Summary
Background:
Perioperative aspiration is a rare but potentially devastating complication, occurring in 1–10 per 10 000 anesthetics based on studies of quality assurance databases. Quality assurance reporting is known to underestimate the incidence of adverse outcomes, but few large studies use supplementary data sources. This study aims to identify the incidence of and risk factors for perioperative aspiration in children using quality assurance data supplemented by administrative billing records, and to examine the utility of billing data as a supplementary data source.
Methods:
Aspiration events for children receiving anesthesia at a tertiary care pediatric hospital between 2008 and 2014 were identified using (i) a perioperative quality assurance database and (ii) hospital administrative billing records with International Classification of Diseases, Ninth Revision Clinical Modification coded diagnoses of aspiration. Records were subject to review by pediatric anesthesiologists. Following identification of all aspiration events, the incidence of perioperative aspiration was calculated and risk factors were assessed.
Results:
47 272 anesthetic cases were evaluated over 7 years. The quality assurance database identified 20 cases of perioperative aspiration occurring in surgical inpatients, same-day admissions, and outpatients. Using hospital administrative data (which excludes outpatients with shorter than a 24-hour stay), 9 cases of perioperative aspiration were identified of which 6 had not been found through quality assurance data. Overall, International Classification of Diseases, Ninth Revision coding demonstrated a positive predictive value of 94.5% for any aspiration event; however, positive predictive value was <4% for perioperative aspiration. A total incidence of 5.5 perioperative aspirations per 10 000 (95% CI: 3.7–8.0 per 10 000) anesthetics was found.
Conclusion:
Quality assurance data offer an efficient way to measure the incidence of rare events, but may underestimate perioperative complications. International Classification of Diseases, Ninth Revision codes for aspiration used as a secondary data source were nonspecific for perioperative aspiration, but when combined with record review yielded a 30% increase in identified cases of aspiration over quality assurance data alone. The use of administrative data therefore holds potential for supplementing quality assurance studies of rare complications.
Keywords: hospitals, intraoperative complications, pediatric, perioperative period, quality assurance, respiratory aspiration, respiratory aspiration of gastric contents
1 |. INTRODUCTION
Perioperative aspiration is currently viewed as a rare but potentially devastating complication, with reports from large, retrospective, quality assurance (QA) database studies showing an incidence of <1 to 4.7 in 10 000 anesthetic cases in adult and mixed age populations.1–5 A subgroup analysis of one of these studies found that children aged 0–9 years old experienced twice the risk of aspiration compared to other ages.2 Subsequent pediatric-specific studies have reported an incidence ranging from ~1 in 10 000 to as high as 10.2 in 10 000.6–12
Analysis of risk factors for aspiration in adults has found ASA status and emergency surgery to be significantly associated with higher incidence of aspiration.4 Studies in children alone as well as in mixed populations confirm with varying consistency these risk factors, and additionally suggest that risk for aspiration is increased in children of younger age and higher body weight.1,7,8,11,12 A recent study, based on the Pediatric Sedation Research Consortium’s database, did not identify lack of nil per os status as a risk factor for aspiration in the largest study to date of pediatric sedation cases.6 Though numerous sequelae have been described in the above pediatric studies, such as unplanned admission, prolonged intubation, sepsis, and other morbidity, there have been no mortalities described.
Published studies examining perioperative pulmonary aspiration in children rely nearly exclusively on data derived from large voluntary databases such as QA databases. While the use of QA databases can efficiently assess rare outcomes in large populations, these data are captured through voluntary reporting from the medical provider, and as a result have been found to underreport complications.13–16 The goals of this study were to (i) determine whether the use of multiple data sources including QA data can enhance the identification of aspiration events at a single tertiary medical center, and (ii) evaluate the incidence of and risk factors for perioperative aspiration in children at our center using multiple sources of aspiration reporting.
2 |. MATERIALS AND METHODS
Following IRB approval, perioperative pulmonary aspiration was identified using 2 independent data sources at Columbia University Medical Center (CUMC): the pediatric quality assurance (QA) database and hospital administrative billing records from January 2008 to December 2014. All patients aged 18 years or younger were included in this study.
2.1 |. Quality assurance database
Perioperative QA data have been recorded for all pediatric operating room and offsite procedures at CUMC beginning in 2008.17 All QA forms are completed by the anesthesia provider at the end of each procedure, with paper QA forms used from 2008 to 2009, and electronic QA reports from 2010 onwards. All QA reports record demographic data including age, height, and weight of the child, sex, American Society of Anesthesiology (ASA) physical status, emergency status, location of procedure (operating room or offsite), and other patient comorbidities. Details of the anesthetic technique, postoperative vital signs, and adverse events including episodes of perioperative pulmonary aspiration are also recorded.
2.2 |. Hospital administrative billing data
Hospital administrative billing data are generated based on information from the medical record, and typically includes patients requiring at least a 24-hour stay in the hospital. Upon discharge, data regarding the principal diagnosis and procedures as well as any additional diagnoses and procedures are extracted from the medical record by professional coders.18 For this study, the hospital administrative data were surveyed for all inpatient admissions in which children received an anesthetic according to anesthesiology departmental billing records from the time period 2008 to 2014. Hospital discharge billing records for all of these admissions were then requested from the hospital Clinical Data Warehouse, which house all hospital administrative data and electronic health records. Cases of aspiration were identified using International Classification of Diseases 9th Revision (ICD-9) codes 997.32 (postprocedural aspiration pneumonia) and 507.0 (pneumonitis due to inhalation of food or vomitus). A formal data collection form was completed to gather data on each ICD-9-coded aspiration.
2.3 |. Chart review of aspiration cases
Cases identified with either of the above ICD-9 codes for aspiration in the hospital discharge billing records were subject to an initial in-depth chart review by a pediatric anesthesiologist to capture any and all potential aspiration events. Aspiration events in the initial chart review were identified as any possible occurrence of pulmonary aspiration of gastric contents with documentation occurring within 7 days of the surgery and anesthesia. This broad review of records up to 1 week postoperatively was performed in order to reduce the risk that any perioperative aspiration events were missed due to delayed reporting. Perioperative aspiration was defined as any documentation of perioperative vomiting, gastric material in the airway, or physical exam or radiographic evidence of findings consistent with aspiration. The records reviewed for each case included the anesthetic record, postanesthesia care unit (PACU) notes, admission and discharge notes, daily progress notes, as well as radiology reports. In addition to identifying potential perioperative aspiration events, the chart review also determined whether a coded aspiration was (i) present on admission based on documentation of aspiration in the admission or emergency room notes, (ii) present prior to the procedure based on documentation of aspiration before the procedure was performed, (iii) occurring outside of the perioperative period defined as aspiration documented in records >7 days after the procedure, or (iv) no aspiration documented in any of the records in the chart.
Records that were identified with any possibility of perioperative aspiration on initial review were subsequently independently reviewed by 2 other pediatric anesthesiologists in order to determine if the event was a verified perioperative aspiration. Confirmation of an aspiration event required documentation of perioperative vomiting and either (i) the presence of gastric material during suctioning, laryngoscopy, or bronchoscopy, or (ii) if the tracheal/bronchial airways were not examined, physical exam or radiographic findings consistent with aspiration.11 Physical exam findings consistent with aspiration included desaturation and new-onset cough, wheeze, or crackles in the chest, while radiographic findings consistent with aspiration included new focal infiltrates, particularly of the right middle lobe.11
The aspiration was deemed perioperative if it occurred between the time at which the patient entered the operating room and 2 hours after completion of the procedure. Any discrepancies resulting from this secondary review were resolved with further review and discussion and required agreement between the 2 reviewers.
These verified perioperative aspiration events were then also assessed to determine patient comorbidities, initial airway management, and phase of detection of aspiration. They were also assessed for escalation of care including treatment with antibiotics,12 additional airway management such as unplanned intubation, unplanned hospital admission, and unplanned ICU admission. Lastly, the cases were evaluated for the presence of any long-term sequelae at discharge such as hypoxic brain injury, new neurologic deficits, complications related to prolonged intubation, or complications of infection/sepsis.
Cases identified as perioperative aspiration in the QA database were subject to detailed review of the electronic medical record to determine patient comorbidities, initial airway management, phase of detection of aspiration, escalation of care, and sequelae at discharge. The validity of the reports of aspiration events recorded in the QA database however were not subject to scrutiny from 2 additional reviewers like the billing data, as they were directly reported by the pediatric anesthesia team caring for the patient at the time of aspiration.
2.4 |. Statistical analysis
The incidence of aspiration was initially calculated using the QA data alone, and then re-calculated after including additional verified aspiration events as identified by the hospital administrative billing records. Confidence intervals for incidence were calculated using a Wilson’s score interval. Positive predictive value (PPV) was calculated for the 507.0 (pneumonitis due to inhalation of food or vomitus) ICD-9 code for recognizing (i) aspiration occurring at some point during the hospitalization (including aspiration as a reason for admission) as well as (ii) perioperative aspiration, according to the following formula: true positives/(true positives + false positives).
The records with aspiration as identified by either of the 2 data sources were then evaluated for risk factors using the demographic data from our QA database. Demographic and clinical variables including age, height, weight, sex, location (operating room or offsite), emergency status, and ASA classification were evaluated to determine the association with an aspiration event. Significant differences in any these variables between children with aspiration and without aspiration were evaluated using T tests for continuous variables and chi-square tests for categorical variables. Significance was set at an a priori P-value of .05. For each variable, children with missing values were excluded from analysis.
The data analysis for this paper was generated using SAS® software (Version 9.4 of the SAS System for Windows. Copyright © 2013 SAS Institute Inc.).
3.|. RESULTS
3.1 |. Incidence of aspiration: quality assurance data
A total of 47 272 pediatric anesthetic cases were recorded in our QA database between 2008 and 2014. An aspiration event was reported in 20 cases, yielding an overall incidence of 4.2 in 10 000 anesthetic cases (95% CI: 2.7–6.5 per 10 000 anesthetics) based on the QA data alone.
3.2 |. Hospital administrative data review
The hospital administrative discharge data for all patients undergoing a procedure over the same 7-year period were reviewed. A total of 254 hospital admissions records were identified containing 1 of the 2 ICD-9 codes consistent with aspiration: 997.32 (postprocedural aspiration pneumonia) and 507.0 (pneumonitis due to inhalation of food or vomitus). The code 997.32 was only identified in a single record, and the code 507.0 was found in the remaining 253 cases. Based on our record review, 94.5% (n = 240) of the hospital records contained evidence of an aspiration event documented in the medical record and 5.5% (n = 14) of records had no mention of any aspiration in the medical record.
Of the 240 records containing evidence of an aspiration event, 50% (n = 120) represented a condition present at the time of admission or as the primary reason for admission, while 41.2% (n = 99) involved aspiration events that occurred outside the perioperative period. The remaining 8.8% (n = 21) of records were identified as a possible aspiration event occurring within the perioperative period during initial review. Upon further detailed review, only 9 records (3.5%) were verified as involving likely perioperative aspirations. The remaining 12 records were deemed to be lacking sufficient evidence based on physical exam, radiographic, or bronchoscopic evidence or that it occurred during the immediate perioperative period and was unlikely to be related to the procedure or anesthetic care. Positive predictive value (PPV) for the ICD-9 code 507.0 for recognizing any aspiration during the hospitalization (including aspiration as a reason for admission) was 95%; however, the PPV for specifically recognizing perioperative aspiration using that code was 3.5%.
3.3 |. Incidence of aspiration: QA and administrative data
Of the 9 verified perioperative aspirations from the administrative data, 3 records had already been reported in the QA database, but there were 6 cases that had not been captured by the QA data. The 6 cases identified by the administrative data coupled with the 20 cases identified with the QA yielded a total of 26 cases of aspiration out of 47 272 anesthetics during this 7-year period, or an incidence of aspiration of 5.5 in 10 000 anesthetics (95% CI: 3.7–8.0 per 10 000 anesthetics). The addition of the hospital administrative data provided a 30% increase in cases of aspiration beyond what was captured by the QA data.
3.4 |. Comparison of children with and without perioperative aspiration
The characteristics of the patient records with and without documented aspiration during hospital admission are presented in Table 1. Children with aspiration were similar in age, height, weight, sex, location (operating room or offsite), emergency status, and ASA status compared with children with no reported aspiration.
TABLE 1.
Risk factors for perioperative pulmonary aspiration
No Aspiration (n = 47 246) | Aspiration (n = 26) | P-value | |
---|---|---|---|
Age (year)a | 6.87 ± 5.4 | 7.05 ± 4.6 | .8 |
Height (cm)a | 114.18 ± 43.6 | 115.33 ± 28.8 | .8 |
Weight (kg)a | 27.15 ± 22.1 | 28.99 ± 20.7 | .67 |
Sex | |||
Male | 27 081 (57%) | 14 (54%) | .7 |
Female | 20 144 (43%) | 12 (46%) | |
(Missing) | 21 (0.04%) | 0 (0%) | |
Location | |||
OR | 28 229 (60%) | 13 (50%) | .17 |
Offsite | 16 598 (35%) | 13 (50%) | |
Emergency status | |||
Emergent | 5668 (12%) | 1 (4%) | .18 |
Elective | 40 054 (85%) | 25 (96%) | |
(Missing) | 1524 (3%) | 0 (0%) | |
ASA status | |||
1 | 10 087 (21%) | 2 (8%) | .1 |
2 | 16 918 (36%) | 8 (31%) | |
3 or greater | 20 191 (43%) | 16 (62%) | |
(Missing) | 50 (0.1%) | 0 (0%) |
Location = Location where procedure performed; ASA Status = American Society of Anesthesiology Physical Status Classification.
The values are means ± SD.
3.5 |. Description of children with perioperative aspiration
The 26 children with reported perioperative aspiration are described in Table 2. Of these children, 46% (n = 12) had preexisting neurologic diseases including developmental delay or cerebral palsy and 23% (n = 6) had preexisting cardiac, pulmonary, or gastrointestinal disease. With regard to the timing for the occurrence of aspiration during the perioperative period, 92% (n = 24) could be determined based on the medical record, with a total of 88% (n = 23) of the cases occurring during the intraoperative period, and (4% [n = 1]) occurring in the postanesthesia care unit (PACU). Intraoperative aspiration occurred during induction of anesthesia in 9 children (35%), during maintenance in 10 (38%), and emergence of anesthesia in 4 children (15%), respectively. The distribution of airway management was endotracheal tube (ETT) in 50% (n = 13) of the cases, laryngeal mask airway in 15% (n = 4) of the cases, and general anesthesia without any airway devices in 35% (n = 9) of the cases.
TABLE 2.
Descriptive data for aspiration episodes
Data (n) | Age, year | Sex | ASA | Comorbidities | Procedure | Initial airway | Timing | Disposition |
---|---|---|---|---|---|---|---|---|
QA data (17) | 15.8 | F | 1 | None | Arthroscopic knee surgery | Natural airway | Unknown | Outpatient as planned |
3.8 | F | 3 | Asthma, heart surgery | Scoliosis surgery | ETT | Induction | ICU admit as planned | |
2.8 | F | 3 | Obstructive sleep apnea, heart transplant | Supraglottoplasty | Natural airwaya | Maintenance | ICU admit as plannedb | |
10.9 | F | 3 | Asthma, developmental delay, heart transplant | Cardiac catheterization | ETT | Induction | Floor admit as planned, antibiotic | |
3.2 | M | 2 | Hypotonia, developmental delay, failure to thrive | MRI | Laryngeal mask airwaya | Maintenance | Floor admit, unplanned | |
3.8 | F | 2 | Developmental delay, cerebral palsy | Tendon lengthening | ETT | Induction | Outpatient as planned | |
12.5 | M | 3 | Leukemia, gastroesophageal reflux | Bilateral orchiectomy | ETT | Emergence | Outpatient as planned | |
6.7 | M | 2 | Developmental delay | MRI | Natural airwaya | Maintenance | Outpatient as planned | |
10.6 | M | 3 | Myelomeningocele, contractures | Right lower extremity osteotomy | ETT | Induction | Floor admit as planned | |
1.8 | F | 3 | Wilm’s tumor | MRI | Laryngeal mask airwaya | Maintenance | Outpatient as planned | |
2.8 | M | 1 | None | Tonsil and adenoidectomy | ETT | Emergence | Floor admit as planned | |
0.2 | F | 3 | Hypoparastalsis (Berdon’s syndrome) | Jejunostomy revision | ETT | Induction | ICU admit as planned, antibiotic | |
3.2 | M | 3 | Brain tumor | MRI | Natural airwaya | Maintenance | Outpatient as planned | |
11.5 | F | 2 | Anxiety, gastroesophageal reflux disease | Upper Endoscopy | Natural airwaya | Induction | Outpatient as planned | |
3.2 | M | 3 | Leukemia, microcephaly | LP with chemo | Natural airway | Emergence | Outpatient as planned | |
7.5 | M | 2 | Developmental delay | Frenulotomy | ETT | Induction | Outpatient as planned | |
8.3 | M | 3 | Attention deficit disorder, anxiety, leukemia | LP, bone marrow biopsy | Laryngeal mask airwaya | Maintenance | Floor admit as planned | |
Both sources (3) | 7.8 | F | 3 | Prior heart surgery | Cardiac catheterization | ETT | Emergence | ICU admit as planned, antibiotic |
17.2 | M | 2 | Developmental delay, anxiety, prior heart surgery | Tendon lengthening | ETT | Maintenance | Floor admit as planned, antibiotic | |
8.2 | F | 3 | Prior small bowel and colonic transplant | Upper Endoscopy | Natural airwaya | Maintenance | Floor admit as planned, antibiotic | |
Billing data (6) | 13.2 | F | 3 | Leukemia with CNS involvement | LP, bone marrow biopsy | Natural airway | Maintenance | Floor admit as planned, antibiotic |
3.4 | F | 3 | Prior heart transplant | Cardiac catheterization | ETT | PACU | ICU admit, unplanned, antibioticb | |
3.2 | M | 3 | Developmental delay, gastrostomy tube | Gastrostomy tube exchange | ETT | Induction | Floor admit, unplanned, antibiotic | |
5 | M | 2 | Lymphoma | Central line removal | ETT | Induction | Floor admit, unplanned, antibiotic | |
10.8 | M | 2 | Asthma | Upper Endoscopy | Natural airway | Unknown | Floor admit as planned, antibiotic | |
5.4 | M | 3 | Leukemia | LP | Laryngeal mask airway | Maintenance | Floor admit as planned, antibiotic |
LP = Lumbar puncture; Unknown = Cases of aspiration in which the timing could not be determined by chart review.
Indicates patient required intraoperative airway management with an ETT following aspiration (extubation upon completion of procedure).
Indicates patient required postoperative airway management with an ETT following aspiration.
3.6 |. Outcomes in children with perioperative aspiration
Among the 26 cases of aspiration, 69% (n = 18) required an escalation of care. Treatment with antibiotics was initiated in 11 children (42%), who received at least 1 dose. Additional airway management was required, including unplanned intubation intra- and postoperatively, in 9 (35%) cases. Of the 12 patients who were scheduled as outpatients, 25% (n = 3) required unplanned hospital admission. Two patients remained intubated postoperatively. There was 1 case in which unplanned ICU admission was required following aspiration. At the time of hospital discharge, no associated mortality or long-term morbidity was identified following perioperative aspiration.
4 |. DISCUSSION
Anesthesia-related pulmonary aspiration was found to be a rare event at our pediatric tertiary care center. Our findings of an incidence of 5.5 aspirations in 10 000 cases is within the range of previously published studies and does not differ substantially from rates reported in adults, while employing a comparable sample size.1–12 However, the incidence of aspiration described in the present study is double that of the most recent large-scale QA-only audit of pediatric cases, completed in another pediatric tertiary care center in Singapore.8 While this discrepancy may be due in part to differences in anesthetic practice between institutions or risk between the 2 populations, underreporting in voluntary QA data likely also played a role. While other studies have reported the incidence and risk factors of perioperative pulmonary aspiration, the novelty of this study lies in the use of administrative data to supplement the QA data. To our knowledge, there are no pediatric studies of aspiration to date which employ secondary data sources to enhance capture of cases of aspiration, as well as no studies to assess the validity of ICD-9 coding of perioperative aspiration either in children or adults.19
The large-scale studies of perioperative aspiration to date have been performed in various populations. Three studies were performed in mixed cohorts of adults and children, 2 exclusively in adults, and 6 focused specifically on children. Of these 11 studies, 9 relied exclusively on voluntary reporting methods such as QA databases or surveys given to anesthesiologists to report complications. The most recent study surveyed providers over a focused 2-week study period from 261 centers in Europe, finding the risk of aspiration events to be within the range of previous reports.12
Two studies however did include some use of a secondary data source to enhance capture of aspiration events. The first, a study in adults, performed a text search of the hospital wide medical archive recording system for keywords “pulmonary aspiration” and “perioperative” or “postoperative”, ultimately identifying 1 additional case outside of their QA data for an 8% increase in yield.3 The second, a mixed study of adults and children, probed the county inpatient register in Stockholm, Sweden, for all cases of “aspiration pneumonitis” and identified 4 additional cases of aspiration beyond what could be identified using their QA data for a 5% increase in yield.2
The above-described alternative methods of detecting additional cases likely share some of the strengths and limitations of billing data. These studies indicate, however, that their added value for detecting perioperative aspirations over QA is quite small (5–8% increased yield). In our study, the use of hospital administrative billing data combined with chart review identified additional cases of perioperative aspiration resulting in a 30% increase in documented aspiration cases beyond what was recorded in the QA database alone. This demonstrates that a significant portion of aspiration events are likely to be missing from self-reported QA data, and that ICD-9 coded administrative data may be a more effective means for discovering missed cases than other secondary data sources. Furthermore, hospital administrative billing data is almost universally available and can likely be obtained in most hospitals in which QA data research is being performed.
While other ICD-9-coded adverse events have been evaluated, validation of the accuracy of ICD-9 codes for aspiration has not yet been performed.19,20 In our population of children who received anesthesia, the positive predictive value (PPV) of the 507.0 (pneumonitis due to inhalation of food or vomitus) ICD-9 code was high (95%) for recognizing aspiration at some point during the hospitalization (including patients with aspiration as a reason for admission). However, when used to identify perioperative aspiration in this cohort, the PPV of the code was low (3.5%). This is not entirely unexpected because that code is not specific to perioperative aspiration. The ICD-9 code specific to perioperative aspiration: 997.32 (postprocedural aspiration pneumonia) was recorded only once during the 7 years surveyed, and that child was ultimately deemed not to have had a verified perioperative aspiration. As a result, this specific code would not be useful in identifying perioperative aspiration.
Hospital administrative billing data typically includes patients who stay in the hospital for at least 24 hours. Thus, children undergoing outpatient procedures who aspirated but did not demonstrate symptoms requiring further inpatient observation were not recorded in our billing data. Billing data were also unable to detect 7 of the QA-reported inpatient perioperative aspirations, due likely in part to limited documentation of these events. One of these cases, for instance, had been documented only on the QA form and not in any subsequent patient notes. Therefore, aspirations discovered through billing data are more likely to represent events with sequelae recognized by the primary team. These severe complications are important to include in studies of adverse outcomes and some were found to be missed by our QA database.
While we were able to identify additional aspiration events using billing data, there are likely to still be unrecognized perioperative aspiration events. This can occur for a number of reasons including the lack of diagnosis while the patient was still in the hospital, the lack of adequate documentation by providers, or lack of recognition by the coder entering the ICD-9 code into the billing records. For example, though all children with the codes for pneumonitis due to the inhalation of food/vomitus and postprocedural aspiration pneumonia were reviewed, it is possible that aspirations could be misclassified as other conditions such as pneumonia or not coded at all.
While over 250 records needed to be reviewed to identify an additional 6 patients with aspiration, changes to hospital billing may improve the efficiency of this method as hospital billing begins to include variables indicating whether certain conditions were “present on admission” (POA).21 The capability to remove cases of aspiration based on POA status would reduce the record review by 50%, as demonstrated by findings at our institution. Hospital billing in the United States has also recently switched to ICD-10 codes on October 1, 2015.22 As medical billing and coding specialists gain experience in using ICD-10 codes, the accuracy of hospital billing data may also change. For example, ICD-10 has a code specifically for anesthesia-related aspiration: (J95.4: Chemical pneumonitis due to anesthesia).
In prior studies, several risk factors have been identified as being associated with perioperative pulmonary aspiration including higher ASA status, younger age, and emergent surgery.1,4,7,8,11 Such associations were not found in the present study. Since perioperative aspiration is an extremely rare event and may depend on the patient populations studied as well as the clinical practice at each institution, it is possible that risk factors may vary between centers, complicating the prediction of aspiration risk. For example, aspiration was noted in our study to occur with equal likelihood during induction as during maintenance, which is in contrast to prior findings regarding timing.1,8,12 In comparing our outcome with previously published findings from years ago, it should also be noted that practices and medications have changed substantially over the past several decades.
In patients with confirmed aspiration, escalation of care included treatment with antibiotics, unplanned intubation intra- or postoperatively, increased length of stay for outpatients, and ICU transfer. Treatment with antibiotics and/or unplanned intraoperative intubation was the most common care escalations, with 31% of patients having no documented escalation of care. None of the patients in whom aspiration occurred were noted to have any long-term sequelae or to have suffered mortality at discharge, and this is largely consistent with the published literature to date.23
While ICD-9 codes for aspiration cannot be used to independently identify perioperative aspiration events, by employing expert review in combination with these codes, we were able to significantly increase the number of aspiration events identified beyond those recorded in our departmental QA database. This finding underscores the fact that many adverse events are likely missed by voluntary reporting methods and that secondary data sources are effective in identifying additional events. Though large-scale QA databases are still valuable for studying rare perioperative outcomes when no other data source is available, it is important to recognize that adverse outcomes are likely to occur at a significantly higher rate than is reported by such studies.
What is already known
Perioperative aspiration is a rare but potentially devastating complication of anesthesia, with studies of rates and risk factors in children based exclusively on quality assurance databases.
Quality assurance databases and other voluntary-reported sources likely underestimate hospital complications.
Secondary data sources have been used with limited efficacy to improve upon voluntary reporting-based studies of aspiration; International Classification of Diseases, Ninth Revision Clinical Modification (ICD-9) coded administrative billing data have not been utilized.
What this article adds
The positive predictive value (PPV) of ICD-9 codes in administrative billing data to identify any cases of aspiration was 94.5% overall, but only 3.5% for aspiration specific to the perioperative period.
Upon expert review of the patients identified through administrative data, we found that quality assurance data underestimated the rate of perioperative aspiration at our institution by at least 30%.
ACKNOWLEDGMENTS
We acknowledge the Tripartite Request Assessment Committee (TRAC) of New York-Presbyterian Hospital and Columbia University Medical Center for their help in obtaining the hospital administrative billing records used in this study.
Funding information
Dr. Caleb Ing is supported by a Herbert Irving Scholars Award as well as the Agency for Healthcare Research and Quality (AHRQ) under award number K08HS022941. The content is solely the responsibility of the authors and does not necessarily represent the official views of the AHRQ.
Footnotes
ETHICAL APPROVAL
Ethics approval for the study was granted on July 21, 2017 by the Columbia University Human Research Protection Office, under protocol AAAD7712(M00Y10).
CONFLICT OF INTEREST
The authors report no conflict of interest.
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