Validity of the I‑FEED classification in assessing postoperative gastrointestinal impairment in patients undergoing elective lumbar spinal surgery with general anesthesia: a prospective observational study (2024)

  • Journal List
  • Perioper Med (Lond)
  • v.13; 2024
  • PMC11145765

As a library, NLM provides access to scientific literature. Inclusion in an NLM database does not imply endorsem*nt of, or agreement with, the contents by NLM or the National Institutes of Health.
Learn more: PMC Disclaimer | PMC Copyright Notice

Validity of the I‑FEED classification in assessing postoperative gastrointestinal impairment in patients undergoing elective lumbar spinal surgery with general anesthesia: a prospective observational study (1)

Link to Publisher's site

Perioper Med (Lond). 2024; 13: 50.

Published online 2024 Jun 3. doi:10.1186/s13741-024-00409-4

PMCID: PMC11145765

PMID: 38831440

Chun-Yu Wu,1,2,3 Chih-Jun Lai,2 Fu-Ren Xiao,3,4 Jen-Ting Yang,5 Shih-Hung Yang,3,4 Dar-Ming Lai,3,4 and Fon-Yih TsuangValidity of the I‑FEED classification in assessing postoperative gastrointestinal impairment in patients undergoing elective lumbar spinal surgery with general anesthesia: a prospective observational study (2)3,4

Author information Article notes Copyright and License information PMC Disclaimer

Associated Data

Data Availability Statement

Abstract

Background

The I-FEED classification, scored 0–8, was reported to accurately describe the clinical manifestations of gastrointestinal impairment after colorectal surgery. Therefore, it is interesting to determine whether the I-FEED scoring system is also applicable to patients undergoing lumbar spine surgery.

Methods

Adult patients undergoing elective lumbar spine surgery were enrolled, and the I-FEED score was measured for 4days after surgery. The I-FEED scoring system incorporates five elements: intake (score: 0, 1, 3), feeling nauseated (score: 0, 1, 3), emesis (score: 0, 1, 3), results of physical exam (score: 0, 1, 3), and duration of symptoms (score: 0, 1, 2). Daily I-FEED scores were summed, and the highest overall score is used to categorize patients into one of three categories: normal (0–2 points), postoperative gastrointestinal intolerance (POGI; 3–5 points), and postoperative gastrointestinal dysfunction (POGD; 6 + points). The construct validity hypothesis testing determines whether the I-FEED category is consistent with objective clinical findings relevant to gastrointestinal impairment, namely, the longer length of hospital stay (LOS), higher inhospital medical cost, more postoperative gastrointestinal medical treatment, and more postoperative non-gastrointestinal complications.

Results

A total of 156 patients were enrolled, and 25.0% of patients were categorized as normal, 49.4% POGI, and 25.6% POGD. Patients with higher I-FEED scores agreed with the four validity hypotheses. Patients with POGD had a significantly longer length of hospital stay (1day longer median stay; p = 0.049) and more inhospital medical costs (approximately 500 Taiwanese dollars; p = 0.037), and more patients with POGD required rectal laxatives (10.3% vs. 32.5% vs. 32.5%; p = 0.026). In addition, more patients with POGD had non-gastrointestinal complications (5.1% vs. 11.7% vs. 30.0%; p = 0.034).

Keywords: Lumbar spine, Ileus, I-FEED, Gastrointestinal impairment, Postoperative gastrointestinal impairment, Postoperative gastrointestinal dysfunction

Introduction

Postoperative ileus is a recognized complication after lumbar spine surgery and is associated with worse postoperative outcomes (Jaber et al. 2021; Fineberg et al. 2014). The incidence of ileus after lumbar spine surgery has been reported across a wide range, between 2 and 33%, in the literature (Fineberg et al. 2014; Bahk et al. 2020; Kiely et al. 2016; Lee et al. 2015; Oh et al. 2015). This huge discrepancy in the reported incidence may stem from ambiguous definitions of postoperative ileus between different studies. Thus, an objective measure that sensitively reflects the spectrum of postoperative gastrointestinal (GI) impairment is clinically relevant to improve the quality of postoperative care.

Recently, the I-FEED classification, a 5-item scoring system of postoperative GI recovery, was proposed by the American Society for Enhanced Recovery and Perioperative Quality Initiative Joint Consensus Statement in 2018 to detect GI dysfunction after elective colorectal surgery (Hedrick et al. 2018). The benefits of the I-FEED classification for detecting postoperative GI impairment were twofold. First, postoperative GI recovery is multidimensional, including nausea, vomiting, intolerance to oral intake, inability to pass flatus or stool, and abdominal distension. Hence, the implication of the I-FEED classification could avoid the dichotomous yes-or-no definition to assess a patient’s GI recovery. Second, this scoring system has been recently validated in two studies with patients undergoing colorectal surgery, and these results not only indicated sufficient sensitivity to detect subtle changes in postoperative GI recovery but also revealed its correlation with clinical outcomes (Alsharqawi et al. 2020; Leung et al. 2021). However, its generalizability to lumbar spine surgery remains unclarified. Therefore, we conducted this prospective observational study to evaluate the validity of the I-FEED score classification for postoperative GI impairment in patients undergoing lumbar spine surgery.

Material and methods

This study was approved by the research ethics committee (the Research Ethics Committee of National Taiwan University Hospital) and registered at clinical.gov (NCT04057599). After obtaining informed consent, adult patients undergoing elective lumbar spine surgery with general anesthesia were enrolled between August 2019 and February 2022. Baseline demographic and clinical data were collected at the time of enrollment. Patients with preoperative functional constipation diagnosed based on the ROME IV criteria (Aziz et al. 2020) were excluded, and surgical invasiveness was scored based on a validated index based on the number of vertebrae decompressed, fused, or instrumented (Mirza et al. 1976).

Perioperative care

Each patient received general anesthesia that was maintained by using a combination of intravenous fentanyl and inhalation of sevoflurane to the anesthetic depth of a bispectral index between 40 and 60. The intraoperative mean arterial pressure was maintained at ≥ 60mmHg by using norepinephrine infusion or iv. fluid challenge (Sessler et al. 2019). Blood transfusion was performed when the patient’s hemoglobin level was less than 9g/dL.

Postoperative pain was managed by using the combination of oral tramadol/paracetamol (Dogar and Khan 2017), nonsteroidal anti-inflammatory drugs, and iv. morphine. The use of prophylactic ondansetron to prevent postoperative nausea and vomiting (PONV) was at the discretion of the attending anesthesiologist. The PONV was managed by using metoclopramide, and a laxative (rectal bisacodyl) may be administered for intolerable abdominal distention with failure to pass flatus for at least 24h (Wiriyakosol et al. 2007).

Study measures and construct validity assessment

Trained research nurses who did not participate in clinical care measured the I-FEED score for 4days after surgery. Table ​Table11 illustrates the I-FEED classification scheme, which incorporates five elements: intake (score: 0, 1, 3), feeling nauseated (score: 0, 1, 3), emesis (score: 0, 1, 3), results of physical exam (score: 0, 1, 3), and duration of symptoms (score: 0, 1, 2). The total score, ranging from 0 to 14, is calculated and summed for each postoperative day, and the highest overall score is used to categorize patients into one of three categories: normal (0–2 points), postoperative gastrointestinal intolerance (POGI; 3–5 points), and postoperative gastrointestinal dysfunction (POGD; 6 + points). These three categories have been applied in colorectal surgery, abdominal surgery, and gynecological surgery to provide a consistent and objective definition of postoperative gastrointestinal function, as well as the trajectory of postoperative gastrointestinal recovery (Alsharqawi et al. 2020; Leung et al. 2021; McLemore et al. 2022; Lu et al. 2021; Gungorduk et al. 2024). A brief explanation of the three categories is summarized below:

  1. Normal (score 0–2): These patients tolerate a diet without symptoms of bloating but may experience transient PONV or mild abdominal distension within 24–48h after surgery.

  2. Postoperative gastrointestinal intolerance (POGI; score 3–5): These patients typically experience nausea, small-volume emesis, and bloating 48h after surgery. However, the majority of these patients tolerated oral liquids.

  3. Postoperative gastrointestinal dysfunction (POGD; score ≥ 6): This is the most severe form of postoperative GI impairment. These patients develop abdominal distention with tympany, nausea resistant to antiemetics, and large-volume bilious emesis.

Table1

The I-FEED classification scheme

Scoring itemIntakeFeeling nauseatedEmesisExamDuration of symptom
Description (score)0: tolerating oral diet0: none0: none0: no abdominal distension0: within 24h
1: limiting tolerance1: responsive to treatment1: one or more episodes of nonbilious emesis less than 100ml1: distension without tympany1: 24–72h
3: complete intolerance3: resistant to treatment3: one or more episodes of emesis less than 100ml or bilious emesis3: significant distension with tympany2: > 72h
Total scoreScore 0–2, normal; score, 3–5 postoperative gastrointestinal intolerance (POGI); score ≥ 6, postoperative gastrointestinal dysfunction (POGD)

Open in a separate window

Because there is no gold standard definition for ileus after lumbar spine surgery, this study aimed to perform construct validity hypothesis testing, which determines the degree to which the I-FEED score is consistent with objective clinical findings relevant to gastrointestinal impairment, which are listed below:

  1. Patients classified as POGD required a longer length of hospital stay (Hedrick et al. 2018).

  2. Patients classified as POGD required a higher medical cost (exclusion of operation-related costs) (Fineberg et al. 2014).

  3. Patients with normal I-FEED scores (0–2) required GI medical treatment (Alsharqawi et al. 2020).

  4. Patients classified as POGD had a higher incidence of postoperative non-GI complications defined by using the International Statistical Classification of Diseases and Related Health Problems 10th Revision (ICD-10) (Hedrick et al. 2018; Alsharqawi et al. 2020).

Since the present study aimed to validate the I-FEED scoring system, the treatment for postoperative gastrointestinal impairment was not tailored based on the three categories to avoid interfering with the validation process.

Statistical analysis

The sample size calculation was guided by previous studies, as the power calculation is not reliable for correlation analysis, but it is recommended that studies investigating construct validity and responsiveness should ideally include at least 100 patients (Terwee et al. 2012). Data are presented as the mean (standard deviation, SD), median (interquartile range, IQR), or number (%). Comparisons for dichotomous variables were performed using χ2. Continuous variables were compared using ANOVA or the Kruskal–Wallis test. All analyses were performed using MedCalc version 20.110 (MedCalc Software, Ostend, Belgium).

Results

There were a total of 156 patients enrolled in this study. The patient characteristics and perioperative profile are listed in Table2. Based on the I-FEED classification, 39 patients (25.0%) were classified as normal, 77 patients (49.4%) were classified as POGI, and 40 patients (25.6%) were classified as POGD. There were more male patients with normal I-FEED scores (61.5% vs. 44.2% vs. 32.5%; p = 0.033). Additionally, a greater proportion of patients in the normal and POGI categories had diabetes compared to those in the POGD category (30.8% vs. 22.2% vs. 2.5%; p = 0.004). The age, body mass index, and comorbidities, including cardiac disease, chronic obstructive lung disease, and cerebral disease, were comparable between the three patient groups.

Table2

Patient characteristics of the study population

Overall (n = 156)Normal (n = 39)POGI (n = 77)POGD (n = 40)p-value
Age61.1 ± 13.558.8 ± 14.861.6 ± 14.162.1 ± 10.90.482
Male (n; %)71 (45.5%)24 (61.5%)34 (44.2%)13 (32.5%)0.033
Body mass index (kg/m2)25.7 ± 3.425.7 ± 3.725.9 ± 3.525.5 ± 3.10.843
Cardiac disease33 (21.2%)11 (28.2%)17 (22.1%)5 (12.5%)0.223
COPD3 (1.9%)1 (2.6%)2 (2.6%)0 (0%)0.948
Smoking16 (10.3%)4 (10.3%)8 (10.4%)4 (10.0%)0.998
Diabetes30 (19.2%)12 (30.8%)17 (22.1%)1 (2.5%)#*0.004
Cerebral disease9 (5.8%)3 (7.7%)5 (6.5%)1 (2.5%)0.570
Surgical type
 Decompression (n; %)32 (20.5%)11 (28.2%)15 (19.5%)6 (15.0%)0.264
 Fusion (n; %)105 (67.3%)21 (53.8%)52 (67.5%)32 (80.0%)
 HIVD (n; %)18 (11.6%)7 (18.0%)9 (11.7%)2 (5.0%)
 Scoliosis (n; %)1 (0.6%)0 (0%)1 (1.3%)0 (0%)
Surgery etiology
 Deformity (n; %)2 (1.3%)1 (2.6%)1 (1.3%)0 (0%)0.513
 Degeneration (n; %)148 (94.8%)36 (92.3%)72 (93.5%)40 (100%)
 Trauma (n; %)2 (1.3%)0 (0%)2 (2.6%)0 (0%)
 Tumor (n; %)4 (2.6%)2 (5.1%)2 (2.6%)0 (0%)

Open in a separate window

COPD chronic obstructive pulmonary disease, POGI postoperative gastrointestinal intolerance, POGD postoperative gastrointestinal dysfunction

#indicates a p-value < 0.05 compared to that of normal I-FEED score; *indicates a p-value < 0.05 compared to that of POGI

Table ​Table33 summarizes the intraoperative profiles. The intraoperative profile, including the spine surgical invasiveness, operation time, anesthetic time, blood loss, transfusion, prophylactic antiemetic use, norepinephrine dose, and opioid requirement, was comparable between patients in the three I-FEED categories. Table ​Table44 presents the details of the I-FEED scores in the three groups. Among the whole cohort, the three most common GI impairment presentations based on the I-FEED classification were as follows: abdominal distension without tympanic percussion (85.2%), limited tolerance to oral intake (73.7%), and nausea responsive to treatment (49.4%). The proportions of patients with limited tolerated oral intake were comparable between patients classified as POGI and POGD but were significantly higher than those who were classified as normal (10.3% vs. 92.2% vs. 100%; p < 0.001). The proportions of patients with nausea responsive to treatment (scored one) were significantly different between the three I-FEED groups (0% vs. 54.5% vs. 87.5%; p < 0.001). There was a high proportion of patients (31/40; 77.5%) classified as POGD who had episodes of high volume (> 100ml) emesis, but no patients with normal I-FEED experienced emesis. By comparison, the presentation of abdominal distension without tympany (scored one) was prevalent among the entire cohort (approximately 86%), and there were comparable proportions of patients as the POGI (11.7%) and POGD (15.0%) with significant distension with tympany (scored 3). Regarding the duration of GI impairment symptoms, only patients with POGI and POGD revealed prolonged symptoms more than 72h after surgery.

Table3

Intraoperative profiles

Overall (n = 156)Normal (n = 39)POGI (n = 77)POGD (n = 40)p-value
Surgical invasiveness7.8 ± 5.66.3 ± 5.38.0 ± 5.98.7 ± 5.00.134
Operation time (min)133 ± 70130 ± 74135 ± 73134 ± 610.932
Blood loss (ml)100 (20–300)20 (20–275)100 (20–300)125 (20–325)0.153
Norepinephrine dose (μg)33.5 ± 135.712.3 ± 30.347.1 ± 183.529.6 ± 76.10.416
Transfusion (n; %)21 (13.5%)4 (10.3%)9 (11.7%)8 (20.0%)0.364
Prophylactic ondansetron (n; %)19 (12.2%)4 (10.3%)11 (14.3%)4 (10.0%)0.731
Fentanyl dose (μg)129 ± 49119 ± 33136 ± 52124 ± 530.178

Open in a separate window

POGI postoperative gastrointestinal intolerance, POGD postoperative gastrointestinal dysfunction

Table4

Details of the I-FEED classification score

Overall (n = 156)Normal (n = 39)POGI (n = 77)POGD (n = 40)p-value
Intakep < 0.001
 0 (n; %)41 (26.3%)35 (89.7%)6 (7.8%)0 (0%)
 1 (n; %)115 (73.7%)4 (10.3%)71 (92.2%)*40 (100%)*
 3 (n; %)0 (0%)0 (0%)0 (0%)0 (0%)
Feeling nauseatedp < 0.001
 0 (n; %)79 (50.6%)39 (100%)35 (45.5%)5 (12.5%)
 1 (n; %)77 (49.4%)0 (0%)42 (54.5%)*35 (87.5%)#*
 3 (n; %)0 (0%)0 (0%)0 (0%)0 (0%)
Emesis (n; %)p < 0.001
 0 (n; %)98 (62.8%)39 (100%)55 (71.4%)4 (10.0%)
 1 (n; %)27 (17.3%)0 (0%)22 (28.6%)5 (12.5%)
 3 (n; %)31 (19.9%)0 (0%)031 (77.5%)#*
Exam (n; %)p < 0.001
 0 (n; %)8 (5.1%)7 (17.9%)1 (1.3%)0 (0%)
 1 (n; %)133 (85.2%)32 (82.1%)67 (87.0%)34 (85.0%)
 3 (n; %)15 (9.6%)0 (0%)9 (11.7%)*6 (15.0%)*
Duration of symptomsp < 0.001
 0 (n; %)54 (34.6%)20 (51.3%)16 (20.8%)18 (45.0%)
 1 (n; %)87 (55.8%)19 (48.7%)57 (74.0%)11 (27.5%)
 2 (n; %)15 (9.6%)0 (0%)4 (5.2%)11 (27.5%)

Open in a separate window

POGI postoperative gastrointestinal intolerance, POGD postoperative gastrointestinal dysfunction

*Indicates p < 0.05 compared to the normal I-FEED score. #Indicates p < 0.05 compared to that of the POGI

Table ​Table55 summarizes the postoperative profiles. Patients with higher I-FEED scores agreed with the four validity hypotheses. Patients with POGD had a significantly longer length of hospital stay [4 (3–5) vs. 5 (4–7) vs. 5 (4–7) days in the normal, POGI and POGD groups, respectively; p = 0.049], more inhospital medical costs [806 (582–1633) vs. 1238 (740–1988) vs. 1319 (907–2303) Taiwanese dollars in the normal, POGI and POGD groups, respectively; p = 0.037], and more patients with POGD required rectal laxative (10.3% vs. 32.5% vs. 32.5% in the normal, POGI and POGD groups, respectively; p = 0.026) than those with normal I-FEED scores. In addition, more patients with POGD had non-GI complications than patients in the other two groups (5.1% vs. 11.7% vs. 30.0%; p = 0.034). The perioperative morphine consumption was comparable between the three I-FEED groups, but although patients with POGD exhibited higher tramadol utilization, this increase did not achieve statistical significance (p = 0.077). Moreover, despite patients with POGD requiring a greater amount of perioperative intravenous fluid administration, this difference also failed to attain statistical significance (1661 ± 1012ml vs. 2183 ± 1433ml vs. 2334 ± 1163ml in the normal, POGI and POGD groups, respectively; p = 0.052).

Table5

Postoperative outcomes

Overall (n = 156)I-FEED
0–2 (n = 39)
I-FEED
3–5 (n = 77)
I-FEED
≧ 6 (n = 40)
p-value
Length of hospital stay (day)5 (3–6)4 (3–5)5 (4–7)5 (4–7)*0.049
Medical cost for GI symptoms (TW dollar)1204 (710–1951)806 (582–1633)1238 (740–1988)1319 (907–2303)*0.037
Laxative requirement (n; %)42 (6.9%)4 (10.3%)25 (32.5%)*13 (32.5%)*0.026
Non-GI complication (n; %)17 (10.9%)1 (2.6%)7 (9.1%)9 (22.5%)0.014
Perioperative morphine consumption (mg)7.7 ± 8.46.7 ± 5.97.9 ± 8.18.2 ± 10.90.703
Perioperative tramadol consumption (mg)112.7 ± 190.267.3 ± 154.4116.7 ± 192.1149.1 ± 212.50.077
Perioperative iv. fluid (ml)1984 ± 12811661 ± 10122183 ± 14882334 ± 11630.052

Open in a separate window

LOS length of hospital stay, TW Taiwanese, GI gastrointestinal

*Indicates p < 0.05 compared to patients with an I-FEED score of 0–2

Discussion

This is the first prospective study to investigate the validity of the I-FEED classification to detect postoperative GI impairment in noncolorectal surgery. We observed potentially adequate validity of this scoring system for assessing postoperative GI impairment after lumbar spine surgery.

The incidence of postoperative ileus after lumbar spine surgery was reported to be between 3 and 15% in the retrospective literature (Jaber et al. 2021; Fineberg et al. 2014; Bahk et al. 2020; Kiely et al. 2016). However, we observed a higher incidence of POGD (approximately 25%). This discrepancy may be due to several reasons. First, it may occur that only the most severe form of bowel obstruction was documented in records in case no daily assessment of GI impairment based on consistent criteria was applied. Second, there is a lack of consistency between various definitions of ileus in the literature. Accordingly, Wolthuis et al. (2016) conducted a systemic review for ileus after colorectal surgery and indicated that there were five different definitions of ileus, and these discrepancies in definition resulted in a wide range of incidence between 2.3 and 61%. Third, retrospective analysis based on the billing code is occasionally associated with lower sensitivity to detect real inhospital pathology (Grams et al. 2014). Therefore, an objective measure with sufficient sensitivity to detect postoperative GI impairment in lumbar spine surgery is highly warranted. Recently, Oh et al. (2015) reported that 32% of patients developed radiographic paralytic ileus after lumbar spine surgery which was close to the incidence of POGD in our cohort. Abdominal plain radiography is sensitive for detecting abdominal obstruction (Kim et al. 2011), but it is associated with more medical costs, and more experienced radiologists are required for evaluation (Thompson et al. 2007). By comparison, the I-FEED classification could be performed at the bedside, and this test required minimal physical examination skills that were familiar to most care providers.

In the present study, we observed an acceptable construct validity of the I-FEED classification, as patients classified as POGD were associated with worse postoperative outcomes related to GI impairment, which was compatible with the original proposal applied to patients undergoing colorectal surgery (Hedrick et al. 2018). Specifically, a higher I-FEED score was associated with a longer hospital stay and more laxative treatment. The I-FEED classification was also devised to reflect the increased cost related to GI impairment (Hedrick et al. 2018). In this study, we observed that patients with higher I-FEED scores required higher inhospital medical costs. Furthermore, the original proposal of the I-FEED-defined POGD was to identify patients with higher risks of postoperative non-GI complications (Hedrick et al. 2018). The postoperative complication rate of the present study (10.9%) was similar to that rate in a recent European report with a larger sample size (15.3–22.3%) (Barbanti-Brodano et al. 2020). We further observed that more than half of the patients who developed non-GI complications were classified as POGD by the I-FEED classification. These associations revealed the I-FEED scoring system as a potentially reliable measure to represent both perioperative GI dysfunction and related clinical burden.

Several risk factors for postoperative ileus were reported in previous retrospective reports, including higher surgical complexity (spine surgical invasiveness), higher blood loss (Fineberg et al. 2014; Bahk et al. 2020), higher iv fluid amount (Fineberg et al. 2014; Kiely et al. 2016), and higher opioid consumption (Gifford et al. 2019). Intraoperative spinal manipulations over upper lumbar levels may damage splanchnic nerves, resulting in decreased GI motility, and hence, higher spine surgical invasiveness may be harmful to postoperative GI motility (Boos and Aebi 2008). Accordingly, surgery with a higher invasiveness score is associated with more blood loss and may influence GI motility more. Increased iv. fluid amount may result in edema, and it has been frequently reported to be related to postoperative ileus in robotic surgery, colorectal surgery, and lumbar spine surgery (Kiely et al. 2016; Koch et al. 2021; VandeHei et al. 2017; Shim et al. 2021). Regarding opioid consumption, oral tramadol may also increase the risk of PONV (Liukkonen et al. 2002). In the present study, we observed a high incidence of PONV (feeling nauseated and emesis). The PONV incidence after lumbar spine surgery has been reported to be more than 50% despite prophylactic 5-HT3 antagonist treatment (Roh et al. 1976). In this study, we accordingly observed that the prophylactic 5-HT3 antagonist was not protective against the development of POGD, and one-third of patients required postoperative antiemetics. This is also compatible with a previous report indicating that prophylactic medication was ineffective in preventing ileus after lumbar spine surgery (Oh et al. 2015). Furthermore, we observed a high incidence of postoperative abdominal distension (approximately 86%) in this study. This is compatible with the recently reported rate of abdominal pain (71%) after lumbar spine surgery in a Korean cohort (Bahk et al. 2020). However, this symptom does not necessarily increase the clinical burden, but the I-FEED classification may be helpful for clinicians to detect clinically relevant risk stratification.

There were limitations in this study. First, this is a single-center study with relatively small numbers of patients. Therefore, this study may be underpowered to detect risk factors of POGD such as the spine surgery invasiveness, blood loss, perioperative iv. fluid amount, and the opioid consumptions. However, the good sensitivity of the I-FEED classification was sufficiently observed. Second, we did not propose a treatment protocol based on the I-FEED score for the management of GI impairment after lumbar spine surgery. It remains unclear whether the I-FEED scoring system could reflect the treatment effects. Third, the “duration of symptoms” item of the I-FEED classification is not scored on a daily basis, as the scored item contains a 3-day time frame. As we observed that more than half of the patients in our cohort had one score in the duration item, we expect that expansion of this category to more subunits may also extend the accuracy of I-FEED classification for risk stratification of patients undergoing lumbar spine surgery.

Conclusion

In summary, we indicated preliminary construct validity evidence for the I-FEED as a measure of postoperative GI impairment in patients undergoing elective lumbar spine surgery. This is the first validated data to support I-FEED other than colorectal surgery. The treatment protocol based on the I-FEED classification may be developed in further studies.

Acknowledgements

Not applicable.

Abbreviations

POGIPostoperative gastrointestinal intolerance
POGDPostoperative gastrointestinal dysfunction
PONVPostoperative nausea and vomiting

Authors’ contributions

Author WYC conceived and designed the analysis. CJL performed the analysis. FJX, SHY, and DML contributed data, and DML also provided administration and supervision. WYC and FYT collected the data and wrote the main manuscripts. All the authors have reviewed the final version of the manuscript and approve it for publication.

Funding

We obtained institutional fund of the National Taiwan University Hospital in this study (NTUH. 110-S4863).

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Declarations

Ethics approval and consent to participate

This study was approved by the research ethics committee (the Research Ethics Committee of National Taiwan University Hospital) and registered at clinical.gov (NCT04057599). After obtaining informed consent, adult patients undergoing elective lumbar spine surgery with general anesthesia were enrolled between August 2019 and February 2022.

Consent for publication

Not applicable.

Competing interests

The authors declare no competing interests.

Footnotes

Publisher’s Note

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

References

  • Alsharqawi N, Alhashemi M, Kaneva P, Baldini G, Fiore JF, Jr, Feldman LS, et al. Validity of the I-FEED score for postoperative gastrointestinal function in patients undergoing colorectal surgery. Surg Endosc. 2020;34(5):2219–2226. doi:10.1007/s00464-019-07011-6. [PubMed] [CrossRef] [Google Scholar]
  • Aziz I, Whitehead WE, Palsson OS, Tornblom H, Simren M. An approach to the diagnosis and management of Rome IV functional disorders of chronic constipation. Expert Rev Gastroenterol Hepatol. 2020;14(1):39–46. doi:10.1080/17474124.2020.1708718. [PubMed] [CrossRef] [Google Scholar]
  • Bahk JH, Kim YH, Park HY, Min HK, Kim SI, Ha KY. Incidence and risk factors of gastrointestinal and hepatobiliary complications after spinal fusion surgery: a retrospective cohort study. J Korean Med Sci. 2020;35(40):e345. doi:10.3346/jkms.2020.35.e345. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
  • Barbanti-Brodano G, Griffoni C, Halme J, Tedesco G, Terzi S, Bandiera S, et al. Spinal surgery complications: an unsolved problem-is the World Health Organization Safety Surgical Checklist an useful tool to reduce them? Eur Spine J. 2020;29(5):927–936. doi:10.1007/s00586-019-06203-x. [PubMed] [CrossRef] [Google Scholar]
  • Boos N, Aebi M. Spinal disorders: fundamentals of diagnosis and treatment. Cham: Springer; 2008. [Google Scholar]
  • Dogar SA, Khan FA. Tramadol-paracetamol combination for postoperative pain relief in elective single-level microdisectomy surgery. J Neurosurg Anesthesiol. 2017;29(2):157–160. doi:10.1097/ANA.0000000000000274. [PubMed] [CrossRef] [Google Scholar]
  • Fineberg SJ, Nandyala SV, Kurd MF, Marquez-Lara A, Noureldin M, Sankaranarayanan S, et al. Incidence and risk factors for postoperative ileus following anterior, posterior, and circumferential lumbar fusion. Spine J. 2014;14(8):1680–1685. doi:10.1016/j.spinee.2013.10.015. [PubMed] [CrossRef] [Google Scholar]
  • Gifford C, Minnema AJ, Baum J, Humeidan ML, Vazquez DE, Farhadi HF. Development of a postoperative ileus risk assessment scale: identification of intraoperative opioid exposure as a significant predictor after spinal surgery. J Neurosurg Spine. 2019;19:1–8. [PubMed] [Google Scholar]
  • Grams ME, Waikar SS, MacMahon B, Whelton S, Ballew SH, Coresh J. Performance and limitations of administrative data in the identification of AKI. Clin J Am Soc Nephrol. 2014;9(4):682–689. doi:10.2215/CJN.07650713. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
  • Gungorduk K, Selimoglu B, Gulseren V, Yasar E, Comba C, Ozdemir IA. Effect of abdominal hot pack application on gastrointestinal motility recovery after comprehensive gynecologic staging surgery. Int J Gynaecol Obstet. 2024;164(3):1108–1116. doi:10.1002/ijgo.15181. [PubMed] [CrossRef] [Google Scholar]
  • Hedrick TL, McEvoy MD, Mythen MMG, Bergamaschi R, Gupta R, Holubar SD, et al. American society for enhanced recovery and perioperative quality initiative joint consensus statement on postoperative gastrointestinal dysfunction within an enhanced recovery pathway for elective colorectal surgery. Anesth Analg. 2018;126(6):1896–1907. doi:10.1213/ANE.0000000000002742. [PubMed] [CrossRef] [Google Scholar]
  • Jaber A, Hemmer S, Klotz R, Ferbert T, Hensel C, Eisner C, et al. Bowel dysfunction after elective spinal surgery: etiology, diagnostics and management based on the medical literature and experience in a university hospital. Orthopade. 2021;50(6):425–434. doi:10.1007/s00132-020-04034-z. [PubMed] [CrossRef] [Google Scholar]
  • Kiely PD, Mount LE, Du JY, Nguyen JT, Weitzman G, Memstoudis S, et al. The incidence and risk factors for post-operative ileus after spinal fusion surgery: a multivariate analysis. Int Orthop. 2016;40(6):1067–1074. doi:10.1007/s00264-016-3148-9. [PubMed] [CrossRef] [Google Scholar]
  • Kim S, Park K, Kim J, Eun C, Park Y, Oh M, et al. Accuracy of plain abdominal radiography in the differentiation between small bowel obstruction and small bowel ileus in acute abdomen presenting to emergency department. Hong Kong J Emerg Med. 2011;18(2):68–79. doi:10.1177/102490791101800202. [CrossRef] [Google Scholar]
  • Koch KE, Hahn A, Hart A, Kahl A, Charlton M, Kapadia MR, et al. Male sex, ostomy, infection, and intravenous fluids are associated with increased risk of postoperative ileus in elective colorectal surgery. Surgery. 2021;170(5):1325–1330. doi:10.1016/j.surg.2021.05.035. [PubMed] [CrossRef] [Google Scholar]
  • Lee TH, Lee JS, Hong SJ, Jang JY, Jeon SR, Byun DW, et al. Risk factors for postoperative ileus following orthopedic surgery: the role of chronic constipation. J Neurogastroenterol Motil. 2015;21(1):121–125. doi:10.5056/jnm14077. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
  • Leung V, Baldini G, Liberman S, Charlebois P, Stein B, Fiore JF, Jr, et al. Trajectory of gastrointestinal function after laparoscopic colorectal surgery within an enhanced recovery pathway. Surgery. 2022;171(3):607–14. doi:10.1016/j.surg.2021.08.062. [PubMed] [CrossRef] [Google Scholar]
  • Liukkonen K, Santanen U, Pere P, Erkola O, Rautoma P. Peroral tramadol premedication increases postoperative nausea and delays home-readiness in day-case knee arthroscopy patients. Scand J Surg. 2002;91(4):365–368. doi:10.1177/145749690209100411. [PubMed] [CrossRef] [Google Scholar]
  • Lu Y, Fang PP, Yu YQ, Cheng XQ, Feng XM, Wong GTC, et al. Effect of intraoperative dexmedetomidine on recovery of gastrointestinal function after abdominal surgery in older adults: a randomized clinical trial. JAMA Netw Open. 2021;4(10):e2128886. doi:10.1001/jamanetworkopen.2021.28886. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
  • McLemore EC, Lee L, Hedrick TL, Rashidi L, Askenasy EP, Popowich D, et al. Same day discharge following elective, minimally invasive, colorectal surgery : a review of enhanced recovery protocols and early outcomes by the SAGES Colorectal Surgical Committee with recommendations regarding patient selection, remote monitoring, and successful implementation. Surg Endosc. 2022;36(11):7898–7914. doi:10.1007/s00464-022-09606-y. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
  • Mirza SK, Deyo RA, Heagerty PJ, Konodi MA, Lee LA, Turner JA, et al. Development of an index to characterize the “invasiveness” of spine surgery: validation by comparison to blood loss and operative time. Spine (Phila Pa 1976) 2008;33(24):2651–61; discussion 62. doi:10.1097/BRS.0b013e31818dad07. [PubMed] [CrossRef] [Google Scholar]
  • Oh CH, Ji GY, Yoon SH, Hyun D, Park HC, Kim YJ. Paralytic ileus and prophylactic gastrointestinal motility medication after spinal operation. Yonsei Med J. 2015;56(6):1627–1631. doi:10.3349/ymj.2015.56.6.1627. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
  • Roh GU, Yang SY, Shim JK, Kwak YL. Efficacy of palonosetron versus ramosetron on preventing opioid-based analgesia-related nausea and vomiting after lumbar spinal surgery: a prospective, randomized, and double-blind trial. Spine (Phila Pa 1976) 2014;39(9):E543–9. doi:10.1097/BRS.0000000000000236. [PubMed] [CrossRef] [Google Scholar]
  • Sessler DI, Bloomstone JA, Aronson S, Berry C, Gan TJ, Kellum JA, et al. Perioperative quality initiative consensus statement on intraoperative blood pressure, risk and outcomes for elective surgery. Br J Anaesth. 2019;122(5):563–574. doi:10.1016/j.bja.2019.01.013. [PubMed] [CrossRef] [Google Scholar]
  • Shim JS, Noh TI, Ku JH, Lee S, Kwon TG, Kim TH, et al. Effect of intraoperative fluid volume on postoperative ileus after robot-assisted radical cystectomy. Sci Rep. 2021;11(1):10522. doi:10.1038/s41598-021-89806-z. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
  • Terwee CB, Mokkink LB, Knol DL, Ostelo RW, Bouter LM, de Vet HC. Rating the methodological quality in systematic reviews of studies on measurement properties: a scoring system for the COSMIN checklist. Qual Life Res. 2012;21(4):651–657. doi:10.1007/s11136-011-9960-1. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
  • Thompson WM, Kilani RK, Smith BB, Thomas J, Jaffe TA, Delong DM, et al. Accuracy of abdominal radiography in acute small-bowel obstruction: does reviewer experience matter? AJR Am J Roentgenol. 2007;188(3):W233–W238. doi:10.2214/AJR.06.0817. [PubMed] [CrossRef] [Google Scholar]
  • VandeHei MS, Papageorge CM, Murphy MM, Kennedy GD. The effect of perioperative fluid management on postoperative ileus in rectal cancer patients. Surgery. 2017;161(6):1628–1632. doi:10.1016/j.surg.2016.11.015. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
  • Wiriyakosol S, Kongdan Y, Euanorasetr C, Wacharachaisurapol N, Lertsithichai P. Randomized controlled trial of bisacodyl suppository versus placebo for postoperative ileus after elective colectomy for colon cancer. Asian J Surg. 2007;30(3):167–172. doi:10.1016/S1015-9584(08)60017-2. [PubMed] [CrossRef] [Google Scholar]
  • Wolthuis AM, Bislenghi G, Fieuws S, de Buck van Overstraeten A, Boeckxstaens G, D'Hoore A. Incidence of prolonged postoperative ileus after colorectal surgery: a systematic review and meta-analysis. Colorectal Dis. 2016;18(1):O1–9. doi:10.1111/codi.13210. [PubMed] [CrossRef] [Google Scholar]

Articles from Perioperative Medicine are provided here courtesy of BMC

Validity of the I‑FEED classification in assessing postoperative gastrointestinal impairment in patients undergoing elective lumbar spinal surgery with general anesthesia: a prospective observational study (2024)

FAQs

When can I vacuum after spinal fusion? ›

Limit your pushing and pulling activities such as vacuuming, sweeping, mowing, and mopping floors for at least six weeks. If you feel more pain than usual after an activity, you may have overdone it. Take it a little easier for a few hours.

Why is spinal fusion not recommended? ›

Spinal fusion often works no better than nonsurgical treatments for back pain with a cause that's not clear. Even when spinal fusion relieves symptoms, it doesn't prevent future back pain. Arthritis causes much of back pain.

What is the recovery time for a spinal fusion? ›

Your Recovery

You may have trouble sitting or standing in one position for very long. It may take 4 to 6 weeks to get back to doing simple activities, such as light housework. It may take 6 months to a year for your back to get better completely. You may need to wear a back brace while your back heals.

How to sit on the toilet after back surgery? ›

Using The Bathroom

Use an elevated toilet seat or commode to raise the level of the toilet. Do NOT lean over your legs while sitting. 2. Wear your brace while using the bathroom.

What can you never do again after spinal fusion? ›

What can you never do again after spinal fusion? Unless you have complications, there are very few things you will never be able to do after a spinal fusion. You probably should not perform powerlifting exercises after spinal fusion or any activity that puts extreme stresses on the spine.

What happens if bones don't fuse after spinal fusion? ›

Many symptomatic cases of failed fusion (pseudarthrosis) result in pain, neurological deficits, or loosened hardware necessitating a revision surgery consisting of extending the prior construct and utilizing additional allografts or autografts to augment the fusion.

What is the hardest surgery to recover from? ›

5 of the Most Difficult Orthopedic Surgeries to Recover From
  1. Total Hip Replacement Surgery: The Journey to Regaining Mobility. ...
  2. Spinal Fusion Surgery: Back to the Basics of Movement. ...
  3. Rotator Cuff Surgery: Reclaiming Shoulder Strength and Flexibility. ...
  4. ACL Reconstruction: ...
  5. Ankle Fusion Surgery.
Dec 18, 2023

How long does it take to walk normally after spinal fusion surgery? ›

Gradually increase the distance you walk and, if weather permits, you may walk outside. You should be able to gradually increase your distance until you can walk about one mile within one to two months after surgery.

Is cervical fusion worth it? ›

Cervical spinal fusion surgery has a high success rate. Most people can return to their usual activities four to six weeks after surgery. If you have neck pain that has not been relieved by medication or physical therapy, talk to your doctor or make an appointment with an orthopedic physician.

What is the most painful spinal surgery? ›

Spinal Fusion:

In order to stabilize the spine, this procedure involves fusing two or more vertebrae together. The healing process can be very difficult and painful, especially in the beginning, even though it can be relieving afterward.

Is it better to lay down or sit after back surgery? ›

The best sleeping position to reduce your back pain after surgery is either on your back with your knees bent and a pillow under your knees or on your side with your knees bent and a pillow between your legs.

What is the newest treatment for spinal stenosis? ›

Stem cell therapy is emerging as a revolutionary treatment for spinal stenosis. It involves extracting the body's fundamental building blocks, isolating them, and subsequently implanting them back into the deteriorated tissue of the spine.

What supplements should you avoid after spinal fusion? ›

After fusion surgery, certain medications should be avoided as well; aspirin, non-steroidal anti-inflammatory agents (like ibuprofen, Voltaren, Nuprin, etc.), Vitamin E supplements, and fish oil supplements should be avoided for 3 months after surgery as these agents can all inhibit bone formation.

What happens if you accidentally bend after spinal fusion? ›

One bend likely won't ruin a spinal fusion procedure, but you should avoid bending or putting any excess strain on your back for 3-6 months after the surgery so everything will heal properly.

What is the best way to poop after spinal surgery? ›

The most effective measures to encourage regular bowel movements are discussed below.
  1. Get up and walk as soon as possible after surgery. ...
  2. Engage in physical therapy and stretching to aid bowel movements. ...
  3. Limit the use of opioid pain medications. ...
  4. Use over-the-counter (OTC) laxatives in moderation. ...
  5. Consider natural laxatives.

What are the restrictions 3 months after spinal fusion surgery? ›

During this time period of about 1 to 3 months after the surgery, the lumbar fusion bone mass is becoming established. While the fusion is growing together and strengthening, these movements should continue to be avoided to prevent stress at the fused segments: Excess lifting (anything over 10 to 15 pounds)

How much weight can you lift after spinal fusion? ›

After surgery, you should lift no more than:

Month 1: 8 pounds. Month 2: 16 Pounds. Month 4: 25 Pounds.

What activities can you not do after spinal fusion? ›

Lifting anything that weighs more than a gallon of milk—about 8 pounds—is not advised. No twisting. Even though many routine activities involve twisting the spine, doing so is to be avoided during this period. No driving.

How do I know if I damaged my spinal fusion? ›

Symptoms may include chronic pain in the back, neck, or legs, which can be dull or sharp, aching, burning, or radiating. The pain may continue after surgery or reappear several days or weeks afterward. It can worsen as scar tissue builds in the spinal nerve roots, which extend from the spinal cord.

References

Top Articles
Latest Posts
Article information

Author: Prof. An Powlowski

Last Updated:

Views: 5612

Rating: 4.3 / 5 (64 voted)

Reviews: 87% of readers found this page helpful

Author information

Name: Prof. An Powlowski

Birthday: 1992-09-29

Address: Apt. 994 8891 Orval Hill, Brittnyburgh, AZ 41023-0398

Phone: +26417467956738

Job: District Marketing Strategist

Hobby: Embroidery, Bodybuilding, Motor sports, Amateur radio, Wood carving, Whittling, Air sports

Introduction: My name is Prof. An Powlowski, I am a charming, helpful, attractive, good, graceful, thoughtful, vast person who loves writing and wants to share my knowledge and understanding with you.