一名患有双相情感障碍 II 和强迫症的女性产后愤怒发作:诊断和治疗难题。

IF 5 2区 医学 Q1 CLINICAL NEUROLOGY
Verinder Sharma
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She denied hypo/manic symptoms; however, she reported a history of bipolar I disorder in a sibling. Due to the history of sustained response to sertraline, we recommended continuation of the current dose (75 mg daily). She took it for several months before discontinuing it during her subsequent pregnancy. She remained well after stopping it but had a recurrence of depression immediately following her delivery. She was prescribed sertraline by her family physician, and after a few weeks, quetiapine 25 mg was added. She was also taking lorazepam 0.5 mg/daily, as needed.</p><p>She was referred to our clinic again 8 months after giving birth to her second child for evaluation of intrusive thoughts of harm coming to her children. She had become increasingly worried about their safety since the abrupt cessation of breastfeeding 4 months earlier. In particular, she was afraid of them dying in a motor vehicle accident, or a fire at home. She had spent thousands of dollars on car seats, strollers, mattresses, baby monitors, car window breakers, and fire alarms to safeguard her children. She also reported a history of compulsive skin-picking and hair-pulling. She had become overly sensitive to noises in the house, such as the dishwasher, breathing sounds, and chewing. On the Mood Disorder Questionnaire, she endorsed all items with co-occurrence and moderate functional impairment. She reported having had brief hypomanic and mixed episodes lasting up to a week since her last delivery. She did not have psychotic features and denied abusing alcohol or using illicit drugs.</p><p>Of her extant symptoms, she was particularly concerned about the daily occurrences of episodes of intense anger toward her husband and children. These episodes lasted 45–60 min and were accompanied by yelling, and destruction of property. There were no acts of violence, but she was afraid that she might harm others. She experienced anger attacks after her first delivery, but these were less intense, and less frequent than her rage attacks over the last few months. Her diagnosis was revised to bipolar II disorder and OCD. The sertraline dose was tapered off over 2 weeks due to lack of effectiveness and concerns about induction of manic/mixed episodes. Her quetiapine dose was gradually increased to 125 mg daily. Within 2 weeks of these changes, her sleep improved, and the rage attacks disappeared. Her partner commented on the overall improvement particularly the dramatic disappearance of rage attacks. She has maintained improvement and continues to take quetiapine. She has also been receiving individual psychotherapy. The patient provided written informed consent after reviewing the contents of this report.</p><p>A rage attack is a sudden, short-lived, intense, emotional reaction to situations or stimuli that cannot be controlled. The behavior is out of proportion to the triggering event. 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Our patient had experienced panic attacks in the past but denied concurrent symptoms of autonomic arousal during rage attacks. The exact prevalence of postpartum rage attacks in women with bipolar disorder is unknown. Due to feelings of guilt and shame, women may not disclose this symptom spontaneously. Caregivers may fail to elicit this information due to the lack of awareness of their occurrence postpartum.</p><p>Childbirth is a potent trigger of the first onset of hypo/manic episodes among women with major depressive disorder especially those with a family history of bipolar disorder. Over a decade, our patient had recurrent episodes of major depression characterized by symptoms such as increased sleep requirement, psychomotor retardation, and appetite changes; however, she experienced the first onset of hypomania only after her second delivery. 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However, collectively symptoms such as anxiety, rage, and insomnia caused clinically significant distress and impairment in her social and occupational functioning. And finally, it was difficult to ascribe certain symptoms to diagnostic categories. For example, she had obsessive thoughts, but these started racing after her second delivery. Similarly, excessive spending, typically a symptom of hypo/mania was rationalized as a compulsive act to deal with distressing obsessions about harm coming to her children. 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Her quetiapine dose was gradually increased to 125 mg daily. Within 2 weeks of these changes, her sleep improved, and the rage attacks disappeared. Her partner commented on the overall improvement particularly the dramatic disappearance of rage attacks. She has maintained improvement and continues to take quetiapine. She has also been receiving individual psychotherapy. The patient provided written informed consent after reviewing the contents of this report.</p><p>A rage attack is a sudden, short-lived, intense, emotional reaction to situations or stimuli that cannot be controlled. The behavior is out of proportion to the triggering event. Rage attacks may result in inappropriate verbal utterances, property damage, or aggressive actions. Sleep loss/insomnia in the postpartum period appears to worsen rage attacks.<span><sup>1</sup></span> While irritability is a common symptom of hypo/manic episodes, the DSM-5-TR does not list rage attacks as a symptom of bipolar disorder. 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引用次数: 0

摘要

一位26岁的初为人母的患者接受了产后抑郁症的评估和治疗。在她第一次去诊所的几周前,医生给她开了舍曲林,这是她以前用来治疗非产褥期抑郁症发作的药物。在每日75毫克的舍曲林重新试验的2周内,抑郁和焦虑症状有明显改善。她也有强迫和强迫症,但这些都没有严重到足以达到强迫症的诊断标准。由于多年来至少有10次发作的病史,确诊为重度抑郁症(见图1)。她曾两次企图自杀,包括服药过量,随后住院治疗。她否认有躁狂症状;然而,她报告了一个兄弟姐妹的双相情感障碍病史。由于对舍曲林有持续反应的病史,我们建议继续使用当前剂量(每日75mg)。她服用了几个月,后来在怀孕期间停药。停药后,她保持良好,但分娩后抑郁症立即复发。家庭医生给她开了舍曲林,几周后又加了25毫克喹硫平。根据需要,她还服用了每天0.5毫克的劳拉西泮。她在生下第二个孩子8个月后再次被转介到我们的诊所评估她的孩子会受到伤害的侵入性想法。自从4个月前突然停止母乳喂养以来,她越来越担心他们的安全。她特别害怕他们死于机动车事故,或者家里失火。为了保护孩子,她花了几千美元买了汽车座椅、婴儿车、床垫、婴儿监视器、车窗破璃器和火警报警器。她还报告有强迫性抠皮肤和拔头发的病史。她对家里的噪音过于敏感,比如洗碗机的声音、呼吸声和咀嚼声。在情绪障碍问卷中,她认可了所有伴有中度功能障碍的项目。她报告说,自上次分娩以来,她有短暂的轻度躁狂和混合性发作,持续时间长达一周。她没有精神病特征,并否认滥用酒精或非法药物。在她现存的症状中,她特别担心的是每天都会对丈夫和孩子产生强烈的愤怒。这些事件持续了45-60分钟,伴随着大喊大叫和破坏财产。没有暴力行为,但她担心她可能会伤害别人。她在第一次分娩后经历了愤怒发作,但没有过去几个月的愤怒发作那么强烈,也没有那么频繁。她的诊断被修改为双相情感障碍和强迫症。由于缺乏有效性和对诱发躁狂/混合性发作的担忧,舍曲林的剂量在2周内逐渐减少。她的喹硫平剂量逐渐增加到每天125毫克。在这些改变后的两周内,她的睡眠改善了,愤怒发作消失了。她的伴侣评论说,整体情况有所改善,尤其是愤怒发作的戏剧性消失。她一直在改善,并继续服用喹硫平。她也一直在接受个人心理治疗。患者在阅读本报告内容后提供了书面知情同意。暴怒发作是一种突然的、短暂的、强烈的、对无法控制的情况或刺激的情绪反应。这种行为与触发事件不成比例。暴怒可能导致不恰当的言语表达、财产损失或攻击性行为。产后睡眠不足/失眠似乎会加重愤怒发作虽然易怒是低躁狂发作的常见症状,但DSM-5-TR并未将愤怒发作列为双相情感障碍的症状。一些作者区分了愤怒攻击(一种功能失调的愤怒)和愤怒攻击。愤怒发作是愤怒的突然爆发,伴有自主神经觉醒的症状,如出汗、颤抖或心动过速。愤怒发作与抑郁症有关,而愤怒发作则被描述为各种精神疾病,尤其是注意力缺陷多动障碍、边缘型人格障碍和双相情感障碍。选择性血清素再摄取抑制剂,特别是氟西汀,被推荐用于治疗愤怒发作。我们的病人过去曾经历过惊恐发作,但否认在愤怒发作期间同时出现自主神经觉醒的症状。双相情感障碍女性产后愤怒发作的确切患病率尚不清楚。由于内疚感和羞耻感,女性可能不会自发地透露这种症状。由于缺乏产后意识,护理人员可能无法引出这些信息。 在患有重度抑郁症的妇女中,尤其是那些有双相情感障碍家族史的妇女中,分娩是首次发作躁狂发作的有力诱因。十多年来,我们的病人有反复发作的重性抑郁症,其特征是睡眠需求增加、精神运动迟缓和食欲改变;然而,她在第二次分娩后才经历了第一次轻度躁狂。然而,有一些“危险信号”包括高频率的抑郁发作,非典型抑郁症状,发病年龄早,以及双相情感障碍的家族史抗抑郁药的使用可能导致双相情感障碍的诊断转换。由于出生的致病作用,包括明显的愤怒/愤怒在内的混合症状在双相情感障碍妇女的产后时期很常见该病例提出了独特的诊断挑战。首先,包括焦虑在内的各种诊断领域的症状同时出现,以及迅速发展的症状学导致了一种可以恰当地描述为万花筒的临床概况。其次,由于症状持续时间短,或症状不充分,我们的患者没有达到诊断双相情感障碍和强迫症以外的阈值。然而,焦虑、愤怒和失眠等症状共同引起临床显著的痛苦和社会和职业功能的损害。最后,很难将某些症状归为诊断类别。例如,她有强迫性的想法,但这些想法在她第二次分娩后开始加速。同样,过度消费,典型的躁狂症状,被合理化为一种强迫性行为,以应对对孩子伤害的痛苦困扰。因此,很难确定情绪障碍或强迫/强迫是否导致社会或职业功能的显著损害。双相情感障碍和强迫症合并症也给治疗带来了挑战,特别是在抗抑郁药的使用方面前瞻性收集的数据包括症状特征、治疗反应的变化,以及来自其他护理人员的附带信息,对于明确双相II型障碍的诊断和为治疗决策提供信息至关重要。我们没有把重点放在双相情感障碍或强迫症的治疗上,而是决定把重点放在解决这些诊断中最痛苦或最有害的症状上。愤怒发作和失眠/睡眠不足是我们的病人表达的最常见和最痛苦的担忧。舍曲林逐渐减少,因为它似乎有助于快速循环并加重愤怒发作。由于喹硫平已被发现对包括双相情感障碍和强迫症在内的各种精神疾病有效,我们决定优化喹硫平的剂量。这个病例说明了在产后对患有双相情感障碍的女性进行强烈愤怒筛查的重要性。相反,出现愤怒发作的女性应该被评估为双相情感障碍。对于产后双相情感障碍、强迫症和愤怒发作的个体,治疗应该个体化,重点关注跨越各种精神诊断的症状。一种包括避免潜在诱因(如抗抑郁药)和控制失眠等长期因素的治疗方法是有效、安全、最重要的是简单的。我们声明没有相互竞争的利益。撰写本文的个人同意参与研究,并已审查并批准该手稿发表。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Postpartum rage attacks in a female with bipolar II disorder and obsessive-compulsive disorder: Diagnostic and treatment challenges

Postpartum rage attacks in a female with bipolar II disorder and obsessive-compulsive disorder: Diagnostic and treatment challenges

A 26-year-old first-time mother was referred for assessment and management of postpartum depression. A few weeks before her first visit to the clinic, she was prescribed sertraline which she had previously taken with for treatment of non-puerperal episodes of depression. Within 2 weeks of the retrial of sertraline 75 mg daily, there was a marked improvement in symptoms of depression and anxiety. She also had obsessions and compulsions, but these were not severe enough to reach the diagnostic criteria of obsessive-compulsive disorder (OCD). The diagnosis of major depressive disorder was confirmed due to the history of at least 10 episodes over as many years (see Figure 1). She had made two suicide attempts including a drug overdose following which she was hospitalized. She denied hypo/manic symptoms; however, she reported a history of bipolar I disorder in a sibling. Due to the history of sustained response to sertraline, we recommended continuation of the current dose (75 mg daily). She took it for several months before discontinuing it during her subsequent pregnancy. She remained well after stopping it but had a recurrence of depression immediately following her delivery. She was prescribed sertraline by her family physician, and after a few weeks, quetiapine 25 mg was added. She was also taking lorazepam 0.5 mg/daily, as needed.

She was referred to our clinic again 8 months after giving birth to her second child for evaluation of intrusive thoughts of harm coming to her children. She had become increasingly worried about their safety since the abrupt cessation of breastfeeding 4 months earlier. In particular, she was afraid of them dying in a motor vehicle accident, or a fire at home. She had spent thousands of dollars on car seats, strollers, mattresses, baby monitors, car window breakers, and fire alarms to safeguard her children. She also reported a history of compulsive skin-picking and hair-pulling. She had become overly sensitive to noises in the house, such as the dishwasher, breathing sounds, and chewing. On the Mood Disorder Questionnaire, she endorsed all items with co-occurrence and moderate functional impairment. She reported having had brief hypomanic and mixed episodes lasting up to a week since her last delivery. She did not have psychotic features and denied abusing alcohol or using illicit drugs.

Of her extant symptoms, she was particularly concerned about the daily occurrences of episodes of intense anger toward her husband and children. These episodes lasted 45–60 min and were accompanied by yelling, and destruction of property. There were no acts of violence, but she was afraid that she might harm others. She experienced anger attacks after her first delivery, but these were less intense, and less frequent than her rage attacks over the last few months. Her diagnosis was revised to bipolar II disorder and OCD. The sertraline dose was tapered off over 2 weeks due to lack of effectiveness and concerns about induction of manic/mixed episodes. Her quetiapine dose was gradually increased to 125 mg daily. Within 2 weeks of these changes, her sleep improved, and the rage attacks disappeared. Her partner commented on the overall improvement particularly the dramatic disappearance of rage attacks. She has maintained improvement and continues to take quetiapine. She has also been receiving individual psychotherapy. The patient provided written informed consent after reviewing the contents of this report.

A rage attack is a sudden, short-lived, intense, emotional reaction to situations or stimuli that cannot be controlled. The behavior is out of proportion to the triggering event. Rage attacks may result in inappropriate verbal utterances, property damage, or aggressive actions. Sleep loss/insomnia in the postpartum period appears to worsen rage attacks.1 While irritability is a common symptom of hypo/manic episodes, the DSM-5-TR does not list rage attacks as a symptom of bipolar disorder. Some authors have distinguished between anger attacks (a form of dysfunctional anger) and rage attacks. An anger attack is a sudden outburst of anger accompanied by symptoms of autonomic arousal such as sweating, trembling, or tachycardia. Anger attacks are associated with depression2 while rage attacks have been described in various psychiatric disorders, especially attention-deficit hyperactivity disorder, borderline personality disorder, and bipolar disorder. Selective serotonin reuptake inhibitors, especially fluoxetine, are recommended for the treatment of anger attacks. Our patient had experienced panic attacks in the past but denied concurrent symptoms of autonomic arousal during rage attacks. The exact prevalence of postpartum rage attacks in women with bipolar disorder is unknown. Due to feelings of guilt and shame, women may not disclose this symptom spontaneously. Caregivers may fail to elicit this information due to the lack of awareness of their occurrence postpartum.

Childbirth is a potent trigger of the first onset of hypo/manic episodes among women with major depressive disorder especially those with a family history of bipolar disorder. Over a decade, our patient had recurrent episodes of major depression characterized by symptoms such as increased sleep requirement, psychomotor retardation, and appetite changes; however, she experienced the first onset of hypomania only after her second delivery. There were however “red flags” including high frequency of depressive episodes, atypical depressive symptoms, early age at illness onset, and a family history of bipolar disorder.3 Antidepressant use may have contributed to the diagnostic switch to bipolar disorder.

Due to the pathoplastic effect of birth, mixed symptoms including marked anger/rage are common in the postpartum period among women with bipolar disorder.4 This case posed unique diagnostic challenges. First, the concurrence of symptoms from various diagnostic domains including anxiety, and the rapidly evolving symptomatology gave rise to a clinical profile that can aptly be described as kaleidoscopic. Second, due to the short duration of symptoms, or insufficient symptoms, our patient did not reach the threshold for diagnoses other than bipolar disorder and OCD. However, collectively symptoms such as anxiety, rage, and insomnia caused clinically significant distress and impairment in her social and occupational functioning. And finally, it was difficult to ascribe certain symptoms to diagnostic categories. For example, she had obsessive thoughts, but these started racing after her second delivery. Similarly, excessive spending, typically a symptom of hypo/mania was rationalized as a compulsive act to deal with distressing obsessions about harm coming to her children. Thus, it was difficult to determine whether the mood disorder or the obsessions/compulsions caused marked impairment in social or occupational functioning.

Bipolar II disorder and obsessive-compulsive comorbidity also poses treatment challenges, especially concerning the use of antidepressants.5 Prospectively collected data including changes in symptom profile, treatment response, and collateral information from other caregivers was crucial in clarifying the diagnosis of bipolar II disorder and informing treatment decisions. Rather than focusing on the treatment of bipolar disorder or OCD, we instead decided to focus on addressing the most distressing or impairing symptom (s) that cut across these diagnoses. Rage attacks and insomnia/sleep loss were the most frequent and distressing concerns expressed by our patient. Sertraline was tapered off as it appeared to contribute to rapid cycling and aggravate the rage attacks. Since quetiapine has been found effective in various psychiatric disorders including bipolar II disorder and OCD, we decided to optimize the quetiapine dose. This case illustrates the importance of screening women with bipolar II disorder for intense anger in the postpartum period. Conversely, women presenting with rage attacks should be assessed for bipolar disorder. For individuals with postpartum bipolar disorder, OCD, and rage attacks, treatment should be individualized with a focus on symptoms that cut across various psychiatric diagnoses. A treatment approach involving avoidance of potential triggers (such as antidepressants) and management of perpetuating factors such as insomnia was effective, safe, and above all simple.

We declare no competing interests.

The individual on whom this paper is written consented to participate in the research and has reviewed and approved this manuscript for publication.

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来源期刊
Bipolar Disorders
Bipolar Disorders 医学-精神病学
CiteScore
8.20
自引率
7.40%
发文量
90
审稿时长
6-12 weeks
期刊介绍: Bipolar Disorders is an international journal that publishes all research of relevance for the basic mechanisms, clinical aspects, or treatment of bipolar disorders and related illnesses. It intends to provide a single international outlet for new research in this area and covers research in the following areas: biochemistry physiology neuropsychopharmacology neuroanatomy neuropathology genetics brain imaging epidemiology phenomenology clinical aspects and therapeutics of bipolar disorders Bipolar Disorders also contains papers that form the development of new therapeutic strategies for these disorders as well as papers on the topics of schizoaffective disorders, and depressive disorders as these can be cyclic disorders with areas of overlap with bipolar disorders. The journal will consider for publication submissions within the domain of: Perspectives, Research Articles, Correspondence, Clinical Corner, and Reflections. Within these there are a number of types of articles: invited editorials, debates, review articles, original articles, commentaries, letters to the editors, clinical conundrums, clinical curiosities, clinical care, and musings.
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