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BMC Neurology

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Effects of clobazam for treatment of refractory status epilepticus

  • Dominik Madžar1Email author,
  • Anna Geyer1,
  • Ruben U. Knappe1,
  • Stephanie Gollwitzer1,
  • Joji B. Kuramatsu1,
  • Stefan T. Gerner1,
  • Hajo M. Hamer1 and
  • Hagen B. Huttner1
BMC NeurologyBMC series – open, inclusive and trusted201616:202

https://doi.org/10.1186/s12883-016-0724-y

Received: 17 March 2016

Accepted: 15 October 2016

Published: 21 October 2016

Abstract

Background

Clobazam (CLB) is a well characterized antiepileptic drug (AED) that differs from other benzodiazepines by its basic chemical structure and pharmacodynamic properties. Only one previous study examined the efficacy of CLB as add-on therapy in refractory status epilepticus (RSE).

Methods

We analyzed RSE episodes treated in our institution between 2001 and 2012. Successful treatment with CLB was scored if CLB was the last AED added to therapy before RSE termination. We assessed the differences between patients with and without CLB and correlated CLB with outcome. Among patients treated with CLB, we studied responders and non-responders and compared our CLB cohort with recently published data.

Results

CLB was part of the AED regimen in 24/70 (34.3 %) RSE episodes. In six of these (25.0 %) RSE resolution was attributed to CLB. Baseline characteristics of episodes with and without CLB treatment showed no significant differences and RSE termination rates were very similar (83.3 % vs. 80.4 %). CLB was administered in clinically more complex RSE with longer RSE duration and worse outcome, but CLB was not related independently to outcome. Comparison of our results with previously published data revealed that baseline characteristics as well as CLB maintenance doses and time of treatment initiation were similar in both cohorts. CLB was less frequently the last AED added to RSE therapy in our patients indicating a lower treatment success rate than previously reported.

Conclusions

CLB represents a reasonable AED and promising add-on agent for treatment of RSE. However, rates of successful CLB response were substantially lower than in a recently published study. Differing RSE characteristics and treatment strategies may account for the discrepancy between study results, as RSE etiologies and seizures types associated with unfavorable prognosis were more common in our cohort, while anesthetics tended to be less frequently applied to achieve seizure control.

Keywords

Refractory status epilepticusClobazamAntiepileptic drugsOutcome

Background

Treatment of refractory status epilepticus (RSE) frequently requires application of more than three antiepileptic drugs (AEDs). As there is a limited number of intravenous AEDs, orally administered AEDs represent a therapeutic option particularly for longer RSE episodes [13]. Recently, clobazam (CLB) has been associated with high rates of RSE termination [4]. CLB is a well characterized benzodiazepine with a unique chemical structure and special pharmacodynamic properties. While various studies investigated the efficacy of CLB for treatment of refractory epilepsy, its potential in status epilepticus (SE) and particularly RSE remains uncertain [5]. We investigated the efficacy of CLB as add-on treatment in RSE and compared results with those of a recently published study.

Methods

Definition of refractory status epilepticus

SE was diagnosed on the basis of clinical and/or electroencephalographic evidence of seizure activity with a duration of at least 5 min, or of a series of seizures without interictal clinical recovery [6]. RSE was defined as SE refractory to administration of at least two properly dosed AEDs [7, 8].

Identification of RSE episodes and inclusion/exclusion criteria

For identification of RSE episodes, we screened all consecutive patients treated for SE between January 2001 and December 2012 by analyzing our institutional databases including hospital records, clinical notes, and EEG reports. RSE due to hypoxic brain damage was excluded as it was considered an entity of its own with a particularly poor prognosis [9]. Furthermore, for reasons of comparability with previous studies on RSE, simple-partial and absence RSE episodes were excluded [7, 10].

Collection of clinical and RSE-specific data

We obtained demographic baseline characteristics, laboratory findings on hospital admission, RSE-specific information, and data on treatment and complications. RSE duration was defined as time from the onset of seizures until termination, the latter being confirmed either electroencephalographically or based on clinical improvement arguing against ongoing seizure activity. RSE etiology was assessed according to ILAE criteria (cryptogenic, acute, remote, or progressive symptomatic) [11] and was considered potentially fatal when fulfilling the criteria proposed by Rossetti and coworkers [12]. Clinical severity was graded according to the Status Epilepticus Severity Score (STESS) and RSE episodes were dichotomized into STESS < 3 and STESS ≥ 3 [13]. For every AED administered, we recorded the date of first application, the duration of treatment, and the dosage. All AEDs used for RSE therapy (including initial benzodiazepines as well as anesthetics) were counted as contributing to the total number of AEDs. In all episodes in which patients received CLB, EEG data were reviewed and the episodes were grouped into the following categories based on the findings on the first EEG: +/− lateralized periodic discharges (LPD), +/− lateralized seizure patterns or lateralized rhythmic delta activity (RDA), +/− generalized periodic discharges (GPD), generalized seizure patterns, or generalized RDA.

Outcome definition and assessment

The primary outcome measure was successful response to CLB, defined as “CLB responders” if CLB was the last AED added to treatment before RSE termination. The secondary outcome measure was functional outcome at last available follow-up. Functional outcome was assessed using the modified Rankin Scale (mRS). Poor outcome was defined when episodes either resulted in an mRS >2 or – in case of a premorbid mRS between 3 and 5 – if there was further functional decline, i.e. increase in the mRS.

Statistical analysis

We compared CLB responders and non-responders, patients treated with and without CLB, and our CLB cohort with the one reported by Sivakumar et al. [4]. Statistics were performed using SPSS Statistics 20.0 (www.spss.com). P values of 0.05 or less were considered statistically significant and all tests were two-sided. For assessment of frequency distributions of categorical variables, Pearson χ2 test, or where appropriate, Fisher’s exact tests were applied. We used the Kolmogorov-Smirnov test to distinguish between normal and non-normal data distribution. Normally distributed data were compared with the Student’s t-test, non-normally distributed data with the Mann-Whitney U test. In order to identify independent predictors of outcome, all variables significant on univariate analysis were entered into a forward inclusion multivariable logistic regression model. Parameters representing components of STESS were not added separately into the model when the overall STESS showed significant association upon univariate analysis.

Results

We identified 71 RSE episodes in 65 patients. We excluded one episode because CLB treatment had been initiated before progression into RSE. Overall, RSE was treated with CLB in 24/70 (34.3 %) episodes. CLB was initiated after a median RSE duration of 2 days (IQR, 0–9 days) with a median maintenance dose of 20 mg/day (IQR, 14–23 mg/day) and was applied for a median of 8 days (IQR, 5–13 days). Therapy was preceded by a median of 4 (IQR, 3–6) other AEDs, while a median of 2 more AEDs (IQR, 0–4) followed CLB.

CLB was the last AED added to therapy and – according to the a priori definition – terminated RSE in 6/24 (25.0 %) episodes. Comparing CLB responders with non-responders revealed a significantly higher rate of acute symptomatic RSE etiology in non-responders, whereas essentially all basic characteristics as well as EEG features were similar among both groups (Table 1).
Table 1

Comparison of clobazam responders and non-responders

Variable

Treated with CLB (n = 24)

CLB responders (n = 6)

CLB non-responders (n = 18)

P value

Demographics

 Gender, female

16 (66.7)

3 (50.0)

13 (72.2)

0.362b

 Age on admission, y

64 (52–72)

70 (59–71)

64 (50–72)

0.820c

 Age ≥ 65 y

11 (45.8)

4 (66.7)

7 (38.9)

0.357b

 Premorbid mRS

4 (1–4)

4 (4–5)

1 (1–4)

0.104c

RSE characteristics

 NCSE in coma

4 (16.7)

1 (16.7)

3 (16.7)

1.000b

 Generalized convulsive SE

8 (33.3)

3 (50.0)

5 (27.8)

0.362b

 Complex-partial SE

12 (50.0)

2 (33.3)

10 (55.6)

0.640b

 Stuporous or comatose

16 (66.7)

4 (66.7)

12 (66.7)

1.000b

 Acute symptomatic etiology

10 (41.7)

0 (0)

10 (55.6)

0.024 b

 History of seizures

10 (41.7)

4 (66.7)

6 (33.3)

0.192b

 Potentially fatal etiology

11 (45.8)

3 (50.0)

8 (44.4)

1.000b

 STESS

3 (1–4)

3 (3–4)

3 (1–4)

0.537c

 STESS ≥ 3

15 (62.5)

5 (83.3)

10 (55.6)

0.351b

EEG features

 Lateralized seizure patterns/RDA

9 (37.5)

2 (33.3)

7 (38.7)

1.000b

 Lateralized periodic discharges

10 (41.7)

4 (66.7)

6 (33.3)

0.192b

 Lateralized periodic discharges or seizure patterns/RDA

19 (79.2)

6 (100)

13 (72.2)

0.280b

Laboratory findings on admission

 Leukocyte count, ×103/μl

8.5 (6.3–12.0)

8.5 (8.0–10.3)

8.8 (5.8–12.2)

0.914c

 C-reactive protein, mg/l

18.0 (4.2–56.2)

3.4 (1.2–56.6)

33.0 (13.8–56.3)

0.446c

 Hemoglobin, g/dl

11.2 (1.6)

10.9 (0.9)

11.3 (1.7)

0.622d

 Serum sodium, mmol/l

136.5 (7.3)

136.8 (4.7)

136.4 (8.1)

0.908d

Treatment and complications

 Duration of RSE, d

16 (8–32)

6 (4–36)

16 (10–27)

0.820c

 Length of hospital stay, d

29 (13–61)

14 (6–53)

29 (14–57)

0.673c

 Mechanical ventilation

13 (54.2)

3 (50.0)

10 (55.6)

1.000b

 Length of mechanical ventilation, d

6 (0–43)

0 (0–30)

6 (0–48)

0.770c

 Use of anesthetics

11 (45.8)

3 (50.0)

8 (44.4)

1.000b

 Induction of burst suppression

11 (45.8)

3 (50.0)

8 (44.4)

1.000b

 Number of AEDs

7 (5–11)

9 (5–14)

7 (4–11)

0.537c

 Use of vasopressors

13 (54.2)

3 (50.0)

10 (55.6)

1.000b

 Sepsis

8 (33.3)

3 (50.0)

5 (27.8)

0.362b

Outcome

 RSE terminated

20 (83.3)

6 (100.0)

14 (77.8)

0.539b

 Poor outcome at follow-upa

18 (78.3)

4 (80.0)

14 (77.8)

1.000b

 In-hospital mortality

4 (16.7)

0 (0.0)

4 (22.2)

0.539b

Values are n (%), mean (±standard deviation) or median (interquartile range); significant (p < 0.05) parameters are expressed in bold

Abbreviations: AED antiepileptic drug, CLB clobazam, mRS modified Rankin Scale score, NCSE noncunvulsive status epilepticus, RDA rhythmic delta activity, RSE refractory status epilepticus, SE status epilepticus, STESS Status Epilepticus Severity Score

aData available for 23 episodes

bFisher’s exact test

cMann-Whitney U-test

dStudent’s t-test

Table 2 summarizes demographics, clinical and RSE-specific characteristics, as well as laboratory findings of episodes treated with or without CLB. RSE termination rates were not significantly different in patients treated with (20/24; 83.3 %) or without (37/46; 80.4 %) CLB. Therapy with CLB was associated with clinically more complex RSE, significantly longer RSE durations, and higher numbers of administered AEDs resulting in worse functional long-term outcome (Table 2; poor outcome CLB: 18/23 (78.3 %) vs. no CLB: 23/45 (51.1 %); p = 0.030). The median period from RSE resolution till last-available follow-up was 12 weeks (IQR, 6–35) and outcome was poor in 60.3 % of all episodes. Upon multivariable analysis, RSE duration (OR 1.10; 95 % CI: 1.00–1.28; p = 0.044), sepsis (OR 10.2; 95 % CI: 1.25–82.46; p = 0.030), and STESS ≥ 3 (OR 11.92; 95 % CI: 1.93–73.56; p = 0.008) – but not use of CLB (OR 1.80; 95 % CI: 0.35–9.13; p = 0.481) – were independently related to outcome.
Table 2

Comparison of episodes treated with and without clobazam

Variable

Total cohort (n = 70)

Treated with CLB (n = 24)

Not treated with CLB (n = 46)

P value

Demographics

 Gender, female

47 (67.1)

16 (66.7)

31 (67.4)

0.951b

 Age on admission, y

70 (49–78)

64 (52–72)

73 (45–80)

0.225d

 Age ≥ 65 y

41 (58.6)

11 (45.8)

30 (65.2)

0.118b

 Premorbid mRS

3 (1–4)

4 (1–4)

3 (1–4)

0.694d

RSE characteristics

 NCSE in coma

9 (12.9)

4 (16.7)

5 (10.9)

0.481c

 Generalized convulsive SE

31 (44.3)

8 (33.3)

23 (50.0)

0.183b

 Complex-partial SE

30 (42.9)

12 (50.0)

18 (39.1)

0.383b

 Stuporous or comatose

44 (62.9)

16 (66.7)

28 (60.9)

0.634b

 Acute symptomatic etiology

31 (44.3)

10 (41.7)

21 (45.7)

0.750b

 History of seizures

37 (52.9)

10 (41.7)

27 (58.7)

0.175b

 Potentially fatal etiology

31 (44.3)

11 (45.8)

20 (43.5)

0.851b

 STESS

3 (2–4)

3 (1–4)

3 (2–4)

0.550d

 STESS ≥ 3

42 (60.0)

15 (62.5)

27 (58.7)

0.758b

Laboratory findings on admission

 Leukocyte count, ×103/μl

9.4 (7.4–12.5)

8.5 (6.3–12.0)

10.1 (7.8–12.9)

0.197d

 C-reactive protein, mg/l

15.7 (3.6–53.0)

18.0 (4.2–56.2)

8.3 (3.2–40.3)

0.273d

 Hemoglobin, g/dl

11.7 (1.7)

11.2 (1.6)

11.9 (1.8)

0.110e

 Serum sodium, mmol/l

136.9 (7.2)

136.5 (7.3)

137.2 (7.3)

0.704e

Treatment and complications

 Duration of RSE, d

9 (4–17)

16 (8–32)

8 (4–14)

0.003 d

 Length of hospital stay, d

18 (10–30)

29 (1361)

18 (1029)

0.071 d

 Mechanical ventilation

44 (62.9)

13 (54.2)

31 (67.4)

0.277b

 Length of mechanical ventilation, d

3 (0–16)

6 (0–43)

6 (0–15)

0.459d

 Use of anesthetics

43 (61.4)

11 (45.8)

32 (69.6)

0.053 b

 Induction of burst suppression

28 (40.0)

11 (45.8)

17 (37.0)

0.472b

 Number of AEDs

6 (5–8)

7 (5–11)

6 (5–8)

0.028 d

 Use of vasopressors

40 (57.1)

13 (54.2)

27 (58.7)

0.716b

 Sepsis

19 (27.1)

8 (33.3)

11 (23.9)

0.400b

Outcome

 RSE terminated

57 (81.4)

20 (83.3)

37 (80.4)

1.000c

 Poor outcome at follow-upa

41 (60.3)

18 (78.3)

23 (51.1)

0.030 b

 In-hospital mortality

12 (17.1)

4 (16.7)

8 (17.4)

1.000c

Values are n (%), mean (±standard deviation) or median (interquartile range); significant (p < 0.05) parameters are expressed in bold, parameters showing a statistical trend (p < 0.1) are expressed in italics

Abbreviations: AED antiepileptic drug, CLB clobazam, mRS modified Rankin Scale score, NCSE noncunvulsive status epilepticus, RSE refractory status epilepticus, SE status epilepticus, STESS Status Epilepticus Severity Score

aData available for 68 episodes

bPearson χ2 test

cFisher’s exact test

dMann-Whitney U-test

eStudent’s t-test

The comparison of our RSE patients treated with CLB with those from the study by Sivakumar and coworkers revealed no significant differences regarding patient age and duration of hospital stay. In our cohort, a history of seizures tended to be rarer and there was a trend toward less frequent use of anesthetics. CLB maintenance doses and days in RSE before initiation of CLB treatment were similar, whereas CLB was the last AED added to therapy in a significantly lower number of patients in our cohort (Table 3).
Table 3

Comparison of clobazam treated patients from the study by Sivakumar et al. and the present study

Variable

Sivakumar et al. (n = 17)

Present study (n = 24)

P value

Age on admission, y

63 (54–70)

64 (52–72)

0.466b

History of seizures

11 (64.7)

10 (41.7)

0.146a

CLB maintenance dose (mg/d)

20 (10–30)

20 (14–23)

0.763b

RSE duration before CLB, d

4 (2–7)

2 (0–9)

0.432b

CLB last AED added to therapy

16 (94.1)

6 (25.0)

<0.001 a

Use of anesthetics

12 (70.6)

11 (45.8)

0.116a

Length of hospital stay, d

30 (17–38)

29 (13–61)

0.672b

Values are n (%), or median (interquartile range); significant (p < 0.05) parameters are expressed in bold

Abbreviations: CLB clobazam, RSE refractory status epilepticus

aPearson χ2 test

bMann-Whitney U-test

Discussion

CLB has an interesting pharmacological profile and its role in the treatment of refractory epilepsy is increasingly studied [5]. The possibility of nasogastral tube administration with excellent bioavailability [14] makes CLB moreover an AED alternative worth considering in RSE. In this study, we analyzed CLB for RSE and aimed to compare our findings with recently published data. We observed less convincing results regarding CLB efficacy in seizure termination. As a consequence of different definitions of CLB treatment success, however, comparing our results with those of Sivakumar and coworkers is difficult. In their study, the latter used a strict definition only attributing RSE termination to CLB when SE was terminated within 24 h of CLB administration without changes in concurrent AEDs. Given that not all of our patients were monitored with continuous EEG and that we felt we could not with certainty exclude modifications in co-administered AEDs in a retrospective approach, we chose to use a surrogate for successful CLB treatment, i.e. whether CLB was the last AED added to therapy before RSE termination. Sivakumar and coworkers reported that CLB was the last AED added in the vast majority of their cases. Compared to our findings, this would equal a significantly higher rate of successful CLB treatment according to our definition (94.1 % vs. 25.0 %; p < 0.001) [4]. As dosing and timing of CLB were similar in both studies, factors not directly associated with CLB treatment seem to substantially contribute to the discrepancies between study findings. A history of seizures, for instance, tended to be rarer in our cohort. As we furthermore excluded simple-partial RSE from analysis, seizure types and RSE etiologies generally associated with a rather unfavorable prognosis [15] were probably more common in our study population. Despite this fact, the number of episodes treated with anesthetics tended to be lower than in the study of Sivakumar et al. which probably reflects diverse RSE treatment strategies and again underscores the difficulty of comparing the two studies.

Regarding our cohort, patients with and without CLB were similar in their baseline characteristics, but there were significant differences in RSE treatment-specific parameters such that CLB treated episodes appeared clinically more complex with longer RSE duration requiring more AEDs. Furthermore, CLB therapy was overrepresented in episodes in which the use of anesthetics was avoided or postponed, presumably to prevent negative side effects of therapeutic coma induction [16]. As far as one can conclude from existing studies, including the present one, it appears that CLB is rather applied in more severe RSE and is currently not considered an early choice AED [4]. Despite a comparatively low success rate, initiation of CLB was still linked to RSE resolution in some episodes and – in light of an internalization of GABA receptors with prolonged seizure activity – CLB appears to still have effects despite RSE refractoriness to benzodiazepines [17]. That we observed no CLB responders among patients with acute symptomatic RSE etiology may potentially suggest different pathophysiological mechanisms involved.

The retrospective nature limits the interpretation of our data and large confidence intervals reflect certain data instability. Moreover, the small number of RSE episodes treated with CLB reduces the generalizability of our findings. Not all of our patients received continuous EEG monitoring; this may cause imprecision in the assessment of time of RSE termination. Given the high median number of AEDs applied, effects of AEDs other than CLB in aborting seizures in our cohort cannot be ruled out in those cases in which CLB was the last AED added to therapy. We compared our patients with a cohort from a previous study which applied different criteria for inclusion and assessment of treatment response. The results of this analysis have therefore to be interpreted with due caution. We used the mRS for outcome assessment. Given a high median premorbid mRS score with some patients having 5 points already prior to admission, it is possible that in certain cases new deficits caused by RSE may have not been reflected adequately.

Conclusions

Even if we were unable to confirm the high rates of RSE resolution reported, CLB remains an interesting AED with evident effects on RSE. Despite CLB representing a reasonable therapeutic option in RSE, based on present data, rapid SE termination – if necessary with the use of anesthetics – should not be delayed for treatment attempts with CLB. Further studies using stronger statistical designs are warranted to determine the clinical efficacy of CLB in SE and RSE.

Abbreviations

AED: 

Antiepileptic drug

CI: 

Confidence interval

CLB: 

Clobazam

EEG: 

Electroencephalography

IQR: 

Interquartile range

mRS: 

Modified Rankin Scale

NCSE: 

Nonconvulsive status epilepticus

RSE: 

Refractory status epilepticus

SE: 

Status epilepticus

STESS: 

Status Epilepticus Severity Score

Declarations

Acknowledgements

Not applicable.

Funding

This work was supported by a research grant (ELAN-13-07-15-1) from the ELAN Fonds University of Erlangen-Nuremberg, Germany.

Availability of data and material

The datasets on which the conclusions of our manuscript rely are stored in our institutional database. We did not obtain permission to deposit these data on publicly available repositories from our institutional Ethics Committee and we can therefore not share them.

Authors’ contributions

DM: study concept and design, data acquisition, analysis and interpretation of data, statistical analysis, manuscript drafting. HBH: study concept and supervision, data interpretation, manuscript drafting. AG: study design, data acquisition and interpretation, manuscript drafting. JBK, STG, RUK, SG and HMH: data interpretation, critical revision for important intellectual content. All authors have read the manuscript, agreed with the contents, and approved the final version of the manuscript.

Competing interests

The authors declare that they have no competing interests.

Consent for publication

Not applicable

Ethics approval and consent to participate

The study was approved by the Local Ethics Committee of the Friedrich-Alexander University Erlangen-Nuremberg, Germany (vote number: 48_15Bc). Given the retrospective nature of the study, the need for informed consent was waived.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Department of Neurology, University Hospital Erlangen

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