Division of Pediatric Hematology-Oncology-BMT, Emory University, Atlanta, Georgia.
Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Atlanta, Georgia.
JAMA Netw Open. 2019 May 3;2(5):e194410. doi: 10.1001/jamanetworkopen.2019.4410.
The hallmark of sickle cell disease (SCD) is vaso-occlusive pain that may be acute and episodic or may progress to chronic, persistent pain with unpredictable and disabling exacerbations. Patients with SCD rely on opioids almost exclusively for acute and chronic pain management.
To understand how the current opioid epidemic and subsequent guidelines from the Centers for Disease Control and Prevention are associated with the management of acute and chronic pain for patients with SCD.
DESIGN, SETTING, AND PARTICIPANTS: Qualitative study using semistructured interview guides. Interviews 1 hour or longer were conducted over the telephone. Participants were adults (aged ≥18 years) diagnosed with SCD who experienced pain on 3 or more days per week recruited from national SCD conferences, symposiums, and 2 sickle cell clinics. Open coding analysis facilitated thematic analysis of interview transcripts. Data collection took place from May 2017 to June 2018.
Participant perspective of any changes to their pain management associated with the 2016 guidelines from the Centers for Disease Control and Prevention.
The 15 adults interviewed had a median (range) age of 32 (21-52) years; 13 (87%) were female; and all were of African American race/ethnicity. Participants reported that recently their opioid prescriptions had become more restrictive, were more closely monitored, and were increasingly difficult to fill in pharmacies. Participants also described increased stigmatization about opioid use and that their medical care was being affected by the physician's exclusive focus on reducing pain medication use. There was an emerging interest among adult patients in the consideration of the use of alternative therapies, including marijuana, to manage pain.
These findings suggest that from the perspective of adults living with SCD, the opioid epidemic may have negatively affected patients' care by increasing barriers to opioids. Patients reported decreased opioid dosing, increased stigmatization regarding opioid use, physician preoccupation with opioid dosage interfering with comprehensive care, and lack of access to alternative therapies.
镰状细胞病(SCD)的标志是血管阻塞性疼痛,可能是急性和间歇性的,也可能进展为慢性、持续性疼痛,并伴有不可预测和使人丧失能力的恶化。SCD 患者几乎完全依赖阿片类药物来治疗急性和慢性疼痛。
了解当前阿片类药物流行以及疾病控制与预防中心随后发布的指南如何与 SCD 患者的急性和慢性疼痛管理相关。
设计、设置和参与者:使用半结构化访谈指南进行定性研究。对在全国 SCD 会议、研讨会和 2 家镰状细胞诊所招募的每周疼痛发作 3 天或以上的成年(年龄≥18 岁)SCD 患者进行了 1 小时或更长时间的电话访谈。开放性编码分析促进了访谈记录的主题分析。数据收集于 2017 年 5 月至 2018 年 6 月进行。
参与者对与疾病控制与预防中心 2016 年指南相关的疼痛管理变化的看法。
接受访谈的 15 名成年人的平均(范围)年龄为 32(21-52)岁;13 名(87%)为女性;所有人均为非裔美国人。参与者报告说,最近他们的阿片类药物处方变得更加受限,受到更密切的监测,并且在药店越来越难以配药。参与者还描述了对阿片类药物使用的污名化增加,以及他们的医疗保健受到医生专注于减少止痛药使用的影响。成年患者对考虑使用替代疗法(包括大麻)来管理疼痛表现出了浓厚的兴趣。
这些发现表明,从患有 SCD 的成年人的角度来看,阿片类药物流行可能通过增加阿片类药物的障碍来对患者的护理产生负面影响。患者报告阿片类药物剂量减少、阿片类药物使用污名化增加、医生专注于阿片类药物剂量会干扰全面护理以及无法获得替代疗法。