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"Humans"

Original Article

Effect of Fascia Penetration in Lateral Femoral Cutaneous Nerve Conduction
Mi-Jeong Yoon, Hye Min Park, Sun Jae Won
Ann Rehabil Med 2020;44(6):459-467.   Published online December 31, 2020
DOI: https://doi.org/10.5535/arm.20022
Objective
To evaluate the effect of fascia penetration and develop a new technique for lateral femoral cutaneous nerve (LFCN) conduction studies based on the fascia penetration point (PP) identified using ultrasound.
Methods
The fascia PP of the LFCN was localized in 20 healthy subjects, and sensory nerve action potentials (SNAPs) were obtained at four different stimulation points—2 cm proximal to the PP (2PPP), PP, 2 cm distal to the PP (2DPP), and 4 cm distal to the PP (4DPP). We compared the stimulation technique based on the fascia penetration point (STBFP) with the conventional technique.
Results
The SNAP amplitude of the LFCN was significantly higher when stimulation was performed at the PP and 2DPP than at other stimulation points. Using the STBFP, SNAP responses were elicited in 38 of 40 legs, whereas they were elicited in 32 of 40 legs using the conventional technique (p=0.041). STBFP had a comparable SNAP amplitude and slightly delayed negative peak latency compared to the conventional technique. In terms of the time required, the time spent on STBFP showed a more consistent distribution than the time spent on the conventional technique (two-sample Kolmogorov–Smirnov test, p<0.05).
Conclusion
SNAP of the LFCN significantly changed near the fascia PP, and stimulation at PP and at 2DPP provided high amplitudes. STBFP can help increase the response rate and ensure stable and consistent procedure time of the LFCN conduction study.

Citations

Citations to this article as recorded by  
  • Meralgia Paresthetica as a Result of Surgery With an Emphasis on Harvesting Iliac Bone Grafts: A Review
    Sonia N. Singh, Ruby R. Taylor, Chaimae Oualid, Mutaz B. Habal, Seth R. Thaller
    Journal of Craniofacial Surgery.2024; 35(7): 1964.     CrossRef
  • Dorsal ulnar cutaneous nerve conduction study based on nerve ultrasound
    Eunjin Park, So-youn Chang, Hye Jung Park, Ho-geon Namgung, Sun Jae Won
    Scientific Reports.2024;[Epub]     CrossRef
  • 7,953 View
  • 130 Download
  • 2 Web of Science
  • 2 Crossref
Case Report
Novel Influenza A (H1N1)-Associated Acute Necrotizing Encephalopathy: A Case Report
Ki Jung Kim, Eun Sook Park, Hyun Jung Chang, Miri Suh, Dong-Wook Rha
Ann Rehabil Med 2013;37(2):286-290.   Published online April 30, 2013
DOI: https://doi.org/10.5535/arm.2013.37.2.286

Several cases of acute necrotizing encephalopathy (ANE) with influenza A (H1N1) have been reported to date. The prognosis of ANE associated with H1N1 is variable; some cases resulted in severe neurologic complication, whereas other cases were fatal. Reports mostly focused on the diagnosis of ANE with H1N1 infection, rather than functional recovery. We report a case of ANE with H1N1 infection in a 4-year-old Korean girl who rapidly developed fever, seizure, and altered mentality, as well as had neurologic sequelae of ataxia, intentional tremor, strabismus, and dysarthria. Brain magnetic resonance imaging showed lesions in the bilateral thalami, pons, and left basal ganglia. To our knowledge, this is the first report of ANE caused by H1N1 infection and its long-term functional recovery in Korea.

Citations

Citations to this article as recorded by  
  • Acute Encephalitis Syndrome with an Unusual Diagnosis
    Mili Thomas, Kamala Swarnam, Gopika Sekhar Remadevi, A Marthanda Pillai
    Journal of Tropical Pediatrics.2020; 66(2): 228.     CrossRef
  • Multi-parametric magnetic resonance imaging in acute necrotizing encephalopathy of children: validity and prognostic value
    Rania S. M. Ibrahim, W. Elzayat, H. M. Seif, H. A. El-Kiki, S. Emad-Eldin, M. Shahin, S. M. Kamel, R. Osama, R. Zakaryia, M. Fatouh, Rania H. Hachem
    Egyptian Journal of Radiology and Nuclear Medicine.2020;[Epub]     CrossRef
  • Acute necrotizing encephalopathy of childhood. Diagnostic and treatment challenges in COVID-19 pandemic
    V. E. Kitaeva, A. S. Kotov
    Almanac of Clinical Medicine.2020; 48: 32.     CrossRef
  • MR imaging of adult acute infectious encephalitis
    A. Bertrand, D. Leclercq, L. Martinez-Almoyna, N. Girard, J.-P. Stahl, T. De-Broucker
    Médecine et Maladies Infectieuses.2017; 47(3): 195.     CrossRef
  • Acute necrotising encephalopathy of childhood: an uncommon cause of childhood encephalopathy with recognisable clinical and radiological features and genetic predisposition
    Nicholas Schindler, Gautam Ambegaonkar
    Archives of Disease in Childhood.2017; 102(3): 292.     CrossRef
  • Decreased Na+ influx lowers hippocampal neuronal excitability in a mouse model of neonatal influenza infection
    Hoyong Park, Ji Eun Yu, Sungmin Kim, Sang-Soep Nahm, ChiHye Chung
    Scientific Reports.2015;[Epub]     CrossRef
  • Acute Necrotizing Encephalopathy: An Underrecognized Clinicoradiologic Disorder
    Xiujuan Wu, Wei Wu, Wei Pan, Limin Wu, Kangding Liu, Hong-Liang Zhang, Kazuhiko Kibayashi
    Mediators of Inflammation.2015;[Epub]     CrossRef
  • Vision Loss Caused by Retinal and Lateral Geniculate Nucleus Infarction in H1N1 Influenza
    Dane A. Breker, Andrew W. Stacey, Ashok Srinivasan, Lulu L. C. D. Bursztyn, Jonathan D. Trobe, Mark W. Johnson
    Journal of Neuro-Ophthalmology.2015; 35(3): 265.     CrossRef
  • Severe post-influenza (H1N1) encephalitis involving pulvinar nuclei in an adult patient
    José Tomás, Maria Carmo Macário, Elsa Gaspar, Isabel Santana
    BMJ Case Reports.2015; 2015: bcr2015212667.     CrossRef
  • Neuroinvasion of the Highly Pathogenic Influenza Virus H7N1 Is Caused by Disruption of the Blood Brain Barrier in an Avian Model
    Aida J. Chaves, Júlia Vergara-Alert, Núria Busquets, Rosa Valle, Raquel Rivas, Antonio Ramis, Ayub Darji, Natàlia Majó, Robyn Klein
    PLoS ONE.2014; 9(12): e115138.     CrossRef
  • 5,835 View
  • 75 Download
  • 10 Crossref
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