Supplementary data: Physical, Emotional and Social Pain Communication by Patients Diagnosed and Living with Multiple Myeloma

Supplementary
Table 1: Definition of aspects of pain
Supplementary Table 2: Thresholds for clinical importance
for the EORTC QLQ-C30 scores
<b>Supplementary Table 3: Health-related
quality of life by multiple myeloma patient self-reported pain severity</b>
<b> </b>
<b>Supplementary Table 4: Level of
agreement between symptoms reported by patients in self-reported symptoms
list and EORTC-QLQ-MY20 (using Cohen's kappa analysis)</b>
<b> </b>
<b>Supplementary Table 6: Level of
agreement between symptoms reported by patients and those recorded by the
treating physician at their face-to-face clinical consultation (using Cohen's
kappa analysis)</b>
<b> </b>
Physical,
Emotional and Social Pain Communication by Patients Diagnosed and Living with
Multiple Myeloma

<b>ABSTRACT</b>
<b> </b>
<b>Background: </b> To
describe physical, social, and emotional aspects of
pain self-reported by patients with multiple myeloma (MM), and patient-physician communication of physical pain.

<b>Methods: </b>We analysed self-reported data
from 330 adults receiving anti-MM therapy in Germany and Italy on
health-related quality of life (EORTC QLQ-C30, -MY20) and bone pain symptoms.

<b>Results: </b>Patients experienced clinically
important physical (69%), emotional (58%) and social (22%) pain. Less than
three-quarters of physicians’ records matched patients’ perception of bone
pain (71.5%), with bone pain not recorded in 19.7% of patients experiencing
it. Nearly half of physicians underestimated bone pain severity.

<b>Conclusion: </b>Patients with MM experience
physical, social and emotional pain.<b> </b>Discordance
regarding bone pain symptoms and severity was observed, suggesting the need for
improved communication.