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Erschienen in: European Spine Journal 3/2024

Open Access 22.11.2023 | Original Article

Predictive value of the five-repetition sit-to-stand test for outcomes after surgery for lumbar disc herniation: prospective study

verfasst von: Anita M. Klukowska, Victor E. Staartjes, Manon Dol, W. Peter Vandertop, Marc L. Schröder

Erschienen in: European Spine Journal | Ausgabe 3/2024

Abstract

Objective

It is unknown whether presence of pre-operative objective functional impairment (OFI) can predict post-operative outcomes in patients with lumbar disc herniation (LDH). We aimed to determine whether pre-operative OFI measured by the five-repetition sit-to-stand test (5R-STS) could predict outcomes at 12-months post-discectomy.

Methods

Adult patients with LDH scheduled for surgery were prospectively recruited from a Dutch short-stay spinal clinic. The 5R-STS time and patient reported outcome measures (PROMs) including Oswestry Disability Index, Roland-Morris Disability Questionnaire, Visual Analogue Scale (VAS) for back and leg pain, EQ-5D-3L health-related quality of life, EQ5D-VAS and ability to work were recorded pre-operatively and at 12-months. A 5R-STS time cut-off of ≥ 10.5 s was used to determine OFI. Mann–Whitney and Chi-square tests were employed to determine significant differences in post-operative outcomes between groups stratified by presence of pre-operative OFI.

Results

We recruited 134 patients in a prospective study. Twelve-month follow-up was completed by 103 (76.8%) patients. Mean age was 53.2 ± 14.35 years and 50 (48.5%) patients were female. Pre-operatively, 53 (51.5%) patients had OFI and 50 (48.5%) did not. Post-operatively, patients with OFI experienced a significantly greater mean change (p < 0.001) across all PROMs compared to patients without OFI, except leg pain (p = 0.176). There were no significant differences in absolute PROMs between groups at 12-months (all p > 0.05).

Conclusions

The presence of OFI based on 5R-STS time does not appear to decrease a patient’s likelihood of experiencing satisfactory post-operative outcomes. The 5R-STS cannot predict how a patient with LDH will respond to surgery at 12-month follow-up.
Hinweise

Supplementary Information

The online version contains supplementary material available at https://​doi.​org/​10.​1007/​s00586-023-08046-z.

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Introduction

Patient-reported outcome measures (PROMs) continue to be a gold-standard during assessment of patients with lumbar disc herniation (LDH) [14]. However, in recent years there has been a shift towards additional implementation of tests of objective functional impairment (OFI), such as Timed-Up-and-Go test or Motorized Treadmill Test (MTT) [5]. Due to their straight-forwardness, short completion time, objectivity, patient preference and their ability to account for symptoms such as foot drop (commonly missed by PROMs), they are an important addition to the clinical setting of lumbar spine-surgery, creating a new dimension of pre-operative assessment [58].
To overcome the restrictions of OFI tests involving the need for space and time as seen in six-minute walk test or specialized equipment during MTT, the five-repetition sit-to-stand test (5R-STS) has been introduced to the field of spinal surgery [911]. Its practicality is linked to relatively quick calculation of the time it takes for a patient to perform five consecutive sitting-to-standing movements [12].
Given how advantageous tests of OFI such as 5R-STS appear to be during assessment in patients with LDH, one can question whether they can also determine patients post-operative outcomes as seen with PROMs [13]. If baseline 5R-STS measurement can predict post-operative outcomes in patients with LDH, it can potentially aid in treatment decision-making and management of patients’ expectations.
Therefore, we carried out a prospective study to determine whether the presence of pre-operative OFI measured by 5R-STS influences post-operative outcomes of patients with LDH at 12-month follow-up.

Materials and methods

Study design and oversight

In this prospective cohort study carried out between November 2020 and May 2022, patients were seen at a Dutch specialized short-stay spine surgery clinic pre-operatively and at 12-month post-operatively. The study (ClinicalTrials.gov Identifier: NCT04660656) was approved by the local institutional review board (Medical Research Ethics Committees United, Registration Number: W17.107 and W17.134) and was conducted according to the Declaration of Helsinki and its later amendments. Informed consent was obtained from all participants.

Study population

All enrolled patients underwent tubular microdiscectomy as described previously [14] and were assessed during outpatient consultations. Inclusion criteria were presence of LDH requiring surgical treatment. Patients who were bedridden, pregnant, had hip or knee prosthetics or required walking aides were excluded.

Testing protocol

The test was performed according to the protocol described by Jones et al. [12] If the patient was unable to perform the test in 30 s, or not at all, this was noted down and the test score was recorded as 30 s. The previously described cut-off of  ≥ 10.5 s was used to describe patients as objectively functionally impaired according to their pre operative 5R-STS time [9] Based on the baseline severity stratification (BSS) of 5R-STS previously published by Staartjes et al. patients were additionally categorized by their levels of OFI (none, ≤ 10.4 s; mild, 10.5–15.2 s; moderate, 15.3–22.0 s; and severe, > 22.0 s) [9].

Outcome measures

After performing the 5R-STS at pre-operative assessment, patients were asked to complete questionnaires containing baseline sociodemographic data (age, gender, body mass index (BMI), height, weight, smoking status, education level, level of spinal pathology, site of surgery, analgesia use, history of pain, work situation, ability to work), as well as PROMs: VAS for back and leg pain severity, validated Dutch versions of ODI, Roland–Morris Disability Questionnaire (RMDQ), and EQ-5D-3L questionnaire—containing the EQ visual analogue scale (EQ-VAS)—to capture pain, subjective functional impairment, and health-related quality of life. At 12-month post-operative follow-up patients were asked to perform 5R-STS and complete the aforementioned PROMs again including “ability to work” section. Every assessment was performed in the outpatient clinic by the same examiner. We did not refer any patients to a physiotherapy or rehabilitation programme postoperatively.

Statistical analysis

Continuous variables are reported as mean ± standard deviation, and categorical variables as numbers and percentages. Mann–Whitney tests were used to assess the intergroup differences in continuous data. The Chi-square test with Yates correction was chosen for categorical data at baseline. To compare the change in categorical outcomes from baseline to 12-months among patients with and without OFI, ordinal logistic regression adjusted for the baseline measurement was used with continuity correction where applicable. As a sensitivity analysis, we also compared outcomes of patients with different levels of OFI according to BSS using Kruskal–Wallis test and Chi-square test. Complete-case analysis was performed, and patients with missing outcome data were excluded. All analyses were carried out using R version 1.4.1003 (The R Foundation for Statistical Computing, Vienna Austria) [15]. A 2-tailed p ≤ 0.05 was considered significant. The statistical code is provided (Supplementary Content 2).

Results

Overview

The study recruited 134 patients. Thirty-one patients were excluded from the final analysis (Fig. 1). Thirty (22.3%) patients were lost to follow-up and one (0.7%) patient could not perform the test 12-months post-operatively due to advanced pregnancy. Overall, 103 patients were analyzed. Baseline patient demographics are presented in Table 1. The mean age of participants was 53.2 ± 14.35 years.
Table 1
Basic demographic data for patients with lumbar disc herniation based on preoperative presence of OFI versus no OFI
Characteristics
All participants
No OFI
OFI
p-value
(n = 103)
(n = 50)
(n = 53)
Age
53.2 ± 14.35
52.7 ± 13.7
53.43 ± 15.1
0.726
Gender
Female
50 (48.5)
21 (42.0)
29 (54.7)
0.274
Male
53 (51.5)
29 (58.0)
24 (45.3)
 
BMI (kg/m2)
27.1 ± 4.0
27.0 ± 4.3
27.1 ± 3.7
0.958
Height (cm)
176.5 ± 10.4
176.6 ± 10.8
176.5 ± 10.2
0.812
Weight (kg)
84.7 ± 16.3
84.7 ± 16.7
84.7 ± 16.1
0.981
Smoking status
Active smoker
20 (19.4)
8 (16.0)
12 (22.6)
 
Ceased smoking
36 (35.0)
15 (30.0)
21 (39.6)
0.252
Never smoked
47 (45.6)
27 (54.0)
20 (37.8)
 
Hernia site
Left
34 (33.0)
16 (32.0)
18 (34.0)
 
Right
27 (26.2)
9 (18.0)
18 (34.0)
0.102
Bilateral
42 (40.8)
25 (50.0)
17 (32.0)
 
Index level
L2-3
4 (3.9)
1 (2.0)
3 (5.5)
 
L2-3 & L3-4
3 (2.9)
1 (2.0)
2 (3.8)
 
L3-4
10 (9.7)
5 (10.0)
5 (9.4)
0.734
L3-4 & L4-5
7 (6.8)
5 (10.0)
2 (3.8)
 
L4-5
41 (39.8)
19 (38.0)
22 (41.5)
 
L5-S1
38 (36.9)
19 (38.0)
19 (36.0)
 
Prior spine surgery
17 (16.5)
10 (20.0)
7 (13.2)
0.508
History of pain
6weeks–3months
8 (7.8)
2 (4.0)
6 (11.3)
 
3months–6months
23 (22.3)
12 (24.0)
18 (34.0)
0.054
6months–1 year
30 (29.1)
9 (18.0)
14 (26.4)
 
 > 1 year
42 (40.8)
27 (54.0)
15 (28.3)
 
Analgesic drug use
Daily
77 (74.8)
34 (68.0)
43 (81.0)
 
Weekly
11 (10.7)
6 (12.0)
5 (4.5)
0.256
Not regularly
15 (14.5)
10 (20.0)
5 (4.5)
 
Education
High-school
48 (46.6)
24 (48.0)
29 (54.7)
 
Higher
53 (51.5)
24 (48.0)
24 (45.2)
0.303
Post-doctoral
2 (1.9)
2 (4)
 
Work situation
Employed
58 (56.3)
27 (54.0)
31 (58.5)
 
Self-employed
3 (2.9)
2 (4.0)
1 (2.0)
 
Retired
25 (24.3)
12 (24.0)
13 (24.5)
0.954
House-worker
5 (4.8)
3 (6.0)
2 (3.8)
 
Unfit
5 (4.8)
2 (4.0)
3 (5.6)
 
Unemployed
7 (6.9)
4 (8.0)
3 (5.6)
 
Ability to work
Full
22 (21.4)
15 (30.0)
7 (13.2)
 
Limited
33 (32.0)
14 (28.0)
19 (35.8)
0.115
Unable
48 (46.6)
21 (42.0)
27 (50.9)
 
EQ5D Anxiety & Depression
1
63 (61.2)
37 (74.0)
26 (49.0)
 
2
34 (33.0)
12 (24.0)
22 (41.5)
0.024
3
6 (5.8)
1 (2.0)
5 (9.5)
 
5R-STS Time (seconds)
13.5 ± 7.3
8.17 ± 1.4
18.6 ± 6.9
 < 0.001
RMDQ
13.9 ± 5.2
11.6 ± 4.9
16.1 ± 4.4
 < 0.001
ODI
44.2 ± 17.2
37.5 ± 13.8
50.4 ± 17.8
 < 0.001
VAS back pain
6.5 ± 2.6
5.5 ± 2.8
7.3 ± 2.0
 < 0.001
VAS leg pain
7.7 ± 1.7
7.5 ± 1.7
7.8 ± 1.8
0.253
EQ5D VAS
51.5 ± 18.8
58.6 ± 19.5
44.8 ± 15.5
 < 0.001
Continuous variables are presented as mean ± standard deviation and categorical variables as percentages (%)
BMI Body mass index, OFI Objective functional impairment, RMDQ Roland Morris disability questionnaire, ODI Oswestry disability index, VAS Visual analogue scale
Statistically significant findings are marked in bold font

Pre-operative

Based on the pre-operative 5R-STS time, 53 (51.5%) patients had OFI. Patients with OFI had significantly higher 5R-STS time compared to patients without OFI (18.6 ± 6.9 s vs. 8.17 ± 1.4 s, p < 0.001). In the OFI group, 27 (51.0%) patients reported presence of anxiety & depression symptoms measured by EQ5D-3L, which was significantly more than in the no-OFI group, where there were 13 (26.0%) of such patients (p = 0.024).

Post-operative

At 12-month follow-up, patients with pre-operative OFI still performed the 5R-STS time slower compared to patients with no pre-operative OFI (10.9 ± 3.6 s vs. 7.8 ± 1.8 s, p < 0.001) (Table 2). Among absolute scores at 12-months, only the 5R-STS time was significantly different between groups (OFI 10.9 ± 3.6 s vs. no-OFI 7.8 ± 1.8 s, p < 0.001). Post-operatively, 102 patients (99.0%) denied presence of anxiety and depression and there were no significant differences in mood symptoms between groups (p = 1.00) (Fig. 2). Patients with pre-operative OFI experienced a significantly greater change in PROMs at 12-months compared to patients without pre-operative OFI, except VAS Leg (− 6.6 ± 2.5 vs. − 6.0 ± 2.4, p = 0.176).
Table 2
Comparison of disease burden and change in scores of patients with lumbar disc herniation at 12 months post-operatively based on presence of pre-operative OFI vs no OFI
Characteristics
At 12 months post-operatively
Change in score
All participants (n = 103)
No OFI (n = 50)
OFI (n = 53)
p-value
All participants (n = 103)
No OFI (n = 50)
OFI (n = 53)
p-value
Ability to work
Full
76 (73.7)
37 (74.0)
39 (73.6)
0.772
54 (245.0)
22 (146.7)
32 (457.0)
0.832
Limited
19 (18.4)
10 (20.0)
9 (17.0)
− 14 (− 42.4)
− 4 (− 28.6)
− 10 (− 52.6)
Unable
8 (7.9)
3 (6.0)
5 (9.4)
− 40 (− 83.3)
− 18 (− 85.7)
− 22 (− 81.4)
EQ5D anxiety & depression
1
102 (99.0)
50 (100.0)
52 (99.0)
1.00
39 (61.9)
13 (35.1)
26 (100.0)
0.532
2
− 34 (− 100.0)
3
1 (1.0)
1 (1.0)
− 5 (− 83.3)
− 5 (− 80.0)
5R-STS Time (seconds)
9.4 ± 3.2
7.8 ± 1.8
10.9 ± 3.6
 < 0.001
− 4.1 ± 6.4
− 0.4 ± 1.4
− 7.7 ± 7.1
 < 0.001
RMDQ
3.7 ± 4.9
4.0 ± 5.0
3.4 ± 4.8
0.528
− 10.2 ± 6.7
− 7.6 ± 6.9
− 12.7 ± 5.6
 < 0.001
ODI
6.2 ± 9.3
6.3 ± 10.0
6.1 ± 8.7
0.834
− 38.0 ± 18.7
− 31.2 ± 14.8
− 44.4 ± 19.8
 < 0.001
VAS back pain
1.0 ± 1.9
1.0 ± 1.9
0.6 ± 1.4
0.272
− 5.7 ± 3.1
− 4.6 ± 3.3
− 6.7 ± 2.6
 < 0.001
VAS leg pain
1.3 ± 1.9
1.4 ± 1.8
1.2 ± 2.0
0.211
− 6.3 ± 2.4
− 6.0 ± 2.4
− 6.6 ± 2.5
0.176
EQ5D VAS
82.7 ± 9.6
82.3 ± 9.1
83.2 ± 10.1
0.497
31.3 ± 20.9
23.7 ± 21.8
38.4 ± 17.3
 < 0.001
Continuous variables are presented as mean ± standard deviation and categorical variables as percentages (%) and percentage change (%) for change in score calculations
BMI Body mass index, OFI Objective functional impairment, RMDQ Roland Morris disability questionnaire, ODI Oswestry disability index, VAS Visual analogue scale
Statistically significant findings are marked in bold font

Sensitivity analysis according to OFI BSS

Results are reported in Supplementary Content 1. There were no statistically significant differences between absolute PROMs scores of different OFI groups at 12-months. Stratification of patients based on their level of pre-operative OFI identified that there were statistically significant changes in PROMs between no, mild, moderate, and severe OFI groups at 12-months, except VAS Leg (no OFI 6.0 ± 2.39, mild OFI 6.5 ± 2.4, moderate OFI 6.4 ± 2.9, severe OFI 7.1 ± 2.1, p = 0.494).

Subgroup analysis

Subgroup analyses were performed to identify predictive value of 5R-STS in patients with LDH according to predominant site of pain at presentation (predominant or equal leg or back pain), history of previous spine surgery and patients with chronic pain (> 3 months) (Supplementary Table 3, 4, 5, 6, 7 and 8).

Discussion

In our prospective cohort study of patients with LDH, individuals with pre-operative OFI as per their 5R-STS time experienced significantly greater improvement in 5R-STS performance, ODI, RMDQ, VAS Back, and EQ5D-VAS at 12-month post-surgery compared to individuals with no pre-operative OFI. However, the overall post-operative absolute PROMs score did not differ significantly across groups, demonstrating that 5R-STS at baseline cannot predict 12-month outcomes.
Although it was hypothesized that patients with pre-operative OFI would have significantly different post-operative outcomes as measured by PROMs compared to their not objectively functionally impaired counterparts, findings in our study contradict that. It is known that surgery can successfully reverse the disability associated with LDH, and it appears that patients with motor deficits may achieve as good post-operative outcomes as if they were not present, even when stratified by different level of OFI as seen in our sensitivity analysis [16]. This information is reassuring for both the surgical team and the patient during consultation [17]. As seen in our study, patients who report worse functionality and pain scores pre-operatively, are sometimes theorized to “have more room for improvement” and hence are more likely to experience an overall higher satisfaction with post-operative outcomes [18, 19]. This can aid in management of patients’ expectations–crucial in the spinal surgery setting as positive expectations appear to be linked to better post-operative PROMs [20, 21].
Interestingly, at 12-month follow-up, patients with pre-operative OFI still performed the 5R-STS slower than patients with no pre-operative OFI, yet in both groups the absolute PROMs at 12-months were not significantly different. Ongoing presence of degree of OFI does not appear to necessarily constitute poor post-operative outcomes. It can be concluded that in the absence of pain, the ongoing OFI is no longer burdensome, and patients can cope with it sufficiently to achieve a satisfactory quality of life.
Nearly all PROMs except VAS Leg differed among patients with OFI vs. no OFI, a pattern seen also in our sensitivity analysis. This agrees with a previous study validating the proposed OFI baseline severity stratification of 5R-STS in patients with lumbar degenerative disease, where again, severity of VAS Leg was not associated with advancement of OFI [10]. This further implies that there may exist a subgroup of patients with LDH with a motor component independent of leg pain that is not captured by commonly used PROMs but is potentially identifiable by the 5R-STS [22].
Although the 5R-STS in itself does not appear to predict post-microdiscectomy outcomes, it complements the pre-operative consultation through an objective assessment of functionality and provides a reference point for analyzing post-surgical recovery and outcomes in both clinical and research setting. The 5R-STS was also shown to be reliable when performed at home by patients [11]. This has created an opportunity for patients to not only monitor their self-improvement but better surgeons’ assessment during telephone consultations that have increased in popularity especially since the SARS-CoV-2 pandemic [23].
The 5R-STS as shown above adds a new objective dimension in the assessment of patients with LDH, but on its own, it cannot predict patients’ post-microdiscectomy outcomes. Findings in our study can, however, reassure the patient that despite presence of OFI, they can still achieve satisfactory results after surgery, and they are not disadvantaged. The 5R-STS appears to have the potential to detect a motor component of LDH independent of leg pain and is a validated tool for assessment and monitoring of patients with LDH in both clinical and research setting.

Limitations

As all our patients were diagnosed with LDH, findings in our study are disease-specific and should not be applied to all diagnoses of lumbar degenerative disease.
In this prospective cohort study, 103 (76.9%) patients out of 134 recruited were followed up at 12-months. This may have introduced attrition bias due to unassessed outcomes in a subgroup of patients which may have impacted the results.
As our data was collected at one specialized Dutch short-stay spinal clinic, findings have limited generalizability in other countries. Populations from different areas may require adjusted outcome measures as seen with EQ-5D or 6MWT [24, 25]. Future studies are encouraged to differentiate between nationalities and ethnicities.
Finally, presence of chronic conditions in patients was not clearly reported. This may have led to overestimation of the impact of LDH on the 5R-STS performance and underestimation of the perceived improvement from the surgery due to ongoing burden of other illnesses. However, our inclusion criteria did not allow to analyze patients whose mobility was markedly affected by chronic comorbidities.

Conclusions

Although at 12-months there were no significant differences in absolute post-operative scores between patients with pre-operative OFI and no OFI, patients with pre-operative OFI experienced a greater improvement in PROM scores. It can be concluded that presence of OFI based on 5R-STS time does not decrease a patient’s likelihood of experiencing satisfactory post-operative outcomes. The 5R-STS cannot predict how a patient with LDH will respond to surgery at 12-month follow-up. The 5R-STS continues to remain an effective tool to assess disease severity of patients with LDH with excellent concurrent validity with PROMs. It can be used in both research setting as an outcome measure to determine treatment effectiveness as well as in clinical setting to complement pre-operative assessment and monitor post-operative recovery.

Acknowledgements

The authors are grateful to all patients participating in this study and generously sharing their time.

Declarations

Conflict of interest

The authors declare that the article and its content were composed in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://​creativecommons.​org/​licenses/​by/​4.​0/​.

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Anhänge

Supplementary Information

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Metadaten
Titel
Predictive value of the five-repetition sit-to-stand test for outcomes after surgery for lumbar disc herniation: prospective study
verfasst von
Anita M. Klukowska
Victor E. Staartjes
Manon Dol
W. Peter Vandertop
Marc L. Schröder
Publikationsdatum
22.11.2023
Verlag
Springer Berlin Heidelberg
Erschienen in
European Spine Journal / Ausgabe 3/2024
Print ISSN: 0940-6719
Elektronische ISSN: 1432-0932
DOI
https://doi.org/10.1007/s00586-023-08046-z

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