Pregled bibliografske jedinice broj: 1183663
Treatment of Sciatica and Lumbar Radiculopathy with an Intervertebral Foramen Opening Protocol: Pilot Study in a Hospital Emergency and In-patient Setting
Treatment of Sciatica and Lumbar Radiculopathy with an Intervertebral Foramen Opening Protocol: Pilot Study in a Hospital Emergency and In-patient Setting // PHYSIOTHERAPY THEORY AND PRACTICE, 1 (2022), 16631, 12 doi:10.1080/09593985.2022.2037797 (međunarodna recenzija, članak, znanstveni)
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Naslov
Treatment of Sciatica and Lumbar Radiculopathy
with an Intervertebral Foramen Opening Protocol:
Pilot Study in a Hospital Emergency and In-patient
Setting
Autori
Shacklock, Michael ; Rade, Marinko ; Poznić, Siniša ; Marčinko, Anita ; Fredericson, Michael ; Kröger , Heikki ; Kankaanpää, Markku ; Airaksinen, Olavi
Izvornik
PHYSIOTHERAPY THEORY AND PRACTICE (0959-3985) 1
(2022);
16631, 12
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Lumbar radiculopathy ; sciatica ; physiotherapy ; rehabilitation
Sažetak
Aims Perform a pilot study of a static nerve root foramen opening protocol for lumbar radiculopathy from disc hernia in an emergency hospital setting to establish if patients could execute the protocol, consistency would occur across outcomes, superior outcomes would occur in the experimental group, and if the protocol would be safe. Methods Patients with sciatica arrived of their own volition at the local emergency hospital department, were admitted for care and were randomized into two groups: 1) control (n = 10): forward bending, walking, and medication ; and 2) experimental (n = 10) as control subjects, plus a static lumbar foramen opening protocol using flexion and contralateral lateral flexion (side- lying). Outcomes were back and leg pain (i.e. visual analog scale), disability (i.e. EuroQol5D5L and Oswestry) and straight leg raise. Results At admission, the baseline outcome variables between groups were not significantly different. All patients had moderate or large disc hernias on MRI and 75% had neurological deficits in electrophysiology. At discharge, patients in the experimental group were significantly better (p ≤ .05) than controls in all outcomes. Statistical analysis of the outcomes produced greater significance, effect sizes and minimal clinically important differences in the experimental group. Patients in the experimental group consumed less medication than control patients (21% versus 79%), including less than half the opioids (tramadol). No adverse responses occurred. Conclusions Patients could perform the protocol and superior outcomes occurred, with no adverse effects. The data support more detailed study of therapeutic efficacy, days in hospital, costs, conversion to surgery, and medication consumption, including opioids
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Osijek,
Sveučilište Jurja Dobrile u Puli
Profili:
Marinko Rade
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE