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1.
J Cutan Pathol ; 48(6): 750-757, 2021 Jun.
Article in English | MEDLINE | ID: mdl-33350497

ABSTRACT

BACKGROUND: Data regarding ethical/professional issues affecting dermatopathologists are lacking despite their importance in establishing policy priorities and educational content for dermatopathology. METHODS: A 14-item cross-sectional survey about ethical/professional issues in dermatopathology was distributed over e-mail to members of the American Society of Dermatopathology from June to September 2019. RESULTS: Two hundred sixteen surveys were completed, with a response rate of 15.3%. Respondents ranked appropriate and fair utilization of healthcare resources (n = 83 or 38.6%) as the most often encountered ethical/professional issue. Conflict of interest was ranked as the most urgent or important ethical/professional issue (n = 83 or 39.3%). One hundred thirty-three (61.6%) respondents felt "somewhat" or "not at all" well equipped to handle ethical dilemmas in practice and 47 (22.8%) respondents identified a major or extreme burden (eg, have considered resigning/retiring) due to ethical challenges. CONCLUSIONS: Areas of priority in ethics and professionalism issues can guide future policy and educational content in dermatopathology.


Subject(s)
Dermatology/organization & administration , Pathology/organization & administration , Professionalism/ethics , Societies, Medical/trends , Conflict of Interest , Cross-Sectional Studies , Female , Humans , Male , Patient Acceptance of Health Care/statistics & numerical data , Resource Allocation/ethics , United States
2.
J Clin Neuromuscul Dis ; 21(2): 69-76, 2019 Dec.
Article in English | MEDLINE | ID: mdl-31743249

ABSTRACT

OBJECTIVE: To determine the feasibility of examining intraepidermal nerve fiber density (IENFD) in postmortem skin. METHODS: From 12 subjects, 3-mm skin punch biopsies were collected 1-4 days postmortem from the proximal leg and distal leg, with a mean (range) interval from the death of 37 (15-91) hours. Causes of death varied broadly, including hepatocellular carcinoma, chronic lymphocytic leukemia, generalized atherosclerosis, progressive supranuclear palsy, Parkinson disease, emphysema, and obesity. The mean (range) number of sections evaluated from each biopsy was 5.08 (2-6) from the proximal leg and 5.92 (5-6) from the distal leg. Sections were stained with PGP 9.5 for blinded counting using bright field microscopy. Qualitative and quantitative assessment of feasibility included a comparison of fiber staining with that in healthy subjects and mean IENFD in postmortem samples. Interobserver reliability was assessed among 3 blinded raters by calculating intraclass correlation coefficients and percentage variability of IENFD in at least 4 sections from biopsies in 5 healthy subjects. RESULTS: Intraobserver and interobserver correlation coefficients of blinded IENFD counts undertaken by 4 authors were consistently >0.80, and the coefficient of variation was ≤10%. The quality of staining in postmortem samples was comparable with that in healthy subjects and was not substantially affected by time from death to specimen collection of up to nearly 4 days. Mean (range) IENFD from postmortem samples in the proximal and distal leg was 2.73 (0-7.65) and 1.93 (0-4.91) fibers/mm of skin, respectively. Two of 3 patients who had received chemotherapy during life showed a nearly complete absence of intraepidermal nerve fibers. CONCLUSIONS: IENFD measurement in postmortem skin is feasible and may be used to study the epidemiology of SFN.


Subject(s)
Epidermis/innervation , Nerve Fibers/ultrastructure , Skin/innervation , Aged , Aged, 80 and over , Biopsy , Cause of Death , Cell Count , Female , Humans , Immunohistochemistry , Male , Middle Aged , Observer Variation , Postmortem Changes , Reproducibility of Results , Skin/cytology , Tissue Fixation
4.
Ann Neurol ; 54(6): 824-8, 2003 Dec.
Article in English | MEDLINE | ID: mdl-14681893

ABSTRACT

We describe a family of Slovenian descent with progressive ataxia, corticospinal signs, axonal sensorimotor neuropathy, and disruption of visual fixation by saccadic intrusions. Chromosome mapping indicated a mutation on 1p36, and this recessive disorder has been designated spinocerebellar ataxia with saccadic intrusions. Affected patients showed overshooting horizontal saccades, macrosaccadic oscillations, and increased velocity of larger saccades; other eye movements were normal. Slowed conduction in axons that are selectively vulnerable to the molecular defect could explain both the sensorimotor neuropathy and the saccadic disorder, which would be caused by delayed feedback control because of slow conduction in cerebellar parallel fibers.


Subject(s)
Genes, Recessive , Ocular Motility Disorders/genetics , Spinocerebellar Degenerations/genetics , Adult , Chromosomes, Human, Pair 1/genetics , Confidence Intervals , Female , Humans , Male , Middle Aged , Ocular Motility Disorders/complications , Ocular Motility Disorders/pathology , Spinocerebellar Degenerations/complications , Spinocerebellar Degenerations/pathology
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