Alessandro Mirra

Dr. Alessandro Mirra

University of Bern, Bern, Switzerland
orcid

Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 February 2019 in Physiology & Behavior
Verified
Journal Article
Closed access
DCDaniela Casoni
Daniela Casoni
AMAlessandro Mirra
Alessandro Mirra
MSMarc Suter
Marc Suter
AGA. Gutzwiller
A. Gutzwiller
CSC. Spadavecchia
C. Spadavecchia

1 February 2018 in Physiology & Behavior
Verified
Journal Article
Closed access
AMAlessandro Mirra
Alessandro Mirra
CSClaudia Spadavecchia
Claudia Spadavecchia
RBRupert Bruckmaier
Rupert Bruckmaier
AGAndreas Gutzwiller
Andreas Gutzwiller
DCDaniela Casoni
Daniela Casoni

1 July 2017 in Veterinary Anaesthesia and Analgesia
Verified
Journal Article
Closed access
FMFABIANA MICIELI
FABIANA MICIELI
BSBruna Santangelo
Bruna Santangelo
FRFabiana Reynaud
Fabiana Reynaud
AMAlessandro Mirra
Alessandro Mirra
GNGiusy Napoleone
Giusy Napoleone
GVGiancarlo Vesce
Giancarlo Vesce

22 February 2018 in Veterinary Anaesthesia and Analgesia
Verified
Journal Article
Closed access
PDF file
AMAlessandro Mirra
Alessandro Mirra
ARAlois von Rotz
Alois von Rotz
MSMarta Schmidhalter
Marta Schmidhalter
LMLara Moser
Lara Moser
DCDaniela Casoni
Daniela Casoni
CSClaudia Spadavecchia
Claudia Spadavecchia

20 January 2022 in Journal of Clinical Monitoring and Computing
Verified
Journal Article
Open access
PDF file
AMAlessandro Mirra
Alessandro Mirra
DCDaniela Casoni
Daniela Casoni
PBP. Barge
P. Barge
DHD. Hight
D. Hight
OLOlivier Levionnois
Olivier Levionnois
CSClaudia Spadavecchia
Claudia Spadavecchia
To investigate the usability of the SedLine® monitor in anaesthetized pigs. Five juvenile healthy pigs underwent balanced isoflurane-based general anaesthesia for surgical placement of a subcutaneous jugular venous port. The SedLine® was applied to continuously monitor electroencephalographic (EEG) activity and its modulation during anaesthesia. Computer tomography and magnetic resonance were performed to investigate the relationship between electrodes’ positioning and anatomical structures. The pediatric SedLine® EEG-sensor could be easily applied and SedLine®-generated variables collected. An EEG Density Spectral Array (DS) was displayed over the whole procedure. During surgery, the EEG signal was dominated by elevated power in the delta range (0.5–4 Hz), with an underlying broadband signal (where power decreased with increasing frequency). The emergence period was marked by a decrease in delta power, and a more evenly distributed power over the 4–40 Hz frequency range. From incision to end of surgery, mean SedLine®-generated values (± standard deviation) were overall stable [23.0 (± 2.8) Patient State Index (PSI), 1.0% (± 3.8%) Suppression Ratio (SR), 8.8 Hz (± 2.5 Hz) Spectral Edge Frequency 95% (SEF) left, 7.7 Hz (± 2.4 Hz) SEF right], quickly changing during emergence [75.3 (± 11.1) PSI, 0.0 (± 0.0) SR, 12.5 (± 6.6) SEF left 10.4 (± 6.6) SEF right]. Based on the imaging performed, the sensor does not record EEG signals from the same brain areas as in humans. SedLine®-DSA and -generated variables seemed to reflect variations in depth of anaesthesia in pigs. Further studies are needed to investigate this correlation, as well as to define the species-specific brain structures monitored by the EEG-sensor.

7 February 2018 in Frontiers in Veterinary Science
Verified
Journal Article
Open access
PDF file
AMAlessandro Mirra
Alessandro Mirra
MBMicaël David Klopfenstein Bregger
Micaël David Klopfenstein Bregger
OLOlivier Louis Levionnois
Olivier Louis Levionnois
A 15-year-old Selle Francais gelding was presented to the equine referral hospital for treatment of a left guttural pouch mycosis previously diagnosed. After induction, the horse was shortly hoisted by all four feet, moved on a padded surgical table, and positioned in right lateral recumbency. In order to reduce the risk of bleeding during surgical manipulation of the carotid and maxillary arteries, a mean arterial pressure between 60 and 70 mmHg was targeted. After surgery, the horse was moved in a padded recovery box keeping the same lateral recumbency. Four unsuccessful attempts were performed, with the horse always returning to sternal recumbency keeping the left hind limb up. At the fifth attempt, performed 120 min after the end of the general anesthesia, the horse stood up correctly but moderate ataxia and absence of weight bearing on the left hind limb were shown. Both the stifle and the fetlock joint were held in a flexed position and could not be extended properly in order to set the foot on the ground, resulting in a very short step. The horse was calm, not sweating, and willing to move; the muscles of the affected limb were relaxed, and the limb was neither warm nor painful at palpation. Occasionally, the horse flexed the affected hind limb in an exaggerated motion with marked abduction. No additional laboratory analyses were performed. Due to a strong suspicion of neuropathy, a sling support was initiated and a supportive bandage associated with flunixine administration was performed until resolution of the symptoms. The horse fully recovered after 3 days. This case report does not clarify the pathogenesis of the possible postanesthetic neuropathy accounted on the non-dependent limb, highlighting the need for future research in this field. Non-dependent limb neuropathy should be an expected problem even after having ruled out the most commonly known causes predisposing to postanesthetic lameness.