol. At the 12-week point, foot and ankle function improved according to scores recorded on the VISA-A (59% vs. 97%) and FADI (102 vs. 127/136). Figure 4 displays pre and post left–right differences in gastrocnemius muscle architecture and contractile properties.
In the injured leg, improvements in MT (1.60 cm vs. 1.76 cm) and PA (22.0° vs. 24.8°) were recorded via US. Improvements in Dm (1.15 mm vs. 1.69 mm) and Tc (16.5 ms vs. 15.4 ms) were recorded via TMG. Calf endurance was lower in both legs and the asymmetry between legs remained (L: 31, R: 34). Pain intensity (mean weekly NRS scores) decreased between week 1 and week 12 (6.6 vs. 2.9), while running scores increased (20 vs. 38) during the same period. The program was maintained up to week 16 at which point mean weekly NRS was 2.2 and running score was 47 (Figure 5).

3. Discussion

The runner in this case report ran for ~2 years with persistent pain and achieved several personal bests. This demonstrates, in this athlete at least, that pain can be managed in a way that allows a high level of athletic function. This underscores the title of this paper which suggests that pain and function are not as closely linked in chronic pain as they may be in pain resulting from traumatic insult. In fact, baseline results of the calf endurance test appear to demonstrate a compensatory mechanism whereby calf endurance in the injured leg was higher than that of the non-injured [25]. Calf endurance, and to a lesser extent PA, may have helped to compensate for the asymmetry in MT and Dm reported.
This athlete did not respond to a high-volume stripping injection, which may suggest that this type of intervention is not as effective in insertional tendinopathy as it appeared to be for mid-portion tendinopathy [10]. It may also reflect intra-individual responses to injection therapy. Overall, pain and function appeared to respond positively as a result of the combined shockwave therapy and eccentric loading protocol administered over the 16-week period. It is difficult to know from a case report whether the effects demonstrated were due to one or both interventions. It should be noted that pain did not begin to lower on a consistent basis until week 7, and all shockwave therapy had been administered by week 5. These findings, combined with the rise in function and fall in pain from ~week 10, suggest that the eccentric loading protocol was the dominant factor in recovery. This suggestion is underpinned by the substantial improvements in neuromuscular function reported.
In the injured leg (right), there were improvements in gastrocnemius medialis MT (~10%) and PA (~12.7%), as measured by US, which appeared to be reflected by the relative improvement in Dm (~47%) and, to a lesser extent, Tc (~6.7%). These findings were expected, as they mirror improvements in muscle size and function in response to resistance exercise [25]. Strength increases prior to changes in muscle size and is usually proportionally greater, i.e., modest gains in muscle size are usually associated with 3–4 times the relative strength gains [26,27]. In the early stages of resistance training, this is suggested to be as a result of an increase in the neural drive to muscle [28]. Häkkinen and colleagues reported the largest motor units to be recruited within the first 7 weeks of resistance training [29]. The force output of a muscle increases in response to the number of sarcomeres in parallel. An increase in PA facilitates more sarcomeres in parallel, i.e., an increase in physiological cross-sectional area (CSA) without a change in anatomical CSA [30]. It is likely that the increase in PA and the overall increase in contractile mass (MT) contributed to the increase in Dm reported in this athlete. However, Dm is not a measure of force but of stiffness and therefore, it is likely to be heavily influenced by the tendon aponeurosis complex and intramuscular connective tissue. These are the structures which transfer muscle force to the bone. Increases in musculotendinous stiffness have previously been reported in response to resistance training [31,32] and likely contribute to changes reported in Dm. These changes in connective tissue stiffness are thought to be primarily driven by an increase in type I collagen synthesis [33].
This interpretation of an increase in Dm representing an increase in stiffness is somewhat at odds with researchers in the field who suggest a lower Dm to be associated with a greater muscle stiffness [34]. These interpretations are based primarily on cross-sectional studies comparing power and endurance athletes [35] and founded on what remains a limited understanding of the physiology that underpins measures obtained from Tensiomyography. In our laboratory, we are still optimizing the standard operating procedures [36,37] in order to obtain stable measurements prior to a more in-depth interpretation of what the data might indicate physiologically. Our experience from this case report and on-going investigations in our laboratory suggest that differences in Dm are dependent on the context in which they are reported. We suggest that in the case of cross-sectional comparisons, as mentioned above, lower Dm is indeed indicative of higher muscle stiffness. However, in the case of training or detraining we suggest that the increase or decrease in contractile mass and PA can lead to an increase in or decrease in Dm. We advise caution in the interpretation of these findings and others, as interpretation of the data obtained from Tensiomyography remains in its infancy.
The modest reduction in Tc might be expected from an intervention that did not challenge the speed of muscle contraction. The improvements reported are likely due to an increase in the number of sarcomeres in series [38] and the increase in PA, which would allow sarcomeres to operate closer to their optimum length [25]. Calf endurance appeared to decline during the 12-week period, which we suggest is due to the initial 5 weeks without running and the gradual buildup of running up to week 12. It is likely that the removal of a stimulus that had been there for ~2 years led to this reduction. The asymmetry between legs remained, suggesting that some of the adaptations which occurred in the painful leg over time remained.
There are several limitations we would like to acknowledge related to the interpretation of this case report. Firstly, although tendon structural abnormalities are present on ultrasound, this cannot be inferred to represent pathology [39]. In fact, the link between findings on imaging and pain in runners is weak for several musculoskeletal conditions [40,41,42]. That being said, the presence of loading specific pain and pain on palpation suggest an accurate diagnosis was received. Secondly, although we suggest the eccentric exercise protocol was the primary driver behind improvements demonstrated in this case, the influence of the injection and the shockwave therapy cannot be ruled out. Recent evidence suggests that high-volume image-guided injections, as used in this case, demonstrate improvements in pain and function with or without steroid in mid-portion AT [43]. This did not appear to be the case in this report. Although pain did not decrease on a consistent basis until week 7, a significant dose of shockwave therapy was administered during the first 5 weeks. Furthermore, there are promising results in terms of medium and long-term follow-up in mid-portion AT following shockwave therapy [44]. There are several mechanisms by which shockwave is speculated to have an effect on pain and tissue healing. The short-term effects on pain are thought to occur due to hyper stimulation analgesia [45]. In the medium term, it has been suggested that a sharp rise in substance P release and a subsequent long decrease may lead to longer lasting relief from pain [46]. Tendon repair is speculated to be promoted post shockwave therapy via an increase in tenocyte proliferation and an induction of growth factors [47]. Finally, tendinopathy is a condition associated with chronic pain. Disability levels associated with chronic musculoskeletal pain are more closely associated with cognitive and behavioral aspects of pain than sensory and biomedical ones. Positive outcomes are associated with changes in psychological distress, fear avoidance beliefs, self-efficacy in controlling pain and coping strategies [48]. Therefore, in this case, the break from running, and the knowledge of a combined shockwave therapy and exercise intervention coupled with an expected timeline of improvement may have had just as big an impact as the intervention itself.

4. Conclusions

This athlete ran at a high level for 2 years with persistent Achilles pain. Even after an evidence-based rehabilitation programme and a gradual return to running, this athlete was never entirely pain-free. The findings in this runner appear to underscore the need for greater awareness among clinicians about the dissociation between pain and function in Achilles tendinopathy. Pain education and limiting fear avoidance may be as important as physical rehabilitation. The neuromuscular adaptations in this study were substantial and the physiology which underpins them is multifactorial. To what extent these neuromuscular adaptations contribute to the reduction in pain and increase in running specific function is unknown and it will perhaps always be an almost impossible research question to answer. However, it is likely that the combination of neuromuscular adaptations and structural adaptations within the tendon itself help to better balance stress on biological tissue preventing overload of a specific portion of tendon.

Author Contributions

Conceptualization, P.F.; methodology, I.T. and A.J.; formal analysis, I.T. and A.J.; writing—original draft preparation, P.F.; writing—review and editing, M.I.J. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Acknowledgments

The authors would like to acknowledge the institutions of Leeds Beckett University and Institute of Technology Carlow for providing the facilities and support in writing the full manuscript respectively.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

References

  1. Francis, P.; Whatman, C.; Sheerin, K.; Hume, P.; Johnson, M.I. The proportion of lower limb running injuries by gender, anatomical location and specific pathology: A systematic review. J. Sports Sci. Med. 2019, 18, 21–31. [Google Scholar] [PubMed]
  2. Lopes, A.D.; Hespanhol Junior, L.C.; Yeung, S.S.; Costa, L.O. What are the main running-related musculoskeletal injuries? A Systematic Review. Sports Med. 2012, 42, 891–905. [Google Scholar] [CrossRef] [PubMed]
  3. Cook, J.L.; Stasinopoulos, D.; Brismee, J.M. Insertional and mid-substance Achilles tendinopathies: Eccentric training is not for everyone-updated evidence of non-surgical management. J. Man. Manip. Ther. 2018, 26, 119–122. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Cook, J.L.; Purdam, C.R. Is tendon pathology a continuum? A pathology model to explain the clinical presentation of load-induced tendinopathy. Br. J. Sports Med. 2009, 43, 409–416. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Cook, J.L.; Rio, E.; Purdam, C.R.; Docking, S.I. Revisiting the continuum model of tendon pathology: What is its merit in clinical practice and research? Br. J. Sports Med. 2016, 50, 1187–1191. [Google Scholar] [CrossRef] [PubMed]
  6. Khan, K.M.; Forster, B.B.; Robinson, J.; Cheong, Y.; Louis, L.; Maclean, L.; Taunton, J.E. Are ultrasound and magnetic resonance imaging of value in assessment of Achilles tendon disorders? A two year prospective study. Br. J. Sports Med. 2003, 37, 149–153. [Google Scholar] [CrossRef] [Green Version]
  7. Silbernagel, K.G.; Thomee, R.; Eriksson, B.I.; Karlsson, J. Continued sports activity, using a pain-monitoring model, during rehabilitation in patients with Achilles tendinopathy: A randomized controlled study. Am. J. Sports Med. 2007, 35, 897–906. [Google Scholar] [CrossRef]
  8. Moseley, G.L.; Butler, D.S. Fifteen years of explaining pain: The past, present, and future. J. Pain 2015, 16, 807–813. [Google Scholar] [CrossRef] [Green Version]
  9. Bussin, E.R.; Cairns, B.; Bovard, J.; Scott, A. Randomised controlled trial evaluating the short-term analgesic effect of topical diclofenac on chronic Achilles tendon pain: A pilot study. BMJ Open 2017, 7, e015126. [Google Scholar] [CrossRef]
  10. Humphrey, J.; Chan, O.; Crisp, T.; Padhiar, N.; Morrissey, D.; Twycross-Lewis, R.; King, J.; Maffulli, N. The short-term effects of high volume image guided injections in resistant non-insertional Achilles tendinopathy. J. Sci. Med. Sport 2010, 13, 295–298. [Google Scholar] [CrossRef]
  11. Rio, E.; Kidgell, D.; Purdam, C.; Gaida, J.; Moseley, G.L.; Pearce, A.J.; Cook, J. Isometric exercise induces analgesia and reduces inhibition in patellar tendinopathy. Br. J. Sports Med. 2015, 49, 1277–1283. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Wiegerinck, J.I.; Kerkhoffs, G.M.; van Sterkenburg, M.N.; Sierevelt, I.N.; van Dijk, C.N. Treatment for insertional Achilles tendinopathy: A systematic review. Knee Surg. Sports Traumatol. Arthrosc. 2013, 21, 1345–1355. [Google Scholar] [CrossRef] [PubMed]
  13. Paquette, M.R.; Peel, S.A.; Smith, R.E.; Temme, M.; Dwyer, J.N. The impact of different cross-training modalities on performance and injury-related variables in high school cross country runners. J. Strength Cond. Res. 2018, 32, 1745–1753. [Google Scholar] [CrossRef] [PubMed]
  14. Beyer, R.; Kongsgaard, M.; Hougs Kjaer, B.; Ohlenschlaeger, T.; Kjaer, M.; Magnusson, S.P. Heavy slow resistance versus eccentric training as treatment for achilles tendinopathy: A randomized controlled trial. Am. J. Sports Med. 2015, 43, 1704–1711. [Google Scholar] [CrossRef]
  15. Alfredson, H.; Pietila, T.; Jonsson, P.; Lorentzon, R. Heavy-load eccentric calf muscle training for the treatment of chronic Achilles tendinosis. Am. J. Sports Med. 1998, 26, 360–366. [Google Scholar] [CrossRef] [Green Version]
  16. Woodley, B.L.; Newsham-West, R.J.; Baxter, G.D. Chronic tendinopathy: Effectiveness of eccentric exercise. Br. J. Sports Med. 2007, 41, 188–198. [Google Scholar] [CrossRef] [Green Version]
  17. Jonsson, P.; Alfredson, H.; Sunding, K.; Fahlstrom, M.; Cook, J. New regimen for eccentric calf-muscle training in patients with chronic insertional Achilles tendinopathy: Results of a pilot study. Br. J. Sports Med. 2008, 42, 746–749. [Google Scholar] [CrossRef]
  18. Rio, E.; Kidgell, D.; Moseley, G.L.; Gaida, J.; Docking, S.; Purdam, C.; Cook, J. Tendon neuroplastic training: Changing the way we think about tendon rehabilitation: A narrative review. Br. J. Sports Med. 2016, 50, 209–215. [Google Scholar] [CrossRef]
  19. O’Neill, S.; Watson, P.J.; Barry, S. Why are eccentric exercises effective for achilles tendinopathy? Int. J. Sports Phys. Ther. 2015, 10, 552–562. [Google Scholar]
  20. Robinson, J.M.; Cook, J.L.; Purdam, C.; Visentini, P.J.; Ross, J.; Maffulli, N.; Taunton, J.E.; Khan, K.M. The VISA-A questionnaire: A valid and reliable index of the clinical severity of Achilles tendinopathy. Br. J. Sports Med. 2001, 35, 335–341. [Google Scholar] [CrossRef]
  21. Martin, R.; Burdett, R.; Irrgang, J. Development of the foot and ankle disability index (FADI). J. Orthop. Sports Phys. Ther. 1999, 29, A32–A33. [Google Scholar]
  22. Hale, S.A.; Hertel, J. Reliability and sensitivity of the Foot and Ankle Disability Index in subjects with chronic ankle instability. J. Athl. Train. 2005, 40, 35–40. [Google Scholar]
  23. Hawker, G.A.; Mian, S.; Kendzerska, T.; French, M. Measures of adult pain: Visual Analog Scale for Pain (VAS Pain), Numeric Rating Scale for Pain (NRS Pain), McGill Pain Questionnaire (MPQ), Short-Form McGill Pain Questionnaire (SF-MPQ), Chronic Pain Grade Scale (CPGS), Short Form-36 Bodily Pain Scale (SF-36 BPS), and Measure of Intermittent and Constant Osteoarthritis Pain (ICOAP). Arthritis Care Res. 2011, 63 (Suppl. S11), S240–S252. [Google Scholar]
  24. Borg, G.; Exertion, B.P.; Scales, P. Champaign; Human Kinetics: Champaign, IL, USA, 1998; pp. 1–104. [Google Scholar]
  25. Blazevich, A.J. Effects of physical training and detraining, immobilisation, growth and aging on human fascicle geometry. Sports Med. 2006, 36, 1003–1017. [Google Scholar] [CrossRef] [PubMed]
  26. Francis, P.; Mc Cormack, W.; Toomey, C.; Norton, C.; Saunders, J.; Kerin, E.; Lyons, M.; Jakeman, P. Twelve weeks’ progressive resistance training combined with protein supplementation beyond habitual intakes increases upper leg lean tissue mass, muscle strength and extended gait speed in healthy older women. Biogerontology 2016, 18, 881–891. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  27. Seynnes, O.R.; de Boer, M.; Narici, M.V. Early skeletal muscle hypertrophy and architectural changes in response to high-intensity resistance training. J. Appl. Physiol. 2007, 102, 368–373. [Google Scholar] [CrossRef] [PubMed]
  28. Gabriel, D.A.; Kamen, G.; Frost, G. Neural adaptations to resistive exercise: Mechanisms and recommendations for training practices. Sports Med. 2006, 36, 133–149. [Google Scholar] [CrossRef]
  29. Hakkinen, K.; Pakarinen, A.; Kraemer, W.J.; Hakkinen, A.; Valkeinen, H.; Alen, M. Selective muscle hypertrophy, changes in EMG and force, and serum hormones during strength training in older women. J. Appl. Physiol. 2001, 91, 569–580. [Google Scholar] [CrossRef] [Green Version]
  30. Aagaard, P.; Andersen, J.L.; Dyhre-Poulsen, P.; Leffers, A.M.; Wagner, A.; Magnusson, S.P.; Halkjaer-Kristensen, J.; Simonsen, E.B. A mechanism for increased contractile strength of human pennate muscle in response to strength training: Changes in muscle architecture. J. Physiol. 2001, 534, 613–623. [Google Scholar] [CrossRef]
  31. Geremia, J.M.; Baroni, B.M.; Bobbert, M.F.; Bini, R.R.; Lanferdini, F.J.; Vaz, M.A. Effects of high loading by eccentric triceps surae training on Achilles tendon properties in humans. Eur. J. Appl. Physiol. 2018, 118, 1725–1736. [Google Scholar] [CrossRef]
  32. Kubo, K.; Kanehisa, H.; Ito, M.; Fukunaga, T. Effects of isometric training on the elasticity of human tendon structures in vivo. J. Appl. Physiol. 2001, 91, 26–32. [Google Scholar] [CrossRef]
  33. Langberg, H.; Ellingsgaard, H.; Madsen, T.; Jansson, J.; Magnusson, S.P.; Aagaard, P.; Kjaer, M. Eccentric rehabilitation exercise increases peritendinous type I collagen synthesis in humans with Achilles tendinosis. Scand. J. Med. Sci. Sports 2007, 17, 61–66. [Google Scholar] [CrossRef]
  34. Macgregor, L.J.; Hunter, A.M.; Orizio, C.; Fairweather, M.M.; Ditroilo, M. Assessment of Skeletal Muscle Contractile Properties by Radial Displacement: The Case for Tensiomyography. Sports Med. 2018, 48, 1607–1620. [Google Scholar] [CrossRef] [Green Version]
  35. Valenzuela, P.L.; Sanchez-Martinez, G.; Torrontegi, E.; Vazquez-Carrion, J.; Montalvo, Z.; Lucia, A. Comment on: Assessment of skeletal muscle contractile properties by radial displacement: The case for tensiomyography. Sports Med. 2019, 49, 973–975. [Google Scholar] [CrossRef]
  36. Wilson, H.V.; Johnson, M.I.; Francis, P. Repeated stimulation, inter-stimulus interval and inter-electrode distance alters muscle contractile properties as measured by Tensiomyography. PLoS ONE 2018, 13, e0191965. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  37. Wilson, H.V.; Jones, A.D.; Johnson, M.I.; Francis, P. The effect of inter-electrode distance on radial muscle displacement and contraction time of the biceps femoris, gastrocnemius medialis and biceps brachii, using Tensiomyography in healthy participants. Physiol. Meas. 2019, 40. [Google Scholar] [CrossRef]
  38. Franchi, M.V.; Atherton, P.J.; Reeves, N.D.; Fluck, M.; Williams, J.; Mitchell, W.K.; Selby, A.; Beltran Valls, R.M.; Narici, M.V. Architectural, functional and molecular responses to concentric and eccentric loading in human skeletal muscle. Acta Physiol. 2014, 210, 642–654. [Google Scholar] [CrossRef]
  39. Docking, S.I.; Ooi, C.C.; Connell, D. Tendinopathy: Is imaging telling us the entire story? J. Orthop. Sports Phys. Ther. 2015, 45, 842–852. [Google Scholar] [CrossRef] [Green Version]
  40. Kornaat, P.R.; Van de Velde, S.K. Bone marrow edema lesions in the professional runner. Am. J. Sports Med. 2014, 42, 1242–1246. [Google Scholar] [CrossRef]
  41. Stahl, R.; Luke, A.; Ma, C.B.; Krug, R.; Steinbach, L.; Majumdar, S.; Link, T.M. Prevalence of pathologic findings in asymptomatic knees of marathon runners before and after a competition in comparison with physically active subjects—A 3.0 T magnetic resonance imaging study. Skelet. Radiol. 2008, 37, 627–638. [Google Scholar] [CrossRef]
  42. Shaikh, Z.; Perry, M.; Morrissey, D.; Ahmad, M.; Del Buono, A.; Maffulli, N. Achilles tendinopathy in club runners. Int. J. Sports Med. 2012, 33, 390–394. [Google Scholar]
  43. Abdulhussein, H.; Chan, O.; Morton, S.; Kelly, S.; Padhiar, N.; Valle, X.; King, J.; Williams, S.; Morrissey, D. High Volume Image Guided Injections with or without steroid for mid-portion Achilles Tendinopathy: A Pilot Study. Clin. Res. Foot Ankle 2017, 5, 249. [Google Scholar] [CrossRef]
  44. Vulpiani, M.C.; Trischitta, D.; Trovato, P.; Vetrano, M.; Ferretti, A. Extracorporeal shockwave therapy (ESWT) in Achilles tendinopathy. A long-term follow-up observational study. J. Sports Med. Phys. Fit. 2009, 49, 171–176. [Google Scholar]
  45. Hausdorf, J.; Schmitz, C.; Averbeck, B.; Maier, M. Molecular basis for pain mediating properties of extracorporeal shock waves. Schmerz 2004, 18, 492–497. [Google Scholar] [CrossRef] [PubMed]
  46. Maier, M.; Averbeck, B.; Milz, S.; Refior, H.J.; Schmitz, C. Substance P and prostaglandin E2 release after shock wave application to the rabbit femur. Clin. Orthop. Relat. Res. 2003, 406, 237–245. [Google Scholar] [CrossRef]
  47. Notarnicola, A.; Moretti, B. The biological effects of extracorporeal shock wave therapy (eswt) on tendon tissue. Muscles Ligaments Tendons J. 2012, 2, 33–37. [Google Scholar]
  48. O’Sullivan, P. It’s time for change with the management of non-specific chronic low back pain. Br. J. Sports Med. 2012, 46, 224–227. [Google Scholar] [CrossRef] [Green Version]
Figure 1. Identification of right-sided medial insertional tendinopathy.
Figure 1. Identification of right-sided medial insertional tendinopathy.
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Figure 2. The use of ultrasonography (US), tensiomyography (TMG) and the calf endurance test in the assessment of (a) muscle architecture, (b) contractile properties, and (c) endurance.
Figure 2. The use of ultrasonography (US), tensiomyography (TMG) and the calf endurance test in the assessment of (a) muscle architecture, (b) contractile properties, and (c) endurance.
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Figure 3. The intervention for the management of medial insertional Achilles tendinopathy.
Figure 3. The intervention for the management of medial insertional Achilles tendinopathy.
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Figure 4. Changes in gastrocnemius muscle architecture ((a) muscle thickness and (b) pennation angle) and contractile properties ((c) muscle displacement and (d) contraction time) pre and post intervention.
Figure 4. Changes in gastrocnemius muscle architecture ((a) muscle thickness and (b) pennation angle) and contractile properties ((c) muscle displacement and (d) contraction time) pre and post intervention.
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Figure 5. Weekly pain (numeric rating scale; NRS) and function (miles*rate of perceived exertion; RPE) response to intervention. Weekly mileage totals began with 9.5 on week 5 and ended with 26 on week 16.
Figure 5. Weekly pain (numeric rating scale; NRS) and function (miles*rate of perceived exertion; RPE) response to intervention. Weekly mileage totals began with 9.5 on week 5 and ended with 26 on week 16.
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MDPI and ACS Style

Francis, P.; Thornley, I.; Jones, A.; I. Johnson, M. Pain and Function in the Runner a Ten (din) uous Link. Medicina 2020, 56, 21. https://doi.org/10.3390/medicina56010021

AMA Style

Francis P, Thornley I, Jones A, I. Johnson M. Pain and Function in the Runner a Ten (din) uous Link. Medicina. 2020; 56(1):21. https://doi.org/10.3390/medicina56010021

Chicago/Turabian Style

Francis, Peter, Isobel Thornley, Ashley Jones, and Mark I. Johnson. 2020. "Pain and Function in the Runner a Ten (din) uous Link" Medicina 56, no. 1: 21. https://doi.org/10.3390/medicina56010021

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