Analysis of Dynamic Plantar Pressure before and after the Occurrence of Neurogenic Intermittent Claudication in Patients with Lumbar Spinal Stenosis: An Observational Study

Wei, Wei; Xu, Chao; Yang, Xiao-Jiang; Lu, Chang-Bo; Lei, Wei; Zhang, Yang

doi:https://doi.org/10.1155/2020/5043583

BioMed Research International

On this page

Abstract Introduction Methods Discussion Conclusions Data Availability Conflicts of Interest Authors’ Contributions Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2020 | Article ID 5043583 | https://doi.org/10.1155/2020/5043583

Analysis of Dynamic Plantar Pressure before and after the Occurrence of Neurogenic Intermittent Claudication in Patients with Lumbar Spinal Stenosis: An Observational Study

Wei Wei,¹Chao Xu,¹Xiao-Jiang Yang,¹Chang-Bo Lu,¹Wei Lei,¹and Yang Zhang¹

Academic Editor: Sheldon Lin

Received11 Mar 2020

Accepted11 Jun 2020

Published02 Jul 2020

Abstract

Lumbar spinal stenosis (LSS) is a common disease in the elderly population; it has been reported that patients with LSS have an abnormal gait pattern due to symptom such as neurogenic intermittent claudication (NIC); however, no detailed reports exist on the plantar pressure distributions in LSS patients with NIC. To analysis the plantar pressure characteristics of LSS patients, the Footscan® pressure system was used to perform dynamic plantar pressure measurements in 20 LSS patients (age, years) before and after the occurrence of NIC. The contact time (CT), foot progression angle (FPA), pressure-time integral (PTI), and contact area (CA) were collected and compared between the LSS patients and age-matched healthy subjects in each measurement. The LSS group showed an increase in forefoot CT%, PTI, and CA% in both measurements compared with those in the control group. After the occurrence of NIC in the LSS group, CT%, PTI, and CA% of the forefoot increased further compared with those before the occurrence of NIC. In addition, after the occurrence of NIC, the PTI and CA% of the forefoot shifted from the medial foot to the lateral foot. The results suggested that the plantar pressure distributions of patients with LSS differs from normal subjects due to the posture of waking with lumbar forward flexion, and the forefoot bears a higher relative load. In addition, the occurrence of NIC could affect the plantar pressure distribution of the patients with LSS, predicting the patient’s risk of falling to the anterior direction and to the symptomatic side.

1. Introduction

Lumbar spinal stenosis (LSS) refers to the nerve compression syndrome, in which the spinal canal narrows and compresses the dural sac, spinal cord, or nerve root [1]. The prevalence of LSS increases with age; it is about 9.3% in the general population and up to 47% in individuals older than 60 years [2, 3]. For individuals older than 65 years, LSS can be the most common cause of lumbar surgery [4]. The incidence of LSS has increased because of the burden of aging population. Patients with LSS may cause negligible economic problems considering their limited daily activities and weakened labor capacity [4, 5]. Therefore, clinicians are focusing more on the diagnosis and treatment of LSS. Magnetic resonance imaging (MRI) technology is often the first choice for LSS due to its superior soft tissue resolution [6]. However, the degree of LSS presented by imaging and the severity of clinical symptoms may have a relatively low correlation. Although some individuals do have anatomical LSS, they may not have relevant clinical symptoms [7]. Therefore, besides imaging data, clinicians should consider the medical records and physical signs of the patients at the same time for the diagnosis of LSS [7, 8].

Patients with LSS usually seek medical treatment because of walking disorders. The poor walking ability indicates severe compression of the spinal cord and nerve. Therefore, assessing the patient’s walking function is essential for the diagnosis and treatment of LSS. Many recent studies investigated the gait patterns of patients with LSS. The findings revealed that the walking patterns of patients with LSS were different from those of ordinary subjects, mainly manifested by wide-based gait, increased gait variability, and balance disturbances [9–11]. In addition, studies have shown that the balance of patients with LSS could get worse after the occurrence of neurogenic intermittent claudication (NIC), leading to a higher risk of falling [11]. However, many gaps still remain in the study of mode changes in gait patterns before and after the occurrence of NIC. Specific mechanisms of gait changes need to be elucidated.

The changes in gait can probably affect the pressure distribution under the foot [12]. As an important substitution of gait analysis, plantar pressure analysis is the basis for analyzing and measuring abnormal plantar pressure distribution and gait. It has significance for the etiology analysis, diagnosis, function, and treatment evaluation of diseases related to walking disorders [13]. However, none of the studies have analyzed the pattern of plantar pressure distribution in patients with LSS or the effect of NIC on the distribution of plantar pressure. This study used the Footscan® pressure system to perform dynamic plantar pressure tests on patients with LSS. The aim of this study was to reveal the changes in the distribution of plantar pressure and the risk of falling before and after the occurrence of NIC in patients with LSS. The differences in plantar pressure distributions and the mechanism of their occurrence should be explained to provide theoretical support and data reference for the diagnosis and treatment of patients with LSS.

2. Methods

2.1. Participants

This observational study is a cross-sectional, uncontrolled intervention. From October 2017 to April 2019, patients with LSS in our institution were routinely analyzed for plantar pressure after admission to improve the database of plantar pressure for patients with LSS. The database was reviewed, and the case group was selected. The inclusion criteria were as follows: (1) L4–L5 level spinal stenosis on imaging examination [11, 14] and a history of intermittent claudication; (2) symptom onset within 1 year with no history of invasive treatment; and (3) no history of lower extremity trauma in the last 1 year. Subjects were excluded if they: (1) had spinal stenosis in other levels of the spine; (2) had spine-related diseases, such as scoliosis, lumbar spondylolisthesis, spinal trauma, and history of surgery; (3) had diseases that could affect walking function, such as neuromusculoskeletal, vestibular, cardiopulmonary disorders, and vascular lesions of the lower limbs, hip, knee, and ankle joints; and (4) could not walk without aid. A group of healthy subjects of the same age was recruited as the control group. Subjects in the control group had no previous history of trauma, surgery, or motor system diseases. The characteristics of participants were collected for comparison, including age, height, weight, foot length, body mass index (BMI), and the T-score of the body mineral density. This study was approved by the Medical Ethics Committee of Xijing Hospital, Air Force Military Medical University, China. Informed consent for the plantar pressure test and data application was obtained from the participants or their immediate relatives.

2.2. Instrumentation and Pedobarographic Analysis

Data were collected using the Footscan® 3D pressure system (RSscan International, Belgium), which has been proved to have good reliability and repeatability [15]. The size of the force plate was , with 16,384 sensors distributed. The minimum measurement area was 0.25 cm², and the sampling frequency was 125 Hz. Before each measurement, the test system was calibrated. The force plate was located at the center of a carpet with the same external dimension to provide a “complete platform,” 4 m in length, to ensure that a minimum of three steps was taken before data collection. The platform was disguised with a thin liner of EVA (ethylene-vinyl acetate copolymer) material to avoid targeting effect [15] (Figure 1). The Footscan® system was calibrated before each measurement session following the manufacturer’s protocol, and all the participants initially completed 2-min acclimatization walking trails along the measuring platform. The plantar pressure data of each participant were measured using two protocols. For the LSS group, the first measurement was performed after resting for 2 min, and the second measurement was performed after continuous walking until the symptoms of NIC occurred. The control group took the measurements after resting for 2 min and after walking for 5 min. During the measurement, each participant was asked to perform the tests barefoot at their comfortable walking pace, looking forward. In each measurement, about 3-4 consecutive steps were captured, only one representative step (complete footprints, heel-strike pattern, and no obvious adjustment) was artificially selected for analysis and processing. For the LSS patients, the symptomatic side or the more severe side was selected; for the control group, the dominant foot was selected [11]. The aforementioned measurement steps were repeated until three sets of valid data were collected.

The Scientific Footscan® software automatically divided the foot into the following 10 areas according to the anatomical structure of the foot (Figure 2): toe 1 (T1), toe 2–toe 5 (T2–T5), metatarsal 1–metatarsal 5 (M1–M5), midfoot (MF), medial heel (MH), and lateral heel (LH). In addition, to facilitate the overall comparison, the foot was divided into three parts based on the front and back edges of the MF: forefoot (T1, T2–T5, and M1–M5), MF, and heel (MH and LH). The longitudinal axis of the foot divided the anterior and posterior feet into two parts: the medial foot (T1, M1, M2, and MH) and the lateral foot (T2–T5, M3–M5, and LH). As the symptomatic side of the patient with LSS was selected for analysis, the lateral side of the foot corresponded to the symptomatic side.

At the same time, the software divided the entire stance phase of the foot into the following four phases according to the sequence of the ground contact time (CT) of each anatomical structure: (1) initial contact phase (ICP), (2) forefoot contact phase (FFCP), (3) foot flat phase (FFP), and (4) forefoot push-off phase (FFPOP) (Figure 3).

2.3. Data Analysis

The following plantar pressure parameters were collected using the software: CT in each subphase, contact area (CA) in each zone, pressure-time integral (PTI) in each zone, and foot progression angle (FPA). Among these, CA was corrected by the proportion of each area in the total plantar area (CA%), and CT was corrected by the proportion of each subphase in the total standing phase of one foot (CT%). The average of each parameter in the three valid data was used as the analysis data of each participant. The data were divided into four groups: first measurement in the LSS group, second measurement in the LSS group, first measurement in the control group, and second measurement in the control group.

2.4. Statistical Analysis

The sample size was determined by a pilot study (6 subjects; LSS group, ; control group, ). The Gpower software (Version 3.1.9.6) was used to calculate the required sample size affording a significance level of 0.05, a power of 0.95, and an effect size of 0.65 (calculated using the of data during the pilot study). The required sample size is 28 subjects (LSS group, ; control group, ).

The data were entered into SPSS 23.0 software, and the Kolmogorov–Smirnov single-sample test and scatter plot test were used. The experimental data conformed to the normal distribution. Therefore, the differences between FPA, CA%, CT%, and PTI in the two measurements of the LSS group and the two measurements of the control group were analyzed using the paired -test. Differences between the LSS group and the control group in the first and second measurements were analyzed using the independent-samples -test, and the differences were statistically significant when .

3. Result

20 patients with LSS (12 males and 8 females) were included in the experimental group (LSS group), aged 56–73 years, with an average age of () years. Five cases of relatively narrow L4–L5 level were found on imaging 15 cases with absolute stenosis [6]. 20 age-matched healthy control subjects were recruited from the community surrounding the hospital. No significant differences in age, height, weight, foot length, BMI, and T-score were observed between the LSS group and the control group (; Table 1).

The comparison results of CT% and total CT in the stance phase of each group are shown in Table 2. Compared with the first measurement results of the LSS group, the CT% of ICP decreased and the CT% of FFPOP increased. The CT% of ICP and FFCP was smaller and that of FFP and FFPOP increased in the LSS group compared with the second measurement results of the control group. Compared with the first measurement in the LSS group, the ICP and FFCP decreased and the proportion of FFP and FFPOP increased. In terms of total CT, the two measurements in the LSS group significantly increased compared with those of the control group, and the second measurement in the LSS group significantly increased compared with the first measurement. No significant differences in CT% and total CT were observed between the two measurements in the control group.

Table 3 presents the comparison of the FPA of the two measurements in each group. The FPA in the LSS group increased significantly relative to the two measurements in the control group. No significant difference was found between the two measurements in the LSS group and the control group.

The comparison results of the PTI in each region of the plantar with two measurements are summarized in Table 4. No significant differences in PTI were observed in the control group between the two measurements. The first measurement results in the LSS group showed an increase in PTI in the M1–M2 region compared with the control group; the second measurement results showed a significant increase in the PTI in the M1–M4 region compared with the control group; and the PTI in the MH and LH regions significantly decreased. The second measurement in the LSS group significantly increased the PTI in the first M1–M4 area, and the PTI in the MH and LH areas decreased significantly.

Regarding the proportion of CA in each area, the control group had no statistically significant difference between the two measurements. Compared with the control group, the CA% in the first measurement results of the LSS group in the M1 and M2 areas increased. In the second measurement results, the CA% significantly increased in the T1, T2–T5, and M1–M4 areas and significantly reduced in the MH and LH areas. The comparison of the CA% of the two measurements in the LSS group showed that the results of the second measurement presented a significant increase in the CA% of the T1, T2–T5, and M1–M4 regions and a significant decrease in the CA% of the MH and LH regions (Table 5).

Overall, the LSS group showed an increase in forefoot CT%, PTI, and CA% in both measurements compared with those in the control group. After the occurrence of NIC in the LSS group, CT%, PTI, and CA% of the forefoot increased further compared with those before the occurrence of NIC. In addition, after the occurrence of NIC symptoms, the PTI and CA% of the forefoot shifted from the medial foot to the lateral foot.

4. Discussion

LSS is a common and disabling disease in the population over the age of 60 [1]. The pathological process is mainly the degeneration and overgrowth of the bones, ligaments, and synovial tissue that constitute the lumbar spinal canal. This gradually leads to the compression of nerves and blood vessels in the spinal canal, or prolapse into the spinal canal due to disc degeneration resulting in a series of clinical symptoms [1, 2, 14]. The complaints of patients with LSS are generally not typical; they can be pain or numbness and weakness in the lower back and buttocks, presenting different degrees of NIC [14, 16]. Although MRI and other imaging examinations can objectively present the state of the lumbar spinal canal and anatomically observe LSS, they cannot reflect the severity of the patient’s symptoms [13], and hence are not enough to accurately diagnose LSS clinically. As the main symptom of LSS [16], NIC is usually found when the patient is walking, making the diagnosis more challenging. Gait analysis, as an emerging detection method, provides a new insight for objectively assessing the walking ability of patients with LSS. However, the parameters for gait and performance of LSS have not been fully defined. Previous studies also focused on the kinematic and kinetic parameters of lower limb joints [17–19]. In this study, the Footscan® pressure system was used to perform a dynamic plantar pressure test on patients with LSS, and the changes in plantar pressure distribution before and after the occurrence of NIC and their differences against those of healthy controls were compared. The plantar pressure distribution of patients with LSS was evaluated objectively, which could better explain the abnormal performance of patients with LSS in kinetics and kinematics, providing an important reference for the application of plantar pressure analysis in LSS.

In the gait analysis study of patients with LSS by Garbelotti et al. [20], patients with LSS had shorter stride length, slower walking speed, and significantly longer stance phase compared with healthy subjects, which could be taken as the compensation strategy. Although the parameters, such as stride length and walking speed, were not directly measured in this study, the results showed that after the occurrence of NIC, the total CT in the LSS group was significantly longer than that in the control group, and no significant difference was found before the occurrence of NIC. This showed that the occurrence of NIC in patients with LSS could result in a decrease in their balance function, causing the patients’ requirement of more time to stabilize the body before entering the next gait cycle [10, 20, 21]. Further, the time distribution of each subphase was examined, and the first measurement of the ICP in the LSS group was found to be smaller than that in the control group and the FFPOP was larger. After the occurrence of NIC in the LSS group, ICP and FFCP decreased significantly and FFP and FFPOP increased significantly. Patients with LSS tended to keep the lumbar forward and flexion walking to reduce the symptoms of nerve root compression [22]. This gait pattern could cause the center of gravity to move in the anterior direction [23]. Hence, the patients needed to transfer the center of pressure from the hindfoot to the forefoot faster, resulting in an increase in the CT of the forefoot. In general, in the LSS group, the proportion of the forefoot area increased and the proportion of the hindfoot area decreased in each subphase time distribution compared with the control group before the occurrence of NIC. This characteristic was more pronounced after the occurrence of NIC, indicating that patients with LSS would maintain mild lumbar forward flexion at the beginning of walking. After the symptoms of lower limbs caused by continuous walking, the patient’s lumbar spine was further forward flexed, the center of gravity shifted more to the anterior direction, and the transfer of loading was faster to reduce symptoms. These results showed that patients with LSS had an anterior-posterior balance disorder, and they might have a higher risk of falling at the same time [23].

In this study, irrespective of the occurrence of NIC, the FPA was larger in the LSS group compared with the control group, and the foot was more externally rotated when walking. FPA referred to the angle between the longitudinal axis of one foot and the walking direction, and its outward rotation indicated that the patient had an “out-toe” gait when walking [24]. Previous studies confirmed that patients with LSS had a wide-based gait [17], which was mainly manifested by awkward and faltering walking patterns. These patterns could reflect the characteristics of patients with unstable trunk and limited dynamic balance [11]. In addition, a large number of studies showed that LSS could affect the balance function of patients [25]. Therefore, it was hypothesized that patients in the LSS group walked in the “out-toe” gait to obtain a wider base and thus maintain balance, so as to reduce the swing from one side to another [26].

Marte et al. [27] and Lai et al. [28] showed that the changes in FPA could affect the distribution of plantar pressure. When FPA was externally rotated, it promoted the transfer of plantar pressure to the forefoot and medial feet. The findings of the present study were consistent with this conclusion to some extent. Before the occurrence of NIC in the LSS group, PTI and CA% increased relative to the M1–M2 area in the control group, showing the transfer of pressure to the forefoot and medial feet. However, after the occurrence of NIC in the LSS group, the forefoot loading and the CA increased further. At the same time, the hindfoot loading decreased and the CA decreased. However, no significant difference in FPA before and after the occurrence of NIC was observed in the LSS group, indicating that the increase in CA and loading in the forefoot of the patients with LSS after the occurrence of NIC could also be caused by the patient’s center of gravity moving to the anterior direction. This corresponded to the CT% result. It was also found that in the LSS group, the loading on the lateral feet increased and the CA increased after the occurrence of NIC compared with those before NIC in the LSS group. This study considered that patients with LSS also had a medial-lateral direction balance disorder. SaSaKi et al. [11] studied the characteristics of postural sway during quiet standing before and after the occurrence of NIC. In addition, they found that the postural sway in the left and right directions of patients with LSS increased after the occurrence of NIC, and the center of pressure shifted to the symptomatic side, implying the patient’s risk of falling to the symptomatic side. Yoshio et al. [18] analyzed the gait analysis of patients with LSS and showed that patients with more severe symptoms of LSS presented a significantly higher swing index reflecting the left-right balance function compared with ordinary subjects. This might be because the symptoms of lower limbs caused by intravertebral compression could affect the load capacity of the affected limbs. In this study, the plantar pressure data of the symptomatic side or the more severe side were selected for analysis. During the entire stance phase, the patient suffered from insufficient muscle strength in the lower limbs due to the weakness, pain, or numbness of the symptomatic side. The body’s center of gravity could be further biased to the symptomatic side, resulting in the transfer of plantar pressure distribution to the lateral side of the symptomatic foot.

Impaired balance in patients with LSS has been demonstrated in multiple studies. Aleksandra et al. [29] and Elisabeth [30] et al. conducted studies on the static and dynamic balance functions of patients with LSS, respectively, and confirmed that these patients had a higher risk of falling compared with ordinary subjects. Based on the aforementioned studies, the causes of changes in the gait cycle and plantar pressure distribution in patients with LSS were further analyzed in this study. Before the occurrence of NIC, patients with LSS maintained a mild lumbar forward flexion posture, and the center of gravity moved to the anterior direction. At this time, their body could maintain balance by adjusting the time distribution of each phase of the stance phase [21, 23, 31], and the plantar pressure distribution was close to that in normal subjects. However, these changes caused pressure to shift to the anterior and medial directions due to the “out-toe” gait [28]. After the occurrence of NIC, the patient further flexed the lumbar spine forward to reduce the symptoms, causing the center of gravity to move more in the anterior direction. At this time, the adjustment of the time distribution of the stance phases in each subphase might not be enough to compensate, so the CA and loading of the hindfoot decreased. By relying on the forefoot to contact the ground, the forefoot could be more susceptible to suffer from overuse injuries or strain diseases [31]. The uneven plantar pressure distribution in the anterior and posterior directions also indicated that the patient was at risk of falling to the anterior direction [11, 21, 23]. In addition, the occurrence of NIC made the lower limb muscles on the side of the symptoms contract with weakness or numbness, pain, and other symptoms. Hence, patients with LSS could not maintain the center of gravity of their bodies. Therefore, they shifted the pressure distribution of the plantar from the medial side to the lateral side of the symptomatic side foot. At the same time, they had a risk of falling to the symptomatic side.

This study had some limitations. Only the plantar pressure analysis was performed on patients with L4–L5 level spinal canal stenosis, considering this to be more common in clinic [1, 2], compared with the other levels of stenosis. Further studies are needed to explore the effects of spinal stenosis in different segments on the plantar pressure distribution of patients. However, previous gait analysis was performed on the selected patients with L4–L5 level stenosis [11, 30, 31]. Therefore, patients with LSS with spinal stenosis of other levels or multiple segments were not included in the experimental group, that is, the sample size was small. Future studies should use large samples and involve a comprehensive analysis. Second, only the symptomatic side or the more severe side foot was selected for analysis, which was not conducive to the overall assessment of the walking and balance functions of patients. Moreover, after the development of symptoms of NIC in patients with LSS, the patients were not asked to continue walking until they could not, which otherwise would have helped better understand NIC. Finally, the relation of the severity of NIC to the distribution of plantar pressure in patients with LSS was not evaluated in this study. This is a promising research direction, which can help create an objective and quantitative symptom assessment method to apply in clinic.

5. Conclusions

In summary, plantar pressure tests were conducted before and after the occurrence of NIC in patients with LSS, and the results were compared with those in healthy adults in this study. The results revealed the following differences in the distribution of plantar pressure: (1) patients with LSS could present the posture of the lumbar forward flexion when walking. As a result, the center of gravity moved in the anterior direction compared with the healthy subjects, increasing the CT and loading of the forefoot. The forefoot might have a higher risk of strain disease or overuse injury. (2) The occurrence of NIC could affect the plantar pressure distribution of the patients with LSS, predicting the patient’s risk of falling to the anterior direction and to the symptomatic side. Future gait analysis studies should focus on investigating the changes in plantar pressure distribution after the occurrence of NIC in patients with LSS and correlate them with patients’ walking functions, such as the maximum walking distance or the level of balance function. It is promising to provide a new objectively method for evaluating the walking capabilities of patients with LSS.

Data Availability

The authors declare all data are fully available without restriction.

Conflicts of Interest

The authors declare that they have no competing interests.

Authors’ Contributions

Wei Wei, Chao Xu, and Xiao-Jiang Yang contributed equally to this work as cofirst authors.

Acknowledgments

The authors would like to thank the participants of this study and also Xi-Xia Cheng for the arrangement of the experiment and help during data acquisition. This study was supported by the National Natural Science Foundation of China (grant no. 81672132). The funding body played no direct role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.

References

Y. Yabe, Y. Hagiwara, A. Ando et al., “Chondrogenic and fibrotic process in the ligamentum flavum of patients with lumbar spinal canal stenosis,” Spine, vol. 40, no. 7, pp. 429–435, 2015.
View at: Publisher Site | Google Scholar
L. Kalichman, R. Cole, D. H. Kim et al., “Spinal stenosis prevalence and association with symptoms: the Framingham Study,” The Spine Journal, vol. 9, no. 7, pp. 545–550, 2009.
View at: Publisher Site | Google Scholar
M. C. Jensen, M. N. Brant-Zawadzki, N. Obuchowski, M. T. Modic, D. Malkasian, and J. S. Ross, “Magnetic resonance imaging of the lumbar spine in people without back pain,” The New England Journal of Medicine, vol. 331, no. 2, pp. 69–73, 1994.
View at: Publisher Site | Google Scholar
R. A. Deyo, D. T. Gray, W. Kreuter, S. Mirza, and B. I. Martin, “United States trends in lumbar fusion surgery for degenerative conditions,” Spine, vol. 30, no. 12, pp. 1441–1445, 2005.
View at: Publisher Site | Google Scholar
R. A. Deyo, S. K. Mirza, B. I. Martin, W. Kreuter, D. C. Goodman, and J. G. Jarvik, “Error in Trends, Major Medical Complications, and Charges Associated With Surgery for Lumbar Spinal Stenosis in Older Adults,” JAMA: The Journal of the American Medical Association, vol. 306, no. 10, pp. 1088–1265, 2011.
View at: Publisher Site | Google Scholar
N. Mamisch, M. Brumann, J. Hodler et al., “Radiologic criteria for the diagnosis of spinal stenosis: Results of a delphi survey,” Radiology, vol. 264, no. 1, pp. 174–179, 2012.
View at: Publisher Site | Google Scholar
Y. Ishimoto, N. Yoshimura, S. Muraki et al., “Associations between radiographic lumbar spinal stenosis and clinical symptoms in the general population: the Wakayama Spine Study,” Osteoarthritis and Cartilage, vol. 21, no. 6, pp. 783–788, 2013.
View at: Publisher Site | Google Scholar
C. Weber, C. Giannadakis, V. Rao et al., “Is There an Association Between Radiological Severity of Lumbar Spinal Stenosis and Disability, Pain, or Surgical Outcome? a Multicenter Observational Study,” Spine, vol. 41, no. 2, pp. E78–E83, 2016.
View at: Publisher Site | Google Scholar
M. R. Lim, R. C. Huang, A. Wu, F. P. Girardi, and F. P. Cammisa Jr., “Evaluation of the Elderly Patient With an Abnormal Gait,” Journal of the American Academy of Orthopaedic Surgeons, vol. 15, no. 2, pp. 107–117, 2007.
View at: Publisher Site | Google Scholar
N. C. Papadakis, D. G. Christakis, G. N. Tzagarakis et al., “Gait variability measurements in lumbar spinal stenosis patients: part A. Comparison with healthy subjects,” Physiological Measurement, vol. 30, no. 11, pp. 1171–1186, 2009.
View at: Publisher Site | Google Scholar
K. Sasaki, M. Senda, Y. Katayama, H. Ota, and Y. Matsuyama, “Characteristics of Postural Sway during Quiet Standing Before and After the Occurrence of Neurogenic Intermittent Claudication in Female Patients with Degenerative Lumbar Spinal Canal Stenosis,” Journal of Physical Therapy Science, vol. 25, no. 6, pp. 675–678, 2013.
View at: Publisher Site | Google Scholar
P. Favre, G. U. Exner, B. Drerup, D. Schmid, H. H. Wetz, and H. A. C. Jacob, “The contralateral foot in children with unilateral clubfoot: a study of pressures and forces involved in gait,” Journal of Pediatric Orthopaedics, vol. 27, no. 1, pp. 54–59, 2007.
View at: Publisher Site | Google Scholar
J. A. Ramirez-Bautista, A. Hernández-Zavala, S. L. Chaparro-Cárdenas, and J. A. Huerta-Ruelas, “Review on plantar data analysis for disease diagnosis,” Biocybernetics and Biomedical Engineering, vol. 38, no. 2, pp. 342–361, 2018.
View at: Publisher Site | Google Scholar
S. Genevay and S. J. Atlas, “Lumbar spinal stenosis,” Best Practice & Research. Clinical Rheumatology, vol. 24, no. 2, pp. 253–265, 2010.
View at: Publisher Site | Google Scholar
C. Xu, X. X. Wen, L. Y. Huang et al., “Normal foot loading parameters and repeatability of the Footscan® platform system,” Journal of Foot and Ankle Research, vol. 10, no. 1, 2017.
View at: Publisher Site | Google Scholar
C. Bagley, M. MacAllister, L. Dosselman, J. Moreno, S. G. Aoun, and T. Y. el Ahmadieh, “Current concepts and recent advances in understanding and managing lumbar spine stenosis,” F1000Research, vol. 8, 2019.
View at: Publisher Site | Google Scholar
H. Hayashi, Y. Toribatake, H. Murakami, T. Yoneyama, T. Watanabe, and H. Tsuchiya, “Gait Analysis Using a Support Vector Machine for Lumbar Spinal Stenosis,” Orthopedics, vol. 38, no. 11, pp. e959–e964, 2015.
View at: Publisher Site | Google Scholar
N. Yokogawa, Y. Toribatake, H. Murakami et al., “Differences in Gait Characteristics of Patients with Lumbar Spinal Canal Stenosis (L4 Radiculopathy) and Those with Osteoarthritis of the Hip,” PLoS One, vol. 10, no. 4, article e0124745, 2015.
View at: Publisher Site | Google Scholar
T. Igawa, J. Katsuhira, A. Hosaka, K. Uchikoshi, S. Ishihara, and K. Matsudaira, “Kinetic and kinematic variables affecting trunk flexion during level walking in patients with lumbar spinal stenosis,” Plos One, vol. 13, no. 5, article e197228, 2018.
View at: Publisher Site | Google Scholar
S. A. Garbelotti, P. R. G. Lucareli, A. Ramalho, W. de Godoy, M. Bernal, and J. M. D’Andréa Greve, “An investigation of the value of tridimensional kinematic analysis in functional diagnosis of lumbar spinal stenosis,” Gait & Posture, vol. 40, no. 1, pp. 150–153, 2014.
View at: Publisher Site | Google Scholar
C. P. Carty, P. Mills, and R. Barrett, “Recovery from Forward Loss of Balance in Young and Older Adults Using the Stepping Strategy,” Gait & Posture, vol. 33, no. 2, pp. 261–267, 2011.
View at: Publisher Site | Google Scholar
D. Hirose, K. Ishida, Y. Nagano, T. Takahashi, and H. Yamamoto, “Posture of the trunk in the sagittal plane is associated with gait in community-dwelling elderly population,” Clinical Biomechanics, vol. 19, no. 1, pp. 57–63, 2004.
View at: Publisher Site | Google Scholar
M. Fujimoto, W. N. Bair, and M. W. Rogers, “Center of pressure control for balance maintenance during lateral waist-pull perturbations in older adults,” Journal of Biomechanics, vol. 48, no. 6, pp. 963–968, 2015.
View at: Publisher Site | Google Scholar
S. J. Khan, S. S. Khan, J. Usman, A. H. Mokhtar, and N. A. Abu Osman, “Effects of different foot progression angles and platform settings on postural stability and fall risk in healthy and medial knee osteoarthritic adults,” Proceedings of the Institution of Mechanical Engineers, Part H: Journal of Engineering in Medicine, vol. 232, no. 2, pp. 163–171, 2018.
View at: Publisher Site | Google Scholar
H.-J. Kim, H.-J. Chun, C.-D. Han et al., “The risk assessment of a fall in patients with lumbar spinal stenosis,” Spine, vol. 36, no. 9, pp. e588–e592, 2011.
View at: Publisher Site | Google Scholar
M. C. Chiu, H. C. Wu, L. Y. Chang, and M. H. Wu, “Center of pressure progression characteristics under the plantar region for elderly adults,” Gait. Posture, vol. 37, no. 3, pp. 408–412, 2013.
View at: Publisher Site | Google Scholar
M. Gimunova, M. Zvonař, and O. Mikeska, “The effect of aging and gender on plantar pressure distribution during the gait in elderly,” Acta of Bioengineering and Biomechanics, vol. 20, no. 4, pp. 139–144, 2018.
View at: Publisher Site | Google Scholar
Y. C. Lai, H. S. Lin, H. F. Pan, W. N. Chang, C. J. Hsu, and J. H. Renn, “Impact of foot progression angle on the distribution of plantar pressure in normal children,” Clinical Biomechanics, vol. 29, pp. 196–200, 2014.
View at: Publisher Site | Google Scholar
A. Truszczyńska, J. Drzał-Grabiec, Z. Trzaskoma, K. Rąpała, A. Tarnowski, and K. Górniak, “A comparative analysis of static balance between patients with lumbar spinal canal stenosis and asymptomatic participants,” Journal of Manipulative and Physiological Therapeutics, vol. 37, no. 9, pp. 696–701, 2014.
View at: Publisher Site | Google Scholar
E. Thornes, H. S. Robinson, and N. K. Vøllestad, “Dynamic balance in patients with degenerative lumbar spinal stenosis; a cross-sectional study,” BMC Musculoskeletal Disorders, vol. 19, no. 1, p. 192, 2018.
View at: Publisher Site | Google Scholar
A. De Cock, D. De Clercq, T. Willems, and E. Witvrouw, “Temporal characteristics of foot roll-over during barefoot jogging: reference data for young adults,” Gait & Posture, vol. 21, no. 4, pp. 432–439, 2005.
View at: Publisher Site | Google Scholar

Copyright

Copyright © 2020 Wei Wei et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

PDF Download Citation

Download other formats

Order printed copies

Views

813

Downloads

1094

Citations