Patient selection
This is a single center retrospective cohort study performed in the University Medical Center Utrecht (UMC Utrecht), an academic teaching hospital in the Netherlands, with around 20,000 ED visits per year. The study period ran from January 2017 until January 2020. The study population included all ED visits of adult patients for whom a standard panel of laboratory tests was ordered (pre-defined in our electronic health record as the “internal medicine lab”) through the order management module of the electronic health record. This standard panel comprises the following 14 tests: hemoglobin, thrombocyte count, leucocyte count, sodium, potassium, urea, creatinine, alkaline phosphatase, gamma glutamyltransferase, alanine transaminase, aspartate transaminase, lactate dehydrogenase, glucose, and C-reactive protein. Other tests can be added to this panel, for instance cardiac markers in patients with suspected myocardial infarction. Only visits in which these standard tests were ordered were included to prevent confounding by indication.
If the standard panel was ordered more than once during an ED visit, the first order was used for the analysis. Visits in which not all of the ordered tests of the standard panel were actually performed were excluded from the analysis. If patients visited the ED more than once in the study period all eligible visits were included in the study and were seen as individual events.
In the ED, the nurses are responsible for the venipuncture and the transportation of the samples to the laboratory by pneumatic tube.
Measures and outcomes
The primary outcome was the EDLOS, defined as the time from arrival in the ED to either discharge, admittance, transfer elsewhere, or death, in minutes.
The TTT was calculated as the time in minutes between the patient’s arriving in the ED and the ordering of laboratory tests. The TAT was calculated as the time in minutes between the time the laboratory tests were ordered at the ED and the time the last result of all tests in the standard panel was reported in the electronic health record.
Furthermore, the TAT was divided into a clinical stage (the time from the ordering of the laboratory tests to the arrival at the laboratory) and a laboratory stage (the time from the arrival of the sample at the laboratory to the results becoming available in the electronic health record). The different times are represented schematically in Fig. 1.
Additionally, data were collected on the date of the visit, the patient’s age and sex, the time of arrival at the ED (recorded as being between 8:00 and 16:59 (day time shift), between 17:00 and 00:59 (evening shift) or between 01:00 and 07:59 (night shift), the Emergency Severity Index level [23], which is used as the triage system in the ED, the number of out-of-range laboratory test results in the panel, the daily total number of ED visits, the destination after the ED visit (discharge home, admittance to hospital, transfer to another facility, or deceased) and the specialty treating the patient at the ED (grouped into medicine, surgery, and other specialties including psychiatry, rehabilitation medicine, pain management, and radiotherapy).
The time of day and the date were used to account for potential confounding due to variations in the laboratory workload and ED crowding both over time and at different times of the day. The Emergency Severity Index level, the specialty, the destination after the ED visit and the number of out-of-range tests were included as proxies for the acuity level, which was identified as a confounder in previous studies [11, 12].
Data acquisition
All determinants were collected by two of the authors through the Utrecht Patient Oriented Database (UPOD) and checked for quality by a third. UPOD is an infrastructure of relational databases that automatically retrieve data from the hospital information system on patient characteristics, hospital discharge diagnoses, medical procedures, medication orders and laboratory tests for all patients treated at the UMC Utrecht since 2004. UPOD data acquisition and management is in accordance with current regulations concerning privacy and ethics. The structure and content of UPOD have been described in more detail elsewhere [24]. All measures regarding ED arrival and discharge and the logistics of the laboratory tests are automatically time stamped in the hospital information system.
Statistical analysis
Baseline characteristics were reported. Means and standard deviations (SD) were calculated for normally distributed data, and medians and interquartile ranges (IQR) for non-normal data. Visits with data suspected to be incorrect (e.g. incorrect time stamps due to the change from daylight savings time) were excluded. In order to handle erratic outliers caused by administrative errors, the data set was trimmed to exclude the top and bottom 0.5% values for the EDLOS and the clinical and laboratory stages of the TAT.
The effect of the total TAT and TTT on the EDLOS was estimated by using linear regression, both in a univariate model as in a multivariate model, controlling for the other variables mentioned above.
The regression model gives estimates for the increase in EDLOS in minutes per 1 minute increases in TAT and TTT, as well as for changes in the other variables. A p-value of < 0.05 was considered significant. A sensitivity analysis was performed by performing the linear regression on the full dataset including the trimmed values. Furthermore, we calculated how much of the total TAT consisted of the clinical and laboratory stages. As a post hoc analysis, we compared the TAT for the different times of day, which was tested using the Kruskal-Wallis test. All analyses were performed in R version 4.0.3.