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Braz J Med Biol Res vol.44 no.4 Ribeirão Preto Apr. 2011
Psychopharmacotherapy of panic disorder: 8-week randomized trial with clonazepam and paroxetine
A.E. Nardi1, A.M. Valença1,3, R.C. Freire1, M.D. Mochcovitch1, R. Amrein1, A. Sardinha1, M.N. Levitan1, I. Nascimento1, V.L. de-Melo-Neto1,4, A.L. King1, A.C. de O. e Silva1,3, A.B. Veras1, G.P. Dias1,2, G.L. Soares-Filho1,5, R.T. da Costa1, M.A. Mezzasalma1, M.R. de Carvalho1, A.C. de Cerqueira1, J.E. Hallak6, J.A. Crippa6 and M. Versiani1
1Laboratório de Pânico e Respiração, Instituto de Psiquiatria, 2Laboratório de Neurobiologia da Retina, Instituto Nacional de Ciência e Tecnologia Translacional em Medicina, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brasil
3Departamento de Psiquiatria, Faculdade de Medicina, Universidade Federal Fluminense, Niterói, RJ, Brasil
4Departamento de Psiquiatria, Faculdade de Medicina, Universidade Federal de Alagoas, Maceió, AL, Brasil
5Unidade de Interconsulta Psiquiátrica, Hospital Pró-Cardíaco, Rio de Janeiro, RJ, Brasil
6Departamento de Neurociência e Comportamento, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, SP, Brasil
The objective of the present randomized, open-label, naturalistic 8-week study was to compare the efficacy and safety of treatment with clonazepam (N = 63) and paroxetine (N = 57) in patients with panic disorder with or without agoraphobia. Efficacy assessment included number of panic attacks and clinician ratings of the global severity of panic disorders with the clinical global impression (CGI) improvement (CGI-I) and CGI severity (CGI-S) scales. Most patients were females (69.8 and 68.4% in the clonazepam and paroxetine groups, respectively) and age (mean ± SD) was 35.9 ± 9.6 years for the clonazepam group and 33.7 ± 8.8 years for the paroxetine group. Treatment with clonazepam versus paroxetine resulted in fewer weekly panic attacks at week 4 (0.1 vs 0.5, respectively; P < 0.01), and greater clinical improvements at week 8 (CGI-I: 1.6 vs 2.9; P = 0.04). Anxiety severity was significantly reduced with clonazepam versus paroxetine at weeks 1 and 2, with no difference in panic disorder severity. Patients treated with clonazepam had fewer adverse events than patients treated with paroxetine (73 vs 95%; P = 0.001). The most common adverse events were drowsiness/fatigue (57%), memory/concentration difficulties (24%), and sexual dysfunction (11%) in the clonazepam group and drowsiness/fatigue (81%), sexual dysfunction (70%), and nausea/vomiting (61%) in the paroxetine group. This naturalistic study confirms the efficacy and tolerability of clonazepam and paroxetine in the acute treatment of patients with panic disorder.
Key words: Paroxetine; Clonazepam; Panic disorder; Efficacy; Safety
Panic disorder is a chronic debilitating illness characterized by severe, recurrent, spontaneous panic attacks with autonomic symptoms, with a lifetime prevalence rate of 5% (1). Panic disorder, both with and without agoraphobia, can be profoundly physically and emotionally disabling for affected individuals, and is associated with substantial costs to society (2-5). The disease has several adverse psychological consequences, including poor general medical and emotional health, increased risk of alcohol abuse, marital and occupational dysfunction, greater use of medication, increased emergency room use, with up to 20% of sufferers attempting suicide (2).
Pharmacotherapy is effective in the treatment of panic disorder compared with placebo (6-8); however, it is problematic for several reasons. Despite pharmacotherapy, 20-40% of patients with panic disorder in clinical trials remain symptomatic and this proportion may be higher in the naturalistic setting (9). In addition, the subtype of panic disorder (respiratory or non-respiratory) can influence the response to pharmacotherapy and affect outcomes (10-12). Furthermore, discontinuation of pharmacotherapy can lead to withdrawal symptoms and a significant number of panic disorder patients suffer relapse flowing cessation of treatment (13,14).
Benzodiazepines (6,8,14) and selective serotonin reuptake inhibitors (SSRIs) (8,15) are two drug classes with proven efficacy in treating panic disorder. In a meta-analysis of 53 studies including 7725 patients with panic disorder who received pharmacotherapeutic treatment, the benzodiazepines and SSRIs showed comparable efficacy (7). SSRIs have been prescribed for panic disorder with or without agoraphobia for over a decade and are recommended as first-line treatment for panic disorder on the basis of their favorable safety profile (16). The efficacy and safety profile of the SSRI paroxetine has been demonstrated in the treatment of panic disorder in a number of randomized controlled trials (17-19). However, the benzodiazepines remain one of the most commonly prescribed therapeutic options for panic disorder (20).
Benzodiazepines are rapidly acting, effective, well tolerated and suitable as monotherapy (11,21) or combination therapy (22). Clonazepam also affects serotonin transmission (23,24) and is the only benzodiazepine on the market for which additional serotonergic activity has been shown, an action that may contribute to its ansiolytic effects (23-25). Benzodiazepines and SSRIs are associated with different adverse event (AE) profiles (6,14). When patients with panic disorder cannot tolerate the AEs associated with a particular drug class, switching to a different drug class can improve the safety outcomes of panic disorder (6,26). Accordingly, which drug to prescribe depends largely on considerations of AE profiles (6).
Although SSRIs and benzodiazepines have been shown to have comparable efficacy in the treatment of panic disorder in a meta-analysis (7), there have been few direct comparisons in clinical trials. Double-blind, placebo-controlled studies have demonstrated the efficacy and safety of clonazepam and of paroxetine individually, but direct comparisons between these drugs have not been made. Therefore, the objective of this study was to compare the efficacy and safety of 8 weeks of treatment with clonazepam and paroxetine in patients with panic disorder in a naturalistic setting, using a randomized, open-label study design. Although the open design has its limitations, it permits careful individual dose adaptation as is done in clinical practice.
The study protocol was approved by the Ethics Committee of the Instituto de Psiquiatria, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil. Written informed consent was obtained from all patients prior to inclusion.
This was a naturalistically designed, prospective, randomized, open-label study. For patients on prior anti-panic medication a 1-week wash-out period was employed, except for those taking fluoxetine for whom a 6-week washout period was used. Patients were initially randomized to receive either 0.5-2 clonazepam or 10-40 mg/day paroxetine, taken after dinner. The planned starting dose was 0.5-1 mg/day clonazepam and 10 mg/day paroxetine. Maintenance doses of 2 mg clonazepam and 40 mg paroxetine were planned to be achieved at the end of the second treatment week, but patients were still kept in the study if these doses were not achieved due to AEs. For every 4 patients entering the trial, two were randomly assigned to clonazepam and two to paroxetine. Neither the patient nor the treating physician had any influence on the drug taken. Treatment was given for 8 weeks and dose adjustment was permitted according to the patient’s symptoms. Clonazepam and paroxetine were chosen for comparison since both are approved for the treatment of panic disorder in Brazil. Generic and branded versions of both drugs are available in Brazil and cost is generally low, which makes their relative efficacy and safety an important factor in the choice of treatment.
Patients were evaluated in the Panic and Respiration Laboratory of the Institute of Psychiatry, Rio de Janeiro, Brazil. Participants were male and female patients aged 18-60 years who met the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, text revision criteria for panic disorder, with or without agoraphobia, as determined by a structured clinical interview. Patients were also required to have at least two panic attacks in the week preceding their inclusion in the study. Patients were excluded if they were unable or unwilling to provide written informed consent, did not complete all the evaluations before study initiation, or if they were diagnosed with comorbidities that could affect clinical evaluation including drug abuse, neurological disorders, or severe personality disorder.
The rating was performed by independent examiners who were blind to the drugs under study. Demographic and clinical features at baseline were compared between groups. Efficacy parameters were recorded at baseline and at weeks 1, 2, 4, and 8. Efficacy assessments included the number of panic attack and clinician ratings of the global severity of panic disorder using the clinical global impression (CGI) and severity (CGI-S) scale. Scores ranged from 1 (not at all ill) to 7 (extremely ill). Global change from the baseline assessment was also rated with the CGI improvement (CGI-I) scale. Scores ranged from 1 (very much improved) to 7 (very much worse). Severity of anxiety was assessed using the Hamilton Anxiety Rating Scale (HAMA) 14-item test.
Regarding safety parameters, a physical examination was performed on day 1 of treatment and at the end of the treatment period or at study discontinuation. Blood pressure and heart rate were measured at every visit. A 12-lead electrocardiogram and laboratory tests (i.e., hematology, chemistry, urinalysis) were obtained at baseline and at week 8. AEs were recorded at baseline and at each defined time during treatment by independent examiners who were blind to the study drugs. AE data were collected by asking about spontaneous complaints and by a subsequent systematic inquiry using a list of AEs that were combined with the Benzodiazepine Discontinuation Symptom Scale (27). The severity of each AE was also recorded; multiple episodes of the same AE were counted only once, but they were rated at the greatest level of severity.
All patients who took at least one dose were included in the final analysis. Patient responses were analyzed based on an intent to treat, last value carried forward approach. Appropriate parametric and non-parametric tests were employed; the Student t-test for independent samples were used for HAMA and for the number of panic attacks. The Cochran-Armitage χ2 test for linear trends was employed for CGI-I and CGI-S. The statistical analyses were two-tailed and 5% was considered to be significant.
A total of 120 patients met the inclusion criteria; 63 were randomized to receive clonazepam and 57 to receive paroxetine. One patient in the clonazepam group and seven patients in the paroxetine group withdrew consent before the first drug intake. These patients had been included in the randomization process but were not considered in the total number of patients. Patient demographics and clinical characteristics were similar for the two groups, with no statistically significant differences between groups for any of the parameters studied (Table 1). Most patients were females (69%), were educated at least to high school level (63%), and were employed (66%). Most patients included had panic disorder plus agoraphobia (93%) and had not received prior therapy (63%). The high proportion of patients suffering from agoraphobia was due to patients with a long history of panic disorder and agoraphobia often being referred to our institute. Of 44 patients with prior therapy, 1 patient in the paroxetine group had failed treatment previously with an SSRI and no patients in the clonazepam group had failed with a benzodiazepine. The mean (± SD) initial dose was 0.97 ± 0.1 mg/day in the clonazepam group and 10.5 ± 2.3 mg/day in the paroxetine group. At week 8, the mean dose was 1.92 ± 0.3 mg/day in the clonazepam group and 38.4 ± 3.7 mg/day in the paroxetine group. Two patients who received paroxetine and 1 patient who received clonazepam withdrew from the study at the end of the first month as a result of poor efficacy; all other patients participated until the end of the 8-week study.
A 1-week wash-out period was included to remove prior anti-panic medication. Less than 25% of the patients in each group were taking anti-panic medication one week before staring the trial (24.6% in the paroxetine group and 12.7% in the clonazepam group). There was no significant difference in the number of panic attacks, CGI, or AEs reported by these patients at screening and at baseline.
After initiation of drug treatment there was a dramatic decrease in the number of weekly panic attacks in both treatment groups, which persisted over the course of the treatment period (Figure 1). At week 4, patients in the clonazepam group had significantly fewer panic attacks (0.1 ± 0.5 per week) than those in the paroxetine group (0.5 ± 0.9 per week; P < 0.01; Table 2). At week 8, patients experienced similarly low numbers of panic attacks with clonazepam and paroxetine (0.2 ± 0.6 vs 0.2 ± 0.4 per week, respectively; P = not significant). The two groups showed a similar average reduction of panic attacks over the first 8 weeks of treatment (Figure 1). The proportion of patients who were panic free following treatment is presented in Figure 2. At week 4, more patients who received clonazepam were free of panic attacks (92.06 vs 70.16%, respectively; P = 0.002).
Clonazepam had a faster onset of action than paroxetine. When CGI-I was assessed, patients treated with clonazepam had significantly greater improvements than those treated with paroxetine at week 1 (2.2 ± 0.8 vs 2.7 ± 1.0; P = 0.003) and week 2 (2.2 ± 1.0 vs 2.7 ± 1.2; P = 0.006; Table 2). CGI-I was further reduced over the course of the study, with values of 1.6 ± 1.0 for clonazepam and 2.9 ± 1.2 for paroxetine (P = 0.04) at week 8. At baseline, the severity of panic disorder as measured by CGI-S was borderline significantly higher in patients randomized to receive clonazepam versus paroxetine (4.5 ± 0.5 vs 4.3 ± 0.5; P = 0.02; Table 2). After 4 weeks of treatment, there was no significant difference between groups; CGI-S was reduced to 2.0 ± 1.0 in the clonazepam group and to 2.2 ± 1.3 in the paroxetine group. At week 8, CGI-S was 1.6 ± 1.0 in the clonazepam group and 1.9 ± 1.2 in the paroxetine group (P = not significant). In agreement with CGI-I, the severity of anxiety measured by HAMA at week 1 was significantly lower in clonazepam-treated patients (10.0 ± 3.5) than in paroxetine-treated patients (12.2 ± 4.2; P = 0.003; Table 2). Significant reductions in the clonazepam group versus the paroxetine group were also observed at week 2 (P = 0.03), but not at week 4 or at the end of the study (10.5 ± 3.9 and 10.4 ± 3.7, respectively).
No patients withdrew because of AEs. More than 60% of patients enrolled in the trial reported AEs at baseline, regardless of the study group, and these were mainly anxiety, insomnia, headache, shaking/trembling, paresthesia, memory/concentration difficulties, nausea/vomiting, sexual dysfunction, and weakness (Table 3).
Patients treated with clonazepam had significantly fewer AEs than patients treated with paroxetine at week 8 (73.0 versus 94.7%, respectively; P = 0.001; Table 3). The most common AEs in the clonazepam group were drowsiness/fatigue (57%), memory/concentration difficulties (24%), and sexual dysfunction (11%). The vast majority of AEs in clonazepam-treated patients were of mild severity, with moderate severity reported for 6 cases of drowsiness/fatigue. The most common AEs in the paroxetine group were drowsiness/fatigue (81%), sexual dysfunction (70%), and nausea/vomiting (61%). Although most AEs in the paroxetine group were of mild severity, there were several cases of moderately severe drowsiness/fatigue, sexual dysfunction, nausea/vomiting, and appetite/weight change. A severe case of sexual dysfunction was also noted with paroxetine. AEs that occurred significantly more frequently in the paroxetine group versus the clonazepam group were drowsiness/fatigue (P = 0.006), sexual dysfunction, nausea/vomiting, appetite/weight change, dry mouth, excessive sweating, diarrhea/constipation, and shaking/trembling/tremor (all P < 0.001). There were no clinically significant changes in laboratory parameters in either group during the study.
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|Table 3. Summary of adverse events (AE) at week 8.|
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The present investigation confirms earlier studies, which have demonstrated the efficacy of clonazepam (11,12,21,28-30) and paroxetine (18,19,31,32) in separate trials in the treatment of panic disorder. The present study compares clonazepam with paroxetine using a parallel methodology with the same team of health providers. There was a small difference in effectiveness in favor of clonazepam between the two treatments. As assessed by CGI-I scores, clonazepam was associated with significantly greater clinical improvement than paroxetine at the end of the 8-week treatment period. Furthermore, clonazepam was associated with a faster response than paroxetine. Although the number of panic attacks experienced was similarly reduced in both treatment groups by week 8, both CGI-I and HAMA scores were significantly better in clonazepam-treated patients than in paroxetine-treated patients at weeks 1 and 2. The slower onset of action of paroxetine is consistent with other studies of paroxetine and other SSRIs, and is often associated with increased agitation and anxiety at the beginning of treatment (14,33). Saeki et al. (34) demonstrated that genetic and pharmacokinetic factors may affect the initial therapeutic response to paroxetine (34). Plasma concentration of paroxetine, serotonin transporter gene-linked polymorphic region (5-HTTLPR) genotype, and co-morbid physical illness were significant factors affecting the initial pharmacotherapeutic effect of paroxetine in Japanese patients (34). In contrast to SSRIs, benzodiazepines are associated with a rapid onset of action (22,35). An SSRI can take 4-6 weeks to become entirely effective, but a benzodiazepine may be combined with an SSRI at the beginning of therapy to overcome this delay, and initial studies have confirmed the suitability of this approach (16,32,36).
An original methodological feature of this trial was the systematic evaluation of AEs prior to as well as during treatment. This allowed us to differentiate drug-induced AEs from pre-existing drug-independent conditions, revealing a completely new picture for some of the reported AEs. Several complaints, typically regarded as AEs, were already frequent before treatment and both investigational products were successful not only in reducing the frequency of panic attacks, but also some of the pre-existing panic attack symptoms such as anxiety, paresthesia, insomnia, weakness, headache, and shaking/trembling. Notably, clonazepam reduced the frequency of nausea/vomiting and memory and concentration difficulties, whereas these events became more frequent under paroxetine. Likewise, clonazepam had no effect on preexisting sexual activity, whereas paroxetine increased the frequency of sexual dysfunction. Both products were associated with drowsiness and/or fatigue. Whereas paroxetine was associated with appetite/weight change, dry mouth, excessive sweating and diarrhea/constipation, clonazepam did not have such effects. To summarize, in this short-term investigation of safety, almost all patients treated with paroxetine experienced AEs compared with three-quarters of patients treated with clonazepam. Furthermore, there were more cases of moderately severe and severe AEs in the paroxetine group versus the clonazepam group.
The AEs reported for clonazepam are typical of those expected from a highly potent benzodiazepine, and consistent with the safety profile of clonazepam observed in other studies (11,22,30). The most frequently reported AEs were drowsiness and lapse in memory/concentration. In memory tests, delayed recall rather than immediate recall was affected by benzodiazepine treatment, and the effect lasted for a short timeframe after administration (22). The AEs observed with paroxetine in the present analysis are consistent with other studies of SSRIs (37). In addition to the drowsiness/fatigue, sexual dysfunction and memory impairment that occurred or persisted with both agents, paroxetine treatment was commonly associated with AEs such as nausea/vomiting, dry mouth, excessive sweating, diarrhea/constipation and tremor/shaking, which were not experienced by any clonazepam-treated patients. In addition, over half of all patients who received paroxetine experienced appetite/weight change compared with only one patient treated with clonazepam.
One of the limitations of this study was the open-label design. Although the open design has its limitations, it allows for careful individual dose adaptation and was also chosen to permit continuation of the study with long-term treatment. Our sample also does not permit generalization of the results. The trial was conducted at a university research center specialized in anxiety and mood disorders. For example, our sample had a high percentage of high school or more education, which is different from the general Brazilian population. The flexible dose design of the study precludes any dose-response findings. Patients with panic disorder are especially sensitive to pharmacotherapy at the initiation of therapy, and many patients begin on half-doses (14). Clonazepam was started at 0.5 or 1 mg/day in the present study; however, all patients in both groups reached the full dose by 8 weeks of treatment.
The present acute study cannot address several important problems that are linked to long-term use of the two drugs. This issue shall be addressed in a continuation study lasting 3 years and followed by drug discontinuation. During long-term use, SSRIs may cause weight gain and sexual dysfunction, primarily anorgasmia and ejaculatory dysfunction (17,38,39), and benzodiazepine therapy in panic disorder may lead to abuse or misuse and physical dependence, and withdrawal and rebound symptoms when treatment is discontinued (40). Previous reports indicate a high level of relapse following discontinuation of panic disorder pharmacotherapy (6,13,14). In a study in patients with panic disorder who received paroxetine for 12 months, 17% of patients experienced one or more panic attacks during the 1-year follow-up period after paroxetine discontinuation (31). The long-term outcomes associated with this study, particularly relapse rates, would be of interest. A comparative study of longer duration would also prove valuable. Both clonazepam (11) and paroxetine (17,31) have been shown to be effective in the treatment of panic disorder over long follow-up periods in separate trials. In a naturalistic 3-year study of 67 patients with panic disorder, clonazepam had a sustained therapeutic effect over the entire treatment period (11). Similarly, paroxetine was effective when given over a 2-year period to 55 patients with panic disorder, with 0.23 ± 0.2 panic attacks per week recorded at the end of the treatment period (31).
To conclude, this naturalistic study confirms the efficacy and tolerability of clonazepam and paroxetine in the acute treatment of patients with panic disorder, with greater clinical improvements, faster onset of action and a more favorable AE profile observed in clonazepam-treated patients.
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We thank Hester van Lier, PhD, of Excerpta Medica who provided editorial/writing support. Research supported by CNPq and INCT Translational Medicine (CNPq). A.E. Nardi, A.M. Valença, I. Nascimento, J.A. Crippa, and M. Versiani are recipients of CNPq productivity fellowship awards. The authors received editorial/writing support solely in the preparation of this manuscript funded by F. Hoffmann-La Roche Ltd. The funding source had no role in the study design, collection, analysis or interpretation of data, nor in the decision to submit the paper for publication.
Address for correspondence: A.E. Nardi, Laboratório de Pânico e Respiração, Instituto de Psiquiatria, UFRJ, INCT-TM (CNPq), Rua Visconde de Piraja, 407/702, 22410-003 Rio de Janeiro, RJ, Brasil. Fax: +55-21-2523-6839. E-mail: email@example.com
Received August 16, 2010. Accepted February 3, 2011. Available online February 2, 2011. Published April 11, 2011.
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