Reviewed by Jerome Thomas, SPT, Tyler Tice, PT, DPT, OCS, ATC

Utilization of total knee arthroplasty (TKA) procedures in the United States has skyrocketed in recent years. According to Cram et. al (2012), the annual volume of TKA surgeries among Medicare beneficiaries increased 161.5% between 1991 and 2010. In this research article, Cram and his colleagues proposed that this dramatic advancement in TKA surgeries could be due to the fact that the TKA procedure is highly reliant on subjective criteria, therefore lending itself to potential over-utilization. Determining whether a TKA surgery is advisable for a patient requires evidence-based appropriateness criteria; however, these specific criteria have never formally been developed for patients undergoing TKAs. The aim of this cohort study is to determine if the current TKA appropriateness criteria is valid and accurately predicts whether a patient should opt for a TKA surgery.

As previously mentioned, there has been no formal appropriateness criteria for TKA procedures in the United States. The most commonly recommended and studied approach is the RAND/UCLA method developed by Escobar and his colleagues in Spain. Escobar et. al constructed their TKA appropriateness algorithm based on several variables: symptom behavior, age, extent of radiographic arthritis, prior medical history, knee joint mobility and stability, and functional status. These researchers in Spain then tested their algorithm against 775 TKA patients and determined their appropriateness based on their specialized criterion. The purpose of this cohort study was to modify Escobar’s system for US TKA patients and analyze its validity in determining whether a patient is a good candidate for a TKA procedure.

For the cohort study, 216 subject data sets were derived from 4,796 possible patients enrolled in the Osteoarthritis Initiative (OAI). In order to assess severity of knee arthritis for each patient, the KL radiographic grading system was utilized: 1 indicated mild (1 to 33%) narrowing, 2 indicated moderate (34–66%) narrowing and 3 indicated severe (67 to 100%) narrowing. The WOMAC Physical Function scale evaluates the functional status of each patient and how their symptoms impact their function:0 = none, 1=mild impairment, 2= moderate impairment, 3=severe impairment, 4=extreme impairment. Additionally, patients were categorized as limited when they had either less than 0° to 90° of knee motion or greater than 5 millimeters of medial or lateral gapping during stress testing.

The results of the cohort study were based on the modifications of Escobar’s appropriateness algorithm. Of 175 subjects with complete data sets, 77 were classified as appropriate TKA surgeries. The majority of patients that were deemed appropriate for TKA surgeries had intense or severe symptoms that impacted functional status, KL arthritis scores of 4 (severe knee joint narrowing), and were greater than 55 years of age. Many patients struggle with the ultimate decision of undergoing a TKA surgery so the researchers of this cohort study wanted to provide evidence-based criteria for patients to aid in their choice.

Clinical Application:

The patient population that are most likely to be deemed appropriate for TKA surgeries are those with intense/severe symptoms that impact functional status, KL arthritis scores of 4 (severe knee joint narrowing shown on radiographic images), and greater than 55 years of age. Other important variables that must be considered before a TKA procedure include psychological readiness for the surgery and the recommendations of all members of the patient’s healthcare team.

References:

Cram P, Lu X, Kates SL, Singh JA, Li Y, Wolf BR. Total knee arthroplasty volume, utilization, and outcomes among Medicare beneficiaries, 1991–2010. JAMA. 2012; 308(12):1227–36.

Escobar A, Quintana JM, Arostegui I, Azkarate J, Guenaga JI, Arenaza JC, et al. Development of explicit criteria for total knee replacement. Int J Technol Assess Health Care. 2003; 19(1):57–70.

Riddle DL, Jiranek WA, Hayes CW. Use of a validated algorithm to judge the appropriateness of total knee arthroplasty in the United States: a multicenter longitudinal cohort study. Arthritis Rheumatol. 2014;66(8):2134-2143.

Reviewed by Austin Mowrey PT, DPT

Introduction:  

Hamstring injuries are common in many sports that require repetitive acceleration and deceleration, including football, soccer, and basketball. There is also a correlation between hamstring mobility and pelvic, knee and low back pain. The aim of this study was to compare foam rolling and proprioceptive neuromuscular facilitation (PNF) to address hamstring mobility deficits.  

Methods and Interventions:  

This study consisted of 80 subjects over 18 years old with no history of hypermobility, hamstring injuries in the past 6 months, a diagnosed orthopedic problems or surgery in the lower limb, back pain or spine surgery, and systemic and neurological disorders. The sample consisted of 53 men and 27 women with an average age of 22.82 years. Subjects were randomly assigned to receive PNF treatment or foam rolling treatment. Hamstring mobility was assessed using a modified sit-and-reach test before interventions, during interventions and 2 minutes after interventions. The subject’s discomfort was also measured using the BORG RPE scale at the end of the intervention.  

The PNF group consisted of 29 men and 11 women with an average age of 22.48. The PNF stretching protocol was performed with each participant in a long sitting position on a plinth. The participant was asked to perform a maximal isometric hamstring muscle contraction for 5 seconds followed by 5 seconds if relaxation and 20 seconds of stretching (30 seconds total). Each participant underwent four repetitions of the PNF stretching in which hamstring length was recorded at baseline, at the end of first repetition, and at the end of the protocol.  

The foam roll group consisted of 24 men and 16 women with an average age of 22.50. For the foam rolling protocol, each participant assumed the long sitting position on a firm and even surface by placing their arms backward and transferring their weight to their palms. The foam roller was placed bilaterally under their hamstrings and slowly moved back forth from the ischial tuberosity and the popliteal fossa for two minutes. Hamstring length was recorded at baseline, 30 seconds from the start of the intervention and at the end of the protocol.  

Results:  

Baseline measurements of hamstring flexibility demonstrated no significant differences between each group, but both groups had statistically significant increase in hamstring flexibility during the interventions and after the intervention. The PNF group demonstrated a 56% total gain of hamstring mobility after the first bout of PNF stretching and the rest during the last three bouts. The foam roll group demonstrated 47% of the total gain after 30 seconds of foam rolling and the rest during the last 90 seconds. When comparing PNF stretching vs foam rolling for hamstring mobility, PNF stretching demonstrated statistically significant results during and after the interventions. There were no statistically significant results when comparing the participants’ perceived exertion between groups or with increased effort and flexibility gained.  

Conclusion:  

The PNF group and foam rolling both experienced statistically significant increase in flexibility in their hamstrings during and after both interventions. When comparing the two groups, the PNF group had significant increase in hamstring flexibility compared to the foam rolling group, but both groups had similar sensation of perceived exertion.  

Take Home Message: 

It is important for clinicians to consider patients’ needs, body size, demographics and goals when deciding on the appropriate intervention. This study concludes that PNF stretching and foam rolling are both effective to improve hamstring flexibility, but PNF is more effective for the population studied. Further research should be performed to assess the duration of the physiological changes noted in this study.  

Reference:  

Pérez-Bellmunt A, Casasayas-Cos O, Ragazzi P, Rodríguez-Sanz J, Hidalgo-García C, Canet-Vintró M, Caballero-Martínez I, Pacheco L, López-de-Celis C. Foam Rolling vs. Proprioceptive Neuromuscular Facilitation Stretching in the Hamstring Flexibility of Amateur Athletes: Control Trials. International Journal of Environmental Research and Public Health. 2023; 20(2):1439. https://doi.org/10.3390/ijerph20021439 

Reviewed by Jerome Thomas, SPT, Tyler Tice, PT, DPT, OCS, ATC

Manual therapy is one of the most common interventions utilized by physical therapists and generally refers to passively applying mechanical forces to the superficial body in order to receive a therapeutic effect. Manual therapy is often implemented in combination with other modalities and interventions to provide a comprehensive, multi-modal approach to musculoskeletal management. Additionally, manual therapy has shown superior clinical outcomes for numerous musculoskeletal disorders in the research that has been conducted on this intervention. However, new evidence in the field of physical therapy has led to a paradigm shift in the way that manual therapy can be utilized. Researchers in physical therapy are asking this pivotal question: Do some specific groups of individuals receive greater therapeutic benefits from manual therapy compared to others?

The International Association for the Study of Pain (IASP) outlines three major pain classifications: nociceptive, nociplastic, and neuropathic. Nociceptive pain is a protective mechanism, caused by physiological activation of pain receptors and is usually attributed to actual tissue damage such as stubbing your toe. Nociplastic pain is often described as increased sensitivity to pain due to the impaired functioning of the pain-processing systems in the central nervous system. This type of pain presentation is commonly seen in chronic conditions such as fibromyalgia. Lastly, neuropathic pain arises from nerve damage or irritation and can often be characterized as shooting, burning, or stabbing pain. There is a prevalent hypothesis that categorizing patients based on these three major pain presentations will allow physical therapists to better tailor their manual therapy techniques for improved patient outcomes.

This detailed study was a consensus-based survey design between the expert clinicians on manual therapy, with group members evaluating one of the three major pain presentations. These group members were tasked with developing an optimal manual therapy treatment framework for each specific pain presentation. These expert clinicians or stakeholders in this study all exhibited high levels of training and experience using manual therapy interventions in clinical practice. Each specific manual therapy framework would outline specific treatment protocols that could be modified based on the patient’s signs and symptoms. As expected, there are both differences and similarities between the theoretical frameworks of the three IASP mechanism-based pain classifications.

The experts came away with several conclusions concerning each specified theoretical framework. The neuropathic and nociplastic frameworks recommended a graded application scheme, with less aggressive techniques early in treatment to monitor patient response; the nociceptive framework recommended approaches that are more aggressive once the patient’s symptoms are improved. For the neuropathic and nociplastic frameworks, it was recommended that you attempt to reconceptualize the pain experience for these patients and create an environment that limits fear and catastrophizing. Additionally, there was an emphasis on “increasing space” for the neuropathic framework as nerve movement increases blood flow in nerve-related conditions.

Clinical Application:

All three frameworks recommended selecting a therapeutic manual therapy approach based on the patient’s unique pain presentation. Patients with neuropathic pain will benefit from graded application of manual therapy and techniques that aim to increase nerve movement for improved blood flow. Patients with nociplastic pain will generally benefit from a reconceptualized view of their pain experience along with less aggressive techniques early on in their treatment plan. Patients with nociceptive pain can be introduced to more aggressive techniques as their symptoms improve; techniques should be selected with the goal of increasing pain-free active range of motion.

Reference:

Cook, C. E., Rhon, D. I., Bialosky, J., Donaldson, M., George, S. Z., Hall, T., … & Puentedura, E. J. (2023). Developing Manual Therapy Frameworks for Dedicated Pain Mechanisms. JOSPT Open, 1(1), 1-15.

Reviewed by Jerome Thomas, SPT, Tyler Tice, PT, DPT, OCS, ATC

Achilles tendinopathy is a very common, overuse injury of the lower extremity that often affects athletes and highly-active individuals that engage in activities such as running, jumping, and other recreational-related tasks. Achilles tendinopathy can consequently become detrimental to a patient’s activity levels and overall functional capacity as many patients may begin to decrease their activity in response to pain or decline in function. There are a very limited number of randomized controlled trials and established treatment protocols for Achilles tendinopathy, despite various forms of modalities and exercise utilized for this patient population. This prospective, randomized controlled trial attempted to evaluate the efficacy of utilizing the Pain-Monitoring Model in combination with a continued, tendon-loading training regimen for patients with Achilles tendinopathy.

In this study, 38 patients with Achilles Tendinopathy were divided into two separate treatment groups: an exercise training group (n=19) and an active rest group (n=19) that was not allowed to perform any physical activity for the first 6 weeks of rehabilitation. However, both treatment groups were rehabilitated with an identical, progressive Achilles tendon-loading program for 12 weeks to 6 months.  As previously mentioned, the exercise training group was allowed to continue loading activities for the Achilles tendon in accordance with the Pain-Monitoring Model in the same timeframe that the active rest group was restricted .

Guidelines for the Pain-Monitoring Model were modified by Silberngael et al. in their 2001 study. According to their guidelines for the pain-monitoring model, pain was not allowed to reach level 5 on the VAS where a 0 indicated no pain and a 10 indicated the worst pain imaginable. Pain after the exercises were allowed to reach a 5 on the VAS but should have subsided by the following morning. Additionally, pain and stiffness in the Achilles tendon were not allowed to increase from week to week. Treatment protocol consisted of a progressive, four-phase program that incorporated the following exercises: 2-legged, 1-legged, eccentric, and fast-rebounding toe raises. Phase 3 allowed the patients to transition to more plyometric-style movements if the subsequent phases were handled with no pain in the tendon insertion or increased morning stiffness. The primary outcomes utilized for the conclusion of this randomized controlled trial were the VISA-A-S score, which was a specialized Achilles assessment questionnaire, as well as pain with hopping measured with the VAS scale.

The results of the trial showed that both treatment groups showed significant improvements in VISA-A-S score and hopping pain in comparison to baseline measurements at 6 weeks, 3 month, 6 month, and 12 month evaluations. More importantly, this study could not demonstrate any negative findings or implications for allowing the patients in the exercise training group to continue Achilles tendon-loading activities in accordance with the Pain-Monitoring Model. Therefore, early implementation of strengthening exercises for the Achilles tendon and plantar flexor complex, as well as moderated activities such as running and jumping, can be utilized to reduce symptoms and improve functional capacity in patients with Achilles tendinopathy. In previous literature, it had been recommended that patients with Achilles tendinopathy take a rest period from the activities that were pain-provoking. However, this study demonstrates that those same activities can be continued as long as the patient with Achilles tendinopathy  is following the protocols set by the Pain-Monitoring Model.

Clinical Application:

Based on this study, we can use the Pain Monitoring Model as a guide to help determine the appropriate amount of activity and exercise for the proper amount of loading to the Achilles tendon with Achilles tendinopathy without “overdoing it”. Below is a graphic that simplifies the explanation of this model:

Reference:

Silbernagel KG, Thomeé R, Eriksson BI, 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 Jun;35(6):897-906. doi: 10.1177/0363546506298279. Epub 2007 Feb 16. PMID: 17307888.

by John Baur, PT, OCS, FAAOMPT

Acetaminophen (APAP) is a commonly used over-the-counter pain reliever that can cause liver damage when taken in high doses. The common brand name for acetaminophen (APAP) is Tylenol and acute liver injury caused by APAP overdose is a serious medical condition that can lead to liver failure and death. Probiotics are live microorganisms that can provide health benefits when consumed in adequate amounts. Bacillus spp. spores are a type of probiotic that have been shown to modulate the gut microbiota and improve overall health. In this report, we will discuss a study that investigated the effects of a probiotic containing Bacillus spp. spores on a rat model of APAP-induced acute liver injury.

Methods

The study used a rat model of APAP-induced acute liver injury. The rats were divided into four groups: a control group, an APAP group, an APAP group treated with the probiotic, and an APAP group treated with N-acetylcysteine (NAC), a standard treatment for APAP-induced liver injury. The probiotic contained Bacillus spp. spores.

The rats were treated with the probiotic or NAC for a period of 3 days. The severity of liver injury was assessed by measuring levels of liver enzymes in the blood and examining liver tissue for signs of damage.

Results

The study found that treatment with the probiotic containing Bacillus spp. spores protected against APAP-induced acute liver injury in rats. The probiotic significantly reduced levels of liver enzymes in the blood and reduced signs of liver damage in the liver tissue. The protective effects of the probiotic were comparable to those of NAC, the standard treatment for APAP-induced liver injury.

The study also found that the probiotic increased the abundance of beneficial bacteria in the gut microbiota, which may have contributed to its protective effects on the liver.

Conclusion

The study suggests that treatment with a probiotic containing Bacillus spp. spores can protect against APAP-induced acute liver injury in rats. The probiotic reduced levels of liver enzymes in the blood and reduced signs of liver damage in the liver tissue. These findings suggest that Bacillus spp. spores could be a promising treatment option for APAP-induced liver injury in humans. Further research is needed to confirm these findings in human clinical trials, but the study provides a promising avenue for future research in the field of probiotics and liver health.

Physical Therapy First recognizes the importance staying well-informed with the latest health and wellness topics that affect our patients.  Megasporebiotic made by Microbiome Labs (microbiomelabs.com) is the first spore-base probiotic with research which supports it use for Acetaminophen (APAP)-induced acute liver injury and many other health conditions.

Reference

Probiotic Bacillus Spores Protect Against Acetaminophen Induced Acute Liver Injury in Rats.Neag MA, Catinean A, Muntean DM, Pop MR, Bocsan CI, Botan EC, Buzoianu AD.Nutrients. 2020 Feb 27;12(3):632. doi: 10.3390/nu12030632.