Background Chronic pain is usually refractory to treatment. Ketamine is often used to treat chronic refractory pain.In France most of the patients are treated in pain units day hospital.
This study aims to evaluate the effectiveness of continuous four days of Ketamine infusion associated with magnesium sulfate for inpatients.
Methods A total of 89 patients received a 4 days continuous subanesthetic IV ketamine infusion associated with 1000 mg/day of magnesium sulfate.Primary outcome was mean pain intensity (Numerical Rating Pain Scale) 30 days after infusion. Patient Impression of Change (PGIC), Anxiety and depression (HADS), Neuropathic Pain (NPSI), quality of life (SF-12) were secondary outcomes.
Results Ketamine continuous infusion was associed with decrease of NRS (7.54 ± 1.35 at d0 to 5.59 ± 2.2 at d30 [26%; p < 0.001]).The PGIC improved in 68.7 % patients (36.2 % reports “much improved” or “very much improved”).There was a significant decrease of Npsi total score (−28% ; p < 0.0001) and an increase of SF12 (Mental health dimension from 31.4 ±7.9 to 36.4 ± 8.9 [+15.9 % ; p < 0.0001]; Physical health dimension from 30.2 ± 6.7 to 32.8 ± 6.8 [+8.6% ; p:0.0007]).The mean HADS Depression decreased from 10 ± 4.5 at d0 to 8.2 ± 4.6 at d30 (−15% ; p:0.0012) ; The mean HADS Anxiety decreased from 11.35 ± 4.7 at d0 to 9.38 ± 4.5 at d30 (−14% ; p < 0.0001).
Conclusions Findings suggests that continuous low-dose infusion of ketamine is effective for chronic pain relief to inpatients.
Competing Interest StatementThe authors have declared no competing interest.
Clinical TrialNCT06131970
Funding StatementThis study did not receive any funding
Author DeclarationsI confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
Yes
The details of the IRB/oversight body that provided approval or exemption for the research described are given below:
The study was conducted in accordance with the Declaration of Helsinki, approved by the local Ethics Committee (centre hospitalier princesse grace)IRB equivalent : 2022-RC-04 in 05/09/2022 and written informed consent was obtained from all participants before procedure.
I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.
Yes
I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
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I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.
Yes
Data AvailabilityAll data produced in the present work are contained in the manuscript
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