Pregabalin for Recurrent Seizures in Critical Illness: A Promising Adjunctive Therapy, Especially for cyclic Seizures
Background Pregabalin (PGB) is an effective adjunctive treatment for focal epilepsy and acts by binding to the alpha2-delta subunit of voltage-gated calcium channels to reduce excitatory neurotransmitter release. Limited data exist on its use in the neurocritical care setting, including cyclic seizu...
Ausführliche Beschreibung
Autor*in: |
Busl, Katharina M. [verfasserIn] |
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Englisch |
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2022 |
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Anmerkung: |
© Springer Science+Business Media, LLC, part of Springer Nature and Neurocritical Care Society 2022 |
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Übergeordnetes Werk: |
Enthalten in: Neurocritical care - New York, NY : Springer, 2004, 37(2022), 1 vom: 25. Feb., Seite 140-148 |
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Übergeordnetes Werk: |
volume:37 ; year:2022 ; number:1 ; day:25 ; month:02 ; pages:140-148 |
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DOI / URN: |
10.1007/s12028-022-01459-6 |
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SPR047584106 |
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520 | |a Background Pregabalin (PGB) is an effective adjunctive treatment for focal epilepsy and acts by binding to the alpha2-delta subunit of voltage-gated calcium channels to reduce excitatory neurotransmitter release. Limited data exist on its use in the neurocritical care setting, including cyclic seizures—a pattern of recurrent seizures occurring at nearly regular intervals. Although the mechanism underpinning cyclic seizures remains elusive, spreading excitation linked to spreading depolarizations may play a role in seizure recurrence and periodicity. PGB has been shown to increase spreading depolarization threshold; hence, we hypothesized that the magnitude of antiseizure effect from PGB is more pronounced in patients with cyclic versus noncyclic seizures in a critically ill cohort with recurrent seizures. Methods We conducted a retrospective case series of adults admitted to two academic neurointensive care units between January 2017 and March 2019 who received PGB for treatment of seizures. Data collected included demographics, etiology of brain injury, antiseizure medications, and outcome. Continuous electroencephalogram recordings 48 hours before and after PGB administration were reviewed by electroencephalographers blinded to the administration of antiseizure medications to obtain granular data on electrographic seizure burden. Cyclic seizures were determined quantitatively (i.e., < 50% variation of interseizure intervals for at least 50% of consecutive seizures). Coprimary outcomes were decrease in hourly seizure burden in minutes and decrease in seizure frequency in the 48 hours after PGB initiation. We used nonparametric tests for comparison of seizure frequency and burden and segmented linear regression to assess PGB effect. Results We included 16 patients; the median age was 69 years, 11 (68.7%) were women, three (18.8%) had undergone a neurosurgical procedure, and five (31%) had underlying epilepsy. All seizures had focal onset; ten patients (62.5%) had cyclic seizures. The median hourly seizure burden over the 48 hours prior to PGB initiation was 1.87 min/hour (interquartile range 1.49–8.53), and the median seizure frequency was 1.96 seizures/hour (interquartile range 1.06–3.41). In the 48 hours following PGB (median daily dose 300 mg, range 75–300 mg), the median number of seizures per hour was reduced by 0.80 seizures/hour (95% confidence interval 0.19–1.40), whereas the median hourly seizure burden decreased by 1.71 min/hour (95% confidence interval 0.38–3.04). When we compared patients with cyclic versus noncyclic seizures, there was a relative decrease in hourly seizure frequency (− 86.7% versus − 2%, p = 0.04) and hourly seizure burden (− 89% versus − 7.8%, p = 0.03) at 48 hours. Conclusions PGB was associated with a relative reduction in seizure burden in neurocritically ill patients with recurrent seizures, especially those with cyclic seizures, and may be considered in the therapeutic arsenal for refractory seizures. Whether this effect is mediated via modulation of spreading depolarization requires further study. | ||
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700 | 1 | |a Fong, Michael W. K. |4 aut | |
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700 | 1 | |a Hirsch, Lawrence J. |4 aut | |
700 | 1 | |a Maciel, Carolina B. |0 (orcid)0000-0002-8763-5839 |4 aut | |
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10.1007/s12028-022-01459-6 doi (DE-627)SPR047584106 (SPR)s12028-022-01459-6-e DE-627 ger DE-627 rakwb eng Busl, Katharina M. verfasserin aut Pregabalin for Recurrent Seizures in Critical Illness: A Promising Adjunctive Therapy, Especially for cyclic Seizures 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer Science+Business Media, LLC, part of Springer Nature and Neurocritical Care Society 2022 Background Pregabalin (PGB) is an effective adjunctive treatment for focal epilepsy and acts by binding to the alpha2-delta subunit of voltage-gated calcium channels to reduce excitatory neurotransmitter release. Limited data exist on its use in the neurocritical care setting, including cyclic seizures—a pattern of recurrent seizures occurring at nearly regular intervals. Although the mechanism underpinning cyclic seizures remains elusive, spreading excitation linked to spreading depolarizations may play a role in seizure recurrence and periodicity. PGB has been shown to increase spreading depolarization threshold; hence, we hypothesized that the magnitude of antiseizure effect from PGB is more pronounced in patients with cyclic versus noncyclic seizures in a critically ill cohort with recurrent seizures. Methods We conducted a retrospective case series of adults admitted to two academic neurointensive care units between January 2017 and March 2019 who received PGB for treatment of seizures. Data collected included demographics, etiology of brain injury, antiseizure medications, and outcome. Continuous electroencephalogram recordings 48 hours before and after PGB administration were reviewed by electroencephalographers blinded to the administration of antiseizure medications to obtain granular data on electrographic seizure burden. Cyclic seizures were determined quantitatively (i.e., < 50% variation of interseizure intervals for at least 50% of consecutive seizures). Coprimary outcomes were decrease in hourly seizure burden in minutes and decrease in seizure frequency in the 48 hours after PGB initiation. We used nonparametric tests for comparison of seizure frequency and burden and segmented linear regression to assess PGB effect. Results We included 16 patients; the median age was 69 years, 11 (68.7%) were women, three (18.8%) had undergone a neurosurgical procedure, and five (31%) had underlying epilepsy. All seizures had focal onset; ten patients (62.5%) had cyclic seizures. The median hourly seizure burden over the 48 hours prior to PGB initiation was 1.87 min/hour (interquartile range 1.49–8.53), and the median seizure frequency was 1.96 seizures/hour (interquartile range 1.06–3.41). In the 48 hours following PGB (median daily dose 300 mg, range 75–300 mg), the median number of seizures per hour was reduced by 0.80 seizures/hour (95% confidence interval 0.19–1.40), whereas the median hourly seizure burden decreased by 1.71 min/hour (95% confidence interval 0.38–3.04). When we compared patients with cyclic versus noncyclic seizures, there was a relative decrease in hourly seizure frequency (− 86.7% versus − 2%, p = 0.04) and hourly seizure burden (− 89% versus − 7.8%, p = 0.03) at 48 hours. Conclusions PGB was associated with a relative reduction in seizure burden in neurocritically ill patients with recurrent seizures, especially those with cyclic seizures, and may be considered in the therapeutic arsenal for refractory seizures. Whether this effect is mediated via modulation of spreading depolarization requires further study. Pregabalin (dpeaa)DE-He213 Antiseizure medication (dpeaa)DE-He213 Antiepileptic drug (dpeaa)DE-He213 Cyclic seizures (dpeaa)DE-He213 Neurocritical care (dpeaa)DE-He213 Nonconvulsive seizures (dpeaa)DE-He213 Fong, Michael W. K. aut Newcomer, Zachary aut Patel, Mitesh aut Cohen, Scott A. aut Jadav, Rakesh aut Smith, Christine N. aut Mitropanopoulos, Sotiris aut Bruzzone, Maria aut Hella, Maria aut Eisenschenk, Stephan aut Robinson, Christopher P. aut Roth, William H. aut Ameli, Pouya Alexander aut Babi, Marc-Alain aut Pizzi, Michael A. aut Gilmore, Emily J. aut Hirsch, Lawrence J. aut Maciel, Carolina B. (orcid)0000-0002-8763-5839 aut Enthalten in Neurocritical care New York, NY : Springer, 2004 37(2022), 1 vom: 25. 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10.1007/s12028-022-01459-6 doi (DE-627)SPR047584106 (SPR)s12028-022-01459-6-e DE-627 ger DE-627 rakwb eng Busl, Katharina M. verfasserin aut Pregabalin for Recurrent Seizures in Critical Illness: A Promising Adjunctive Therapy, Especially for cyclic Seizures 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer Science+Business Media, LLC, part of Springer Nature and Neurocritical Care Society 2022 Background Pregabalin (PGB) is an effective adjunctive treatment for focal epilepsy and acts by binding to the alpha2-delta subunit of voltage-gated calcium channels to reduce excitatory neurotransmitter release. Limited data exist on its use in the neurocritical care setting, including cyclic seizures—a pattern of recurrent seizures occurring at nearly regular intervals. Although the mechanism underpinning cyclic seizures remains elusive, spreading excitation linked to spreading depolarizations may play a role in seizure recurrence and periodicity. PGB has been shown to increase spreading depolarization threshold; hence, we hypothesized that the magnitude of antiseizure effect from PGB is more pronounced in patients with cyclic versus noncyclic seizures in a critically ill cohort with recurrent seizures. Methods We conducted a retrospective case series of adults admitted to two academic neurointensive care units between January 2017 and March 2019 who received PGB for treatment of seizures. Data collected included demographics, etiology of brain injury, antiseizure medications, and outcome. Continuous electroencephalogram recordings 48 hours before and after PGB administration were reviewed by electroencephalographers blinded to the administration of antiseizure medications to obtain granular data on electrographic seizure burden. Cyclic seizures were determined quantitatively (i.e., < 50% variation of interseizure intervals for at least 50% of consecutive seizures). Coprimary outcomes were decrease in hourly seizure burden in minutes and decrease in seizure frequency in the 48 hours after PGB initiation. We used nonparametric tests for comparison of seizure frequency and burden and segmented linear regression to assess PGB effect. Results We included 16 patients; the median age was 69 years, 11 (68.7%) were women, three (18.8%) had undergone a neurosurgical procedure, and five (31%) had underlying epilepsy. All seizures had focal onset; ten patients (62.5%) had cyclic seizures. The median hourly seizure burden over the 48 hours prior to PGB initiation was 1.87 min/hour (interquartile range 1.49–8.53), and the median seizure frequency was 1.96 seizures/hour (interquartile range 1.06–3.41). In the 48 hours following PGB (median daily dose 300 mg, range 75–300 mg), the median number of seizures per hour was reduced by 0.80 seizures/hour (95% confidence interval 0.19–1.40), whereas the median hourly seizure burden decreased by 1.71 min/hour (95% confidence interval 0.38–3.04). When we compared patients with cyclic versus noncyclic seizures, there was a relative decrease in hourly seizure frequency (− 86.7% versus − 2%, p = 0.04) and hourly seizure burden (− 89% versus − 7.8%, p = 0.03) at 48 hours. Conclusions PGB was associated with a relative reduction in seizure burden in neurocritically ill patients with recurrent seizures, especially those with cyclic seizures, and may be considered in the therapeutic arsenal for refractory seizures. Whether this effect is mediated via modulation of spreading depolarization requires further study. Pregabalin (dpeaa)DE-He213 Antiseizure medication (dpeaa)DE-He213 Antiepileptic drug (dpeaa)DE-He213 Cyclic seizures (dpeaa)DE-He213 Neurocritical care (dpeaa)DE-He213 Nonconvulsive seizures (dpeaa)DE-He213 Fong, Michael W. K. aut Newcomer, Zachary aut Patel, Mitesh aut Cohen, Scott A. aut Jadav, Rakesh aut Smith, Christine N. aut Mitropanopoulos, Sotiris aut Bruzzone, Maria aut Hella, Maria aut Eisenschenk, Stephan aut Robinson, Christopher P. aut Roth, William H. aut Ameli, Pouya Alexander aut Babi, Marc-Alain aut Pizzi, Michael A. aut Gilmore, Emily J. aut Hirsch, Lawrence J. aut Maciel, Carolina B. (orcid)0000-0002-8763-5839 aut Enthalten in Neurocritical care New York, NY : Springer, 2004 37(2022), 1 vom: 25. Feb., Seite 140-148 (DE-627)478509855 (DE-600)2176033-0 1556-0961 nnns volume:37 year:2022 number:1 day:25 month:02 pages:140-148 https://dx.doi.org/10.1007/s12028-022-01459-6 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 37 2022 1 25 02 140-148 |
allfields_unstemmed |
10.1007/s12028-022-01459-6 doi (DE-627)SPR047584106 (SPR)s12028-022-01459-6-e DE-627 ger DE-627 rakwb eng Busl, Katharina M. verfasserin aut Pregabalin for Recurrent Seizures in Critical Illness: A Promising Adjunctive Therapy, Especially for cyclic Seizures 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer Science+Business Media, LLC, part of Springer Nature and Neurocritical Care Society 2022 Background Pregabalin (PGB) is an effective adjunctive treatment for focal epilepsy and acts by binding to the alpha2-delta subunit of voltage-gated calcium channels to reduce excitatory neurotransmitter release. Limited data exist on its use in the neurocritical care setting, including cyclic seizures—a pattern of recurrent seizures occurring at nearly regular intervals. Although the mechanism underpinning cyclic seizures remains elusive, spreading excitation linked to spreading depolarizations may play a role in seizure recurrence and periodicity. PGB has been shown to increase spreading depolarization threshold; hence, we hypothesized that the magnitude of antiseizure effect from PGB is more pronounced in patients with cyclic versus noncyclic seizures in a critically ill cohort with recurrent seizures. Methods We conducted a retrospective case series of adults admitted to two academic neurointensive care units between January 2017 and March 2019 who received PGB for treatment of seizures. Data collected included demographics, etiology of brain injury, antiseizure medications, and outcome. Continuous electroencephalogram recordings 48 hours before and after PGB administration were reviewed by electroencephalographers blinded to the administration of antiseizure medications to obtain granular data on electrographic seizure burden. Cyclic seizures were determined quantitatively (i.e., < 50% variation of interseizure intervals for at least 50% of consecutive seizures). Coprimary outcomes were decrease in hourly seizure burden in minutes and decrease in seizure frequency in the 48 hours after PGB initiation. We used nonparametric tests for comparison of seizure frequency and burden and segmented linear regression to assess PGB effect. Results We included 16 patients; the median age was 69 years, 11 (68.7%) were women, three (18.8%) had undergone a neurosurgical procedure, and five (31%) had underlying epilepsy. All seizures had focal onset; ten patients (62.5%) had cyclic seizures. The median hourly seizure burden over the 48 hours prior to PGB initiation was 1.87 min/hour (interquartile range 1.49–8.53), and the median seizure frequency was 1.96 seizures/hour (interquartile range 1.06–3.41). In the 48 hours following PGB (median daily dose 300 mg, range 75–300 mg), the median number of seizures per hour was reduced by 0.80 seizures/hour (95% confidence interval 0.19–1.40), whereas the median hourly seizure burden decreased by 1.71 min/hour (95% confidence interval 0.38–3.04). When we compared patients with cyclic versus noncyclic seizures, there was a relative decrease in hourly seizure frequency (− 86.7% versus − 2%, p = 0.04) and hourly seizure burden (− 89% versus − 7.8%, p = 0.03) at 48 hours. Conclusions PGB was associated with a relative reduction in seizure burden in neurocritically ill patients with recurrent seizures, especially those with cyclic seizures, and may be considered in the therapeutic arsenal for refractory seizures. Whether this effect is mediated via modulation of spreading depolarization requires further study. Pregabalin (dpeaa)DE-He213 Antiseizure medication (dpeaa)DE-He213 Antiepileptic drug (dpeaa)DE-He213 Cyclic seizures (dpeaa)DE-He213 Neurocritical care (dpeaa)DE-He213 Nonconvulsive seizures (dpeaa)DE-He213 Fong, Michael W. K. aut Newcomer, Zachary aut Patel, Mitesh aut Cohen, Scott A. aut Jadav, Rakesh aut Smith, Christine N. aut Mitropanopoulos, Sotiris aut Bruzzone, Maria aut Hella, Maria aut Eisenschenk, Stephan aut Robinson, Christopher P. aut Roth, William H. aut Ameli, Pouya Alexander aut Babi, Marc-Alain aut Pizzi, Michael A. aut Gilmore, Emily J. aut Hirsch, Lawrence J. aut Maciel, Carolina B. (orcid)0000-0002-8763-5839 aut Enthalten in Neurocritical care New York, NY : Springer, 2004 37(2022), 1 vom: 25. Feb., Seite 140-148 (DE-627)478509855 (DE-600)2176033-0 1556-0961 nnns volume:37 year:2022 number:1 day:25 month:02 pages:140-148 https://dx.doi.org/10.1007/s12028-022-01459-6 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 37 2022 1 25 02 140-148 |
allfieldsGer |
10.1007/s12028-022-01459-6 doi (DE-627)SPR047584106 (SPR)s12028-022-01459-6-e DE-627 ger DE-627 rakwb eng Busl, Katharina M. verfasserin aut Pregabalin for Recurrent Seizures in Critical Illness: A Promising Adjunctive Therapy, Especially for cyclic Seizures 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer Science+Business Media, LLC, part of Springer Nature and Neurocritical Care Society 2022 Background Pregabalin (PGB) is an effective adjunctive treatment for focal epilepsy and acts by binding to the alpha2-delta subunit of voltage-gated calcium channels to reduce excitatory neurotransmitter release. Limited data exist on its use in the neurocritical care setting, including cyclic seizures—a pattern of recurrent seizures occurring at nearly regular intervals. Although the mechanism underpinning cyclic seizures remains elusive, spreading excitation linked to spreading depolarizations may play a role in seizure recurrence and periodicity. PGB has been shown to increase spreading depolarization threshold; hence, we hypothesized that the magnitude of antiseizure effect from PGB is more pronounced in patients with cyclic versus noncyclic seizures in a critically ill cohort with recurrent seizures. Methods We conducted a retrospective case series of adults admitted to two academic neurointensive care units between January 2017 and March 2019 who received PGB for treatment of seizures. Data collected included demographics, etiology of brain injury, antiseizure medications, and outcome. Continuous electroencephalogram recordings 48 hours before and after PGB administration were reviewed by electroencephalographers blinded to the administration of antiseizure medications to obtain granular data on electrographic seizure burden. Cyclic seizures were determined quantitatively (i.e., < 50% variation of interseizure intervals for at least 50% of consecutive seizures). Coprimary outcomes were decrease in hourly seizure burden in minutes and decrease in seizure frequency in the 48 hours after PGB initiation. We used nonparametric tests for comparison of seizure frequency and burden and segmented linear regression to assess PGB effect. Results We included 16 patients; the median age was 69 years, 11 (68.7%) were women, three (18.8%) had undergone a neurosurgical procedure, and five (31%) had underlying epilepsy. All seizures had focal onset; ten patients (62.5%) had cyclic seizures. The median hourly seizure burden over the 48 hours prior to PGB initiation was 1.87 min/hour (interquartile range 1.49–8.53), and the median seizure frequency was 1.96 seizures/hour (interquartile range 1.06–3.41). In the 48 hours following PGB (median daily dose 300 mg, range 75–300 mg), the median number of seizures per hour was reduced by 0.80 seizures/hour (95% confidence interval 0.19–1.40), whereas the median hourly seizure burden decreased by 1.71 min/hour (95% confidence interval 0.38–3.04). When we compared patients with cyclic versus noncyclic seizures, there was a relative decrease in hourly seizure frequency (− 86.7% versus − 2%, p = 0.04) and hourly seizure burden (− 89% versus − 7.8%, p = 0.03) at 48 hours. Conclusions PGB was associated with a relative reduction in seizure burden in neurocritically ill patients with recurrent seizures, especially those with cyclic seizures, and may be considered in the therapeutic arsenal for refractory seizures. Whether this effect is mediated via modulation of spreading depolarization requires further study. Pregabalin (dpeaa)DE-He213 Antiseizure medication (dpeaa)DE-He213 Antiepileptic drug (dpeaa)DE-He213 Cyclic seizures (dpeaa)DE-He213 Neurocritical care (dpeaa)DE-He213 Nonconvulsive seizures (dpeaa)DE-He213 Fong, Michael W. K. aut Newcomer, Zachary aut Patel, Mitesh aut Cohen, Scott A. aut Jadav, Rakesh aut Smith, Christine N. aut Mitropanopoulos, Sotiris aut Bruzzone, Maria aut Hella, Maria aut Eisenschenk, Stephan aut Robinson, Christopher P. aut Roth, William H. aut Ameli, Pouya Alexander aut Babi, Marc-Alain aut Pizzi, Michael A. aut Gilmore, Emily J. aut Hirsch, Lawrence J. aut Maciel, Carolina B. (orcid)0000-0002-8763-5839 aut Enthalten in Neurocritical care New York, NY : Springer, 2004 37(2022), 1 vom: 25. Feb., Seite 140-148 (DE-627)478509855 (DE-600)2176033-0 1556-0961 nnns volume:37 year:2022 number:1 day:25 month:02 pages:140-148 https://dx.doi.org/10.1007/s12028-022-01459-6 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 37 2022 1 25 02 140-148 |
allfieldsSound |
10.1007/s12028-022-01459-6 doi (DE-627)SPR047584106 (SPR)s12028-022-01459-6-e DE-627 ger DE-627 rakwb eng Busl, Katharina M. verfasserin aut Pregabalin for Recurrent Seizures in Critical Illness: A Promising Adjunctive Therapy, Especially for cyclic Seizures 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer Science+Business Media, LLC, part of Springer Nature and Neurocritical Care Society 2022 Background Pregabalin (PGB) is an effective adjunctive treatment for focal epilepsy and acts by binding to the alpha2-delta subunit of voltage-gated calcium channels to reduce excitatory neurotransmitter release. Limited data exist on its use in the neurocritical care setting, including cyclic seizures—a pattern of recurrent seizures occurring at nearly regular intervals. Although the mechanism underpinning cyclic seizures remains elusive, spreading excitation linked to spreading depolarizations may play a role in seizure recurrence and periodicity. PGB has been shown to increase spreading depolarization threshold; hence, we hypothesized that the magnitude of antiseizure effect from PGB is more pronounced in patients with cyclic versus noncyclic seizures in a critically ill cohort with recurrent seizures. Methods We conducted a retrospective case series of adults admitted to two academic neurointensive care units between January 2017 and March 2019 who received PGB for treatment of seizures. Data collected included demographics, etiology of brain injury, antiseizure medications, and outcome. Continuous electroencephalogram recordings 48 hours before and after PGB administration were reviewed by electroencephalographers blinded to the administration of antiseizure medications to obtain granular data on electrographic seizure burden. Cyclic seizures were determined quantitatively (i.e., < 50% variation of interseizure intervals for at least 50% of consecutive seizures). Coprimary outcomes were decrease in hourly seizure burden in minutes and decrease in seizure frequency in the 48 hours after PGB initiation. We used nonparametric tests for comparison of seizure frequency and burden and segmented linear regression to assess PGB effect. Results We included 16 patients; the median age was 69 years, 11 (68.7%) were women, three (18.8%) had undergone a neurosurgical procedure, and five (31%) had underlying epilepsy. All seizures had focal onset; ten patients (62.5%) had cyclic seizures. The median hourly seizure burden over the 48 hours prior to PGB initiation was 1.87 min/hour (interquartile range 1.49–8.53), and the median seizure frequency was 1.96 seizures/hour (interquartile range 1.06–3.41). In the 48 hours following PGB (median daily dose 300 mg, range 75–300 mg), the median number of seizures per hour was reduced by 0.80 seizures/hour (95% confidence interval 0.19–1.40), whereas the median hourly seizure burden decreased by 1.71 min/hour (95% confidence interval 0.38–3.04). When we compared patients with cyclic versus noncyclic seizures, there was a relative decrease in hourly seizure frequency (− 86.7% versus − 2%, p = 0.04) and hourly seizure burden (− 89% versus − 7.8%, p = 0.03) at 48 hours. Conclusions PGB was associated with a relative reduction in seizure burden in neurocritically ill patients with recurrent seizures, especially those with cyclic seizures, and may be considered in the therapeutic arsenal for refractory seizures. Whether this effect is mediated via modulation of spreading depolarization requires further study. Pregabalin (dpeaa)DE-He213 Antiseizure medication (dpeaa)DE-He213 Antiepileptic drug (dpeaa)DE-He213 Cyclic seizures (dpeaa)DE-He213 Neurocritical care (dpeaa)DE-He213 Nonconvulsive seizures (dpeaa)DE-He213 Fong, Michael W. K. aut Newcomer, Zachary aut Patel, Mitesh aut Cohen, Scott A. aut Jadav, Rakesh aut Smith, Christine N. aut Mitropanopoulos, Sotiris aut Bruzzone, Maria aut Hella, Maria aut Eisenschenk, Stephan aut Robinson, Christopher P. aut Roth, William H. aut Ameli, Pouya Alexander aut Babi, Marc-Alain aut Pizzi, Michael A. aut Gilmore, Emily J. aut Hirsch, Lawrence J. aut Maciel, Carolina B. (orcid)0000-0002-8763-5839 aut Enthalten in Neurocritical care New York, NY : Springer, 2004 37(2022), 1 vom: 25. Feb., Seite 140-148 (DE-627)478509855 (DE-600)2176033-0 1556-0961 nnns volume:37 year:2022 number:1 day:25 month:02 pages:140-148 https://dx.doi.org/10.1007/s12028-022-01459-6 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 37 2022 1 25 02 140-148 |
language |
English |
source |
Enthalten in Neurocritical care 37(2022), 1 vom: 25. Feb., Seite 140-148 volume:37 year:2022 number:1 day:25 month:02 pages:140-148 |
sourceStr |
Enthalten in Neurocritical care 37(2022), 1 vom: 25. Feb., Seite 140-148 volume:37 year:2022 number:1 day:25 month:02 pages:140-148 |
format_phy_str_mv |
Article |
institution |
findex.gbv.de |
topic_facet |
Pregabalin Antiseizure medication Antiepileptic drug Cyclic seizures Neurocritical care Nonconvulsive seizures |
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Neurocritical care |
authorswithroles_txt_mv |
Busl, Katharina M. @@aut@@ Fong, Michael W. K. @@aut@@ Newcomer, Zachary @@aut@@ Patel, Mitesh @@aut@@ Cohen, Scott A. @@aut@@ Jadav, Rakesh @@aut@@ Smith, Christine N. @@aut@@ Mitropanopoulos, Sotiris @@aut@@ Bruzzone, Maria @@aut@@ Hella, Maria @@aut@@ Eisenschenk, Stephan @@aut@@ Robinson, Christopher P. @@aut@@ Roth, William H. @@aut@@ Ameli, Pouya Alexander @@aut@@ Babi, Marc-Alain @@aut@@ Pizzi, Michael A. @@aut@@ Gilmore, Emily J. @@aut@@ Hirsch, Lawrence J. @@aut@@ Maciel, Carolina B. @@aut@@ |
publishDateDaySort_date |
2022-02-25T00:00:00Z |
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SPR047584106 |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">SPR047584106</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230520012324.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">220715s2022 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/s12028-022-01459-6</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)SPR047584106</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(SPR)s12028-022-01459-6-e</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Busl, Katharina M.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Pregabalin for Recurrent Seizures in Critical Illness: A Promising Adjunctive Therapy, Especially for cyclic Seizures</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2022</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">© Springer Science+Business Media, LLC, part of Springer Nature and Neurocritical Care Society 2022</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Background Pregabalin (PGB) is an effective adjunctive treatment for focal epilepsy and acts by binding to the alpha2-delta subunit of voltage-gated calcium channels to reduce excitatory neurotransmitter release. Limited data exist on its use in the neurocritical care setting, including cyclic seizures—a pattern of recurrent seizures occurring at nearly regular intervals. Although the mechanism underpinning cyclic seizures remains elusive, spreading excitation linked to spreading depolarizations may play a role in seizure recurrence and periodicity. PGB has been shown to increase spreading depolarization threshold; hence, we hypothesized that the magnitude of antiseizure effect from PGB is more pronounced in patients with cyclic versus noncyclic seizures in a critically ill cohort with recurrent seizures. Methods We conducted a retrospective case series of adults admitted to two academic neurointensive care units between January 2017 and March 2019 who received PGB for treatment of seizures. Data collected included demographics, etiology of brain injury, antiseizure medications, and outcome. Continuous electroencephalogram recordings 48 hours before and after PGB administration were reviewed by electroencephalographers blinded to the administration of antiseizure medications to obtain granular data on electrographic seizure burden. Cyclic seizures were determined quantitatively (i.e., < 50% variation of interseizure intervals for at least 50% of consecutive seizures). Coprimary outcomes were decrease in hourly seizure burden in minutes and decrease in seizure frequency in the 48 hours after PGB initiation. We used nonparametric tests for comparison of seizure frequency and burden and segmented linear regression to assess PGB effect. Results We included 16 patients; the median age was 69 years, 11 (68.7%) were women, three (18.8%) had undergone a neurosurgical procedure, and five (31%) had underlying epilepsy. All seizures had focal onset; ten patients (62.5%) had cyclic seizures. The median hourly seizure burden over the 48 hours prior to PGB initiation was 1.87 min/hour (interquartile range 1.49–8.53), and the median seizure frequency was 1.96 seizures/hour (interquartile range 1.06–3.41). In the 48 hours following PGB (median daily dose 300 mg, range 75–300 mg), the median number of seizures per hour was reduced by 0.80 seizures/hour (95% confidence interval 0.19–1.40), whereas the median hourly seizure burden decreased by 1.71 min/hour (95% confidence interval 0.38–3.04). When we compared patients with cyclic versus noncyclic seizures, there was a relative decrease in hourly seizure frequency (− 86.7% versus − 2%, p = 0.04) and hourly seizure burden (− 89% versus − 7.8%, p = 0.03) at 48 hours. Conclusions PGB was associated with a relative reduction in seizure burden in neurocritically ill patients with recurrent seizures, especially those with cyclic seizures, and may be considered in the therapeutic arsenal for refractory seizures. 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Pregabalin for Recurrent Seizures in Critical Illness: A Promising Adjunctive Therapy, Especially for cyclic Seizures Pregabalin (dpeaa)DE-He213 Antiseizure medication (dpeaa)DE-He213 Antiepileptic drug (dpeaa)DE-He213 Cyclic seizures (dpeaa)DE-He213 Neurocritical care (dpeaa)DE-He213 Nonconvulsive seizures (dpeaa)DE-He213 |
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Busl, Katharina M. Fong, Michael W. K. Newcomer, Zachary Patel, Mitesh Cohen, Scott A. Jadav, Rakesh Smith, Christine N. Mitropanopoulos, Sotiris Bruzzone, Maria Hella, Maria Eisenschenk, Stephan Robinson, Christopher P. Roth, William H. Ameli, Pouya Alexander Babi, Marc-Alain Pizzi, Michael A. Gilmore, Emily J. Hirsch, Lawrence J. Maciel, Carolina B. |
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pregabalin for recurrent seizures in critical illness: a promising adjunctive therapy, especially for cyclic seizures |
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Pregabalin for Recurrent Seizures in Critical Illness: A Promising Adjunctive Therapy, Especially for cyclic Seizures |
abstract |
Background Pregabalin (PGB) is an effective adjunctive treatment for focal epilepsy and acts by binding to the alpha2-delta subunit of voltage-gated calcium channels to reduce excitatory neurotransmitter release. Limited data exist on its use in the neurocritical care setting, including cyclic seizures—a pattern of recurrent seizures occurring at nearly regular intervals. Although the mechanism underpinning cyclic seizures remains elusive, spreading excitation linked to spreading depolarizations may play a role in seizure recurrence and periodicity. PGB has been shown to increase spreading depolarization threshold; hence, we hypothesized that the magnitude of antiseizure effect from PGB is more pronounced in patients with cyclic versus noncyclic seizures in a critically ill cohort with recurrent seizures. Methods We conducted a retrospective case series of adults admitted to two academic neurointensive care units between January 2017 and March 2019 who received PGB for treatment of seizures. Data collected included demographics, etiology of brain injury, antiseizure medications, and outcome. Continuous electroencephalogram recordings 48 hours before and after PGB administration were reviewed by electroencephalographers blinded to the administration of antiseizure medications to obtain granular data on electrographic seizure burden. Cyclic seizures were determined quantitatively (i.e., < 50% variation of interseizure intervals for at least 50% of consecutive seizures). Coprimary outcomes were decrease in hourly seizure burden in minutes and decrease in seizure frequency in the 48 hours after PGB initiation. We used nonparametric tests for comparison of seizure frequency and burden and segmented linear regression to assess PGB effect. Results We included 16 patients; the median age was 69 years, 11 (68.7%) were women, three (18.8%) had undergone a neurosurgical procedure, and five (31%) had underlying epilepsy. All seizures had focal onset; ten patients (62.5%) had cyclic seizures. The median hourly seizure burden over the 48 hours prior to PGB initiation was 1.87 min/hour (interquartile range 1.49–8.53), and the median seizure frequency was 1.96 seizures/hour (interquartile range 1.06–3.41). In the 48 hours following PGB (median daily dose 300 mg, range 75–300 mg), the median number of seizures per hour was reduced by 0.80 seizures/hour (95% confidence interval 0.19–1.40), whereas the median hourly seizure burden decreased by 1.71 min/hour (95% confidence interval 0.38–3.04). When we compared patients with cyclic versus noncyclic seizures, there was a relative decrease in hourly seizure frequency (− 86.7% versus − 2%, p = 0.04) and hourly seizure burden (− 89% versus − 7.8%, p = 0.03) at 48 hours. Conclusions PGB was associated with a relative reduction in seizure burden in neurocritically ill patients with recurrent seizures, especially those with cyclic seizures, and may be considered in the therapeutic arsenal for refractory seizures. Whether this effect is mediated via modulation of spreading depolarization requires further study. © Springer Science+Business Media, LLC, part of Springer Nature and Neurocritical Care Society 2022 |
abstractGer |
Background Pregabalin (PGB) is an effective adjunctive treatment for focal epilepsy and acts by binding to the alpha2-delta subunit of voltage-gated calcium channels to reduce excitatory neurotransmitter release. Limited data exist on its use in the neurocritical care setting, including cyclic seizures—a pattern of recurrent seizures occurring at nearly regular intervals. Although the mechanism underpinning cyclic seizures remains elusive, spreading excitation linked to spreading depolarizations may play a role in seizure recurrence and periodicity. PGB has been shown to increase spreading depolarization threshold; hence, we hypothesized that the magnitude of antiseizure effect from PGB is more pronounced in patients with cyclic versus noncyclic seizures in a critically ill cohort with recurrent seizures. Methods We conducted a retrospective case series of adults admitted to two academic neurointensive care units between January 2017 and March 2019 who received PGB for treatment of seizures. Data collected included demographics, etiology of brain injury, antiseizure medications, and outcome. Continuous electroencephalogram recordings 48 hours before and after PGB administration were reviewed by electroencephalographers blinded to the administration of antiseizure medications to obtain granular data on electrographic seizure burden. Cyclic seizures were determined quantitatively (i.e., < 50% variation of interseizure intervals for at least 50% of consecutive seizures). Coprimary outcomes were decrease in hourly seizure burden in minutes and decrease in seizure frequency in the 48 hours after PGB initiation. We used nonparametric tests for comparison of seizure frequency and burden and segmented linear regression to assess PGB effect. Results We included 16 patients; the median age was 69 years, 11 (68.7%) were women, three (18.8%) had undergone a neurosurgical procedure, and five (31%) had underlying epilepsy. All seizures had focal onset; ten patients (62.5%) had cyclic seizures. The median hourly seizure burden over the 48 hours prior to PGB initiation was 1.87 min/hour (interquartile range 1.49–8.53), and the median seizure frequency was 1.96 seizures/hour (interquartile range 1.06–3.41). In the 48 hours following PGB (median daily dose 300 mg, range 75–300 mg), the median number of seizures per hour was reduced by 0.80 seizures/hour (95% confidence interval 0.19–1.40), whereas the median hourly seizure burden decreased by 1.71 min/hour (95% confidence interval 0.38–3.04). When we compared patients with cyclic versus noncyclic seizures, there was a relative decrease in hourly seizure frequency (− 86.7% versus − 2%, p = 0.04) and hourly seizure burden (− 89% versus − 7.8%, p = 0.03) at 48 hours. Conclusions PGB was associated with a relative reduction in seizure burden in neurocritically ill patients with recurrent seizures, especially those with cyclic seizures, and may be considered in the therapeutic arsenal for refractory seizures. Whether this effect is mediated via modulation of spreading depolarization requires further study. © Springer Science+Business Media, LLC, part of Springer Nature and Neurocritical Care Society 2022 |
abstract_unstemmed |
Background Pregabalin (PGB) is an effective adjunctive treatment for focal epilepsy and acts by binding to the alpha2-delta subunit of voltage-gated calcium channels to reduce excitatory neurotransmitter release. Limited data exist on its use in the neurocritical care setting, including cyclic seizures—a pattern of recurrent seizures occurring at nearly regular intervals. Although the mechanism underpinning cyclic seizures remains elusive, spreading excitation linked to spreading depolarizations may play a role in seizure recurrence and periodicity. PGB has been shown to increase spreading depolarization threshold; hence, we hypothesized that the magnitude of antiseizure effect from PGB is more pronounced in patients with cyclic versus noncyclic seizures in a critically ill cohort with recurrent seizures. Methods We conducted a retrospective case series of adults admitted to two academic neurointensive care units between January 2017 and March 2019 who received PGB for treatment of seizures. Data collected included demographics, etiology of brain injury, antiseizure medications, and outcome. Continuous electroencephalogram recordings 48 hours before and after PGB administration were reviewed by electroencephalographers blinded to the administration of antiseizure medications to obtain granular data on electrographic seizure burden. Cyclic seizures were determined quantitatively (i.e., < 50% variation of interseizure intervals for at least 50% of consecutive seizures). Coprimary outcomes were decrease in hourly seizure burden in minutes and decrease in seizure frequency in the 48 hours after PGB initiation. We used nonparametric tests for comparison of seizure frequency and burden and segmented linear regression to assess PGB effect. Results We included 16 patients; the median age was 69 years, 11 (68.7%) were women, three (18.8%) had undergone a neurosurgical procedure, and five (31%) had underlying epilepsy. All seizures had focal onset; ten patients (62.5%) had cyclic seizures. The median hourly seizure burden over the 48 hours prior to PGB initiation was 1.87 min/hour (interquartile range 1.49–8.53), and the median seizure frequency was 1.96 seizures/hour (interquartile range 1.06–3.41). In the 48 hours following PGB (median daily dose 300 mg, range 75–300 mg), the median number of seizures per hour was reduced by 0.80 seizures/hour (95% confidence interval 0.19–1.40), whereas the median hourly seizure burden decreased by 1.71 min/hour (95% confidence interval 0.38–3.04). When we compared patients with cyclic versus noncyclic seizures, there was a relative decrease in hourly seizure frequency (− 86.7% versus − 2%, p = 0.04) and hourly seizure burden (− 89% versus − 7.8%, p = 0.03) at 48 hours. Conclusions PGB was associated with a relative reduction in seizure burden in neurocritically ill patients with recurrent seizures, especially those with cyclic seizures, and may be considered in the therapeutic arsenal for refractory seizures. Whether this effect is mediated via modulation of spreading depolarization requires further study. © Springer Science+Business Media, LLC, part of Springer Nature and Neurocritical Care Society 2022 |
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Continuous electroencephalogram recordings 48 hours before and after PGB administration were reviewed by electroencephalographers blinded to the administration of antiseizure medications to obtain granular data on electrographic seizure burden. Cyclic seizures were determined quantitatively (i.e., < 50% variation of interseizure intervals for at least 50% of consecutive seizures). Coprimary outcomes were decrease in hourly seizure burden in minutes and decrease in seizure frequency in the 48 hours after PGB initiation. We used nonparametric tests for comparison of seizure frequency and burden and segmented linear regression to assess PGB effect. Results We included 16 patients; the median age was 69 years, 11 (68.7%) were women, three (18.8%) had undergone a neurosurgical procedure, and five (31%) had underlying epilepsy. All seizures had focal onset; ten patients (62.5%) had cyclic seizures. The median hourly seizure burden over the 48 hours prior to PGB initiation was 1.87 min/hour (interquartile range 1.49–8.53), and the median seizure frequency was 1.96 seizures/hour (interquartile range 1.06–3.41). In the 48 hours following PGB (median daily dose 300 mg, range 75–300 mg), the median number of seizures per hour was reduced by 0.80 seizures/hour (95% confidence interval 0.19–1.40), whereas the median hourly seizure burden decreased by 1.71 min/hour (95% confidence interval 0.38–3.04). When we compared patients with cyclic versus noncyclic seizures, there was a relative decrease in hourly seizure frequency (− 86.7% versus − 2%, p = 0.04) and hourly seizure burden (− 89% versus − 7.8%, p = 0.03) at 48 hours. Conclusions PGB was associated with a relative reduction in seizure burden in neurocritically ill patients with recurrent seizures, especially those with cyclic seizures, and may be considered in the therapeutic arsenal for refractory seizures. 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