Neurological complications due to beta-propiolactone (BPL)-inactivated antirabies vaccination: Clinical, electrophysiological and therapeutic aspects

Seventy six patients with neuroparalytic accidents due to antirabies vaccination (ARV) with BPL vaccine were studied. The mean age of incidence was 26.9 ± 15.7 years. The suspected source of infection was by the bite of a dog in 72 (97.3%) out of 74. The mean duration of interval between the first d...

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Veröffentlicht in:Journal of the neurological sciences 1984, Vol.63 (1), p.111-128
Hauptverfasser: Swamy, H.Satyanarayana, Shankar, S.K., Chandra, P.Satish, Aroor, Suresh Rao, Krishna, A.Shivarama, Perumal, V.G.Kalia
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container_end_page 128
container_issue 1
container_start_page 111
container_title Journal of the neurological sciences
container_volume 63
creator Swamy, H.Satyanarayana
Shankar, S.K.
Chandra, P.Satish
Aroor, Suresh Rao
Krishna, A.Shivarama
Perumal, V.G.Kalia
description Seventy six patients with neuroparalytic accidents due to antirabies vaccination (ARV) with BPL vaccine were studied. The mean age of incidence was 26.9 ± 15.7 years. The suspected source of infection was by the bite of a dog in 72 (97.3%) out of 74. The mean duration of interval between the first dose of ARV and onset of neurological deficits was 12.2 ± 8.4 days. The number of doses was 7 or less in 49 (65.3%) cases and more than 7 in 26 (34.7%) cases. With regard to neurological deficits, 6 (7.9%) had encephalopathy, 23 (30.3%) had encephalomyeloradiculopathy, 7 (9.2%) had myelopathy, 21 (27.6%) had myeloradiculopathy, 18 (23.7%) had polyradiculopathy and one had bilateral 7th cranial nerve palsies. Lumbar CSF analysis was done in 67 patients and was abnormal in 47 (70.1%) patients in the form of pleocytosis or raised protein or both. EEG, done in 30 patients, was abnormal in 13 (43.3%) and the abnormalities were not related to clinical features in 6. Electroneuromyography (ENMG) was done in 25 and was abnormal in 21 cases. Visual evoked potentials (VEP) was done in 11 cases and was abnormal in two. Sixty eight patients received steroids and 17 patients received cyclophosphamide in addition to steroids, 14 during the first admission and 3 during follow up when the recovery with steroids was not satisfactory. The therapeutic results were better in those who received cyclophosphamide and was statistically significant. Fourteen (18.4%) patients died and 6 were autopsied. The pathological features were essentially myeloradiculopathies, with variable degree of encephalic involvement. Two showed distinct necrotising myelopathy of immune type.
doi_str_mv 10.1016/0022-510X(84)90113-8
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The mean age of incidence was 26.9 ± 15.7 years. The suspected source of infection was by the bite of a dog in 72 (97.3%) out of 74. The mean duration of interval between the first dose of ARV and onset of neurological deficits was 12.2 ± 8.4 days. The number of doses was 7 or less in 49 (65.3%) cases and more than 7 in 26 (34.7%) cases. With regard to neurological deficits, 6 (7.9%) had encephalopathy, 23 (30.3%) had encephalomyeloradiculopathy, 7 (9.2%) had myelopathy, 21 (27.6%) had myeloradiculopathy, 18 (23.7%) had polyradiculopathy and one had bilateral 7th cranial nerve palsies. Lumbar CSF analysis was done in 67 patients and was abnormal in 47 (70.1%) patients in the form of pleocytosis or raised protein or both. EEG, done in 30 patients, was abnormal in 13 (43.3%) and the abnormalities were not related to clinical features in 6. Electroneuromyography (ENMG) was done in 25 and was abnormal in 21 cases. Visual evoked potentials (VEP) was done in 11 cases and was abnormal in two. Sixty eight patients received steroids and 17 patients received cyclophosphamide in addition to steroids, 14 during the first admission and 3 during follow up when the recovery with steroids was not satisfactory. The therapeutic results were better in those who received cyclophosphamide and was statistically significant. Fourteen (18.4%) patients died and 6 were autopsied. The pathological features were essentially myeloradiculopathies, with variable degree of encephalic involvement. 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The mean age of incidence was 26.9 ± 15.7 years. The suspected source of infection was by the bite of a dog in 72 (97.3%) out of 74. The mean duration of interval between the first dose of ARV and onset of neurological deficits was 12.2 ± 8.4 days. The number of doses was 7 or less in 49 (65.3%) cases and more than 7 in 26 (34.7%) cases. With regard to neurological deficits, 6 (7.9%) had encephalopathy, 23 (30.3%) had encephalomyeloradiculopathy, 7 (9.2%) had myelopathy, 21 (27.6%) had myeloradiculopathy, 18 (23.7%) had polyradiculopathy and one had bilateral 7th cranial nerve palsies. Lumbar CSF analysis was done in 67 patients and was abnormal in 47 (70.1%) patients in the form of pleocytosis or raised protein or both. EEG, done in 30 patients, was abnormal in 13 (43.3%) and the abnormalities were not related to clinical features in 6. Electroneuromyography (ENMG) was done in 25 and was abnormal in 21 cases. Visual evoked potentials (VEP) was done in 11 cases and was abnormal in two. Sixty eight patients received steroids and 17 patients received cyclophosphamide in addition to steroids, 14 during the first admission and 3 during follow up when the recovery with steroids was not satisfactory. The therapeutic results were better in those who received cyclophosphamide and was statistically significant. Fourteen (18.4%) patients died and 6 were autopsied. The pathological features were essentially myeloradiculopathies, with variable degree of encephalic involvement. Two showed distinct necrotising myelopathy of immune type.</description><subject>Adult</subject><subject>Allergic encephalomyelitis</subject><subject>Antirabies vaccine</subject><subject>Brain - pathology</subject><subject>Cyclophosphamide</subject><subject>Electrodiagnosis</subject><subject>Female</subject><subject>Humans</subject><subject>Immunisation</subject><subject>Lactones - adverse effects</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Necrotising myelitis</subject><subject>Nervous System Diseases - etiology</subject><subject>Nervous System Diseases - pathology</subject><subject>Paralysis - etiology</subject><subject>Paralysis - pathology</subject><subject>Propiolactone - adverse effects</subject><subject>Rabies</subject><subject>Rabies Vaccines - adverse effects</subject><subject>Spinal Cord - pathology</subject><subject>Spinal Nerve Roots - pathology</subject><subject>Vaccination</subject><issn>0022-510X</issn><issn>1878-5883</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1984</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9UU1LAzEQDaLUWv0HCjm24Opk024TD4IWv6CoBwVvIZtMNbLdLJu00B_i_zWrpaeZxxvezLxHyCmDCwasuATI82zC4GMoxiMJjPFM7JE-E1ORTYTg-6S_GzkkRyF8A0AhhOyRXlFIWUxYn_w846r1lf90RlfU-GVTpS46XwdqV0ijpyVGnTWtb5yvtIm-Rjq8fZ2PMlcn6NY6oqW6jq7VpcNA19qYRHUaV3RWubqTPqdYoYlJ5WsT3G6hri2NX9jqBlfRGapDk6bCMTlY6CrgybYOyPv93dvsMZu_PDzNbuYZ5gWL2WI60UUpp1DycQ55-q60pbSG8YXliGjATDmC1cAlZyJBCaVhCwCZM84LPiBn_7rNqlyiVU3rlrrdqK09ib_-5zEdsXbYqmAc1gata9OdynqnGKguDtV5rTqvlRirvziU4L-ljX_9</recordid><startdate>1984</startdate><enddate>1984</enddate><creator>Swamy, H.Satyanarayana</creator><creator>Shankar, S.K.</creator><creator>Chandra, P.Satish</creator><creator>Aroor, Suresh Rao</creator><creator>Krishna, A.Shivarama</creator><creator>Perumal, V.G.Kalia</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>1984</creationdate><title>Neurological complications due to beta-propiolactone (BPL)-inactivated antirabies vaccination: Clinical, electrophysiological and therapeutic aspects</title><author>Swamy, H.Satyanarayana ; Shankar, S.K. ; Chandra, P.Satish ; Aroor, Suresh Rao ; Krishna, A.Shivarama ; Perumal, V.G.Kalia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-e261t-f75a6b970b34202006bdb9dc13fd3eeec0c73e0da039318c0c90bc1f009213363</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1984</creationdate><topic>Adult</topic><topic>Allergic encephalomyelitis</topic><topic>Antirabies vaccine</topic><topic>Brain - pathology</topic><topic>Cyclophosphamide</topic><topic>Electrodiagnosis</topic><topic>Female</topic><topic>Humans</topic><topic>Immunisation</topic><topic>Lactones - adverse effects</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Necrotising myelitis</topic><topic>Nervous System Diseases - etiology</topic><topic>Nervous System Diseases - pathology</topic><topic>Paralysis - etiology</topic><topic>Paralysis - pathology</topic><topic>Propiolactone - adverse effects</topic><topic>Rabies</topic><topic>Rabies Vaccines - adverse effects</topic><topic>Spinal Cord - pathology</topic><topic>Spinal Nerve Roots - pathology</topic><topic>Vaccination</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Swamy, H.Satyanarayana</creatorcontrib><creatorcontrib>Shankar, S.K.</creatorcontrib><creatorcontrib>Chandra, P.Satish</creatorcontrib><creatorcontrib>Aroor, Suresh Rao</creatorcontrib><creatorcontrib>Krishna, A.Shivarama</creatorcontrib><creatorcontrib>Perumal, V.G.Kalia</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Journal of the neurological sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Swamy, H.Satyanarayana</au><au>Shankar, S.K.</au><au>Chandra, P.Satish</au><au>Aroor, Suresh Rao</au><au>Krishna, A.Shivarama</au><au>Perumal, V.G.Kalia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neurological complications due to beta-propiolactone (BPL)-inactivated antirabies vaccination: Clinical, electrophysiological and therapeutic aspects</atitle><jtitle>Journal of the neurological sciences</jtitle><addtitle>J Neurol Sci</addtitle><date>1984</date><risdate>1984</risdate><volume>63</volume><issue>1</issue><spage>111</spage><epage>128</epage><pages>111-128</pages><issn>0022-510X</issn><eissn>1878-5883</eissn><abstract>Seventy six patients with neuroparalytic accidents due to antirabies vaccination (ARV) with BPL vaccine were studied. The mean age of incidence was 26.9 ± 15.7 years. The suspected source of infection was by the bite of a dog in 72 (97.3%) out of 74. The mean duration of interval between the first dose of ARV and onset of neurological deficits was 12.2 ± 8.4 days. The number of doses was 7 or less in 49 (65.3%) cases and more than 7 in 26 (34.7%) cases. With regard to neurological deficits, 6 (7.9%) had encephalopathy, 23 (30.3%) had encephalomyeloradiculopathy, 7 (9.2%) had myelopathy, 21 (27.6%) had myeloradiculopathy, 18 (23.7%) had polyradiculopathy and one had bilateral 7th cranial nerve palsies. Lumbar CSF analysis was done in 67 patients and was abnormal in 47 (70.1%) patients in the form of pleocytosis or raised protein or both. EEG, done in 30 patients, was abnormal in 13 (43.3%) and the abnormalities were not related to clinical features in 6. Electroneuromyography (ENMG) was done in 25 and was abnormal in 21 cases. Visual evoked potentials (VEP) was done in 11 cases and was abnormal in two. Sixty eight patients received steroids and 17 patients received cyclophosphamide in addition to steroids, 14 during the first admission and 3 during follow up when the recovery with steroids was not satisfactory. The therapeutic results were better in those who received cyclophosphamide and was statistically significant. Fourteen (18.4%) patients died and 6 were autopsied. The pathological features were essentially myeloradiculopathies, with variable degree of encephalic involvement. Two showed distinct necrotising myelopathy of immune type.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>6699651</pmid><doi>10.1016/0022-510X(84)90113-8</doi><tpages>18</tpages></addata></record>
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source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects Adult
Allergic encephalomyelitis
Antirabies vaccine
Brain - pathology
Cyclophosphamide
Electrodiagnosis
Female
Humans
Immunisation
Lactones - adverse effects
Male
Middle Aged
Necrotising myelitis
Nervous System Diseases - etiology
Nervous System Diseases - pathology
Paralysis - etiology
Paralysis - pathology
Propiolactone - adverse effects
Rabies
Rabies Vaccines - adverse effects
Spinal Cord - pathology
Spinal Nerve Roots - pathology
Vaccination
title Neurological complications due to beta-propiolactone (BPL)-inactivated antirabies vaccination: Clinical, electrophysiological and therapeutic aspects
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