Follow-up score, change score or percentage change score for determining clinical important outcome following surgery? An observational study from the Norwegian registry for Spine surgery evaluating patient reported outcome measures in lumbar spinal stenosis and lumbar degenerative spondylolisthesis.
Back pain
Leg pain
Lumbar degenerative spondylolisthesis (LDS)
Lumbar spinal stenosis (LSS)
Minimal clinically important difference (MCID)
Oswestry disability index (ODI)
Patient reported outcome measures (PROMs)
Success criteria
Journal
BMC musculoskeletal disorders
ISSN: 1471-2474
Titre abrégé: BMC Musculoskelet Disord
Pays: England
ID NLM: 100968565
Informations de publication
Date de publication:
18 Jan 2019
18 Jan 2019
Historique:
received:
24
11
2017
accepted:
19
12
2018
entrez:
20
1
2019
pubmed:
20
1
2019
medline:
3
5
2019
Statut:
epublish
Résumé
Assessment of outcomes for spinal surgeries is challenging, and an ideal measurement that reflects all aspects of importance for the patients does not exist. Oswestry Disability Index (ODI), EuroQol (EQ-5D) and Numeric Rating Scales (NRS) for leg pain and for back pain are commonly used patients reported outcome measurements (PROMs). Reporting the proportion of individuals with an outcome of clinical importance is recommended. Knowledge of the ability of PROMs to identify clearly improved patients is essential. The purpose of this study was to search cut-off criteria for PROMs that best reflect an improvement considered by the patients to be of clinical importance. The Global Perceived Effect scale was utilized to evaluate a clinically important outcome 12 months after surgery. The cut-offs for the PROMs that most accurately distinguish those who reported 'completely recovered' or 'much improved' from those who reported 'slightly improved', unchanged', 'slightly worse', 'much worse', or 'worse than ever' were estimated. For each PROM, we evaluated three candidate response parameters: the (raw) follow-up score, the (numerical) change score, and the percentage change score. We analysed 3859 patients with Lumbar Spinal Stenosis [(LSS); mean age 66; female gender 50%] and 617 patients with Lumbar Degenerative Spondylolisthesis [(LDS); mean age 67; 72% female gender]. The accuracy of identifying 'completely recovered' and 'much better' patients was generally high, but lower for EQ-5D than for the other PROMs. For all PROMs the accuracy was lower for the change score than for the follow-up score and the percentage change score, especially among patients with low and high PROM scores at baseline. The optimal threshold for a clinically important outcome was ≤24 for ODI, ≥0.69 for EQ-5D, ≤3 for NRS leg pain, and ≤ 4 for NRS back pain, and, for the percentage change score, ≥30% for ODI, ≥40% for NRS leg pain, and ≥ 33% for NRS back pain. The estimated cut-offs were similar for LSS and for LDS. For estimating a 'success' rate assessed by a PROM, we recommend using the follow-up score or the percentage change score. These scores reflected a clinically important outcome better than the change score.
Sections du résumé
BACKGROUND
BACKGROUND
Assessment of outcomes for spinal surgeries is challenging, and an ideal measurement that reflects all aspects of importance for the patients does not exist. Oswestry Disability Index (ODI), EuroQol (EQ-5D) and Numeric Rating Scales (NRS) for leg pain and for back pain are commonly used patients reported outcome measurements (PROMs). Reporting the proportion of individuals with an outcome of clinical importance is recommended. Knowledge of the ability of PROMs to identify clearly improved patients is essential. The purpose of this study was to search cut-off criteria for PROMs that best reflect an improvement considered by the patients to be of clinical importance.
METHODS
METHODS
The Global Perceived Effect scale was utilized to evaluate a clinically important outcome 12 months after surgery. The cut-offs for the PROMs that most accurately distinguish those who reported 'completely recovered' or 'much improved' from those who reported 'slightly improved', unchanged', 'slightly worse', 'much worse', or 'worse than ever' were estimated. For each PROM, we evaluated three candidate response parameters: the (raw) follow-up score, the (numerical) change score, and the percentage change score.
RESULTS
RESULTS
We analysed 3859 patients with Lumbar Spinal Stenosis [(LSS); mean age 66; female gender 50%] and 617 patients with Lumbar Degenerative Spondylolisthesis [(LDS); mean age 67; 72% female gender]. The accuracy of identifying 'completely recovered' and 'much better' patients was generally high, but lower for EQ-5D than for the other PROMs. For all PROMs the accuracy was lower for the change score than for the follow-up score and the percentage change score, especially among patients with low and high PROM scores at baseline. The optimal threshold for a clinically important outcome was ≤24 for ODI, ≥0.69 for EQ-5D, ≤3 for NRS leg pain, and ≤ 4 for NRS back pain, and, for the percentage change score, ≥30% for ODI, ≥40% for NRS leg pain, and ≥ 33% for NRS back pain. The estimated cut-offs were similar for LSS and for LDS.
CONCLUSION
CONCLUSIONS
For estimating a 'success' rate assessed by a PROM, we recommend using the follow-up score or the percentage change score. These scores reflected a clinically important outcome better than the change score.
Identifiants
pubmed: 30658613
doi: 10.1186/s12891-018-2386-y
pii: 10.1186/s12891-018-2386-y
pmc: PMC6339296
doi:
Types de publication
Journal Article
Observational Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
31Références
Spine (Phila Pa 1976). 2000 Nov 15;25(22):2940-52; discussion 2952
pubmed: 11074683
Spine (Phila Pa 1976). 2000 Dec 15;25(24):3100-3
pubmed: 11124724
Spine (Phila Pa 1976). 2000 Dec 15;25(24):3167-77
pubmed: 11124733
Mayo Clin Proc. 2002 Apr;77(4):371-83
pubmed: 11936935
Psychol Methods. 2002 Jun;7(2):147-77
pubmed: 12090408
J Rehabil Med. 2003 Sep;35(5):241-7
pubmed: 14582557
Best Pract Res Clin Rheumatol. 2005 Aug;19(4):593-607
pubmed: 15949778
Med Decis Making. 2005 May-Jun;25(3):250-61
pubmed: 15951453
Qual Life Res. 2007 Feb;16(1):131-42
pubmed: 17033901
Spine (Phila Pa 1976). 2007 Jan 1;32(1):1-8
pubmed: 17202885
N Engl J Med. 2007 May 31;356(22):2257-70
pubmed: 17538085
J Pain. 2008 Feb;9(2):105-21
pubmed: 18055266
Spine J. 2008 Mar-Apr;8(2):305-10
pubmed: 18082461
Spine (Phila Pa 1976). 2008 Jan 1;33(1):90-4
pubmed: 18165753
Spine J. 2008 Nov-Dec;8(6):968-74
pubmed: 18201937
N Engl J Med. 2008 Feb 21;358(8):794-810
pubmed: 18287602
J Bone Joint Surg Am. 2008 Sep;90(9):1839-47
pubmed: 18762642
Spine J. 2009 Jul;9(7):609-14
pubmed: 19447684
J Clin Epidemiol. 2010 May;63(5):524-34
pubmed: 19926446
J Clin Epidemiol. 2010 Jul;63(7):760-766.e1
pubmed: 20056385
Spine J. 2010 Apr;10(4):321-7
pubmed: 20362248
Spine J. 2010 Apr;10(4):328-9
pubmed: 20362249
Acta Orthop. 2011 Feb;82(1):56-63
pubmed: 21189113
Expert Rev Pharmacoecon Outcomes Res. 2011 Apr;11(2):163-9
pubmed: 21476818
BMJ. 2011 May 19;342:d2786
pubmed: 21596740
J Clin Epidemiol. 2012 Mar;65(3):253-61
pubmed: 22014888
J Neurosurg Spine. 2013 Jan;18(1):102-6
pubmed: 23157276
Acta Orthop. 2013 Apr;84(2):196-201
pubmed: 23506164
Bone Joint J. 2013 Jul;95-B(7):960-5
pubmed: 23814250
J Man Manip Ther. 2012 Aug;20(3):160-6
pubmed: 23904756
J Orthop Surg Res. 2013 Nov 14;8:40
pubmed: 24225254
J Clin Epidemiol. 2014 May;67(5):508-15
pubmed: 24598378
J Pain. 2015 Feb;16(2):116-23
pubmed: 25419989
J Clin Epidemiol. 2015 May;68(5):518-24
pubmed: 25544741
Spine (Phila Pa 1976). 2015 Apr 15;40(8):514-20
pubmed: 25608246
J Orthop Surg Res. 2015 Feb 03;10:24
pubmed: 25645576
Acta Orthop. 2015;86(5):534-44
pubmed: 25909475
Spine (Phila Pa 1976). 2015 May 15;40(10):710-8
pubmed: 25955088
Spine J. 2016 Apr;16(4 Suppl):S12-8
pubmed: 26850172
Control Clin Trials. 1989 Dec;10(4):407-15
pubmed: 2691207
N Engl J Med. 2016 Apr 14;374(15):1413-23
pubmed: 27074066
N Engl J Med. 2016 Apr 14;374(15):1424-34
pubmed: 27074067
Spine J. 2016 Oct;16(10):1221-1230
pubmed: 27343730
Eur Spine J. 2017 Feb;26(2):404-413
pubmed: 27421276
BMC Musculoskelet Disord. 2017 Mar 21;18(1):121
pubmed: 28327114
Eur Spine J. 2018 Mar;27(3):554-563
pubmed: 29058135
BMJ. 1994 Jul 16;309(6948):188
pubmed: 8044101
Health Econ. 1996 Mar-Apr;5(2):141-54
pubmed: 8733106
BMJ. 1998 Feb 28;316(7132):690-3
pubmed: 9522799
Phys Ther. 1998 Nov;78(11):1186-96
pubmed: 9806623