TY - JOUR
T1 - Dextrose Prolotherapy for Symptomatic Knee Osteoarthritis
T2 - Feasibility, Acceptability, and Patient-Oriented Outcomes in a Pilot-Level Quality Improvement Project
AU - Rabago, David
AU - Kansariwala, Ina
AU - Marshall, David
AU - Nourani, Bobby
AU - Stiffler-Joachim, Mikel
AU - Heiderscheit, Bryan
N1 - Funding Information:
Margaret Smith, BS, Stephanie Lakritz, BS, and Supriya Hayer, MD, contributed to the early clinical and administrative work of this project. This project received funding from the Small Grant Program of the University of Wisconsin Department of Family Medicine and Community Health, the UW Department of Family Medicine and Community Health Summer Student Research and Student Assistantship Program, and the UW Prolotherapy Education and Research Lab (UW-PEARL). Members of the Hackett-Hemwall-Patterson Foundation provided advice about the injection protocol. Special acknowledgment goes to the staff of the Northeast Family Medical Center in Madison, WI, who facilitated this and many other projects in prolotherapy over the years.
Publisher Copyright:
© 2019, Mary Ann Liebert, Inc., publishers 2019.
PY - 2019/4/1
Y1 - 2019/4/1
N2 - Knee osteoarthritis (KOA) is a growing health problem with limited nonsurgical treatment options. Prolotherapy is an injection-based technique for chronic KOA pain; health plan coverage is limited, presenting an access barrier. A local health plan recently included coverage for prolotherapy for KOA, but uptake and treatment response in routine care are unknown. The authors conducted a pilot-level quality improvement (QI) project to explore the feasibility, acceptability, and effects of prolotherapy for painful KOA in a primary care setting. Design: QI prospective case series. Setting/Location: Outpatient: invitation letters were sent to symptomatic KOA patients with a primary care provider whose health plan covered prolotherapy. Subjects: Primary care patients with KOA. Intervention: Intra- and extra-articular prolotherapy injections: patients received up to six prolotherapy sessions. Outcome measures: Primary: Feasibility: response rate to invitation to utilize prolotherapy. Acceptability: patient adherence to, and satisfaction with, three or more prolotherapy sessions. Secondary: Survey based (the Western Ontario McMaster University Osteoarthritis Index, WOMAC, 0-100; EuroQOL 5-D). Objectively assessed: function (30-sec chair stand, 4 × 10 m walk, 9-step stair-climb), overall activity (ActiGraph wGT3X accelerometer), treadmill gait analysis, and preferred walking speed. Outcome analysis (paired t-test) was per protocol, comparing follow-up and baseline outcome data at ∼8 months. Results: Thirty-nine patients were invited, 11 responded, and 7 patients (59.6 ± 9.3 years, 6 female) received 5.0 ± 1.1 prolotherapy sessions. Satisfaction was high. Their WOMAC scores improved by 27.6 ± 19.5 points (p = 0.02) at 8.4 months. Functional testing improved by 8.0 ± 3.6 sec (p = 0.003) in the 4 × 10 m walk. There were no group differences between baseline and follow-up in chair stand, stair-climb, accelerometry, or gait outcomes. Five patients increased their preferred walking speed (p = 0.001). Conclusions: These data suggest that prolotherapy in this primary care clinic is feasible and acceptable. Self-reported improvement is similar to that of efficacy studies; office-based, objectively assessed functional assessment can be performed. Further evaluation is warranted.
AB - Knee osteoarthritis (KOA) is a growing health problem with limited nonsurgical treatment options. Prolotherapy is an injection-based technique for chronic KOA pain; health plan coverage is limited, presenting an access barrier. A local health plan recently included coverage for prolotherapy for KOA, but uptake and treatment response in routine care are unknown. The authors conducted a pilot-level quality improvement (QI) project to explore the feasibility, acceptability, and effects of prolotherapy for painful KOA in a primary care setting. Design: QI prospective case series. Setting/Location: Outpatient: invitation letters were sent to symptomatic KOA patients with a primary care provider whose health plan covered prolotherapy. Subjects: Primary care patients with KOA. Intervention: Intra- and extra-articular prolotherapy injections: patients received up to six prolotherapy sessions. Outcome measures: Primary: Feasibility: response rate to invitation to utilize prolotherapy. Acceptability: patient adherence to, and satisfaction with, three or more prolotherapy sessions. Secondary: Survey based (the Western Ontario McMaster University Osteoarthritis Index, WOMAC, 0-100; EuroQOL 5-D). Objectively assessed: function (30-sec chair stand, 4 × 10 m walk, 9-step stair-climb), overall activity (ActiGraph wGT3X accelerometer), treadmill gait analysis, and preferred walking speed. Outcome analysis (paired t-test) was per protocol, comparing follow-up and baseline outcome data at ∼8 months. Results: Thirty-nine patients were invited, 11 responded, and 7 patients (59.6 ± 9.3 years, 6 female) received 5.0 ± 1.1 prolotherapy sessions. Satisfaction was high. Their WOMAC scores improved by 27.6 ± 19.5 points (p = 0.02) at 8.4 months. Functional testing improved by 8.0 ± 3.6 sec (p = 0.003) in the 4 × 10 m walk. There were no group differences between baseline and follow-up in chair stand, stair-climb, accelerometry, or gait outcomes. Five patients increased their preferred walking speed (p = 0.001). Conclusions: These data suggest that prolotherapy in this primary care clinic is feasible and acceptable. Self-reported improvement is similar to that of efficacy studies; office-based, objectively assessed functional assessment can be performed. Further evaluation is warranted.
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U2 - 10.1089/acm.2018.0361
DO - 10.1089/acm.2018.0361
M3 - Article
C2 - 30688517
AN - SCOPUS:85064211072
SN - 1075-5535
VL - 25
SP - 406
EP - 412
JO - Journal of Alternative and Complementary Medicine
JF - Journal of Alternative and Complementary Medicine
IS - 4
ER -