TY - JOUR
T1 - A Brief Nonmotor Screen Combined with Transcranial Ultrasound may Improve Diagnostic Accuracy of Parkinson’s Disease
AU - Hayes, Michael
AU - Puhl, Peter
AU - Hagenah, Johann
AU - Russo, Robert
N1 - Funding Information:
Ethical Compliance Statement: We confirm that we have read the Journal’s position on issues involved in ethical publication and affirm that this work is consistent with those guidelines. All authors have been substantively involved in the study or preparation of the manuscript. There are no ghost writers. All authors have also seen and approved the submitted version of the paper and accept responsibility for its content and agree to the order of author’s names. Funding Sources and Conflicts of Interest: The authors report no sources of funding and no conflicts of interest. Financial Disclosures for previous 12 months: M.H. has been employed by Sydney Local Health District as a staff specialist (Neurology) and served on the Advisory Board for Global Kinetics Corporation. P.P. has been employed by the Northern Sydney Area Health Service and the Adventist Hospital, Wahroonga, NSW, and has received a travel grant for the Asia-Pacific Masterclass 2015, Tokyo 05.-06.2016, UCB Australia. R.R. has been employed by Sydney Local Health District; has received travel grants from Pfizer, Bristol Myers Squibb, UCB, and AbbVie to attend educational meetings; and has been on an advisory board with Pfizer.
Publisher Copyright:
© 2016 International Parkinson and Movement Disorder Society
Copyright:
Copyright 2019 Elsevier B.V., All rights reserved.
PY - 2017/5/1
Y1 - 2017/5/1
N2 - Background: The addition of a simple nonmotor symptom (NMS) screen and transcranial sonography (TCS) to standard clinical assessment may improve the diagnostic accuracy of Parkinson's disease (PD). Methods: Sixty-nine subjects (23 established PD group, 23 healthy controls, and 23 possible PD) were enrolled. All completed 3 “yes-no” NMS questions (score, 0–3) and had a transcranial ultrasound assessing nigral hyperechogenicity (score, 0–1). A combined PD risk score of 0 to 4 was obtained for each subject. A PD risk score of ≥2 was used as the diagnostic cutoff for PD. Results: In the established PD group, there was an average of 2 NMSs per person or a group total of 46 of 69 possible NMSs, but only 4 of 69 NMSs in the healthy control group. Of the technically satisfactory TCS, 16 of 20 (80%) of the established PD group and 2 of 16 (12.5%) of the healthy control group were TCS positive. Using ≥2 NMSs alone as the cutoff identified 17 of 23 (74%) of the established PD and 100% of the healthy controls. The PD risk score of ≥2 identified 21 of 23 (91%) of the established PD as PD and 22 of 23 (96%) of the healthy control group as non-PD. In the possible PD group, the PD risk score identified 9 of 18 (50%) of those with a final clinical diagnosis of PD and 4 of 5 (80%) of non-PD. Conclusions: The combination of a brief NMS screen and TCS discriminated well between normal healthy controls and established PD. A positive TCS and one NMS, or a negative TCS with two NMSs, indicated a likely diagnosis of PD.
AB - Background: The addition of a simple nonmotor symptom (NMS) screen and transcranial sonography (TCS) to standard clinical assessment may improve the diagnostic accuracy of Parkinson's disease (PD). Methods: Sixty-nine subjects (23 established PD group, 23 healthy controls, and 23 possible PD) were enrolled. All completed 3 “yes-no” NMS questions (score, 0–3) and had a transcranial ultrasound assessing nigral hyperechogenicity (score, 0–1). A combined PD risk score of 0 to 4 was obtained for each subject. A PD risk score of ≥2 was used as the diagnostic cutoff for PD. Results: In the established PD group, there was an average of 2 NMSs per person or a group total of 46 of 69 possible NMSs, but only 4 of 69 NMSs in the healthy control group. Of the technically satisfactory TCS, 16 of 20 (80%) of the established PD group and 2 of 16 (12.5%) of the healthy control group were TCS positive. Using ≥2 NMSs alone as the cutoff identified 17 of 23 (74%) of the established PD and 100% of the healthy controls. The PD risk score of ≥2 identified 21 of 23 (91%) of the established PD as PD and 22 of 23 (96%) of the healthy control group as non-PD. In the possible PD group, the PD risk score identified 9 of 18 (50%) of those with a final clinical diagnosis of PD and 4 of 5 (80%) of non-PD. Conclusions: The combination of a brief NMS screen and TCS discriminated well between normal healthy controls and established PD. A positive TCS and one NMS, or a negative TCS with two NMSs, indicated a likely diagnosis of PD.
UR - http://www.scopus.com/inward/record.url?scp=85067374627&partnerID=8YFLogxK
U2 - 10.1002/mdc3.12450
DO - 10.1002/mdc3.12450
M3 - Journal articles
AN - SCOPUS:85067374627
SN - 2330-1619
VL - 4
SP - 397
EP - 402
JO - Movement Disorders Clinical Practice
JF - Movement Disorders Clinical Practice
IS - 3
ER -