Study Population
This investigation was a retrospective, 15-year observational cohort study from January 1990 until December 2005. Data were obtained for patients admitted to participating Pennsylvania Trauma Society hospitals as collected by the Pennsylvania Trauma Society Foundation (PTSF) trauma registry. The PTSF was established by the Pennsylvania Emergency Services Act of 1985 to accredit trauma centers in Pennsylvania and is currently composed of 26 designated Level I and Level II trauma centers. In addition to its accreditation mission, the PTSF also collects data from trauma centers to determine the demographics of trauma throughout the state and to provide a measure of quality and outcome.
All the data elements of the Major Trauma Outcomes Study of the American College of Surgeons Committee on Trauma are included in the registry [21]. Patients entered into the database include all trauma deaths, all intensive care unit admissions, all admissions with a length of stay greater than 72 h, all trauma patients transferred in or out of a participating institution and all patients dead on arrival. As part of their charter, trauma centers are mandated to report the requested data elements to the PTSF and their continued accreditation depends on compliance. Database fidelity is monitored by annual external audits of each participating site by the PTSF. In addition, most programs also perform routine internal audits. As of December 31, 2007, the sum total of all trauma patients submitted to the PTSF database since its inception in 1985 was 460,471.
For the above study period, we obtained the data records on all patients with a Glasgow Coma Score (GCS) of less than or equal to eight and evidence of a head injury. We then selected all patients that had undergone a tracheostomy at some point during their hospitalization. To make the study group more homogenous and because there were very few patients with isolated head injury in this cohort, we then chose to focus our analysis on those patients that had an associated injury to at least one other body system. This group was then divided into an Early Tracheostomy Group (ETG), defined as having a tracheostomy performed during hospital days one through seven, and a Late Tracheostomy Group (LTG), defined as having a tracheostomy performed greater than 7 days after admission.
Baseline demographics and presenting characteristics, including injury type and pre-existing conditions were recorded. Clinical status at presentation in the form of GCS and Injury Severity Score (ISS) was also documented. ISS is an anatomical scoring system that provides an overall score for patients with multiple injuries. Each injury is assigned an Abbreviated Injury Scale (AIS) score and is allocated to one of six body regions (Head, Face, Chest, Abdomen, Extremities (including Pelvis), and External). Only the highest AIS score in each body region is used. The three most severely injured body regions have their score squared and added together to produce the ISS score.
Outcome Measures
The following clinical variables collected by the PTSF, discharge status, number of ICU days, number of hospital days, functional status, and types of adverse events were recorded as outcome measures.
Functional status as acquired by the PTSF is based on a modification of the Functional Independence Measure (FIM) Score. The PTSF modification assesses five categories: feeding, locomotion, expression, transfer mobility, and social interaction. Each category is scored on a four-point scale, with a score of 4 meaning complete independence, 3 meaning independence with a device, 2 meaning modified dependence, and 1 meaning complete dependence. For the purposes of our analysis, the score was dichotomized, with a total score of 5 to 10 considered “dependent” and a score of greater than 10 considered “independent.”
We then analyzed the impact of tracheostomy timing (early vs. late) on discharge status (alive vs. dead), functional status at discharge (independent vs. dependent), number of ICU days, and total number of hospital days. In addition, we assessed the impact of tracheostomy timing on four classes of adverse events or “occurrences” as defined by the PTSF: pulmonary, cardiovascular, infectious, and neurological. Adverse pulmonary occurrences recorded in the PTSF database include adult respiratory distress syndrome (ARDS), acute respiratory failure, aspiration/aspiration pneumonia, atelectasis, pleural effusion, pneumonia, pneumothorax, and pulmonary embolus. Cardiovascular occurrences were listed as cardiopulmonary arrest, acute arterial occlusion, major arrhythmia, deep venous thrombosis, and myocardial infarction. Infectious occurrences included empyema, sepsis, septicemia, and acute sinusitis. Adverse neurological events included central nervous system infections, progression of original neurological insult, and seizures.
Finally, since our initial primary endpoints yielded mixed results, we created a composite five-point ranked ordinal scale based on a combination of discharge status, functional status, and hospital days, to arrive at a summary patient outcome measure, referred to as the Composite Outcome Score (COS). The scale parallels the Glasgow Outcome Scale (GOS), with a grade of 1 being the worst and a grade of 5 being the best (Table 1). Grade 5 patients were discharged alive and independent within 30 days of admission. Grade 4 patients were discharged alive and independent more than 30 days after admission. Grade 3 patients were discharged alive and dependent less than 30 days after admission. Grade 2 patients were discharged alive and dependent more than 30 days after admission. Grade 1 patients died during their acute hospitalization.
Table 1 Composite outcome scale
Statistical Analysis
The primary outcomes for the study were discharge status (alive vs. dead), functional status at discharge (independent vs. dependent), and ICU and hospital days dichotomized at their respective median values. The chi-square test was used to compare the timing of tracheostomy with dichotomous variables and the Mantel–Haenszel chi-square test was used to compare the timing of tracheostomy with ordinal variables. Comparisons with a P value < 0.20 from these chi-square tests were considered potential confounders, i.e., the distributions of timing of tracheostomy groups differed, to be controlled for in a multivariable analysis. These potential confounders were Injury Severity Score (ISS) (stratified as <15, 15–25, 26–40 and >40), age (dichotomized as 18–50 and >50 based on clinical grounds), pre-existing conditions (dichotomized as 0–1 pre-existing condition and >1 pre-existing condition), race (White, Black, other), sex, and injury type (blunt, penetrating, burn), as well as presence or absence of face, neck, thorax, abdominal, or spine injuries. Multiple logistic regression models were fit to assess the association of the timing of tracheostomy with each of the primary outcomes adjusting for the potential confounders, with results quantified using adjusted odds ratios (OR) and 95% confidence intervals (CI).