Hanna Ashraf F, Bolling Danielle, Tadros Mariam
Pain Management/Anesthesiology, Florida Spine Institute, Clearwater, USA.
Pain Management, University of South Florida (USF) Health Morsani College of Medicine, Tampa, USA.
Cureus. 2024 Apr 30;16(4):e59397. doi: 10.7759/cureus.59397. eCollection 2024 Apr.
Stiff Person Syndrome (SPS) is a rare autoimmune condition marked by extremely painful muscle spasms, stiffness, and rigidity throughout the body. Its rarity often translates to limited treatment options for patients and, occasionally, challenges in obtaining a definitive diagnosis. SPS also impacts patients' mental health, social and economic involvement, and overall quality of life. A 43-year-old man was initially being seen for lumbar radicular pain. A clinical diagnosis of SPS was made by a neurologist and confirmed by in-clinic follow-ups and anti-glutamic acid decarboxylase (anti-GAD) antibody testing. The Pain Management doctor agreed with this diagnosis and offered intravenous (IV) ketamine treatment, which he has found to positively impact the treatment of similar disorders. After an initial 10-day infusion, the patient reported improvement in pain and function. For almost two years, the patient received intravenous immunoglobulin (IVIg) and IV ketamine treatments to manage their condition and maintain pain control as well as quality of life. When the patient's symptoms began worsening after IVIg infusions, the decision to withdraw IVIg infusions and continue ketamine infusions was made. After discontinuing IVIg infusions, the patient reported improvement in function and pain level and continues to receive monthly two-day ketamine boosters. Outside of the infusions, the patient was able to discontinue the use of fentanyl patches and continued taking ketamine lozenges, oxycodone-acetaminophen, and dextromethorphan for at-home pain management. The patient's symptoms continue to be managed effectively with their current regimen, enabling their return to work and experiencing an enhanced quality of life. This case illustrates the potential benefits of IV ketamine treatment for patients with treatment-resistant SPS and similar neurologic and autoimmune disorders. Understanding and examining treatment alternatives for rare syndromes is crucial for achieving optimal patient outcomes. Additionally, documenting such cases offers valuable insights into the mechanism of ketamine, extending beyond these syndromes.
僵人综合征(SPS)是一种罕见的自身免疫性疾病,其特征是全身出现极其疼痛的肌肉痉挛、僵硬和强直。因其罕见,患者的治疗选择往往有限,偶尔在获得明确诊断时也会面临挑战。SPS还会影响患者的心理健康、社会和经济参与度以及整体生活质量。一名43岁男性最初因腰椎神经根性疼痛就诊。神经科医生做出了SPS的临床诊断,并通过门诊随访和抗谷氨酸脱羧酶(抗GAD)抗体检测得以确诊。疼痛管理医生认同这一诊断,并提供了静脉注射氯胺酮治疗,他发现这种治疗对类似疾病的治疗有积极影响。经过最初为期10天的输注后,患者报告疼痛和功能有所改善。近两年来,该患者接受静脉注射免疫球蛋白(IVIg)和静脉注射氯胺酮治疗以控制病情、维持疼痛控制以及生活质量。当患者在接受IVIg输注后症状开始恶化时,决定停止IVIg输注并继续氯胺酮输注。停止IVIg输注后,患者报告功能和疼痛水平有所改善,并继续每月接受为期两天的氯胺酮强化治疗。在输注之外,患者能够停用芬太尼透皮贴剂,并继续服用氯胺酮含片、羟考酮 - 对乙酰氨基酚和右美沙芬用于居家疼痛管理。患者的症状通过当前治疗方案仍得到有效控制,使其能够重返工作岗位并体验到更高的生活质量。该病例说明了静脉注射氯胺酮治疗对难治性SPS及类似神经和自身免疫性疾病患者的潜在益处。了解和研究罕见综合征的治疗替代方案对于实现最佳患者预后至关重要。此外,记录此类病例可为氯胺酮的作用机制提供有价值的见解,其作用机制并不局限于这些综合征。