Department of Pathology, Haukeland University Hospital, Jonas Lies Vei 65, Bergen, 5021, Norway.
Department of Pathology, Haukeland University Hospital, Jonas Lies Vei 65, Bergen, 5021, Norway; Department of Clinical Medicine, University of Bergen, Jonas Lies Vei 87, Bergen, 5021, Norway.
Hum Pathol. 2021 Oct;116:102-111. doi: 10.1016/j.humpath.2021.07.009. Epub 2021 Jul 28.
The polymer polyvinylpyrrolidone (PVP) is an excipient widely used in prescription drugs. Depending on the molecular weight (MW), parenterally administered PVP may accumulate in various tissues. Consequently, moderate and high MW PVP have only been used in oral preparations since the late 1970s. Surprisingly, starting in 2009, pathology departments in Norway received biopsies revealing PVP deposition, all from patients with a history of intravenous drug use. We identified 13 patients with PVP deposition and re-evaluated 31 biopsies and two autopsies. Common indications for biopsy were renal insufficiency, anemia, pathological fractures, and abdominal complaints. We observed PVP deposits in all biopsies (kidney, hematopoietic bone marrow, bone, gastrointestinal tract, lymph node, and skin) and all sampled tissue from the autopsies. Overall, the clinical findings could be related to PVP deposits in the biopsies. In the most seriously affected patients, PVP deposition caused severe organ dysfunction and contributed to the fatal outcomes of two patients. All patients except for one were prescribed opioid substitution drugs (OSDs), and most of the patients admitted to having injected such medications. Several OSDs contain PVP. One methadone formulation that was marketed in Norway from 2007 to 2014 contained large amounts of very high MW PVP, making it the most likely source of PVP deposition. Although the presumed source of PVP in these patients has now been withdrawn from the market, pathologists should be aware of PVP deposits when evaluating biopsies from this patient group.
聚合物聚乙烯吡咯烷酮(PVP)是一种广泛用于处方药的赋形剂。根据分子量(MW)的不同,注射用 PVP 可能会在各种组织中蓄积。因此,自 20 世纪 70 年代末以来,中、高分子量 PVP 仅用于口服制剂。令人惊讶的是,自 2009 年以来,挪威的病理科开始收到显示 PVP 沉积的活检报告,所有患者均有静脉药物使用史。我们确定了 13 例 PVP 沉积患者,并重新评估了 31 例活检和 2 例尸检。活检的常见指征包括肾功能不全、贫血、病理性骨折和腹部不适。我们在所有活检(肾、造血骨髓、骨、胃肠道、淋巴结和皮肤)和尸检的所有取样组织中都观察到 PVP 沉积。总的来说,临床发现可能与活检中的 PVP 沉积有关。在受影响最严重的患者中,PVP 沉积导致严重的器官功能障碍,并导致两名患者死亡。除一名患者外,所有患者均被开处阿片类药物替代药物(OSD),且大多数患者承认注射过此类药物。几种 OSD 含有 PVP。一种 2007 年至 2014 年在挪威上市的美沙酮制剂含有大量非常高分子量的 PVP,这使其成为 PVP 沉积的最可能来源。尽管这些患者 PVP 的推测来源已从市场上撤出,但病理学家在评估来自该患者群体的活检时应注意 PVP 沉积。