Neurophysiological aspects in SARS-CoV-2–induced acute respiratory distress syndrome

Patients with coronavirus disease 2019 (COVID-19) often develop acute respiratory failure and acute respiratory distress syndrome (ARDS) that requires intensive care unit (ICU) hospitalization and invasive mechanical ventilation, associated with a high mortality rate. In addition, many patients fail early weaning attempts, further increasing ICU length of stay and mortality. COVID-19 related ARDS can be complicated by neurological involvement with mechanisms of direct central nervous system (CNS) infection and with overlapping para-infective mechanisms of the peripheral nervous system (PNS). We aimed to evaluate the possible involvement of the brainstem and PNS in patients with COVID-19 related ARDS and difficulty in weaning from mechanical ventilation. We evaluated electroencephalogram (EEG), brainstem auditory evoked potentials (BAEPs), electroneurography of the four limbs and the phrenic nerve in 10 patients with respiratory insufficiency due to SARS-CoV-2. All were admitted to intensive care unit and were facing prolonged weaning from mechanical ventilation. All ten patients showed a mild diffuse non-specific slowing of brain electrical activity on the EEG. Four patients had an acute motor axonal neuropathy with absent or reduced amplitude phrenic nerve CMAP while four patients showed impairment of the BAEPs. A patient with peripheral nerve impairment suggestive of Guillain-Barré syndrome (GBS) underwent an intravenous immunoglobulin (IVIg) cycle that led to an improvement in the weaning process and progressive motor improvement. The inclusion of a comprehensive neurological evaluation in COVID-19 patients in ICU facilitated the early identification and effective management of Nervous System involvement

Prevalence of anisakid parasites in fish collected from Apulia region (Italy) and quantification of nematode larvae in flesh

Abstract Anisakis spp. and Hysterothylacium spp. are nematodes that commonly parasitize several fish species. Nematode larvae can be recovered in coelomic cavity and viscera, but also in flesh and have an important economic and public health impact. A total of 1144 subjects of wild teleosts, 340 samples of cephalopods and 128 specimens of farmed fish collected from Apulia region were analysed for anisakid larvae detection by visual inspection of coelomic cavity and viscera and by digestion of the flesh. No nematode larvae were found in farmed fish and cephalopod molluscs. All examined wild-caught fish species were parasitized, except for 5 species for each of which only a few subjects belonging to the same batch were sampled, therefore the results are just indicative. A total of 6153 larvae were isolated; among these, 271 larvae were found in the muscular portion. Larvae were identified by morphological method as belonging to the genera Anisakis (97.2%) (type I and type II) and Hysterothylacium (2.8%). Both nematodes could be found in all fish species, except for round sardinella (Sardinella aurita), infected only by Hysterothylacium spp. and for Mediterranean scaldfish (Arnoglossus laterna), little tunny (Euthynnus alleteratus) and chub mackerel (Scomber japonicus) infected only with Anisakis spp.. A sample of 185 larvae was sent to the National Reference Centre for Anisakiasis (C.Re.N.A.) of Sicily for identification at the species level: 180 larvae belonged to the species A. pegreffii and 2 larvae to A. physeteris. The remaining 3 larvae were identified at genus level as Hysterothylacium. Statistical indices such as prevalence, mean intensity and mean abundance were calculated. Chub mackerel (S. japonicus) was the species with the highest prevalence and mean intensity. Moreover, the average and the median values of larvae per 100 g of edible part for each fish species were determined to estimate the consumer exposure to Anisakis spp.. The obtained values were then recalculated by referring to the edible part of all specimens (infected and non-infected) forming a single parasitized batch, getting more realistic and objective data useful for risk assessment. Our results indicate that the consumption of raw or undercooked wild fish caught off Apulian coasts could result in the acquisition of anisakiasis; on the contrary, farmed fish and cephalopods appear to be safer for the consumer

Ulnar Goniometer Device: Confronto tra elettro-neurografia ed ecografia.

Obbiettivo Il nostro studio mira a estendere la ricerca precedente e confrontare due metodi diagnostici eseguiti sul nervo ulnare per convalidare l'uso del goniometro ulnare nella pratica elettromiografica come strumento ausiliario diagnostico. Confrontando il metodo elettro-neurografico, ottenuto attraverso studi sulla velocità di conduzione (VC), con l'ecografia del nervo ulnare al canale cubitale e in corrispondenza del terzo medio dell’avambraccio, miriamo a quantificare l'affidabilità del goniometro ulnare rispetto al metodo diagnostico dell'ecografia del nervo. Materiali E Metodi l'operatore ha eseguito l'esame con l'uso del Goniometro Ulnare, rilevando la velocità di conduzione motoria dal polso al gomito e la velocità sopra il gomito (AE), sotto il gomito (BE) e successivamente ha eseguito l'ecografia del nervo ulnare nell'avambraccio e nel gomito. Abbiamo calcolato il grado di omogeneità tra le misurazioni. Risultati Valutando 30 partecipanti di entrambi i sessi con sintomi parestesici tipici di compressione del nervo ulnare al gomito, Il 100% delle misurazioni mostra che una diminuzione di MCV al di sotto di 50 m/s è associata a un aumento di CSA. Inoltre, nell'89% dei casi, una riduzione di MCV wBE e BEAE di più di 10 m/s è correlata a un aumento di CSA. Discussione e Conclusioni La misurazione dell'angolo sotto il gomito (BE) e sopra il gomito (AE) utilizzando il Goniometro Ulnare ci fornisce una Velocità di Conduzione Motoria (MCV) rallentata che è in accordo con i dati ecografici che mostrano un aumento della cosiddetta Cross Sectional Area (CSA)  ossia la sezione trasversale misurata in mm2 del nervo ulnare in quel segmento, come accade  nella Sindrome del Tunnel Cubitale (CTS)

Ulnar Goniometer Device: Comparison between electro-neurography and ultrasound.

OBJECTIVE Our study aims to extend the previous research and compare two diagnostic methods performed on the ulnar nerve to validate the use of the ulnar goniometer in electromyographic diagnostic practice. Comparing the electroneurographic method, obtained through conduction velocity (CV) studies with ultrasound of the ulnar nerve in the area above the elbow and at the wrist, we aim to quantify the reliability of the ulnar goniometer compared to the diagnostic method ultrasound of the nerve. MATERIALS AND METHODS The operator examined with the use of the Ulnar Goniometer, detecting the wrist-below-elbow motor conduction speed and the above-elbow speed (AE), below-elbow speed (BE) and subsequently performed an ultrasound examination of the ulnar nerve in the forearm and elbow. We calculated the degree of homogeneity between measurements. RESULTS Evaluating 30 participants of both genders with typical paresthetic symptoms of ulnar nerve compression at the elbow, 100% of the measurements show that a decrease in Motor Conduction Velocity (MCV) below 50 m/s is associated with an increase in Cross-Sectional Area (CSA). Additionally, in 89% of cases, a reduction in MCV wBE and BEAE by more than 10 m/s is correlated with an increase in CSA. DISCUSSION AND CONCLUSIONS The measurement of the angle below the elbow (BE) and above the elbow (AE) using the Ulnar Goniometer provides us with a slowed Motor Conduction Velocity (MCV) that is by ultrasound data showing an increase in the Cross-Sectional Area (CSA) of the ulnar nerve in that segment, as observed in Cubital Tunnel Syndrome (CTS)

Ulnar Goniometer: a simple device for better neurophysiological evaluation of the Motor Conduction Velocity of the Ulnar Nerve.

OBJECTIVE The use of the Ulnar Goniometer standardizes the method of detecting the Motor Conduction Velocity (MCV) of the Ulnar nerve by keeping the elbow flexed at a fixed angle, thus enabling an easier and more precise measurement. MATERIALS AND METHODS The stimulations were performed by two independent operators. We evaluated 30 participants of both genders with paresthetic symptoms of the upper limbs and 30 healthy and asymptomatic volunteers. Each operator performed the examination without and with the use of the Ulnar Goniometer, detecting the velocity of motor conduction wrist-below elbow and the speed above-elbow (AE) below-elbow (BE). Agreement between the measurements was assessed with intraclass correlation coefficient (ICC). RESULTS The repeatability of the measurements between operators was modest without the use of the support (ICC = 0.152) while a good agreement was found when the operators used the support (ICC = 0.499). DISCUSSION AND CONCLUSIONS The most obvious results of the study were the reduction of the difference between operators using the Ulnar goniometer, the increase in the repeatability of the measurements and the specificity of the test

Goniometro Ulnare: un semplice dispositivo per una migliore valutazione neurofisiologica della velocità di conduzione motoria del nervo ulnare.

OBIETTIVO L’utilizzo del Goniometro Ulnare ha l’obiettivo standardizzare il metodo di rilevazione della Velocità di Conduzione Motoria (VCM) del nervo Ulnare mantenendo il gomito flesso ad un’angolazione standardizzata, favorendo così una più agevole e precisa misurazione. MATERIALI E METODI Le stimolazioni sono state eseguite da due diversi operatori; ogni operatore ha eseguito l'esame senza e con l'uso del Goniometro Ulnare, rilevando la Velocità di conduzione motoria polso-sotto gomito e la velocità sovragomito (above-elbow AE) sottogomito (below-elbow, BE). Abbiamo calcolato il grado di omogeneità tra le misurazioni e il coefficiente di correlazione intraclasse. RISULTATI Valutando 30 partecipanti di ambo i sessi con sintomi parestetici degli arti superiori e 30 volontari sani e asintomatici, la ripetibilità delle misurazioni tra operatori è stata modesta senza l'uso del supporto (ICC = 0,152) mentre si è riscontrato un buon accordo quando gli operatori hanno utilizzato il supporto (ICC = 0,499).. CONCLUSIONI I risultati più evidenti dello studio sono stati la riduzione della differenza tra operatori utilizzando il goniometro Ulnare, l’aumento della riproducibilità della misurazione e della specificità del test

Ulnar Goniometer Device: Confronto tra elettro-neurografia ed ecografia.

Obbiettivo Il nostro studio mira a estendere la ricerca precedente e confrontare due metodi diagnostici eseguiti sul nervo ulnare per convalidare l'uso del goniometro ulnare nella pratica elettromiografica come strumento ausiliario diagnostico. Confrontando il metodo elettro-neurografico, ottenuto attraverso studi sulla velocità di conduzione (VC), con l'ecografia del nervo ulnare al canale cubitale e in corrispondenza del terzo medio dell’avambraccio, miriamo a quantificare l'affidabilità del goniometro ulnare rispetto al metodo diagnostico dell'ecografia del nervo. Materiali E Metodi l'operatore ha eseguito l'esame con l'uso del Goniometro Ulnare, rilevando la velocità di conduzione motoria dal polso al gomito e la velocità sopra il gomito (AE), sotto il gomito (BE) e successivamente ha eseguito l'ecografia del nervo ulnare nell'avambraccio e nel gomito. Abbiamo calcolato il grado di omogeneità tra le misurazioni. Risultati Valutando 30 partecipanti di entrambi i sessi con sintomi parestesici tipici di compressione del nervo ulnare al gomito, Il 100% delle misurazioni mostra che una diminuzione di MCV al di sotto di 50 m/s è associata a un aumento di CSA. Inoltre, nell'89% dei casi, una riduzione di MCV wBE e BEAE di più di 10 m/s è correlata a un aumento di CSA. Discussione e Conclusioni La misurazione dell'angolo sotto il gomito (BE) e sopra il gomito (AE) utilizzando il Goniometro Ulnare ci fornisce una Velocità di Conduzione Motoria (MCV) rallentata che è in accordo con i dati ecografici che mostrano un aumento della cosiddetta Cross Sectional Area (CSA)  ossia la sezione trasversale misurata in mm2 del nervo ulnare in quel segmento, come accade  nella Sindrome del Tunnel Cubitale (CTS)

Ulnar Goniometer Device: Comparison between electro-neurography and ultrasound.

OBJECTIVE Our study aims to extend the previous research and compare two diagnostic methods performed on the ulnar nerve to validate the use of the ulnar goniometer in electromyographic diagnostic practice. Comparing the electroneurographic method, obtained through conduction velocity (CV) studies with ultrasound of the ulnar nerve in the area above the elbow and at the wrist, we aim to quantify the reliability of the ulnar goniometer compared to the diagnostic method ultrasound of the nerve. MATERIALS AND METHODS The operator examined with the use of the Ulnar Goniometer, detecting the wrist-below-elbow motor conduction speed and the above-elbow speed (AE), below-elbow speed (BE) and subsequently performed an ultrasound examination of the ulnar nerve in the forearm and elbow. We calculated the degree of homogeneity between measurements. RESULTS Evaluating 30 participants of both genders with typical paresthetic symptoms of ulnar nerve compression at the elbow, 100% of the measurements show that a decrease in Motor Conduction Velocity (MCV) below 50 m/s is associated with an increase in Cross-Sectional Area (CSA). Additionally, in 89% of cases, a reduction in MCV wBE and BEAE by more than 10 m/s is correlated with an increase in CSA. DISCUSSION AND CONCLUSIONS The measurement of the angle below the elbow (BE) and above the elbow (AE) using the Ulnar Goniometer provides us with a slowed Motor Conduction Velocity (MCV) that is by ultrasound data showing an increase in the Cross-Sectional Area (CSA) of the ulnar nerve in that segment, as observed in Cubital Tunnel Syndrome (CTS)

Isolation and characterization of Yersinia enterocolitica from foods in Apulia and Basilicata regions (Italy) by conventional and modern methods

Yersiniosis is the third most reported food-borne zoonosis in Europe. The aim of the present study was to perform the search for Yersinia enterocolitica in food samples collected from Apulia and Basilicata regions (Southern Italy) and to characterize any isolates by classical and modern analytical methods. A total of 130 samples were analyzed between July 2018 and July 2019: most of them were raw milk and dairy products made from it. Furthermore, 8 out of 130 samples were individual milk samples collected from bovines reared in a Brucella-free farm which showed false positive serological reaction for brucellosis due to the presence of pathogenic Y. enterocolitica O:9 biotype 2 in faeces. The Real Time PCR targeting the ail gene and the culture method were performed to detect pathogenic Y. enterocolitica. Isolates were subjected to API 20E (Biomerieux) and MALDI-TOF MS (Matrix Assisted Laser Desorption Ionization Time-of-Flight) for species identification. All samples were negative for the ail gene. The culture method allowed to isolate suspicious colonies from 28 samples. The API 20E system and the MALDI-TOF MS technique identified 20 Y. enterocolitica and 1 Y. intermedia in a concordant way. The remaining 7 strains were all identified as Y. enterocolitica by the API 20E system, while the MALDI-TOF MS recognized 4 Y. intermedia, 1 Y. bercovieri and 2 Y. massiliensis. Genotypic characterization of the discordant strains was performed by rMLST and it confirmed the MALDI-TOF MS’ results. Only non-pathogenic Y. enterocolitica biotype 1A strains were found, although with a non-negligible prevalence (P = 0.15 with CI 95% = ± 0.06). This study indicates a poor circulation of pathogenic Y. enterocolitica in food products made and marketed in the investigated areas. However, the small number of samples, insufficient for some food categories such as meat and vegetable, does not allow to exclude the presence of pathogenic strains at all

Isolation and characterization of Yersinia enterocolitica from foods in Apulia and Basilicata regions (Italy) by conventional and modern methods.

Yersiniosis is the third most reported food-borne zoonosis in Europe. The aim of the present study was to perform the search for Yersinia enterocolitica in food samples collected from Apulia and Basilicata regions (Southern Italy) and to characterize any isolates by classical and modern analytical methods. A total of 130 samples were analyzed between July 2018 and July 2019: most of them were raw milk and dairy products made from it. Furthermore, 8 out of 130 samples were individual milk samples collected from bovines reared in a Brucella-free farm which showed false positive serological reaction for brucellosis due to the presence of pathogenic Y. enterocolitica O:9 biotype 2 in faeces. The Real Time PCR targeting the ail gene and the culture method were performed to detect pathogenic Y. enterocolitica. Isolates were subjected to API 20E (Biomerieux) and MALDI-TOF MS (Matrix Assisted Laser Desorption Ionization Time-of-Flight) for species identification. All samples were negative for the ail gene. The culture method allowed to isolate suspicious colonies from 28 samples. The API 20E system and the MALDI-TOF MS technique identified 20 Y. enterocolitica and 1 Y. intermedia in a concordant way. The remaining 7 strains were all identified as Y. enterocolitica by the API 20E system, while the MALDI-TOF MS recognized 4 Y. intermedia, 1 Y. bercovieri and 2 Y. massiliensis. Genotypic characterization of the discordant strains was performed by rMLST and it confirmed the MALDI-TOF MS' results. Only non-pathogenic Y. enterocolitica biotype 1A strains were found, although with a non-negligible prevalence (P = 0.15 with CI 95% = ± 0.06). This study indicates a poor circulation of pathogenic Y. enterocolitica in food products made and marketed in the investigated areas. However, the small number of samples, insufficient for some food categories such as meat and vegetable, does not allow to exclude the presence of pathogenic strains at all