Patients with Parkinson disease are increasingly recognized to suffer from non-motor symptoms in addition to motor symptoms. Many non-motor symptoms fluctuate in parallel with motor symptoms and in relationship to plasma levodopa levels. Though these symptoms are troublesome and result in reduced quality of life to patients and their caregivers, there has not been an objective method of recognizing and quantifying non-motor fluctuations (NMFs). This study sought to develop a patient-based instrument that would accurately capture the experience of patients with NMFs. Patient-based nominal group technique sessions, focus groups, and expert opinion were utilized in developing this questionnaire.
Non-motor symptoms in Parkinson Disease (PD) are increasingly recognized as a major source of disability for patients with moderate to advanced PD. Disability due to these symptoms arises as a result of problems with, among other difficulties, sleep, cognitive and mood disturbances, pain and other sensory complaints, as well as bowel and bladder dysfunction [
Non-motor fluctuations (NMFs), in contrast, are non-motor symptoms that vary according to plasma dopaminergic tone in a manner similar to motor fluctuations [
As individuals with motor fluctuations are thought to be at greater risk for NMFs, individuals with motor fluctuations were recruited by (i) mailing pamphlets about the study and its eligibility criteria to all the Parkinson's Disease Research, Education & Clinical Center (PADRECC) patients at the Philadelphia VA Medical Center (PVAMC), (ii) distributing similar pamphlets at PD patient and caregiver support groups, and at the Pennsylvania Hospital Movement Disorders Center reception area, and by (iii) direct questioning of patients during a routine health care visit if they were listed as having symptoms of NMFs in the PADRECC electronic database. A screening questionnaire was administered to those with motor fluctuations who expressed interest in study participation to verify the presence of motor fluctuations and to assess level of awareness and knowledge about non-motor symptoms. Anyone with substantial cognitive impairment, defined as a Mini-Mental Status Exam (MMSE) score ≤24 (whereby scores had been obtained by any health care provider in the previous six months), was excluded [
The study was approved by the Institutional Review Boards (IRB) of the PVAMC and the Pennsylvania Hospital. All participants signed the IRB-approved, written informed consent form before participation.
Three group discussions were held to generate content for the questionnaire. Three to four unique patient and partner/caregiver dyads were recruited for each session (Figure
NMF questionnaire development schema. NGT: nominal group technique. *Focus group consisted of both new subjects and original members of the NGT sessions.
Participants were asked to identify and record on paper all NMFs affecting them with particular attention paid to those NMFs that affected day-to-day life and/or life quality. Participants then took turns presenting their written responses such that with each cycle around the table the participant offered a single response. Every response offered by a group member was discussed by the whole group until all participants understood the NMF symptom offered and reached consensus on the language best describing that symptom. Precipitating and aggravating factors for each NMF symptom was discussed as was whether it was correlated with a particular motor state (e.g., ON versus OFF).
“Round-robins” continued until all unique responses were exhausted, after which a (secret ballot) vote took place to determine which symptoms were most frequent and disabling. A final composite list for each session was compiled before the group discussion ended and the group reviewed the findings. Group discussions not only identified content for instrument construction using lay language, they also applied meaning to the content and provided a sense of its relative perceived importance.
The complete list of all candidate symptoms identified by patient and caregivers were subjected to further critique by clinicians with expertise in PD. The clinicians were selected from the panel on non-motor symptoms of PD of the Quality Standards Subcommittee of the American Academy of Neurology [
The initial questionnaire was presented to two focus groups that consisted both of previous participants from NGT sessions and new patients. Participants were asked to critique the questionnaire for item relevance and ease of understanding, and whether response choices were both exhaustive and mutually exclusive. Important gaps in content were identified along with suggestions for questions that should be included to capture the content. Unnecessary or duplicative questions also were identified and removed. Following this process, a revised questionnaire was distributed to clinician experts for a final review.
An additional goal of the final questionnaire was to create response options that would allow differentiation between non-motor symptoms that were present but did not fluctuate according to plasma dopaminergic tone, and those that did fluctuate. A scoring scheme was developed that consisted of imputing one to three points (mild, moderate, severe) for each endorsed item that indicated a symptom that fluctuated by “ON” versus “OFF” status, and 0 for all other options. As such, higher scores would reflect a greater number and severity of NMFs. A total NMF score ranges from 0 to 84, and subscores (mood/cognition, autonomic, sensory, sleep, and fatigue) could be generated in the “ON” and “OFF” periods.
Baseline characteristics of patient-participants are detailed in Table
Characteristics of patient-participants.
Characteristics | Patients ( |
---|---|
Mean age, years | 74 |
Mean age onset of PD, years | 64 |
Mean PD stage (H + Y), years | 3 |
Mean LEDD, mg/d | 770 |
Sex, % men | 91 |
Table
Ranking of non-motor fluctuations (NMFs) symptoms by study participants*.
Rank | Symptom | Frequency¶ | Importance score* | Summary score† |
---|---|---|---|---|
1 | Pain (OFF) | 10 | 50 | 500 |
2 | Confusion (OFF) | 9 | 42 | 378 |
3 | Poor concentration (OFF) | 9 | 41 | 369 |
4 | Frustration (OFF) | 8 | 40 | 320 |
5 | Urinary frequency (ON); urgency/incontinence (OFF) | 7 | 33 | 231 |
6 | Word-finding difficulty (OFF) | 7 | 33 | 231 |
7 | Word-finding difficulty (OFF) | 7 | 25 | 175 |
8 | Drooling (OFF) | 6 | 23 | 138 |
9 | Poor short-term memory (OFF) | 5 | 25 | 125 |
10 | Obsessive/compulsive behavior (OFF) | 6 | 20 | 120 |
11 | Poor judgment (OFF) | 5 | 15 | 75 |
12 | Depression (OFF) | 5 | 14 | 70 |
13 | Mood swings/emotional lability/irritability (OFF) | 5 | 12 | 60 |
14 | Insomnia (ON, OFF) | 3 | 14 | 42 |
15 | Agitation/irritability/impatience (OFF) | 3 | 10 | 30 |
16 | Lack of interest (OFF) | 3 | 9 | 27 |
17 | Decreased laughter (apathy?) (OFF) | 2 | 12 | 24 |
18 | Difficulty breathing (OFF) | 2 | 11 | 22 |
19 | Fatigue (OFF) | 3 | 7 | 21 |
20 | Hallucinations (OFF) | 2 | 10 | 20 |
21 | Increased perspiration/odor (ON) | 2 | 7 | 14 |
22 | Paranoia (OFF) | 2 | 6 | 12 |
23 | Double/blurry vision (OFF) | 2 | 5 | 10 |
24 | Decreased communication/social withdrawal (OFF) | 1 | 7 | 7 |
25 | Decreased reading comprehension (OFF) | 1 | 6 | 6 |
26 | Reduced coping skills (OFF) | 1 | 6 | 6 |
27 | Reduced sense of taste (OFF) | 1 | 5 | 5 |
28 | Tingling (OFF) | 1 | 5 | 5 |
29 | Constipation (ON) | 1 | 5 | 5 |
30 | Change in hearing (OFF) | 1 | 3 | 3 |
31 | Intermittently sleepy (OFF) | 1 | 3 | 3 |
32 | Numbness (OFF)‡ | 0 | 0 | 0 |
33 | Restlessness (ON) | 0 | 0 | 0 |
*Summation of individual scores.
†Summary score: frequency X score.
‡Mentioned as symptom but not ranked in top 7.
¶Frequency: number of subjects ranking symptom.
19 participants asked to rank symptoms from 1–7 (least to most important).
133 total possible.
121/133—some subjects did not rank all 7.
Clinician experts collapsed some items they believed to be assessing the same underlying concept into one single item (e.g., decreased reading comprehension and poor concentration and decreased communication and word-finding difficulties) and removed other items they thought were not highly prevalent in clinical practice (e.g., altered hearing). In those situations where multiple same-construct symptoms were collapsed into a single item, wording was revised to capture the concept appropriately.
The final revised questionnaire resulting from focus groups with patient/caregiver/ and feedback from clinician experts is shown in the appendix. Twenty-eight items were included in the final questionnaire.
Outcome assessments based on patient perceptions and self-reports are increasingly incorporated into clinical trials of patients with PD. No instrument existed previously to allow assessment of NMFs in patients with PD. This study has led to the creation of such an instrument, the Non-motor Fluctuations Assessment instrument (NoMoFA), which can be used as a patient-based outcome measure in both research and clinical practice. While this instrument was developed using methods that impart substantial face and construct validity, reliability and additional validity assessments of the instrument necessarily must follow. To that end, a recent effort to identify wearing off phenomena both motor and non-motor, determined through expert consensus and literature review, identified similar symptoms to our patient-derived items [
Though patients have long complained of non-motor symptoms to their health-care providers, only recently have they been recognized as important and disabling [
Due to the recent increased attention given to NMFs, a new effort has sought to incorporate evaluation of non-motor symptoms into the standardized PD evaluation protocol [
In developing the NoMoFA, we sampled a heterogeneous group of patients with diverse backgrounds. In addition, we received feedback from experts providing revisions with an effort to maximize clinical relevance. We believe this has increased the likelihood the NoMoFA is an accurate, understandable, comprehensive compilation of NMFs experienced by PD patients. Further work needs to be performed to ensure that the NoMoFA is reliable and valid before it can be incorporated into standard research and clinical evaluations of patients.
Many people with Parkinson disease have symptoms related to their muscles (movement symptoms). These include stiffness, slowness in carrying out movements, and trouble with walking, getting up from a chair, or using their hands. However, people living with Parkinson disease can also have symptoms that are not related to their movement (nonmovement symptoms). These nonmovement symptoms include things like problems in thinking and memory, pain, abnormal body sensations, difficulty with emptying bowels or troubles with the bladder. Many people do not know that these other symptoms (nonmovement symptoms) may be related to Parkinson disease or to how their body responds to medications taken for Parkinson disease (levodopa, prolopa, Sinemet).
For people experiencing nonmovement symptoms that change in response to Parkinson disease medications, symptoms may only occur or may get worse when medications are either working or not working.
This questionnaire only asks about the nonmovement symptoms that come and go in response to effects of Parkinson disease medications.
For each question, if the symptom was present in the past week, you will be asked to rate how bothersome it was for you. The choices of answers are mild, moderate, or severe.
The symptom did not affect my ability to carry out normal daily tasks or social activities
The symptom affected but did not prevent me from carrying out normal daily tasks or social activities
Symptom prevented me from carrying out normal daily tasks or social activities.
Investigator:
Subject ID:
Date Performed:
Day Month
In the last week, did you
Yes No
If you answered “yes”, did this get better or worse after you took your levodopa?
Yes No
Was
Please rate the severity.
Mild Moderate Severe
Was
Please rate the severity.
Mild Moderate Severe
In the last week, did you get
Yes No
If you answered “yes”, did this get better or worse after you took your levodopa?
Yes No
Was
Please rate the severity.
Mild Moderate Severe
Was
Please rate the severity.
Mild Moderate Severe
In the last week, did you have
Yes No
If you answered “yes”, did this get better or worse after you took your levodopa?
Yes No
Was
Please rate the severity.
Mild Moderate Severe
Was
Please rate the severity.
Mild Moderate Severe
In the last week, were you
Yes No
If you answered “yes”, did this get better or worse after you took your levodopa?
Yes No
Was
Please rate the severity.
Mild Moderate Severe
Was
Please rate the severity.
Mild Moderate Severe
In the last week, were you
Yes No
If you answered “yes”, did this get better or worse after you took your levodopa?
Yes No
Was
Please rate the severity.
Mild Moderate Severe
Was
Please rate the severity.
Mild Moderate Severe
In the last week, did you have
Yes No
If you answered “yes”, did this get better or worse after you took your levodopa?
Yes No
Was
Please rate the severity.
Mild Moderate Severe
Was
Please rate the severity.
Mild Moderate Severe
In the last week, were you
Yes No
If you answered “yes”, did this get better or worse after you took your levodopa?
Yes No
Was
Please rate the severity.
Mild Moderate Severe
Was
Please rate the severity.
Mild Moderate Severe
In the last week, did you
Yes No
If you answered “yes”, did this get better or worse after you took your levodopa?
Yes No
Was
Please rate the severity.
Mild Moderate Severe
Was
Please rate the severity.
Mild Moderate Severe
In the last week, did you
Yes No
If you answered “yes”, did this get better or worse after you took your levodopa?
Yes No
Was
Please rate the severity.
Mild Moderate Severe
Was
Please rate the severity.
Mild Moderate Severe
In the last week, did you
Yes No
If you answered “yes”, did this get better or worse after you took your levodopa?
Yes No
Was
Please rate the severity.
Mild Moderate Severe
Was
Please rate the severity.
Mild Moderate Severe
In the last week, were you more likely to
Yes No
If you answered “yes”, did this get better or worse after you took your levodopa?
Yes No
Was
Please rate the severity.
Mild Moderate Severe
Was
Please rate the severity.
Mild Moderate Severe
In the last week, did you
Yes No
If you answered “yes”, did this get better or worse after you took your levodopa?
Yes No
Was
Please rate the severity.
Mild Moderate Severe
Was
Please rate the severity.
Mild Moderate Severe
In the last week, did you
Yes No
If you answered “yes”, did this get better or worse after you took your levodopa?
Yes No
Was
Please rate the severity.
Mild Moderate Severe
Was
Please rate the severity.
Mild Moderate Severe
In the last week, were you more likely to
Yes No
If you answered “yes”, did this get better or worse after you took your levodopa?
Yes No
Was
Please rate the severity.
Mild Moderate Severe
Was
Please rate the severity.
Mild Moderate Severe
In the last week, were you more likely to
Yes No
If you answered “yes”, did this get better or worse after you took your levodopa?
Yes No
Was
Please rate the severity.
Mild Moderate Severe
Was
Please rate the severity.
Mild Moderate Severe
In the last week, did you have
Yes No
If you answered “yes”, did this get better or worse after you took your levodopa?
Yes No
Was
Please rate the severity.
Mild Moderate Severe
Was
Please rate the severity.
Mild Moderate Severe
In the last week, did you have
Yes No
If you answered “yes”, did this get better or worse after you took your levodopa?
Yes No
Was
Please rate the severity.
Mild Moderate Severe
Was
Please rate the severity.
Mild Moderate Severe
In the last week, did you
Yes No
If you answered “yes”, did this get better or worse after you took your levodopa?
Yes No
Was
Please rate the severity.
Mild Moderate Severe
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Do you have any other nonmovement symptoms that come and go depending on when you took your Parkinson medications that you feel are important and that were
Please only respond to this section if this is the Today, are your PD movement symptoms Today, are your PD nonmovement symptoms Are you taking the same PD medication today compared to last week? If not, please list the changes.
The authors thank Dr. A. Siderowf for facilitation of data acquisition at Pennsylvania Hospital. They also wish to thank the clinician expert panel members: Drs. Anderson, Miyasaki, Samuel, Siderowf, Shulman, Stacy, Voon, and Weiner. This study was supported by a competitive pilot project grant from the Philadelphia VA Medical Center.