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ClinicoEconomics and Outcomes Research: CEOR logoLink to ClinicoEconomics and Outcomes Research: CEOR
. 2021 Apr 1;13:227–239. doi: 10.2147/CEOR.S304037

Factors and Economic Outcomes Associated with Documented Difficult Intubation in the United States

Marilyn A Moucharite 1,, Jianying Zhang 1, Robert Giffin 1
PMCID: PMC8021135  PMID: 33833535

Abstract

Purpose

Establishing good mechanical ventilation is a critical component and prerequisite to a wide range of surgical and medical interventions. Yet difficulties in intubating patients, and a variety of associated complications, are well documented. The economic burden resulting from difficult intubation (DI), however, is not well understood. The current study examines the economic burden of documented DI during inpatient surgical admissions and explores factors that are associated with DI.

Patients and Methods

Using data from the Premier Healthcare Database, adult patients with inpatient surgical admissions between January 1, 2016 and December 31, 2018 were selected. International Classification of Diseases, Tenth Edition, Clinical Modification (ICD-10-CM) diagnosis codes were used to classify the patients into matched cohorts of DI and non-DI patients.

Results

Patients in the DI group have mean inpatient costs and intensive care unit (ICU) costs that are substantially higher than patients without difficult intubations ($14,468 and $4,029 higher, respectively). Mean hospital length of stay and ICU length of stay were 3.8 days and 2.0 days longer, respectively (all p<0.0001, except ICU cost p=0.0001) in the DI group. Obesity, other chronic conditions, and larger hospital size were significantly associated with DI.

Conclusion

DI is associated with higher average cost and longer average length of stay.

Keywords: cost burden, difficult intubation, airway management, health economics

Plain Language Summary

In this study, we compared the difference in hospital cost and length of hospital stay between two groups of patients. Both groups of patients were admitted to the hospital because of the need for a surgical procedure. When an anesthesiologist inserts a tube into the airway to ventilate a patient before administering anesthesia, the anesthesiologist might encounter some patients for whom the tube is difficult to insert. Patients with this characteristic were designated to the “difficult intubation” (DI) group. Patients without this characteristic were designated to the “non-difficult intubation” (non-DI) group. We made sure these two groups of patients were comparable in terms of similar age, gender, and disease conditions, and stayed in similar types of hospitals and had similar procedures. We found that when we compared the DI group to the non-DI group, on average, the hospital cost was $14,468 more and length of hospital stay was 3.8 days longer for the DI group. This study highlights the significant cost burden associated with difficult intubation and suggests that further research to enhance clinicians’ ability to predict DI would be beneficial.

Introduction

During tracheal intubation, an anesthetist inserts a tube through the mouth or nose and down the trachea into the lungs. This is a common procedure for patients who undergo surgical procedures. Difficult intubation (DI), which increases the number of laryngoscopic attempts during tracheal intubation, has been associated with a variety of complications including oxygen desaturation, hypertension, dental damage, admission to the intensive care unit (ICU), and complications at extubation, as well as arrhythmias, bronchospasm, airway trauma, CICV (“can’t intubate, can’t ventilate”), and sequela of hypoxia (cardiac arrest, brain damage, and death).1

Many factors influence the success rate of intubation. Studies have shown that the first-pass success rate of intubation in the operating room ranges from only 63% to 85%.2 Up to 93% of difficult intubations are unanticipated.3 Patient risk factors, such as restrictions on neck movement, mouth opening, mallampati class4 and thyromental distance and neck extension are common factors.5 Many studies have tried to establish the best and most feasible method to predict difficult intubation, including Cormack-Lehane classification system6 and the Intubation Difficulty Scale (IDS).7 One study of experienced anesthesiologists, utilizing the widely used Cormack–Lehane classification system, found they did not score the same patients consistently over time, and that only 25% could correctly define all four grades of the Cormack–Lehane classification system.8 Under certain emergency circumstances (e.g., severe head trauma or suspected cervical spine injury), it may be impossible to fully utilize these various classification systems during physical examination to predict the difficulty of tracheal intubation.9

Before the advent of the ICD-10-CM coding system (International Classification of Diseases, Tenth Revision, Clinical Modification), there was no mechanism to quantify the cost burden of failed or difficult intubation from medical claims data. The implementation of ICD-10-CM introduced codes specific to DI, which enables researchers to identify cases with documented DI during surgical procedures. To our knowledge, there is no study currently available that examines the cost and healthcare utilization outcomes associated with difficult intubation in the hospital operating room setting. We utilized the ICD-10-CM coding system to classify patients into two groups, those with and without DI, to conduct a retrospective matched cohort study to fill this knowledge gap. This study will shed light from a hospital provider economic perspective on the consequence of DI in the inpatient hospital setting. The objective of this study was two-fold: First, to examine the healthcare utilization and cost associated with DI during an inpatient surgical procedure; and second, to explore the major patient characteristics and hospital characteristics of cases that were reported as DI.

Patients and Methods

Construction and Content

A retrospective observational cohort study was conducted using three years of data (2016–2018) from the Premier Healthcare Database® (Premier, Inc., Washington, D.C.).

Data Source

The Premier® Database contains data from more than 600 United States (US) hospitals and includes de-identified Universal Billing (UB-04) data for approximately 1 out of every 5 discharges in the U.S.10 It also includes information for each discharge describing patient demographics, hospital characteristics, payer information, Medicare Severity-Diagnosis Related Group (MS-DRG), ICD-10-CM primary and secondary diagnosis and procedure codes, admission and discharge calendar quarter and year, and detailed hospital department-level billing and cost data for each discharge. As an administrative database containing de-identified data, institutional review board or ethics committee approval was not required for this study. Cost data represent the actual total costs to treat the patient and include both fixed and variable costs.10 Approximately 60% of hospitals in the Premier database report costs. For the remaining hospitals, costs are calculated by Premier using charges reported to Premier and department-specific cost-to-charge ratios reported by hospitals to the Centers for Medicare & Medicaid Services.

Cohort Selection

All adult patients who underwent inpatient surgical procedures between January 1, 2016 and December 31, 2018 were included in the initial cohort selection. Patients with difficult intubation (DI group) were identified using three ICD-10 codes on the discharge record, which correspond to “failed or difficult intubation” on an initial encounter (T88.4XXA), subsequent encounter (T88.4XXD), or sequela (T88.4XXS). The following patients were excluded from the study: 1) Pregnant women; 2) Cases where general anesthesia was not indicated in the master charge file; 3) Patients with a primary procedure that indicates the Major Diagnostic Category (MDC) was a) not documented, b) “Unrelated Operating Room Procedures” or c) “Invalid or Ungroupable MS-DRG”; and 4) “Pre-MDC” which included all organ transplants or tracheotomies. These exclusion criteria applied to both the DI group and the non-DI group. In addition, the DI group excluded patients with diagnosis code indicating failed or difficult intubation (ICD-10 codes: T88.4XXA, T88.4XXD, T88.4XXS) was present on admission and the non-DI group excluded patients with primary procedures that were not present in the DI group.

Pregnant women were excluded from the study because the level of difficulty of intubation and procedure type likely differ for pregnant women compared to non-pregnant adults. Admissions with primary procedures not in the DI group were excluded because the risk adjustment process includes an exact match on primary procedure as well as a match on propensity score between the DI and non-DI groups to ensure that cost difference is based on comparison of cases with the same primary procedure. The reasons for implementing the remaining exclusion criteria were to make the cohort groups comparable by ensuring all patients in the study underwent general anesthesia during a surgical procedure, all cases were inpatient admissions, and all patients in the DI group experienced difficult intubation during rather than prior to the admission.

Multiple steps were applied to identify the comparison group, non-DI, and implement risk adjustment to confirm comparison of demographically and clinically similar patients. The risk adjustment process involved two steps:

  1. Exact match between DI and non-DI patients on primary surgical procedures: to qualify for the non-DI group, patients must have the same primary procedure, identified using the ICD-10-PCS (International Classification of Diseases, Tenth Revision, Procedure Coding System) code, as in the DI group (Supplementary Table 1).

  2. One to one DI vs non-DI propensity score matching within each primary procedure. The matching process between the DI and non-DI groups matched cases within each primary procedure based on propensity scores using a nearest neighbor matching method. The propensity score was calculated using a multivariable logistic regression model which included as predictor variables both patient characteristics (age group, gender, race, admission type (Urgent/Emergent or Elective), insurance type, comorbid conditions), and hospital characteristics (region of the country, teaching status, number of beds, urban/rural designation). The 12 comorbid conditions included in the propensity score model were obesity, cancer, congestive heart failure (CHF), chronic obstructive pulmonary disease (COPD), cardiovascular disease, diabetes, diabetes with sequela, hypertension, peripheral vascular disease, mild liver disease, moderate/severe liver disease, and paralysis. These 12 comorbid conditions were selected from the 17 comorbid conditions that make up the Charlson Comorbidity Index (CCI) using a “purposeful selection” process.

The “purposeful selection” process of determining which predictor variables to include in a logistic regression model was developed by researchers at the University of Arkansas for Medical Sciences the and University of Massachusetts, Amherst11 and implemented for this research using an automated SAS macro developed by Bursac et al.12 The “purposeful selection” process begins with a univariate analysis of the candidate predictive variables, in this case the 17 comorbid conditions. The initial model includes variables with p-values that fall below the pre-defined threshold for statistical significance (p < 0.25). An iterative process adds the variables that were not initially found to be statistically significant into the model one at a time to evaluate each variable for statistical significance in the new model, using a p-value threshold of p < 0.1, and confounding, which is defined as a 15% change in a parameter estimate in the new model compared to the original model. The variables that are statistically significant or determined to be confounders are retained in the new model. This iterative process results in a final variable selection that includes significant variables and important confounding variables.11 The threshold values recommended by the authors of the “purposeful selection” process11 were used to determine which variables to include–p < 0.25 for inclusion in the initial model, p < 0.1 to remain in the model after being added back in, and 15% change in a predictor variable.

Outcome Measures

Primary outcome measures were average cost of admission, hospital length of stay (LOS), post-operative Intensive Care Unit (ICU) admission rate, cost of ICU stay, and length of ICU stay. Post-operative ICU was defined as ICU admissions that occurred on the same day of surgery or within two days post-surgery. Costs for admissions in 2016 and 2017 were adjusted to 2018 dollars using the US Bureau of Labor Statistics Consumer Price Index for Medical Care.

Statistical Analysis

Descriptive univariate analysis was used to compare baseline patient demographics, clinical characteristics, and hospital characteristics between the DI and non-DI groups. Chi-squared test was used for categorical variables and the two sample t-test was used for continuous variables such as LOS or cost. A multivariable logistic regression model was used to calculate adjusted odds ratios (OR) to examine patient and hospital characteristics that are associated with documented DI. Variables modeled in the logistic regression included (1) patient characteristics: age group, gender, race, admission type (Urgent/Emergent or Elective), insurance type, comorbid conditions and (2) hospital characteristics: region, teaching status, number of beds, urban/rural designation. Statistical significance was defined as p-value <0.05. All statistical analyses were conducted using SAS® 9.4 for UNIX (SAS Institute Inc Cary, NC, USA).

This study did not directly involve human subjects. All patient data were de-identified and were compliant with the Health Insurance Portability and Accountability Act (HIPAA). Therefore, this study was exempt from Institutional Review Board (IRB) approval (45 CFR § 46.0001(b) (4)).

Results

Characteristics of the DI and Non-DI Groups Before Propensity Score Matching

A total of 2,233,751 cases met the eligibility criteria for the analysis. Of these, 609 cases were in the DI group and 2,233,142 cases were in the non-DI group. Patient and provider characteristics, and economic outcomes associated with each cohort, are described in Figure 1 and Table 1.

Figure 1.

Figure 1

Patient selection criteria for inclusion in the study.

Abbreviations: DI, difficult intubation; MDC, major diagnostic category; OR, operating room.

Table 1.

Patient and Hospital Demographic Characteristics and Logistic Regression Outputs Prior to Risk Adjustment Matching

Patient Characteristics Without Difficult Intubation With Difficult Intubation p-valuea Comparing Difficult Intubation to No Difficult Intubation
2,233,142 609
Number of Patients Percent of Patients Number of Patients Percent of Patients Odds Ratio 95% Confidence Limits p-valuea
Age Category
 < 65 years 1,166,440 52% 347 57% 0.019 N/A N/A
 ≥ 65 years 1,066,702 48% 262 43% 0.841 0.666 1.062 0.1454
Reference group=Age<65
Gender
 Male 1,009,182 45% 358 59% <0.0001 1.652 1.396 1.953 <0.0001
 Female 1,223,960 55% 251 41% N/A N/A N/A N/A
Reference group=Female
Race
 Black 226,988 10% 125 21% <0.0001 2.069 1.679 2.551 <0.0001
 White 1,775,839 80% 422 69% N/A N/A N/A N/A
 Other 192,258 9% 52 9% 1.062 0.792 1.424 0.6894
 Unspecified 38,057 2% 10 2% 1.01 0.538 1.895 0.9748
Reference group=White
Insurance Type
 Medicaid 213,795 10% 74 12% 0.004 1.103 0.808 1.505 0.538
 Managed Care 746,579 33% 183 30% 1.045 0.815 1.339 0.7294
 Uninsured 71,561 3% 32 5% 1.562 1.032 2.363 0.0349
 Other ins 90,998 4% 29 5% 1.162 0.775 1.742 0.4684
 Medicare 1,110,209 50% 291 48% N/A N/A N/A N/A
Reference group=Managed care
Admission Type
 Elective 1,361,309 61% 279 46% <0.0001 N/A N/A N/A N/A
 Urgent/Emergent 871,833 39% 330 54% 1.587 1.335 1.886 <0.0001
Reference group=Elective
Hospital Characteristics Hospital Characteristics
Hospital Region
 South 1,060,938 48% 303 50% 0.006 N/A N/A N/A N/A
 Northeast 280,004 13% 63 10% 0.862 0.647 1.147 0.3072
 Midwest 516,277 23% 117 19% 0.868 0.696 1.083 0.2089
 West 375,923 17% 126 21% 1.52 1.221 1.893 0.0002
Reference group=South
Teaching Hospital
 Teaching Hospital 1,039,632 47% 331 54% 0.0001 1.107 0.914 1.34 0.2981
 Non-Teaching Hospital 1,193,510 53% 278 46% N/A N/A N/A N/A
Reference group=Teaching Hospital
Bed Size
 500+ beds 777,012 35% 305 50% <0.0001 1.567 1.25 1.965 <0.0001
 300–500 671,676 30% 147 24% 0.94 0.746 1.185 0.6014
 <300 784,454 35% 157 26% N/A N/A N/A N/A
Reference group=<300
Urban vs Rural
 Urban 2,004,270 90% 558 92% 0.127 1.038 0.774 1.393 0.8038
 Rural 228,872 10% 51 8% N/A N/A N/A N/A
Reference group=Urban

Note: aChi-square test was used to calculate p-value.

Abbreviation: N/A, not applicable.

Prior to matching, patients in the DI group were more likely be male (59% vs. 45%, p<0.0001), black (21% vs. 10%, p<0.0001), less than 65 years old (57% vs. 52%, p=0.019) and have urgent or emergent admissions (54% vs. 39% p=<.0001) (Table 1). Notably, patients in the DI group were more likely to have comorbidities such as obesity (44% vs. 26%), cancer (14% vs. 9%), CHF (22% vs.12%), COPD (29% vs. 18%) and renal disease (20% vs.11%), compared to patients in the non-DI group. All p-values for these comorbidities were <0.0001 (Table 2). Compared to patients in the non-DI group, patients who were treated in a teaching hospital or a large hospital (500 beds or more) were more likely to be documented as DI patients, 54% vs. 47% (p=0.0001) and 50% vs. 35% (p<0.0001) respectively (Table 1).

Table 2.

Distribution of Comorbidities for Patients with and without Difficult Intubation Prior to Risk Adjustment Matching

Patient Comorbidities Number of Patients without Difficult Intubation Percent of Patients without Difficult Intubation Number of Patients with Difficult Intubation Percent of Patients with Difficult Intubation p-valuea Odds Ratiob Lower 95% Confidence Limits Upper 95% Confidence Limits p-valuea
Obesity 582,344 26% 265 44% <0.0001 2.202 1.857 2.612 <0.0001
Cancer 190,379 9% 86 14% <0.0001 1.886 1.458 2.44 <0.0001
Acquired Immune Deficiency Disease 2,484 0% 2 0% 0.108 1.654 0.41 6.67 0.4796
Congestive Heart Failure 265,728 12% 135 22% <0.0001 1.236 0.989 1.545 0.0621
Chronic Obstructive Pulmonary Disease 408,685 18% 176 29% <0.0001 1.553 1.295 1.861 <0.0001
Cardiovascular Disease 107,398 5% 55 9% <0.0001 1.419 1.054 1.911 0.0211
Diabetes 447,307 20% 177 29% <0.0001 1.146 0.954 1.378 0.145
Diabetes with Sequela 178,372 8% 107 18% <0.0001 1.432 1.109 1.849 0.006
Hypertension 1,389,328 62% 452 74% <0.0001 1.3 1.061 1.592 0.0114
Metastatic Solid Tumor 49,571 2% 24 4% 0.0039 1.123 0.712 1.772 0.6183
Myocardial Infarction 223,036 10% 94 15% <0.0001 0.988 0.777 1.255 0.9201
Peripheral Vascular Disease 173,699 8% 83 14% <0.0001 1.289 1.007 1.649 0.0439
Renal Disease 250,842 11% 120 20% <0.0001 1.048 0.815 1.348 0.7135
Mild Liver Disease 79,086 4% 38 6% 0.0003 1.157 0.811 1.651 0.422
Moderate/Severe Liver Disease 9,014 0% 10 2% <0.0001 2.344 1.193 4.606 0.0134
Paralysis 30,879 1% 20 3% <0.0001 1.435 0.896 2.298 0.1332
Dementia 61,454 3% 16 3% 0.8509 0.919 0.553 1.527 0.7431

Notes: aChi-square test was used to calculate p-value. bReference group for comorbidity odds ratio is patients without the comorbidity for each comorbid condition.

Patients in the DI group had significantly higher mean cost of hospital inpatient stay ($45,251 ± $43,613 vs. $22,056 ± $27,008); longer LOS (10.7 ± 12.1 days vs. 4.5 ± 5.8 days); higher post-operative ICU admission rate (60% vs. 16%); higher ICU costs ($11,657 ± $15,653 vs. $7,049 ± $9,386) and longer length of stay in the ICU (5.4 ± 5.8 days vs. 3.4 ± 3.9 days). All p-values were <0.0001 (Table 3).

Table 3.

Cost and Utilization Differences Between Patients with and without Difficult Intubation Before and After Risk Adjustment

Before Risk Adjustment
Difficult Intubation No Difficult Intubation
N Mean ICU Admission Rate 95% Lower CI 95% Upper CI STD N Mean ICU Admission Rate 95% Lower CI 95% Upper CI STD p-value Mean Difference
Admission Cost (US Dollars) 609 $45,251 $41,780 $48,722 $43,613 2,233,142 $22,056 $22,020 $22,091 $27,008 <0.0001 $23,196
Admission Length of Stay (Days) 609 10.7 60% 9.7 11.7 12.1 2,233,142 4.5 16% 4.5 4.5 5.8 <0.0001 6.2
ICU Cost (US Dollars) 367 $11,657 $10,051 $13,264 $15,653 358,359 $7,049 $7,018 $7,079 $9,386 <0.0001 $4,609
ICU Length of Stay (Days) 367 5.4 4.8 6.0 5.8 358,359 3.4 3.3 3.4 3.9 <0.0001 2.0
After Risk Adjustment
Difficult Intubation No Difficult Intubation
N Mean ICU Admission Rate 95% Lower CI 95% Upper CI STD N Mean ICU Admission Rate 95% Lower CI 95% Upper CI STD p-value Mean Difference
Admission Cost (US Dollars) 606 $45,233 $41,748 $48,717 $43,679 606 $30,765 $28,242 $33,288 $31,624 <0.0001 $14,468
Admission Length of Stay (Days) 606 10.7 60% 9.8 11.7 12.1 606 6.9 33% 6.3 7.5 7.7 <0.0001 3.8
ICU Cost (US Dollars) 364 $11,662 $10,043 $13,280 $15,702 198 $7,633 $6,393 $8,873 $8,849 0.0001 $4,029
ICU Length of Stay (Days) 364 5.4 4.8 6.0 5.8 198 3.4 2.9 4.0 3.8 <0.0001 2.0

Notes: ICU admission rate, cost (US dollars), and length of stay (days) are reported for patients who had an ICU admission 0–2 days after the primary surgery.

Abbreviations: CI, confidence interval; ICU, intensive care unit; N, number of patients; STD, standard deviation.

Results Based on Matched Cohorts of Patients

Propensity score matching reduced the number of patients in each cohort to 606 (Table 3). The matching process accounted for most differences in the distribution of demographic and hospital characteristics (Table 4) and comorbid conditions (Table 5). The difference between DI and non-DI matched cohorts for all outcome measures remained significant. Compared to the non-DI patient group, patients in the DI group had $14,468 higher mean cost of hospital inpatient stay ($45,233 ± $43,679 vs. $30,765 ± $31,624); 3.8 days longer LOS (10.7 ± 12.1 days vs. 6.9 ± 7.7 days); higher post-operative ICU admission rate (60% vs. 33%); $4029 higher ICU costs ($11,662 ± $15,702 vs. $7,633 ± $8,849); and 2.0 days longer length of stay in the ICU (5.4 ± 5.8 days vs. 3.4 ± 3.8 days). All p-values were <0.0001 (Table 3).

Table 4.

Demographic Characteristics of Patients with Difficult Intubation Hospital Inpatient Admissions for Patients After Risk Adjustment Matching

Patient Characteristics Without Difficult Intubation With Difficult Intubation p-valuea Comparing Difficult Intubation to No Difficult Intubation
606 606 95% Confidence Limits
Number of Patients Percent of Patients Number of Patients Percent of Patients Odds Ratio Lower Limit Upper Limit p-valuea
Age Category
 < 65 years 324 53% 346 57% 0.204 N/A N/A
 ≥ 65 years 282 47% 260 43% 0.948 0.676 1.331 0.7591
Reference group=Age<65
Gender
 Male 359 59% 356 59% 0.861 0.994 0.783 1.262 0.9595
 Female 247 41% 250 41% N/A N/A N/A N/A
Reference group=Female
Race
 Black 114 19% 125 21% 0.691 1.162 0.854 1.582 0.3384
 White 437 72% 420 69% N/A N/A N/A N/A
 Other 48 8% 51 8% 1.145 0.738 1.775 0.5456
 Unspecified 7 1% 10 2% 1.453 0.532 3.971 0.4661
Reference group=White
Insurance Type
 Medicaid 87 14% 74 12% 0.293 0.822 0.528 1.279 0.3856
 Managed Care 149 25% 182 30% 1.192 0.832 1.709 0.3392
 Uninsured 34 6% 32 5% 0.958 0.534 1.72 0.8863
 Other ins 29 5% 29 5% 1.036 0.578 1.855 0.9065
 Medicare 307 51% 289 48% N/A N/A N/A N/A
Reference group=Managed care
Admission Type
 Elective 272 45% 277 46% 0.773 N/A N/A N/A N/A
 Urgent/Emergent 334 55% 329 54% 0.951 0.743 1.217 0.688
Reference group=Elective
Hospital Characteristics
Hospital Region
 South 325 54% 301 50% 0.495 N/A N/A N/A N/A
 Northeast 59 10% 62 10% 1.178 0.771 1.802 0.4486
 Midwest 100 17% 117 19% 1.287 0.926 1.788 0.1338
 West 122 20% 126 21% 1.126 0.821 1.545 0.462
Reference group=South
Teaching Hospital
 Teaching Hospital 347 57% 330 54% 0.325 0.884 0.667 1.17 0.3869
 Non-Teaching Hospital 259 43% 276 46% N/A N/A N/A N/A
Reference group=Teaching
Bed Size
 500+ beds 319 53% 303 50% 0.638 1.027 0.735 1.435 0.8758
 300–500 141 23% 146 24% 0.99 0.705 1.39 0.9526
 <300 146 24% 157 26% N/A N/A N/A N/A
Reference group=<300
Urban vs Rural
 Urban 558 92% 555 92% 0.753 0.939 0.609 1.447 0.7753
 Rural 48 8% 51 8% N/A N/A N/A N/A
Reference group=Urban

Note: aChi-square test was used to calculate p-value.

Abbreviation: N/A, not applicable.

Table 5.

Patient and Hospital Demographic Characteristics and Logistic Regression Outputs After Risk Adjustment Matching

Patient Comorbidities Number of Patients without Difficult Intubation Percent of Patients without Difficult Intubation Number of Patients with Difficult Intubation Percent of Patients with Difficult Intubation p-valuea Odds Ratiob Lower 95% Confidence Limits Upper 95% Confidence Limits p-valuea
Obesity 217 36% 264 44% 0.0058 1.251 0.975 1.606 0.0781
Cancer 97 16% 86 14% 0.3775 0.96 0.665 1.386 0.8268
Acquired Immune Deficiency Disease - 0% 2 0% 0.157 N/A N/A N/A 0.9794
Congestive Heart Failure 119 20% 133 22% 0.3217 1.16 0.845 1.594 0.3579
Chronic Obstructive Pulmonary Disease 180 30% 175 29% 0.7523 0.948 0.73 1.232 0.6907
Cardiovascular Disease 59 10% 54 9% 0.6213 0.877 0.571 1.35 0.5518
Diabetes 147 24% 176 29% 0.0596 1.201 0.909 1.587 0.1979
Diabetes with Sequela 85 14% 106 17% 0.0978 1.242 0.843 1.828 0.2727
Hypertension 447 74% 450 74% 0.8442 0.947 0.707 1.268 0.7141
Metastatic Solid Tumor 32 5% 24 4% 0.2737 0.788 0.424 1.465 0.4517
Myocardial Infarction 85 14% 94 16% 0.4662 1.109 0.788 1.562 0.553
Peripheral Vascular Disease 92 15% 83 14% 0.462 0.87 0.614 1.232 0.4315
Renal Disease 116 19% 120 20% 0.7717 0.915 0.642 1.304 0.6234
Mild Liver Disease 35 6% 38 6% 0.7172 1.244 0.724 2.14 0.429
Moderate/Severe Liver Disease 16 3% 10 2% 0.2342 0.556 0.226 1.365 0.2003
Paralysis 19 3% 20 3% 0.8707 1.188 0.583 2.418 0.6358
Dementia 19 3% 16 3% 0.6068 0.918 0.449 1.878 0.8145

Notes: aChi-square test was used to calculate p-value. bReference group for comorbidity odds ratio is patients without the comorbidity for each comorbid condition.

Abbreviation: N/A, not applicable.

Factors Associated with Documented DI

Both patient characteristics and hospital characteristics were independently associated with the likelihood of documented DI. Compared to patients who were white, female, or having elective surgical procedure, the odds of being in the DI group were 2.1 times higher for black patients (OR: 2.1, 95% CI: 1.7–2.6; p<0.0001); 1.7 times higher for male patients (OR: 1.7, 95% CI: 1.4–2.0, p<0.0001); and 1.6 times higher for patients with urgent or emergent admission (OR: 1.6; 95% CI: 1.3–1.9, p<0.0001) (Table 1). Additionally, when evaluating the risk associated with specific chronic conditions, the risk was higher for patients with the chronic condition than for patients without the specific condition. The risk was 2.2 times higher for patients with obesity (OR: 2.2; 95% CI: 1.9–2.6; p<0.0001); 1.9 times higher for patients with cancer (OR: 1.9; 95% CI: 1.5–2.4; p<0.0001); 1.6 times higher for patients with COPD (OR: 1.6; 95% CI: 1.3–1.9; p<0.0001); and 1.4 times higher for patients with cardiovascular disease (OR: 1.4; 95% CI: 1.1–1.9; p=0.02) (Table 2). Hospital factors included hospital size and US Census Region. Compared to patients in hospitals with fewer than 300 beds, patients at hospitals with more than 500 beds were 1.6 times more likely to have documented DI cases (OR: 1.6, 95% CI: 1.3–2.0; p<0.0001) and patients at hospitals in the West region were 1.5 times more likely to have documented DI cases compared to hospitals in the South region (OR: 1.5, 95% CI: 1.2–1.9, p<0.0001) (Table 1).

Discussion

Airway management is fundamental to safe anesthetic practice. Difficult intubation, failed intubation, and wrongly placed tracheal tubes account for 2.3% of all anesthesia-related deaths.13 Problems with tracheal intubation were the most frequently recorded primary airway problem, which accounted for 39% of all events during anesthesia.9 To the best of our knowledge, this is the first study to use ICD-10-CM diagnosis codes to identify documented DI and explore factors associated with DI using Real World Data (RWD), and to examine the difference in healthcare utilization between DI and non-DI patient groups. This new information highlights the significant cost burden associated with DI. The variance in both cost and length of stay measures was high in the DI and non-DI groups, suggesting that while the average patient in the DI group experiences higher costs and length of stay compared to the average patient in the non-DI group, at the individual patient level, these differences may be more difficult to detect.

Our finding of obesity as a risk factor for DI is consistent with other studies which have indicated that patients with obesity were at increased risk of an adverse airway event.9,14–16 Reasons for this include mechanical difficulty in securing the airway, increased risk of aspiration, increased risk of airway obstruction during intubation, and accelerated speed and extent of oxygen desaturation during airway obstruction.17–19 The current study also suggests that patient gender, race, and other chronic conditions are associated with risk of DI. This is consistent with previous reports that increasing age, American Society of Anesthesiologists physical status, and CCI are associated with failed and difficult intubation.20,21 Importantly, many of the factors associated with DI in our study are linked to obesity, including diabetes, cardiovascular disease, cancer, and liver disease.22–25 Further prospective research is required to determine whether some of the chronic conditions are directly related to DI, or if they are confounding factors associated with a major predictor of DI, such as obesity. Other conditions, including the presence of head and neck cancer, arthritis, ankylosing spondylitis, and diabetes with limited joint mobility, which can alter the patient’s ability to lie flat are also associated with failed and difficult intubation, due to narrowing of the airway and challenges in positioning during intubation.26–28 In addition, large hospitals with >500 beds were more likely to have documented DI cases, which may reflect more consistent reporting standards often instituted at large hospitals. Although risk factors associated with DI have been identified, prediction of DI is a challenging task, and additional research to understand the predictors for DI would be beneficial, allowing clinicians to choose the appropriate method and device for patient airway management in challenging cases.16,29–31

Implications and Future Actions

DI may occur in any type of surgical procedure and it can be costly when it happens. Our research highlights a need for clinicians who perform tracheal intubations to carefully consider options that could improve the chances of successful intubation on the first attempt. The advances in new technology in tracheal intubation in a hospital setting may provide alternative options. For example, several studies demonstrated the benefits of video laryngoscopy, including a shorter time required for tracheal intubation, a higher rate of successful intubations, and a reduced need for external manipulation of the larynx or other maneuvers in the case of an expected DI.32–35 The benefits and costs associated with alternative technologies should be considered through future research.

The use of administrative data for retrospective analysis has both strengths and weaknesses. Due to the large number of hospitals, we have a good representation of hospitals in all regions of the United States, as well as good representation of patients with different types of insurance coverage. However, we expect the administrative data to suffer significant under-documentation of DI in the medical claims data. Only 0.03% of admissions in this study were found to have documented DI. Elsewhere, the reported incidence of DI has been estimated to be 1.5–8.5%, while failed intubation occurred in 0.13–0.3% of the general population.36 This discrepancy between expected and documented DI suggests that in our analysis, some admissions with DI may be assigned to the cohort assumed to have no DI. It is also possible that admissions that have documented DI have more serious complications resulting from DI than admissions that may have experienced undocumented DI. Therefore, the cost differential identified in the current study may be a conservative estimate overall, but not generalizable beyond cases of documented DI. Finally, our analysis did not include access to patient electronic medical records, limiting our ability to evaluate patient clinical characteristics to the data available in the administrative dataset.

Conclusion

In conclusion, the current study demonstrates the significant cost burden averaging $14,468 and increased post-operative LOS averaging 3.8 days for patients with documented difficult tracheal intubation.

Funding Statement

There is no funding to report.

Abbreviations

DI, difficult intubation; CFR, Code Of Federal Regulations; CHF, congestive heart failure; CI, confidence interval; CICV, can’t intubate can’t ventilate; COPD, chronic obstructive pulmonary disease; HIPAA, Health Insurance Portability and Accountability Act; ICD-10-CM, International Classification Of Diseases, Tenth Edition, Clinical Modification; ICU, intensive care unit; IRB, Institutional Review Board; LOS, length of stay; MDC, Major Diagnostic Category; MS-DRG, Medicare Severity-Diagnosis Related Group; RWD, real world data; US, United States.

Data Sharing Statement

The data that support the findings of this study are available from Premier Inc. but restrictions apply to the availability of these data, which were used under license for the current study, and so are not publicly available. Data may be available from the authors upon reasonable request and with permission of Premier Inc.

Ethics Approval and Informed Consent

This is a retrospective cohort study using medical billing/encounter data. No registry was used in current study. The data we used are de-identified and complied with Health Insurance Portability and Accountability Act (HIPAA) confidentiality requirements. Per US Title 45 CFR (Code of Federal Regulations) Part 46.101, institutional review board (IRB) approval for this study was not required under the exemption that this research involved the study of existing data and that the information was recorded in such a manner that the subjects could not be identified, directly or through identifiers linked to the subjects.

Author Contributions

All authors made substantial contributions to conception and design, acquisition of data, or analysis and interpretation of data; took part in drafting the article or revising it critically for important intellectual content; agreed to submit to the current journal; gave final approval of the version to be published; and agree to be accountable for all aspects of the work.

Disclosure

All 3 authors are paid employees of Medtronic. The authors report no other conflicts of interest in this work.

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