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1.
Arch Phys Med Rehabil ; 81(3): 258-64, 2000 Mar.
Article in English | MEDLINE | ID: mdl-10724067

ABSTRACT

OBJECTIVES: To determine the interexaminer reliability of palpation of three characteristics of trigger points (taut band, local twitch response, and referred pain) in patients with subacute low back pain, to determine whether training in palpation would improve reliability, and whether there was a difference between the physiatric and chiropractic physicians. DESIGN: Reliability study. SETTING: Whittier Health Campus, Los Angeles College of Chiropractic. PARTICIPANTS: Twenty-six nonsymptomatic individuals and 26 individuals with subacute low back pain. INTERVENTION: Twenty muscles per individual were first palpated by an expert and then randomly by four physician examiners. MAIN OUTCOME MEASURES: Palpation findings. RESULTS: Kappa scores for palpation of taut bands, local twitch responses, and referred pain were .215, .123, and .342, respectively, between the expert and the trained examiners, and .050, .118, and .326, respectively, between the expert and the untrained examiners. Kappa scores for agreement for palpation of taut bands, twitch responses, and referred pain were .108, -.001, and .435, respectively, among the nonexpert, trained examiners, and -.019, .022, and .320, respectively, among the nonexpert, untrained examiners. CONCLUSIONS: Among nonexpert physicians, physiatric or chiropractic, trigger point palpation is not reliable for detecting taut band and local twitch response, and only marginally reliable for referred pain after training.


Subject(s)
Muscle, Skeletal/physiopathology , Myofascial Pain Syndromes/diagnosis , Palpation , Adult , Female , Humans , Low Back Pain/etiology , Low Back Pain/physiopathology , Male , Middle Aged , Reproducibility of Results
2.
Qual Assur ; 4(4): 336-9, 1995 Dec.
Article in English | MEDLINE | ID: mdl-8890363

ABSTRACT

A successful computer validation program requires a solid foundation of policies, guidelines, and procedures. An unstructured approach to validation may yield adequate results for a specific computerized system, but it will not sustain ongoing, consistent computer validation activities over time. The evolution of a strong computer validation program starts with an awareness of the need for such a program and builds on that established base. One approach is a step-by-step method in which each new step builds on the results of one or more of the previous steps. However, the order of events is not as important as the ultimate completion of all the building blocks. A strong computer validation program requires a companywide policy and an administrator who provides oversight and chairs the computer validation committee. The committee should be established to provide departmental leadership and to develop company guidelines for computer validation. Committee members will also create system inventories and classify and prioritize those systems in terms of the need for validation. Departmental standard operating procedures must be developed to provide standardized methods for routine validation activities. Finally the quality assurance unit should have procedures in place that provide for its involvement in the computer validation process.


Subject(s)
Computer Systems/standards , Laboratories/standards , Management Audit/methods , Software Validation , Humans , Industry , Institutional Management Teams , Laboratories/organization & administration
3.
Biopolymers ; 28(6): 1043-58, 1989 Jun.
Article in English | MEDLINE | ID: mdl-2525053

ABSTRACT

The velocity and orientation of T4 and lambda DNA have been measured for the first 20 s during pulsed-field gel electrophoresis in order to clarify the DNA motions that occur. For a square pulse with field strength E = 10 V/cm, the velocity of lambda DNA increases gradually to 10.5 microns/s in 1.0 s, declines to 8.6 microns/s, and then rises to a plateau value of 9.3 microns/s after 4 s. T4 DNA behaves similarly, but more slowly. Parallel measurements of fluorescence-detected linear dichroism show that the DNA becomes substantially aligned with its chain axis parallel to the electrophoretic field E after the pulse is applied. The alignment also shows an overshoot, an undershoot, and a plateau comparable to those seen for velocity. When the field strength increases, both the velocity and the alignment reach their peaks more quickly. For all field strengths and both molecular weights, the velocity peak occurs when the molecular center of mass has moved 0.3 to 0.5 L, where L is the chain contour length. A qualitative model is provided.


Subject(s)
DNA, Viral/isolation & purification , Bacteriophage lambda , Electrophoresis, Agar Gel/methods , Escherichia coli , T-Phages
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