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Karnes, Jeannine L.

Mayo Clinic

Mayo Clinic

Citations 9

A 4, 2, and 1 stepping algorithm for quick and accurate estimation of cutaneous sensation threshold
Dyck, P. James B. , O’Brien, Peter C. , Kosanke, Jon L., Gillen, D. A., Karnes, Jeannine L.

Neurology | May 13, 2012 | Volume: 43 | Issue: 8 | Pages: 1508-1508

10.1212/wnl.43.8.1508 Get It

Cool, warm, and heat‐pain detection thresholds
Dyck, Peter James , Zimmerman, I. R., Gillen, D. A., Johnson, David M. , Karnes, Jeannine L., O’Brien, Peter C.

Neurology | May 13, 2012 | Volume: 43 | Issue: 8 | Pages: 1500-1500

10.1212/wnl.43.8.1500 Get It

Comparison of algorithms of testing for use in automated evaluation of sensation
Dyck, P. James B. , Karnes, Jeannine L., Gillen, D. A., O’Brien, Peter C. , Zimmerman, I. R., Johnson, David M.

Neurology | May 13, 2012 | Volume: 40 | Issue: 10 | Pages: 1607-1607

10.1212/wnl.40.10.1607 Get It

Longitudinal study of neuropathic deficits and nerve conduction abnormalities in hereditary motor and sensory neuropathy type 1
Dyck, P. James B. , Karnes, Jeannine L., Lambert, Edward H.

Neurology | May 13, 2012 | Volume: 39 | Issue: 10 | Pages: 1302-1302

10.1212/wnl.39.10.1302 Get It

Neuropathy Symptom Profile in health, motor neuron disease, diabetic neuropathy, and amyloidosis
Dyck, P. James B. , Karnes, Jeannine L., O’Brien, Peter C. , Swanson, C

Neurology | May 13, 2012 | Volume: 36 | Issue: 10 | Pages: 1300-1300

10.1212/wnl.36.10.1300 Get It

Motor neuron disease (ALS)
Mulder, Donald W., Bushek, Wilfred, Spring, Eileen M, Karnes, Jeannine L., Dyck, Peter James

Neurology | May 13, 2012 | Volume: 33 | Issue: 12 | Pages: 1625-1625

10.1212/wnl.33.12.1625 Get It

The prevalence by staged severity of various types of diabetic neuropathy, retinopathy, and nephropathy in a population‐based cohort
Dyck, P. James B. , Kratz, K. M., Karnes, Jeannine L., Litchy, William J. , Pach, John M., Wilson, Derrick, OʼBrien, P. C., Melton, L. Joseph, Klein, Ronald

Neurology | May 13, 2012 | Volume: 43 | Issue: 4 | Pages: 817-817

10.1212/wnl.43.4.817 Get It

Vibratory and Cooling Detection Thresholds Compared With Other Tests in Diagnosing and Staging Diabetic Neuropathy
Dyck, P. James B. , Bushek, Wilfred, Spring, Eileen M, Karnes, Jeannine L., Litchy, William J. , Service, F John, O'Brien, Peter A. , Service, F John

Diabetes Care | March 5, 2007 | Volume: 10 | Issue: 4 | Pages: 432-440

10.2337/diacare.10.4.432 Get It

Increasingly more tests are being used to detect and characterize diabetic polyneuropathy, but their value in setting minimal criteria for the diagnosis of neuropathy and for staging severity remains inadequately studied. In 180 diabetics, we compared the percentage of patients with test abnormalities and associations among test results, evaluating neuropathic symptoms [neuropathy symptom score (NSS) and neuropathy scale of neuropathy symptom profile (NNSP)], deficits [neurologic disability score (NDS) and vibratory (VDT) and cooling (CDT) detection thresholds], or nerve dysfunction [nerve conduction (NC)]. The percentage of patients that were abnormal varied considerably depending on criteria for abnormality and the tests used. Abnormality (≥ 3 SD of 1 or more parameters) of NC of one or more of four nerves occurred in 80%, of two or more in 69%, of three or more in 46%, and of four in 21%. Similarly, for other tests, the rate of abnormality decreased with use of increasingly stringent criteria. Setting the criteria for abnormal NC at abnormality of two or more nerves, NSS at ≥ 1, NDS at > 6, NNSP at ≥ 97.5th percentile, and at ≥ 95th percentile for the other tests, NC was abnormal in 69%, NSS in 54%, NDS in 48%, NNSP in 47%, VDT in 44%, and CDT in 35%. Abnormality of any two or more of the six tests evaluated occurred in 64% of patients. We estimated that at least 16% of patients without abnormal NC (<2 abnormal nerves) had other findings indicative of neuropathy. By regression analysis, results of one test were in almost all cases associated with those of another test, but the association was not close enough to be predictive. Therefore, although NC provides objective and repeatable results, symptoms and deficits must be measured independently. Assuming no differences between groups of patients, the standardized and validated test (NNSP, VDT, or CDT) should provide the same results at different medical centers. By contrast, the results of NSS or NDS tests, with less standardized approaches and based on the judgment of physicians, might not provide the same results at different medical centers. Tests such as the ones described here may be used to define minimal criteria for the diagnosis of polyneuropathy and for staging its severity.