Poole Brolin B, Hamilton Leslie A, Brockman Megan M, Byrd Debbie C
PGY1 Pharmacy Resident, Department of Pharmacy, University of Tennessee Medical Center , Knoxville, Tennessee.
Assistant Professor, Department of Clinical Pharmacy, University of Tennessee College of Pharmacy , Knoxville, Tennessee.
Hosp Pharm. 2014 Oct;49(9):847-50. doi: 10.1310/hpj4909-847.
The use of gemcitabine may lead to numerous adverse effects ranging from mild to very severe, such as interstitial pneumonitis. The diagnosis of this complication is based on multiple laboratory findings, radiographic evidence, and high clinical suspicion. Presented is a case report of a patient who met these criteria and had onset consistent with drug-induced interstitial pneumonitis.
A 76-year-old White female was treated with gemcitabine for pancreatic cancer. Two months after the initiation of therapy, she was admitted to the hospital for worsening dyspnea and cough. High clinical suspicion, bilateral interstitial opacities on chest x-ray, worsening pulmonary status, and onset 2 months after initiation of therapy led to the diagnosis of gemcitabine-induced interstitial pneumonitis. Steroid therapy with prednisone was initiated, and the patient's clinical symptoms and radiographic findings improved.
Gemcitabine-induced interstitial pneumonitis is well described in the literature. It is a rare but serious complication associated with gemcitabine therapy in which patients present with worsening dyspnea. Most patients only require supportive care and discontinuation of the drug for treatment, but in severe cases supplemental oxygen and steroid therapy must be used before resolution of symptoms. It is important to obtain an accurate medication history to evaluate for other potentially pulmonary toxic medications. Radiographic findings such as bilateral infiltrates should be completely resolved after therapy.
Radiographic findings, clinical symptoms, and clinical suspicion can lead to early recognition of interstitial pneumonitis from gemcitabine. Physician awareness of this adverse effect and early recognition are keys to providing prompt treatment in resolving symptoms and decreasing mortality.
吉西他滨的使用可能会导致从轻度到非常严重的多种不良反应,如间质性肺炎。这种并发症的诊断基于多项实验室检查结果、影像学证据以及高度的临床怀疑。本文报告了一例符合这些标准且发病情况与药物性间质性肺炎相符的患者。
一名76岁的白人女性因胰腺癌接受吉西他滨治疗。治疗开始两个月后,她因呼吸困难和咳嗽加重入院。高度的临床怀疑、胸部X光显示的双侧间质模糊影、肺部状况恶化以及治疗开始两个月后发病,导致诊断为吉西他滨诱导的间质性肺炎。开始使用泼尼松进行类固醇治疗,患者的临床症状和影像学表现有所改善。
吉西他滨诱导的间质性肺炎在文献中有详细描述。这是一种与吉西他滨治疗相关的罕见但严重的并发症,患者表现为呼吸困难加重。大多数患者仅需支持治疗并停用药物即可,但若病情严重,则必须在症状缓解前使用补充氧气和类固醇治疗。获取准确的用药史以评估其他潜在的肺毒性药物非常重要。治疗后,如双侧浸润等影像学表现应完全消退。
影像学表现、临床症状和临床怀疑可促使早期识别吉西他滨所致的间质性肺炎。医生对这种不良反应的认识以及早期识别是及时治疗以缓解症状和降低死亡率的关键。