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. Author manuscript; available in PMC: 2018 Aug 1.
Published in final edited form as: J Hand Surg Am. 2017 Jun 28;42(8):623–629.e1. doi: 10.1016/j.jhsa.2017.05.006

Diagnostic Testing Requested Before Surgical Evaluation for Carpal Tunnel Syndrome

Erika D Sears 1,2,3, Yu-Ting Lu 1, Shannon M Wood 1, Jacob S Nasser 1, Rodney A Hayward 2,3,4, Kevin C Chung 1,3, Eve A Kerr 2,3,4
PMCID: PMC5545070  NIHMSID: NIHMS878027  PMID: 28666673

Abstract

Purpose

We sought to evaluate how often physicians who perform carpal tunnel release (CTR) in the State of Michigan routinely request electrodiagnostic studies (EDS) or other diagnostic tests prior to an initial consultation, and whether provider or practice characteristics had an influence on requirements for pre-consultation diagnostic tests.

Methods

Through online data sources, we identified 356 providers in 261 practices throughout the State of Michigan with profiles confirming hand surgery practice or surgical treatment of carpal tunnel syndrome (CTS). We recorded American Society for Surgery of the Hand (ASSH) membership, teaching facility status, practice size, and primary specialty for each provider. Using a standardized telephone script, 219 providers were contacted by telephone to determine whether any diagnostic tests were needed before an appointment. Using multivariable logistic regression, we evaluated the relationship between the requirement for pre-consultation testing and surgeon and practice characteristics.

Results

Among the 134 providers who were confirmed to perform CTR, 57% (n=76) required and 9% (n=12) recommended a diagnostic test prior to the initial consultation. Of the 88 physicians who required/recommended testing, 85% (n=75) requested EDS, 22% (n=19) requested an MRI, 13% (n=11) requested a CT scan, and 9% (n=8) requested an X-ray. Patients were asked to have multiple studies by 19 (22%) of the 88 surgeons who requested/recommended testing. In the multivariable analysis, ASSH membership, size of practice and teaching facility status did not have a significant relationship with the requirement for pre-consultation testing.

Conclusions

Most surgeons who treat CTS in the State of Michigan routinely request EDS before evaluation, rather than reserving the test for cases where the diagnosis is unclear.

Keywords: Diagnostic tests, electrodiagnostic studies, carpal tunnel syndrome

INTRODUCTION

Electrodiagnostic Studies (EDS) are commonly used to evaluate patients with suspected carpal tunnel syndrome (CTS), with approximately 70% of American Society for Surgery of the Hand (ASSH) members reporting routine use of EDS prior to carpal tunnel release (CTR) in 2015.1 However, there is no reference standard diagnostic test for CTS. Current evidence consistently reports that information gathered from the history and physical exam has similar if not better sensitivity and specificity for CTS diagnosis compared to modalities such as EDS, MRI, and ultrasound, often with EDS having the highest false positive and false negative rates of the commonly used testing modalities.27 Although EDS is not associated with a high risk of harm, it is an unpleasant experience for patients. Furthermore, EDS may provide little value in patients who have classic symptoms and exam findings consistent with CTS, given the delay in surgery and added costs seen in patients who have EDS prior to CTR.8

The 2016 American Academy of Orthopaedic Surgeons (AAOS) Clinical Practice Guidelines (CPG) on the Management of Carpal Tunnel Syndrome supports the use of either EDS or a diagnostic questionnaire to aid the diagnosis of CTS.9 Although previous versions of the AAOS CPG recommended EDS for patients being considered for CTR,10 this recommendation does not appear in the latest guideline. The impact of previous recommendations on the routine use of EDS in current clinical practice for patients with suspected CTS is unknown. Furthermore, it is unknown how often surgeons are using EDS or other diagnostic tests prior to an initial patient evaluation, rather than ordering the tests selectively based on information obtained in the history and physical examination.

We sought to evaluate how often physicians who perform CTR in the State of Michigan routinely request EDS and/or other diagnostic tests prior to an initial consultation. Secondarily, we aimed to determine whether provider or practice characteristics had an influence on requirements for pre-consultation diagnostic tests. We hypothesized that EDS for CTS would be widely utilized before an initial consultation regardless of surgeon or practice factors.

MATERIALS AND METHODS

Dataset and Study Selection

This study received non-regulated status by the Institutional Review Board. We identified surgeons who potentially perform CTR in the State of Michigan through online data sources. ASSH members practicing in Michigan were identified using the ASSH membership directory.11 Non-ASSH members were identified by using two online physician search engines, DocSpot12 and HealthGrades.13 The search engines were chosen to compile a sample of physicians who potentially perform CTR by using related search terms unique to each site. The terms “hand surgery,” “carpal tunnel release,” and “carpal tunnel” were chosen to identify prospective providers on DocSpot and the terms “orthopaedic hand surgery,” “plastic surgery of the hand,” and “neuroplasty (limited to neurosurgeons)” were chosen to identify prospective providers on HealthGrades. We recorded publicly-available data from the physician profiles and verified each element on the physician’s personal website when available, including the physician name, practice name, address, phone number for appointment scheduling, teaching facility status, size of the practice (the number of surgeons in the same practice performing CTR), and primary specialty (plastic surgery, orthopaedic surgery, neurosurgery, or general surgery). Providers were excluded if their profile or personal webpage did not indicate that they performed CTR or hand surgery. We identified 356 providers in 261 practices who met the inclusion criteria (Figure 1).

Figure 1.

Figure 1

Inclusion and Exclusion Criteria of Physician Sample Contacted by Phone. CTR: carpal tunnel release. *All practices with 3 or more surgeons were included (150 surgeons from 42 practices). An additional 58 solo and two-provider practices were randomly sampled (69 surgeons from 58 solo or two-provider practices).

We categorized practices as solo (N = 176), two-provider (N=43 practices), or group practices (3+ providers; N=42 practices). We included all the identified group practices (N=42 practices) to allow evaluation of within-group practice variation. Furthermore, 58 solo or two-provider practices were randomly sampled to provide a total of 100 practices for inclusion (Figure 1). The sample size had sufficient power to detect differences in proportions of at least 25% between two groups for the outcome of recommending or requesting any diagnostic test, with power (beta) of 0.8 and alpha of 0.05. Using a standardized telephone script (Appendix A), three trained research assistants contacted the office staff of providers who practiced in one of the 100 selected practices by telephone between June 28th and July 15th, 2016. The assistants posed as a patient who was seeking to be seen for surgical evaluation for CTS and first verified that the physician/practice information was correct and that the provider performed CTR. The assistants asked whether any diagnostic tests were needed before an appointment with the provider and recorded the specific tests that were requested or recommended. Physicians who did not perform CTR (N=30) or who could not be reached by phone (N=55) were excluded from further analyses.

Study Variables

We extracted provider and practice characteristics from the online data sources and verified the characteristics during the phone calls to increase the completeness and accuracy of the recorded data. The provider characteristics recorded included ASSH membership and primary specialty, including plastic surgery, general surgery, orthopaedic surgery, and neurosurgery. The practice characteristics recorded included involvement in teaching and the number of providers in the practice. We categorized physicians working with residents or fellows as working in a teaching facility. The size of practice represented the number of surgeons in the same clinic who performed CTR. We recorded the reported requirements for pre-consultation diagnostic testing for each provider, including the need for EDS testing and/or alternative study (CT, MRI, ultrasound, X-ray). We categorized diagnostic testing requirements into the following three groups: test required, test recommended, and test not required. Diagnostic tests were defined as being required when the clinic requested that the caller have a test ordered by the surgeon or primary care provider prior to an initial evaluation. We defined the test as recommended if the clinic indicated that a test would be helpful prior to the initial appointment.

Statistical Analysis

We used descriptive statistics to summarize the prevalence of required pre-consultation tests. Among physicians performing CTR, we compared providers with no testing requirements to a combined group of providers who recommended or required pre-consultation studies. We used Fischer’s exact test for unadjusted statistical comparisons of the association between patient and provider attributes with pre-consultation testing. Independent (adjusted) associations were estimated using multiple logistic regression. Adjusted predicted probabilities of pre-consultation testing (average marginal effects) were calculated using the multiple logistic model.

RESULTS

Of 477 physicians identified by the search strategy, 121 physicians who did not perform hand surgery or did not practice in Michigan were excluded. Among the 219 physicians from 100 solo or group practices contacted, the phone questionnaire could be completed for 207 (95%) providers. Information could not be confirmed on the phone for 43 providers, 30 physicians did not perform CTR, and invalid phone numbers were present for 12 providers, all of whom were excluded from the final analysis. Among the 219 physicians contacted by phone, 61% (n=134) were confirmed to perform CTR (Figure 1).

Among the 134 providers who performed CTR, 57% (n=76) required and 9% (n=12) recommended a diagnostic test prior to the initial consultation. Only 34% (n=46) of providers did not require or recommend any diagnostic testing prior to the initial consultation. Two clinics asked the caller about symptoms before requesting a diagnostic test. Respondent characteristics based on pre-consultation diagnostic testing requirements are outlined in Table 1. Among the 134 physicians who performed CTR, 55% (n=28) of ASSH members and 72% (n=60) of non-ASSH members required or recommended diagnostic testing prior to the initial evaluation. In measuring practice differences by specialty, neurosurgeons were significantly more likely to require/recommend pre-consultation tests (92%) compared to orthopaedic and plastic surgeons (53% and 59%, respectively; P<0.05). No significant differences in pre-consultation testing recommendations were found by practice size or teaching status (Table 1). Among the non-solo provider practices, 50% (6/12 two-provider practices and 9/18 group practices) did not have any variation of diagnostic testing required between providers within the practice, meaning that all the surgeons in the practice had similar practices regarding pre-consultation testing recommendations.

Table 1.

Provider Characteristics Based On Requirement for Diagnostic Testing Before Carpal Tunnel Syndrome Consultation

Test Required/
Recommended
Test Not Required Total

ASSH Member
  Yes 28 (55%) 23 (45%) 51
  No 60 (72%) 23 (28%) 83

Specialty*
  General Surgery 2 (100%) 0 (0%) 2
  Neurosurgery 33 (92%) 3 (8%) 36
  Orthopaedic Surgery 34 (53%) 30 (47%) 64
  Plastic Surgery 19 (59%) 13 (41%) 32

Size of Practice
  1 provider 25 (65%) 13 (34%) 38
  2 providers 16 (67%) 8 (33%) 24
  3+ providers 47 (65%) 25 (34%) 72

Teaching Facility
  Yes 47 (65%) 25 (35%) 72
  No 41 (66%) 21 (34%) 62

Total 88 46 134
*

P-value < 0.05 in Fisher's Exact Test

The specific pre-consultation diagnostic tests required/recommended by surgeons are outlined in Table 2. Of the 88 physicians who required/recommended testing, 85% (n=75) requested EDS, 22% (n=19) requested an MRI, 13% (n=11) requested a CT scan, and 9% (n=8) requested an X-ray. Patients were asked to have multiple studies by 19 (22%) of the 88 surgeons who requested/recommended testing. Furthermore, CT, MRI, or both were requested by nearly a quarter of providers who requested or recommended testing (Table 2). In the multivariable analysis, ASSH membership, size of practice and teaching facility status did not have a significant relationship with the requirement for pre-consultation testing. We found no significant difference in plastic surgeons and orthopaedic surgeons in pre-consultation testing practices in the adjusted model. The neurosurgeon specialty was the only significant independent predictor associated with testing requirements (adjusted probability of 93% [95% CI: 64% – 99%] of required/recommended pre-consultation testing, Table 3).

Table 2.

Combinations of Pre-consultation Diagnostic Tests Required/Recommended for Carpal Tunnel Syndrome

ASSH Members Non-ASSH Members Total Percent

EDS only 25 42 67 76%
MRI + CT 0 6 6 7%
EDS + MRI 1 2 3 3%
MRI + X-ray 0 3 3 3%
EDS + MRI + CT 1 1 2 2%
EDS + MRI + X-ray 1 1 2 2%
MRI + CT + X-ray 0 2 2 2%
MRI only 0 1 1 1%
X-ray only 0 1 1 1%
EDS + CT 0 1 1 1%

Total 28 60 88 100%

Table 3.

Multivariable Logistic Regression of Pre-Consultation Test Requirement (n=132)*

Adjusted OR (95% CI) P Predicted Probability

ASSH Member
  Yes 0.82 (0.29 – 2.28) 0.71 0.70 (0.45 – 0.87)
  No Reference 0.74 (0.56 – 0.86)

Specialty
  Neurosurgery 14.08 (2.86 – 69.38) <0.05 0.93 (0.64 – 0.99)
  Plastic Surgery 1.37 (0.40 – 4.76) 0.64 0.56 (0.21 – 0.86)
  Orthopaedic Surgery Reference 0.48 (0.26 – 0.72)

Size of Practice
  1 provider 0.34 (0.09 – 1.34) 0.13 0.60 (0.35 – 0.81)
  2 providers 0.56 (0.13 – 2.48) 0.45 0.71 (0.40 – 0.90)
  3+ providers Reference 0.81 (0.63 – 0.92)

Teaching Facility
  Yes 0.89 (0.29 – 2.77) 0.84 0.70 (0.50 – 0.85)
  No Reference 0.73 (0.51 – 0.87)
*

Multivariable logistic regression modeled outcome of requiring/recommending pre-consultation test prior to consultation.

DISCUSSION

Although the 2016 AAOS CPG suggests that EDS and/or diagnostic questionnaires could be used to aid the diagnosis of CTS and no longer recommends routine use of EDS for patients undergoing CTR, the findings of this study suggest that the majority of surgeons who treat CTS in the State of Michigan request EDS before evaluation, rather than reserving the test for cases where the diagnosis is unclear. The requirement for pre-consultation testing was common regardless of ASSH member status, specialty, practice size, and teaching facility status. Furthermore, studies that are not recommended by the current and previous CPG for diagnosis of CTS (CT, MRI, or both) were requested or recommended by nearly a quarter of surgeons who requested tests.

Our findings support previous research suggesting that a substantial number of physicians routinely obtain EDS for patients undergoing CTR.1, 14, 15 Munns et al1 found that 72% of hand surgeons routinely obtained preoperative EDS in a 2015 survey of 716 ASSH members. A 2014 survey of 705 ASSH members also found that 55% of respondents believed EDS was usually necessary to provide sufficient justification to indicate a surgery in addition to a supporting history and physician exam. However, 64% of surgeons surveyed indicated that they were more likely to order EDS based on the CPG recommendations at the time, and most were concerned about medicolegal consequences created by the guidelines.14 Similarly, Shin et al15 found that 81% of respondents routinely ordered EDS prior to elective surgery for CTS in a 2012 survey of 123 members of the American Association for Hand Surgery. While these studies described high rates of EDS use for patients prior to surgery, no previous study examined whether providers ordered EDS prior to or after an initial consultation. The current study highlights the prevalent practice of indiscriminant EDS use among the surgeons in the study sample, rather than reserving the test to aid diagnosis for clinically uncertain cases.

Although the previous CPG suggested that EDS should be obtained if surgical management was being considered,10 we hypothesize that providers apply EDS more broadly to improve efficiency of establishing a treatment recommendation at the time of the initial evaluation. However, no test has been shown to be superior to clinical evaluation for diagnosis of CTS. For example, Graham6 found that EDS did not change the probability of CTS diagnosis for most patients who were diagnosed with CTS based on history and physician examination alone. Of 142 patients referred for upper extremity EDS evaluation, 73% had a pretest probability of CTS diagnosis greater than 0.8 as estimated by the CTS-6 diagnostic questionnaire. Among these patients with a high pretest probability of CTS diagnosis, the average change in probability of CTS diagnosis was 0.02. In addition, EDS lowered the post-test probability of CTS diagnosis in patients who already had a low (<0.5) pretest probability of diagnosis. In other words, EDS testing is unlikely to impact the probability of CTS diagnosis in patients with a high probability of diagnosis based on history and physical exam criteria.

A latent class analysis by Fowler2 showed that EDS had similar sensitivity (91%) compared to ultrasound (US) and the CTS-6 diagnostic questionnaire (91% and 95%, respectively), whereas EDS had the lowest specificity (83%) compared to US and CTS-6 (94%, and 91%, respectively). Similarly, a study comparing the diagnostic accuracy of EDS, US, CT and MRI in CTS, compared to clinical diagnosis as a reference standard, showed that these four tests had similar accuracy for the diagnosis of CTS.16 The existing evidence does not support using either EDS or imaging tests over history and physical exam for CTS diagnosis. Furthermore, EDS prior to CTR was associated with prolonged time to surgery, additional out of pocket costs, and greater total costs in a national study.8

This study had several limitations. The study sample included physicians limited to the State of Michigan and did not directly evaluate national practices. However, given that the overall rates of testing used prior to surgery was similar in our studies to other national surveys, we expect that our findings reflect national practices of using EDS and other diagnostic tests prior to CTS evaluation. The sample size was likely underpowered to detect small differences in provider and practice characteristics, but expanding the sample size would likely show a similarly common practice of requesting pre-consultation diagnostic tests. In addition, the study design prevented us from evaluating the impact of insurance type on the requirement for pre-consultation diagnostic tests. Furthermore, we do not know the reason that patients were asked to obtain diagnostic tests prior to a consultation and whether providers would offer surgery without prior testing. Some providers may advocate for routine EDS to measure severity of CTS or to predict improvement after surgical intervention, even if the test may not influence treatment recommendations. Others may routinely request diagnostic studies before evaluating a patient with CTS to establish a treatment plan at the time of the consultation and avoid the need for return visits with the surgeon. However, many patients likely receive diagnostic tests that have no bearing on the treatment plan. Although the study was conducted shortly after the new AAOS CPG were published, wide dissemination of new guidelines takes several months. It is possible that some surgeons in this study who requested pre-consultation EDS were influenced by the previous AAOS CPG that recommended EDS testing for patients being considered for surgery. The impact of diagnostic testing self-referral was outside the scope of this study, but also may influence provider practices given potential financial incentives. Lastly, it is possible that clerical staff could ask a patient to obtain a test even if the surgeon personally would not order a test. This may be more plausible in a group practice where individual surgeon practices differ. However, it is worth noting that the majority of office representatives ask patients to obtain tests before scheduling an appointment. It is unknown whether the support staff might be gatekeepers and inappropriately ask for tests in the interest of perceived office efficiency. Regardless of whether the office staff represent the true preferences of the surgeon, the requests that office staff make of patients calling for an appointment will have a direct impact on the tests that patients obtain before an appointment.

Despite these limitations, this study shows the prevalent practice of routinely requesting EDS and other diagnostic tests prior to CTS consultation. There is a need to highlight the change in the AAOS CPG and the responsibility of providers to advocate for more judicious EDS and diagnostic testing use. Given the cost and inconvenience of diagnostic tests, patients should be included in the decision to obtain tests if they are used for purposes other than informing treatment decisions. It is likely that a transition to bundled, episode-based payment for CTR will include any diagnostic testing performed. Greater clarity in the appropriateness of indications for EDS and other preoperative tests will help both primary care providers and surgeons to order tests that patients need, but not those from which patients are not likely to benefit. In the quest for high value care, providers must consider whether the benefit of the test likely outweighs the costs, inconvenience, and potential for treatment delay.

Clinical Relevance.

In the quest for high value care, providers must consider whether the benefit of diagnostic tests for carpal tunnel syndrome likely outweighs the costs, inconvenience, and potential for treatment delay.

Acknowledgments

Support for this study was provided in part by the grants from the National Institute of Arthritis and Musculoskeletal and Skin Diseases of the National Institutes of Health under Award Number 2 K24-AR053120-06, a Midcareer Investigator Award in Patient-Oriented Research (to Dr. Kevin C. Chung). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health, the University of Michigan, or the Department of Veterans Affairs.

Appendix

Appendix A.

Appendix A

Footnotes

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Disclosure: None of the authors have any financial interest or conflicts of interest to declare in relation to the content of this article.

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