Downbeat Nystagmus Associated with Intravenous Patient-Controlled Administration of Morphine

2000 ◽  
Vol 91 (3) ◽  
pp. 691-692 ◽  
Author(s):  
Robert D. Henderson ◽  
Eelco F. M. Wijdicks
Keyword(s):  
2004 ◽  
Vol 35 (03) ◽  
Author(s):  
R Kalla ◽  
S Glasauer ◽  
M Strupp ◽  
U Büttner ◽  
T Brandt
Keyword(s):  

2005 ◽  
Vol 32 (S 4) ◽  
Author(s):  
P Schlindwein ◽  
C Best ◽  
S Bense ◽  
H.G Buchholz ◽  
T Siessmeier ◽  
...  

2006 ◽  
Vol 33 (S 1) ◽  
Author(s):  
A. Sprenger ◽  
H. Rambold ◽  
T. Sander ◽  
S. Marti ◽  
K. Weber ◽  
...  
Keyword(s):  

2021 ◽  
pp. 464-469
Author(s):  
Dominik Péus ◽  
Dominik Straumann ◽  
Alexander Huber ◽  
Christopher J. Bockisch ◽  
Vincent Wettstein

Downbeat nystagmus (DBN) observed in head-hanging positions, may be of central or peripheral origin. Central DBN in head-hanging positions is mostly due to a disorder of the vestibulo-cerebellum, whereas peripheral DBN is usually attributed to canalolithiasis of an anterior semicircular canal. Here, we describe an atypical case of a patient who, after head trauma, experienced severe and stereotypic vertigo attacks after being placed in various head-hanging positions. Vertigo lasted 10–15 s and was always associated with a robust DBN. The provocation of transient vertigo and DBN, which both showed no decrease upon repetition of maneuvers, depended on the yaw orientation relative to the trunk and the angle of backward pitch. On a motorized, multi-axis turntable, we identified the two-dimensional Helmholtz coordinates of head positions at which vertigo and DBN occurred (<i>y</i>-axis: horizontal, space-fixed; <i>z</i>-axis: vertical, and head-fixed; <i>x</i>-axis: torsional, head-fixed, and unchanged). This two-dimensional area of DBN-associated head positions did not change when whole-body rotations took different paths (e.g., by forwarding pitch) or were executed with different velocities. Moreover, the intensity of DBN was also independent of whole-body rotation paths and velocities. So far, therapeutic approaches with repeated liberation maneuvers and cranial vibrations were not successful. We speculate that vertigo and DBN in this patient are due to macular damage, possibly an unstable otolithic membrane that, in specific orientations relative to gravity, slips into a position causing paroxysmal stimulation or inhibition of macular hair cells.


1991 ◽  
Vol 1991 (Supplement42) ◽  
pp. 56-66 ◽  
Author(s):  
Satoshi Yoshio ◽  
Koji Tokumasu ◽  
Akito Fujino ◽  
Hideaki Naganuma ◽  
Kentaro Nitta ◽  
...  
Keyword(s):  

2013 ◽  
Vol 260 (8) ◽  
pp. 1992-1996 ◽  
Author(s):  
Jens Claassen ◽  
Katharina Feil ◽  
Stanislav Bardins ◽  
Julian Teufel ◽  
Rainer Spiegel ◽  
...  

2014 ◽  
Vol 343 (1-2) ◽  
pp. 187-191 ◽  
Author(s):  
Seo Young Choi ◽  
Seong-Ho Park ◽  
Hyo-Jung Kim ◽  
Ji-Soo Kim
Keyword(s):  

1991 ◽  
Vol 54 (4) ◽  
pp. 367-369 ◽  
Author(s):  
M Rousseaux ◽  
T Dupard ◽  
F Lesoin ◽  
P Barbaste ◽  
J C Hache
Keyword(s):  

2017 ◽  
Vol 264 (9) ◽  
pp. 2024-2026 ◽  
Author(s):  
Sun-Uk Lee ◽  
Hyo-Jung Kim ◽  
Eek-Sung Lee ◽  
Jeong-Yoon Choi ◽  
Ji-Soo Kim

2019 ◽  
Vol 2019 ◽  
pp. 1-3
Author(s):  
Akihide Ichimura ◽  
Shigeto Itani

Here, we report a patient with persistent positional upbeat nystagmus in a straight supine position with no evident abnormal central nervous system findings. A 43-year-old woman with rotatory positional vertigo and nausea visited our clinic 7 days after the onset. Initially, we observed persistent upbeat nystagmus in straight supine position with a latency of 2 s during the supine head roll test. However, an upbeat nystagmus disappeared on turning from straight to the left ear-down supine position, and while turning from the left to right ear-down position, an induced slight torsional nystagmus towards the right for >22 s was observed. In the Dix–Hallpike test, the left head-hanging position provoked torsional nystagmus towards the right for 50 s. In prone seated position, downbeat nystagmus with torsional component towards the left was observed for 45 s. Neurological examination and brain computed tomography revealed no abnormal findings. We speculated that persistent positional upbeat nystagmus in this patient was the result of canalolithiasis of benign paroxysmal positional vertigo of bilateral posterior semicircular canals.


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