Painful Diabetic Peripheral Neuropathy Study of Chinese Outpatients (PDNSCOPE): A Multicentre Cross-Sectional Registry Study of Clinical Characteristics and Treatment in Mainland China

被引:15
作者
Zhang, Yuanjin [1 ]
Zhang, Shaowei [2 ]
Pan, Liya [3 ]
Wang, Baojun [4 ]
Sun, Yuanlin [5 ]
Gao, Lijun [6 ]
Wang, Ling [7 ]
Cui, Lijuan [8 ]
Zhang, Qing [9 ]
Shang, Heng [10 ]
Jin, Suqin [11 ]
Qin, Xing [12 ]
Geng, Deqin [13 ]
Yu, Xiaorong [14 ]
Yang, Lin [15 ]
Li, Li [16 ]
Li, Zuoxiao [17 ]
Yan, Chaoli [18 ]
Sun, Hongbin [19 ]
Sun, Tao [20 ]
Du, Baoxin [21 ]
Cao, Junying [22 ]
Hu, Fengyun [23 ]
Ma, Jianhua [24 ]
Zhou, Shengnian [25 ]
Zhao, Fengli [26 ]
Li, Wei [27 ]
Zheng, Jianming [28 ]
Yi, Yanhui [29 ]
Xu, Jianguo [30 ]
Hu, Bo [31 ]
Sheng, Baoying [32 ]
Li, Zhaohui [33 ]
Zhao, Zhong [34 ]
Yang, Ting [35 ]
Wang, Ni [36 ]
Zhao, Hongdong [37 ]
Mima, Dunzhu [38 ]
Qu, Huaiqian [39 ]
Wang, Yi [40 ]
Song, Fuxia [41 ]
Li, Xinyi [42 ]
Li, Nan [43 ]
Fan, Dongsheng [1 ]
机构
[1] Peking Univ Third Hosp, Dept Neurol, 49th North Garden Rd, Beijing, Peoples R China
[2] Shenyang Weikang Hosp, Dept Endocrinol, Shenyang, Peoples R China
[3] Guangxi Med Univ, Dept Neurol, Affiliated Hosp 4, Liuzhou, Peoples R China
[4] Baotou Cent Hosp, Dept Neurol, Baotou, Peoples R China
[5] Panjin Cent Hosp, Dept Neurol, Panjin, Peoples R China
[6] Chengde Med Univ, Dept Neurol, Affiliated Hosp, Chengde, Peoples R China
[7] Liaoning Hlth Ind Grp, Dept Endocrinol, Fukuang Gen Hosp, Fushun, Peoples R China
[8] Liaoning Hlth Ind Grp, Dept Endocrinol, Bengang Gen Hosp, Benxi, Peoples R China
[9] Ningxia Med Univ, Dept Neurol, Gen Hosp, Yinchuan, Ningxia, Peoples R China
[10] Cangzhou Peoples Hosp, Dept Gastroenterol, Cangzhou, Peoples R China
[11] Shandong Univ, Dept Neurol, Hosp 2, Jinan, Peoples R China
[12] Xi An Jiao Tong Univ, Dept Neurol, Affiliated Hosp 1, Xian, Peoples R China
[13] Xuzhou Med Univ, Dept Neurol, Affiliated Hosp, Xuzhou, Jiangsu, Peoples R China
[14] Linfen Peoples Hosp, Dept Neurol, Linfen, Shanxi, Peoples R China
[15] Hosp Dali Univ, Dept Neurol, First Affiliated, Dali, Peoples R China
[16] First Peoples Hosp, Dept Gastroenterol, Tai An, Shandong, Peoples R China
[17] Southwest Med Univ, Dept Neurol, Affiliated Hosp, Luzhou, Peoples R China
[18] Inner Mongolia Med Univ, Dept Endocrinol, Affiliated Hosp, Hohhot, Peoples R China
[19] Sichuan Acad Med Sci, Sichuan Prov Peoples Hosp, Dept Neurol, Chengdu, Peoples R China
[20] Shandong Prov Hosp, Pain Dept, Jinan, Peoples R China
[21] Guangdong Tradit Chinese Med Hosp, Dept Neurol, Guangzhou, Peoples R China
[22] Tianjin Gangkou Hosp, Dept Neurol, Tianjin, Peoples R China
[23] Shanxi Prov Peoples Hosp, Dept Neurol, Taiyuan, Peoples R China
[24] Xinjiang Med Univ, Dept Neurol, Affiliated Hosp 1, Urumqi, Peoples R China
[25] Shandong Univ, Dept Neurol, Qilu Hosp, Jinan, Peoples R China
[26] Yuncheng Cent Hosp, Dept Neurol, Yuncheng, Peoples R China
[27] Henan Prov Peoples Hosp, Dept Neurol, Zhengzhou, Peoples R China
[28] Fujian Med Univ, Dept Neurol, Mindong Hosp, Ningde, Peoples R China
[29] Second Peoples Hosp Hunan Prov, Brain Hosp Hunan Prov, Dept Neurol, Changsha, Peoples R China
[30] Guiyang Sixth Hosp, Dept Neurol, Guiyang, Peoples R China
[31] Huazhong Univ Sci & Technol, Dept Neurol, Union Hosp, Tongji Med Collage, Wuhan, Peoples R China
[32] Jiamusi Univ, Dept Neurol, Affiliated Hosp 1, Jiamusi, Peoples R China
[33] Peoples Hosp Xinxing Country, Dept Neurol, Yunfu, Peoples R China
[34] Suzhou Municipal Hosp, Dept Neurol, Suzhou, Peoples R China
[35] Tianjin Xiqing Hosp, Dept Neurol, Tianjin, Peoples R China
[36] Cent Hosp Wafangdian, Dept Neurol, Dalian, Peoples R China
[37] Nanjing First Hosp, Dept Neurol, Nanjing, Peoples R China
[38] Tibet Autonomous Reg Peoples Hosp, Dept Neurol, Lhasa, Peoples R China
[39] Liaocheng Peoples Hosp, Dept Neurol, Liaocheng, Shandong, Peoples R China
[40] Fudan Univ, Dept Neurol, Huashan Hosp, Shanghai, Peoples R China
[41] Yantai Yuhuangding Hosp, Dept Neurol, Yantai, Peoples R China
[42] Shanxi Bethune Hosp, Dept Neurol, Taiyuan, Peoples R China
[43] Peking Univ Third Hosp, Res Ctr Clin Epidemiol, 49th North Garden Rd, Beijing, Peoples R China
关键词
Age; Anxiety; Depression; DN4; Newly diagnosed; Painful diabetic neuropathy; Peripheral artery disease; Visual analogue scale; RISK-FACTORS; AMERICAN ASSOCIATION; NATURAL-HISTORY; PREVALENCE; COMPLICATIONS; DEPRESSION; DIAGNOSIS; PHENOTYPE; MELLITUS; BURDEN;
D O I
10.1007/s40122-021-00281-w
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction This aim of this study was to delineate current clinical scenarios of painful diabetic peripheral neuropathy (PDN) and associated anxiety and depression among patients in Mainland China, and to report current therapy and clinical practices. Methods A total of 1547 participants were enrolled in the study between 14 June 2018 and 11 November 2019. Recruitment was conducted using a multilevel sampling method. Participants' demographics, medical histories, glucose parameters, Douleur Neuropathique 4 Questionnaire (DN4) scores, visual analogue scale (VAS) pain scores, Patient Health Questionnaire 9 (PHQ-9) scores, Generalised Anxiety Disorder 7 (GAD-7) scores and therapies were recorded. Results The male-to-female ratio was 1.09:1 (807:740), and the mean age at onset was 61.28 +/- 11.23 years. The mean DN4 score (+/- standard deviation) was 4.91 +/- 1.88. The frequencies of DN4 sub-item phenotypes were: numbness, 81%; tingling, 68.71%; pins and needles, 62.90%; burning, 53.59%; hypoaesthesia to touch, 50.16%; electronic shocks, 43.31%; hypoaesthesia to pinprick, 37.94%; brushing, 37.82%; painful cold, 29.61%; and itching, 25.86%. Age, diabetic duration, depression history, PHQ-9 score and GAD-7 score were identified as risk factors for VAS pain score. Peripheral artery disease (PAD) was a protective factor for VAS pain score. For all participants currently diagnosed with PDN and for those previously diagnosed PDN, fasting blood glucose (FBG) was a risk factor for VAS; there was no association between FBG and VAS pain score for PDN diagnosed within 3 months prior to recruitment. Utilisation rate of opium therapies among enrolled participants was 0.71% , contradiction of first-line guideline recommendation for pain relief accounted for 9.43% (33/350) and contradiction of second-line guideline recommendation for opium dosage form was 0.57% (2/350). Conclusion Moderate to severe neuropathic pain in PDN was identified in 73.11% of participants. Age, diabetic duration, depression history, PHQ-9 score, GAD-7 score and FBG were risk factors for VAS pain scores. PAD was protective factor. The majority of pain relief therapies prescribed were in accordance with guidelines.
引用
收藏
页码:1355 / 1373
页数:19
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