Objectives To determine (1) the proportion and number of clinically relevant alarms based on the type of monitoring device; (2) whether patient clinical severity, based on the sequential organ failure assessment (SOFA) score, affects the proportion of clinically relevant alarms and to suggest; (3) methods for reducing clinically irrelevant alarms in an intensive care unit (ICU).
Design A prospective, observational clinical study.
Setting A medical ICU at the University of Tokyo Hospital in Tokyo, Japan.
Participants All patients who were admitted directly to the ICU, aged ≥18 years, and not refused active treatment were registered between January and February 2012.
Methods The alarms, alarm settings, alarm messages, waveforms and video recordings were acquired in real time and saved continuously. All alarms were annotated with respect to technical and clinical validity.
Results 18 ICU patients were monitored. During 2697 patient-monitored hours, 11 591 alarms were annotated. Only 740 (6.4%) alarms were considered to be clinically relevant. The monitoring devices that triggered alarms the most often were the direct measurement of arterial pressure (33.5%), oxygen saturation (24.2%), and electrocardiogram (22.9%). The numbers of relevant alarms were 12.4% (direct measurement of arterial pressure), 2.4% (oxygen saturation) and 5.3% (electrocardiogram). Positive correlations were established between patient clinical severities and the proportion of relevant alarms. The total number of irrelevant alarms could be reduced by 21.4% by evaluating their technical relevance.
Conclusions We demonstrated that (1) the types of devices that alarm the most frequently were direct measurements of arterial pressure, oxygen saturation and ECG, and most of those alarms were not clinically relevant; (2) the proportion of clinically relevant alarms decreased as the patients’ status improved and (3) the irrelevance alarms can be considerably reduced by evaluating their technical relevance.
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Strengths and limitations of this study
We evaluated the technical and clinical relevance of each alarm by using 24 h video monitoring. This technique reduced bias introduced by bedside evaluations.
This study was limited by the small sample size (18 patients, total).
In an intensive care unit (ICU) setting, a large number of medical devices are attached to patients, generating numerous alarm signals every day. Several studies have demonstrated that most of these alarms are not clinically relevant1–,3 and tend to lower the attentiveness of the medical staff and, in turn, lower patient safety.4 ,5 In addition, alarm sounds are associated not only with patient delirium,6–,10 which increases mortality,11 but also with medical staff memory and judgement disturbances, decreased sensitivity and exhaustion.6 ,7 Many attempts have been made to reduce the number of clinically meaningless alarms by using statistical methods and artificial intelligence systems.5 ,12 Some examples include extending the time between the incident and the sounding of the alarm, shutting off alarms prior to performing procedures on patients, and calibrating machines to detect gradual changes in the patient condition. However, alarm devices having high sensitivity and specificity have not been developed because discrepancies remain between the priorities of equipment manufacturers, who are seeking devices with high sensitivity, and those of medical professionals, who desire machines with high specificity.
Previous studies have demonstrated that of the three types of alarms—threshold alarms, arrhythmia alarms and technical alarms—clinical relevance is the lowest for threshold alarms.13 However, the impact of patient clinical severity on the proportion of clinically relevant alarms remains unknown. Our objectives were (1) to determine if the number and proportion of clinically relevant alarms differ based on the type of monitoring device; (2) to determine whether patient clinical severity, based on the sequential organ failure assessment (SOFA) score, affects the proportion of clinically relevant alarms and (3) to suggest methods for reducing clinically irrelevant alarms. To answer these questions, we used video monitors to collect 24 h continuous data from ICU patients.
Materials and methods
Study setting and patient population
This study was conducted in a 6-bed, mixed ICU at the University of Tokyo Hospital, where patients are mainly admitted following ambulance transport. The study ICU is organised in an ‘I’ shape, with two individual patient rooms on the west side and two double patient rooms on the east side, with a central monitoring station. The doors to the patient rooms are left open unless procedures are being performed or privacy is required. The unit is staffed with one nurse for every two patients. Most patients monitored during the study had sepsis, respiratory failure, acute respiratory distress syndrome, multisystem organ failure, renal failure, heart failure or trauma.
The following inclusion criteria were used to enrol patients in the study: (1) admitted directly to the University of Tokyo Hospital mixed ICU, not stepped-down from other ICUs and (2) age ≥18 years. Patients were excluded if they were (1) already admitted to this ICU or (2) the patient refused active treatment. This study was approved by the Ethics Committee of the University of Tokyo Hospital, and all patients or their family provided signed informed consent before the beginning of the recordings.
General patient information, such as age, gender and disease, was recorded. All patients were continuously videotaped using a network of cameras (JVC-Kenwood, V.NET@Web, Tokyo, Japan), attached to the ceiling above each bed, to record patient and/or system manipulations. Each patient was monitored for heart rate, invasive or closely monitored non-invasive arterial blood pressure, respiratory rate, oxygen saturation (SpO2), end-tidal carbon dioxide (ETCO2) and temperature. In addition, any changes in the equipment used for each patient were recorded throughout the study period. In addition, the acute physiology and chronic health evaluation (APACHE II) score14 was calculated for each patient within 24 h of admission, and the SOFA score15 was calculated every 8 h. Patient data were pseudonymised and the electronic files and videos were stored in locked, encrypted hard drives.
Alarm systems and settings
During the study period, all patients were monitored with a standard cardiovascular monitoring system (BSM-9101 & CNS-9701, Nihon Koden, Tokyo, Japan). The numerical measurements, waveforms, alarms, alarm settings and alarm messages were acquired in real time and saved continuously (CNS-9600 & CAP-2100, Nihon Koden). The alarm information consisted of the parameter causing the alarm and the alarm message (table 1). The alarm messages were divided into three types: threshold alarms, arrhythmia alarms and technical alarms. The technical alarms indicated technical problems, such as a disconnected probe.
The initial alarm limits and every modification of these during the observation period were registered with corresponding time stamps and automatically recorded (CNS-9600 & CAP-2100, Nihon Koden). Chambrin et al1 determined the initial limits for heart rate and systolic arterial pressure by using the rule, ‘initial value observed during a stable period ±30%’. This rule was used in this study as well. When the prehospital patient heart rates and arterial pressures were not obtained, the initial limits were 156/56 mm Hg (120/80±30%) for systolic arterial pressure/diastolic pressure and 78 and 43 bpm (60±30%) for upper and lower heart rate limits, respectively. In addition, the SpO2 limit was 93%, except for patients with chronic obstructive pulmonary disease or acute respiratory distress syndrome, where the limit was 90%; a temperature limit of 38.3°C was also used. After these initial settings, the alarm limits could be modified; any changes were automatically recorded.
After completion of the data collection for a particular patient, two nurses and two intensivists, with at least 6 years’ experience in intensive care medicine, annotated the data. The two nurses first analysed the technical validity of the alarms, and divided the alarms into three categories, technically true, technically false and indeterminable. They referred to the multimonitoring wave shapes or pulse rate when the monitor described alarm messages, rather than using the video record. Alarms were classified as technically false, unnecessary alarms if the monitor referred to other waveforms or pulse rates at the same time.
The classifications were defined, in detail, according to the following criteria. For ECG, SpO2, direct measurements of arterial pressure and ETCO2, if the waveform was obviously an artefact produced by movements or procedures, the alarm was determined to be technically false. For waveforms in which the origin of the artefact(s) or arrhythmia(s) was uncertain, other waveforms or pulse rates (eg, a direct measurement of arterial pressure (ART) or SpO2) at the time of alarm generation were also referenced. Alarms that did not meet any of the above criteria were considered technically true. All technical evaluations that could not be determined from the relevant monitor's waveform recording were defined as indeterminable. For temperature alarms, all upper and lower limits of the temperature alarms were defined as technically true. Finally, for non-invasive blood pressure (NIBP) determinations, if an apparently abnormal value was obtained for the NIBP measurement, the patient's movements and concurrent procedures were also considered. Other values, for example, ART or SpO2 were also referenced as they may have triggered the upper and lower limit alarms. In such instances, these alarms were considered technically false.
After the technical analyses, the two physicians divided the alarms into three types. These types were relevant alarms, helpful alarms that were not relevant and irrelevant alarms; these were classified by referring to the video and medical records. In this study, an alarm was defined as relevant when an immediate clinical examination plus diagnostic or therapeutic decision (eg, ECG, echocardiography or drug administration) were necessary. When the situation required clinical examination but did not require a diagnostic or therapeutic decision, it was classified as a helpful alarm but not relevant. Intensivists determining the clinical relevance could see the result of technical validity.
All included patient characteristics were described using means and SDs for continuous variables, along with medians and ranges. After obtaining the descriptive statistics regarding the alarm counts and their proportions, the bivariate relationship of the alarms (the total number of alarms and the proportions of relevant alarms) to patient (SOFA) scores was examined by fitting cross-sectional, time-series models for panel data. Alarms from different monitoring devices were examined separately and together. In a preliminary analysis, the numbers and proportions of alarm types were regressed against SOFA scores by fitting either fixed-effects or random-effects models, using the Hausman test. The Hausman test indicated that the random-effects estimates were consistently more appropriate than the fixed-effects estimates.16 Therefore, the results obtained by the random-effects model were adopted. The interpretation of the statistical significance of relationships was made following multiple comparisons using the Bonferroni method.17 The NIBP data were not suited for univariate analysis because the amount of data and statistical power were inadequate.
The intraobserver and interobserver variabilities between the two physicians performing the clinical annotations of alarms, and the two nurses performing the technical annotations of the alarms were judged by a κ test.18 To evaluate the intraobserver variability, 300 alarm situations were reannotated by the same observer after a period of approximately 6 months. Statistical analyses were conducted using STATA Special Edition V.12.1 (StataCorp, College Station, Texas, USA).
Between January and February 2012, a total of 15 229 alarms were recorded for 20 patients. Two patients were excluded because of their poor clinical condition at the time of admission and of their families’ lack of expected benefit from invasive treatment. Therefore, a total of 11 591 alarms for 18 patients were included in this study, corresponding to 2697 person-monitored hours. The observation time for the cases averaged 150±113 h. Table 2 describes patient characteristics on admission. During their treatment in the ICU, 66.7% of the patients improved (SOFA scores decreased), while 22.2% deteriorated (SOFA scores increased). The ECG, SpO2 and NIBP devices were attached to all ICU patients throughout their time in the ICU.
The interobserver variabilities in the technical and clinical annotations, as estimated by the κ coefficient, were 0.98 and 0.68. Similarly, the intraobserver validities were 0.95 and 0.73. These values are within the range of substantial (0.61–0.80) or almost perfect (0.81–1.00) agreement.
In addition, false-negative situations were not recorded during the 2697 patient-monitored hours.
A total of 11 591 alarms were included in the analysis, classified as technically true (71%), technically false (21.4%) and indeterminable (7.7%) alarms (figure 1 and table 3). The overall contribution of each alarm type to the 11 591 alarms is shown in table 3. Only 6.4% of all alarms were relevant, whereas 32.8% were helpful alarms but not relevant, and 60.8% of all alarms were irrelevant. During an 8 h shift, on average, ICU nurses would hear a total of approximately 32 alarms, of which only two were relevant.
The monitoring devices that triggered alarms the most often were ART (33.5%), SpO2 (24.2%) and ECG (22.9%; figure 2). The numbers of relevant alarms were 12.4% (ART), 2.4% (SpO2) and 5.3% (ECG).
Effect of patient status on the alarms
The results of the cross-sectional time-series analysis are shown in table 4. ART demonstrated a positive correlation between the SOFA score and the proportion of relevant alarms, as well as between the SOFA score and the total number of alarms, and also between the SOFA score and the total number of relevant alarms. The SpO2 and ECG monitors demonstrated positive correlations only between the SOFA score and the proportion of relevant alarms.
All the devices demonstrated that the SOFA scores had statistically significant positive coefficients when regressed against the total number of relevant alarms (p<0.0001), as well as against the total number of alarms (p=0.0061) and the proportion of relevant alarms (p<0.0001). The results indicated that as the SOFA score decreased, the number of alarms, the number of relevant alarms and the proportion of relevant alarms decreased; the converse was also true.
The inclusion of a regression variable that indicated whether an event occurred during a day or night shift, in the time-series model, indicated that the time of the alarm did not demonstrate a statistically significant relationship with the SOFA score.
Relevant alarms comprised those that were technically true and those that were indeterminable, but did not include those that were technically false. Thus, the irrelevant alarms could be reduced by 21.4% by evaluating their technical relevance.
ICU patients are surrounded by medical devices that regularly sound alarms, but most of the alarms are not clinically relevant.1–,3 These irrelevant alarms cause a lower quality of patient care by distracting the medical staff4–,7 and contributing to patient delirium.9 ,10 Thus, attempts to reduce the number of clinically irrelevant alarms are important as solutions for this national problem are sought.19 The present study demonstrated that (1) the devices that alarm the most frequently are ART, SpO2 and ECG; (2) the proportion of relevant alarms decreases as patient status improves and (3) the irrelevant alarms can be reduced by combining the data for the waveforms or pulse rates of each device.
Prior to this study, Siebig et al13 were the first to record data with a 24 h video monitor, with the help of two physicians, to evaluate the clinical relevance of alarms. This technique reduced the possible bias introduced by bedside evaluations. The same method of evaluation was used in this study, with the added evaluation of alarm frequency for each device, and the determination of the fluctuations in alarm relevance and clinical severity for individual patients.
Alarm types and their relevance
The vast majority of alarms triggered in the ICU is either false alarms or are irrelevant for patient treatment. The present study shows that only 6.4% of all alarms triggered in the ICU were relevant. These data are similar to the results of multiple prior studies from various institutions, which indicated that approximately 10% of alarms are relevant.1–,3 ,20 The number of alarms that were technically annotated as being indeterminable was 7.7%. When the amplitude of waveforms was small or when the arrhythmia indications and noises were mixed, the technical annotations were difficult.
The ART alarms had a positive correlation between the SOFA score and the number and proportion of relevant alarms. In contrast, the SpO2 and ECG alarms only showed positive correlations between the SOFA score and the number of alarms. These findings indicate that the SpO2 and ECG alarms sound regardless of the clinical severity. Therefore, the SpO2 and ECG alarms are the primarily clinically irrelevant alarms, especially in patients with decreasing SOFA scores. However, this study revealed that the ECG and SpO2 devices were attached to all ICU patients, for safety reasons, from the time of their ICU admission. Therefore, establishing criteria for removing these devices would be difficult.
How can we reduce the noise in the ICU?
We demonstrated that clinically irrelevant alarms were reduced by 21.4% by evaluating their theoretical technical relevance. When evaluating technical relevance, two nurses combined the data for waveforms or pulse rates for each device. After annotation, their intraobserver and interobserver correlations demonstrated almost perfect agreement and the relevant alarms comprised those that were technically true and indeterminable, but not those that were technically false. Thus, manufacturers can decrease the number of technically false alarms by combining the data from each device. In particular, the ART monitor is often used in the ICU setting, and a reduction in the number of clinically irrelevant alarms might be possible by combining the ART waveform with the data from the SpO2 monitor and ECG.
The number of ART monitor alarms and the proportion of relevant alarms that were associated with the patient SOFA scores implied that there should be a criterion established to remove this device when the SOFA score has decreased to some appropriate level. We found that when the SOFA scores were ≤2, there were no relevant ART alarms. Thus, when the SOFA scores are ≤2 and the patient's condition is not likely to change suddenly, the ART device may be removed. As a general rule, if the sensitivity and specificity of a given test are constant, the positive predictive value (PPV) is assumed to increase as the (true) prevalence/incidence becomes higher. According to this rule, if alarms are being triggered constantly, then PPV is higher when the patient illness severity is higher. Thus, as the patient illness severity increases, the number of alarms increases, and these alarms include a large number of relevant alarms. In contrast, as the patient illness severity decreases, the number of alarms decreases, but these alarms include only a small number of relevant alarms. If the significance of medical treatment, measured by the alarms, is constant, the PPV would be more desirably held constant regardless of the patient's condition. Thus, when the patient illness severity is low, an increase in PPV is important, strictly according to the standards of sensitivity and specificity.
Why has this problem not resolved over the past decade?
The most serious problem encountered with these alarms was that although they provided PPVs (relevant alarms/all alarms), their sensitivity and specificity cannot be ascertained. These data cannot be ascertained because the evaluation of false negatives and true negatives are not possible in cases where the monitor does not alarm in clinical practice. Therefore, manufacturers need to produce alarmed devices that have higher sensitivities in order to avoid medical accidents. In this study, we did not detect false-negative situations. According to studies by Tsien3 and Siebig et al13 the sensitivity of the current alarms is close to 100%. However, their specificity, which is important for medical staff, could not be determined. Another reason for the failure to reduce the number of clinically irrelevant alarms is that physicians may be relatively insensitive to alarm problems because they do not stand by patient beds as often as nurses. Thus, physicians, nurses, researchers and medical companies need to establish an evidence-based practice model and find a mutually acceptable solution to this matter.
his study has several limitations. The first is that the sample size was small, with only 18 patients. The second limitation is that although a determination could be made regarding whether an alarm was technically true or false, a strict definition of the clinical annotations was more difficult. There are relevant alarms that require clinical examination, plus diagnostic or therapeutic decision, but this annotation may differ from a definition considered by intensivists. Finally, we did not analyse ventilator and infusion pump alarms, because detailed ventilator alarm messages were not recorded by our system; thus, annotation of their clinical relevance could not be performed. In addition, infusion pump alarms could not connect our system. These irrelevant alarms also need to be decreased,21 and should be the subject of a future study.
Excessive alarms in clinical settings are linked to lower medical attentiveness and poorer treatment environments. Manufacturers should work to decrease the number of technically false alarms by combining waveform data with the device measurement, especially for ART. Physicians should remove ART when patient conditions improve sufficiently and they are not likely to change suddenly.
The authors are deeply grateful to Yugo Tamura for collecting data, and would like to thank Yohei Hashimoto, Kikuo Furuta and Hiroko Hagiwara for their support. The authors would also like to thank all participating intensive care unit members at the University of Tokyo Hospital for their support.
Review history and Supplementary material
Contributors RI conceived of the study, RI and HS designed the analysis plan and performed the statistical analyses. RI wrote the first draft of the study, RI, YN, ME, AT, TI, TM, KD, MG, TH, KN, YK, SN and NY contributed to patient management. KS, MU, and NY critically reviewed the manuscript. All authors contributed to the design, interpretation of results and critical revision of the article for intellectually important content.
Funding This work was supported by a Grant-in-Aid for Young Scientists (C) (127100000424), and a Health Labour Sciences Research Grant.
Competing interests None.
Patient consent Obtained.
Provenance and peer review Not commissioned; externally peer reviewed.
Data sharing statement The technical appendix, statistical code and dataset are available from the corresponding author at Dryad repository; a permanent, citable and open access home for the dataset will be provided.
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