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A preliminary assessment of vital-signs-integrated patient-assisted intravenous opioid analgesia (VPIA) for postsurgical pain: a case series
Ban Leong SNG
KK Women's and Children's Hospital
Corresponding Author
ORCiD: https://orcid.org/0000-0001-5374-4271
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Background We developed a Vital-signs-integrated Patient-assisted Intravenous opioid Analgesia (VPIA) analgesic infusion pump, a closed-loop vital signs monitoring and drug delivery system which embodied in a novel algorithm that took into account patients’ vital signs (oxygen saturation, heart rate). The system aimed to allow responsive titration of personalized pain relief to optimize pain relief and reduce the risk of respiratory depression. Moreover, the system would be important to enable continuous monitoring of patients during delivery of opioid analgesia.
Methods Nineteen patients who underwent elective gynecological surgery with postoperative patient controlled analgesia (PCA) with morphine were recruited. The subjects were followed up from their admission to the recovery room/ ward for at least 24 hours until assessment of patient satisfaction on the VPIA analgesic infusion pump.
Results The primary outcome measure of incidence of oxygen desaturation showed all patients had at least one episode of oxygen desaturation (<95%) during the study period. Only 6 (31.6%) patients had oxygen desaturation that persisted for more than 5 minutes. The median percentage time during treatment that oxygen saturation fell below 95% was 1.9%. Fourteen (73.7%) out of 19 patients encountered safety pause, due to transient oxygen desaturation or bradycardia. The patients’ median [IQR] pain scores at rest and at movement after post-op 24 hours were 0.0 [2.0] and 3.0 [2.0], respectively. The average morphine consumption in the first 24 hours was 12.5 ± 7.1mg. All patients were satisfied with their experience with the VPIA analgesic infusion pump.
Conclusions The use of VPIA analgesic infusion pump, when integrated with continuous vital sign monitor and variable lockout algorithm, was able to provide pain relief with good patient satisfaction.
Keywords
infusion pump, postoperative pain, vital sign monitoring, oxygen desaturation
Figure 1
Figure 2
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Figure 4
More than 230 million major surgeries are performed annually in the world that could result in moderate to severe post-surgical pain [1]. Patient-controlled analgesia (PCA) with an opioid pump is often the commonly used technique, as it allows greater autonomy in managing pain, potentially leading to less analgesic consumption, greater pain relief efficacy and improved patient’s satisfaction [2-4]. However, 10% of patients who received PCA still experienced severe pain [5]. Inadequate postoperative pain management accounted for unwanted physiological and psychological effect such as increased postoperative morbidity, delayed recovery to normal daily living, and reduced patient satisfaction. Importantly, it led to persistent pain after surgery, increased the use of healthcare resources and healthcare costs [6].
Opioids adverse effects such as nausea, vomiting, sedation and respiratory depression may occur especially in high risk patients. The risk of opioid-induced respiratory depression was significantly increased in patients with advanced age, respiratory disease and obstructive sleep apnoea [7, 8], leading to the increased length of stay and overall costs [9]. Intermittent monitoring measures were highly labor intensive, yet not reliably recognized opioid-induced respiratory depression in the postoperative period [5]. According to Anaesthesia Patient Safety Foundation, patients having vital signs charted every 4 hours were usually left unmonitored >90% of the time. Since these patients were commonly administered with supplemental oxygen, this might eventually complicate the monitoring by masking hypoventilation, causing the signs of respiratory depression to be recognized only in its later stage [10].
Our overall aim was to develop a Vital-signs-integrated Patient-assisted Intravenous opioid Analgesia (VPIA) analgesic infusion pump with closed-loop vital signs monitoring and drug delivery system which embodied a novel algorithm that accounted for patients’ vital signs (oxygen saturation, heart rate). In this preliminary study, our primary aim was to investigate the incidence of oxygen desaturation (defined as oxygen saturation <95% in a patient for more than 60 seconds) in post-operative patients using our VPIA analgesic infusion pump. The side effects of opioid administration (nausea, vomiting and sedation), patients’ satisfaction and vital signs monitoring data were also evaluated.
This study was approved by the SingHealth Centralized Institutional Review Board, Singapore (SingHealth CIRB Ref: 2015/3062), and registered on Clinicaltrials.gov (NCT02804022). Written informed consent was obtained from every patient before any study procedure. The study period was between January 2017 and June 2017 and was conducted at KK Women’s and Children’s Hospital, Singapore
We recruited female patients aged 21 to 70 years old with American Society of Anesthesiologists (ASA) status I or II, undergoing elective surgery and intending to use postoperative PCA with morphine for postoperative analgesia. The exclusion criteria were patients with allergies to morphine, history of significant respiratory disease or obstructive sleep apnea, unwilling to wear oxygen saturation monitoring devices throughout the study duration, pregnancy and unable to comprehend the use of PCA. Recruitment was performed either in the pre-operative assessment clinic or on the same day of surgery if they had not attended pre-operative assessment clinic. An information brochure describing the use of VPIA analgesic infusion pump for post-operative analgesia, including potential side effects and complications was provided to patients.
Setting up of Infusion Pump
The algorithm and the VPIA analgesic infusion pump (“Intellifuse pump”; Model: Opiva) was designed by Innovfusion Pte Ltd, Singapore (Figure 1). Intravenous morphine used in the VPIA analgesic infusion pump was administered according to institutional guidelines: morphine diluted in normal saline to a concentration of 1 mg/ml, with bolus doses of 1 mg morphine delivered as per patient demand. In the VPIA analgesic infusion pump, vital signs monitoring (oxygen saturation, pulse rate) was programmed into the VPIA variable lockout algorithm, in which a temporary pause to the pump was triggered when vital signs safety threshold was breached; and subsequently the lockout interval was increased upon re-starting thereby improving the safety of intravenous morphine administration. That means when the vital signs were within normal range, the system was able to increase or decrease the lockout interval according to the analgesic needs of the patient. This lockout interval was a safety mechanism that limited the frequency of demands. By allowing an adequately long interval between each dose, patients were given sufficient time to achieve the opioid’s effects before the next dose. However, if the interval were prolonged, the effectiveness of patient controlled analgesia would be reduced.
The detailed VPIA variable lockout algorithm was illustrated in Figure 2. The bolus lockout interval was empirically set at 7 minutes, and was adjusted automatically according to the patient successful demands and the patient safety in the event of abnormal vital signs monitoring. The monitoring data was performed by taking average epochs of 15 seconds to summarize the vital signs. Missing vital signs were dropped from the analysis. However, if there was no available vital sign for the whole duration of each epoch, a safety pause would be triggered. The VPIA variable lockout algorithm reassessed for the recovery of the patient’s’ vital signs at the end of the safety lockout period. If the patient’s vital signs did not recover to safe levels, the pump automatically raised the on-board alarm. Conversely, if the patient’s vital signs recovered beyond the threshold limits by the end of the safety lockout period, the lockout interval would be prolonged. If at any time, there were critically abnormal vital sign parameters, the system would trigger the “emergency safety stop” function to cease the patient’s boluses. The system would be manually restarted by the clinician or the nurse after reviewing the patient.
All patients had established intravenous access before surgery. The patients were instructed on the use of the VPIA analgesic infusion pump prior to the study and educated to press the demand button whenever they needed pain relief. While in the recovery room after surgery, the VPIA analgesic infusion pump was secured with a 50 ml syringe filled with1 mg/ml morphine that was connected to the patient’s intravenous line for analgesia. The patient’s oxygen saturation and heart rate was continuously monitored by the VPIA analgesic system at least for 24 hours after surgery.
Data Collection
We collected and analyzed three sets of data: (1) patient demographic, surgical and anesthetic characteristics; (2) VPIA analgesic infusion pump data including opioid consumption, patient demands, successful demands, pattern of demands, oxygen saturation and heart rate; and (3) VPIA analgesic infusion pump user feedback survey that was conducted at the end of the study.
Following the initiation of VPIA analgesic infusion pump, attending nurses who were educated on the usage and side effects of morphine therapy would monitor the patient at regular intervals and document pain scores (0-10 numeric rating scale), blood pressure, heart rate, oxygen saturation and sedation score (0 for “awake, alert”, 1 for “occasionally drowsy, easy to rouse, responds to calling”, 2 for “occasionally drowsy, difficult to rouse, responds to shaking only”; 3 for “unresponsive and unarousable-- defined as no response to voice or physical stimulation”; D for “distressed -- defined as awake and in great pain”). Side effects such as nausea and vomiting were also recorded.
An independent observer would assess the patient during the period she was placed on the VPIA analgesic infusion pump. The patient’s overall satisfaction (numerical score between 0-100%) with the postoperative analgesia provided, the feedback on pain relief effectiveness and any side effect from the therapy were also gathered. Once the indications for PCA opioid for pain management were deemed unnecessary by the patient’s primary care team, the VPIA analgesic infusion pump was disconnected.
Sample size calculation and statistical analysis
The primary outcome measure of the study was the incidence of oxygen desaturation (defined as oxygen saturation < 95% in a patient for more than 60 seconds) in patients using the VPIA analgesic infusion pump. The secondary outcome measures were bradycardia, sedation, nausea/vomiting, pain scores, total consumption of morphine, patient’s satisfaction score. Patient’s oxygen saturation and heart rate were measured every minute for at least 24 hours. Assuming that a patient had < 3% oxygen desaturation, 0.005 width of interval and 95% confidence interval, we would require 18,000 oxygen saturation readings. Each patient would provide at least 1200 readings. Therefore, the study was adequately powered for 18 patients with 1200 readings (= 18 X 1200 ~ 21,600) for both primary and secondary aims.
Patient demographics, surgical and anesthetic characteristics were summarized as frequency with corresponding proportion, as mean ± standard deviation (SD) or median [range], whichever applicable. The incidence rate and 95% confidence intervals (CI) of binary outcomes (such as desaturation, bradycardia) were estimated based on the exact method by Wilson [11], which demonstrated to have good statistical properties even for small number of subjects and/or extreme probabilities [12, 13]. Significance level was set at 0.05 and all tests were two-tailed. SAS version 9.3 software (SAS Institute; Cary, North Carolina, USA) was used for the analysis.
Nineteen patients were recruited for this study over a 6-month period (January 2017 to June 2017), with their baseline and demographic characteristics shown in Table 1. The mean age of patients was 51.5 ± 8.8 years (range 36 - 66 years), the average body mass index (BMI) was 24.7 ± 4.4 kg/m2. All patients recruited went through scheduled open surgery, with the majority (n=15) under total abdominal hysterectomy and bilateral salpingo-oophorectomy (TAHBSO). The rest were open myomectomy (n=2) and salpingo-oophorectomy (n=2). Intraoperative morphine and fentanyl was administered with a meandosage of 8.7 ± 1.3 mg and 102.0 ± 35.3mcg respectively.
The patients were offered pain relief via VPIA analgesic infusion pump once they were transferred to the Post-Anesthesia Care Unit (PACU; Table 2). The average morphine consumption during the stay was 3.6 ± 3.0 mg, whereas the last pain score before sending to ward was 3 [0 - 6]. Minimal to moderate sedation was observed in 15 patients, whereas 4 other patients exhibited no sedation, having an median of overall sedation scoring of 1 [0 - 2]. Only one patient showed nausea or vomiting during this period.
At 12 hours post-surgery, the pain score at rest and movement in 19 patients was 2 [0 - 6] and 5 [0 -10], respectively (Table 2). At 24 hours post-surgery, patients had pain scores of 0 [0 - 7] and 3 [0 - 8] at rest and movement, respectively. The average morphine consumption in the first 24 hours was 12.5 ± 7.1 mg.
The primary outcome measure of incidence of oxygen desaturation (Figure 3) showed that all patients had at least one episode of oxygen saturation (SpO2) below 95% transiently during the study period. Only 13 (68.4%, 95%CI 46.0% - 84.6%) patients had oxygen desaturations that persisted for more than 60 seconds. However, only 8 (42.1%, 95%CI 23.1% - 63.7%) and 6 (31.6%, 95%CI 15.4% - 54.0%) patients had persisted oxygen desaturation for 3 and 5 minutes, respectively. The median total time spent and percentage of time that SpO2 fell below 95% was 35.3 minutes and 1.9%, respectively. During the 1st 4 hours post-surgery, the median time period and percentage of time that SpO2 fell below 95% was 2.08 minutes and 0.87%, respectively; whereas the median time period and percentage of time that SpO2 fell below 95% was 26.8 min and 1.4%, respectively after 4 hours until the removal of VPIA infusion pump.
All patients had at least one episode of heart rate (HR) <60/min with 3 (15.8%, 95%CI 5.5% - 37.6%) patients experiencing their HR < 60/min for longer than 60 seconds duration (Figure 4). The median time period and percentage of time that HR fell below 60/min was 1.2 minutes and 0.13%, respectively. Only 1 (5.3%, 95%CI 1.0% - 24.6%) patient had HR <60 for both 3 and 5 minutes. There was no clinically significant respiratory event of note.
Fourteen out of 19 (73.7%) patients encountered safety pause, whereas ten (52.6%) patients had experienced emergency safety stop during the study period. Median [range] number of safety pause was 5 [1 - 21]. Reasons for safety pause included either occurrence of oxygen desaturation or bradycardia. Eleven (57.9%) patients had safety pause due to SpO2 < 95% but all had HR > 60/min during the episode. Six (31.6%) patients had HR < 60/min but all had SpO2 > 95% during the episode. There were 2 (10.6%) patients experiencing oxygen desaturation <90% for more than one minute. Post-operative side effects included nausea / vomiting (6/19) and pruritus (1/19).
The median number of demands of bolus was 21 per patient. User feedback received on VPIA analgesic infusion pump showed that all patients agreed that the pump was safe and effective to use, although they remained neutral on the mobility of the pole where the pump was mounted onto (Table 3).
We presented a case series on a novel drug delivery system with a novel reactive clinical algorithm that integrated with continuous physiological monitoring. This system was able to provide appropriate response to any breach in continuous vital signs monitoring during post-operative pain management. VPIA analgesic infusion pump comprised in-built vital signs monitors and an adaptive algorithm that modulated the patient’s consumption of analgesic by varying the lockout time of patient’s bolus (and therefore the dose of analgesic). The results of the present study suggested that the use of VPIA analgesic infusion pump, when integrated with a VPIA variable lockout algorithm, was able to provide pain relief with good patient satisfaction in post-operative acute pain management. No significant adverse event was observed in this study.
Several studies have evaluated the incidence of oxygen desaturation after different types of analgesia, but few has analyzed the oxygen saturation continuously for 24-60 hours after surgery [14]. Our results showed that all patients had at least one episode of oxygen desaturation (SpO2 < 95%) transiently, whereas only 13 (68.4%) patients had persistent oxygen desaturations more than 60 seconds. Moreover, only 8 (42.1%) and 6 (31.6%) patients had persisted oxygen desaturation for 3 and 5 minutes, respectively. It was important to understand the percentage of time spent with oxygen desaturation. Motamed et al [15] demonstrated that the time spent with SpO2 <95% was about 65% and 40% during 1st and 2nd postoperative night, respectively. This was much higher than our results that showed the median time period and percentage of time that SpO2 fell below 95% was 35.3 minutes and 1.9%, respectively. The reason behind this might due to our novel VPIA analgesic infusion system that integrated with continuous vital sign monitor and variable lockout algorithm.
Respiratory depression was reported in up to 5% patients with the use of PCA opioids [5, 16]. A retrospective study on Chinese patients receiving PCA intravenous morphine showed that the incidence of respiratory depression (as defined by oxygen desaturation < 90% for longer than one minute) was 1.62% (20/1233). This study showed a higher incidence due to differences in definition of oxygen desaturation and continuous monitoring system, because conventional intermittent routine monitoring could under-diagnose the events of oxygen desaturation [17].
We used a closed-loop system with safety pause to lock out patient demands when vital signs safety threshold was breached. These vital signs safety thresholds could be adjusted by the healthcare provider for high risk populations (elderly patients with respiratory disease or morbidly obese). While optimizing the size of bolus dose appeared to provide good pain relief with minimal side effects, there were limited data available concerning the effects of various doses. Owen et al. examined the effects of different demand morphine bolus and found that the patients who were prescribed 0.5 mg demand dose were unable to achieve adequate analgesia, whereas a high incidence of respiratory depression was reported in those who received 2 mg. Hence, an optimal PCA bolus dose for morphine of 1 mg was proposed [18]. This study concentrated on varying the duration of the lockout interval as a safety mechanism. This safety of margin allowed an interval to be long enough for patient to receive the drug effect from the bolus dose before the next bolus was delivered. There was no recommended optimal lockout interval, hence this would need to be individualized to the patient’s pain relief and safety requirements [19]. We also gathered patient centric outcomes through patient’s feedback on device setup (patient handset, pole stand) and overall treatment experiences (interference with treatment, safety and effectiveness). The overall feedback was positive, but patients remained neutral on the reduced mobility of the pump due to vital signs monitor integration. Future design of a more portable setup would be desirable.
Hospital practice of intermittent vital signs monitoring with opioid delivery became an increasing concern. More than 75% of patients with moderate to severe sleep apnea are undiagnosed, and conventional risk stratification for heightened post-op monitoring could potentially miss patients at increased risk of respiratory depression [20]. This could result in increased length of stay, risk of hospital-acquired infections and increased costs [21]. Furthermore, the medical legal implications associated with respiratory depression are huge. Opioid related respiratory depression reportedly had payment to the plaintiff in 45% of claims, with a median payment of USD$216,750 [22].
Our results also showed that the morphine consumption was lower than other groups. Chou et al. found that 80 patients that underwent total abdominal hysterectomy and later given acute postoperative morphine analgesia (1-mg bolus of morphine solution with lockout time of 5 min and a maximum dosage of 15 mg within a 4-hour period in the absence of background infusion) had an average pain score (visual analogue scale VAS; at rest) of 3.75 and 2.8 at 6 hour and 24 hour post-operatively, scorings of 0.9 and 0.5 in nausea and sedation respectively, and a further 15% (12/80) in vomiting [23]. The same study also found an average morphine consumption of 40mg in 48 hours, which was higher than our present data. Another study on patients after total knee arthroplasty showed an approximate VAS pain score of 2 and 1.5 at 12 and 24 hours, respectively as well as an average morphine consumption of 27 mg in 48 hours, indicating the different opioid consumption and pain scores across various surgical procedures [24].
The limitations of the study would be the small sample size as this study was conducted in gynecological surgeries. Patients with different gender and surgical procedures would need to be investigated in future larger trials that may require different predefined critical values. More details on the episodes of oxygen desaturation, such as the when and where the events happen should be included in the future studies. The present system might have artifacts interfering with the algorithms and led to false alert to the users. Future study plans will also include refining new vital signs sensors, incorporating respirator rate monitoring and better integration with the delivery system to ensure better data capture.
In conclusion, this VPIA analgesic infusion pump system was able to detect and automatically respond to oxygen desaturation and bradycardia by instituting safety pause. This pilot study pump had positive user feedback. Future research and development would be needed to assess the cost-effective value of the system in providing safe and effective opioid delivery during postoperative pain management.
ASA: American Society of Anesthesiologists; BMI: Body mass index; CI: Confidence intervals; IQR: Interquartile range; PACU: Post-Anesthesia Care Unit; PCA: Patient controlled analgesia; SD: Standard deviation; SpO2: Oxygen saturation; TAHBSO: Total Abdominal Hysterectomy and Bilateral Salpingo-oophorectomy; VAS: Visual analogue scale; VPIA: Vital-signs-integrated Patient-assisted Intravenous opioid Analgesia.
Ethical approval and consent to participate
This study was approved by the SingHealth Centralized Institutional Review Board, Singapore (SingHealth CIRB Ref: 2015/3062), and registered on Clinicaltrials.gov (NCT02804022). Written informed consent was obtained from all participants prior to start of the study. This work was conducted in accordance with the Declaration of Helsinki.
Consent to publish
Not applicable.
Availability of data and materials
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
Competing interests
Ban Leong Sng is an associate editor of BMC Anesthesiology. Ban Leong Sng and Alex Sia Tiong Heng have filed a patent related to this work (SG 10201801161P, filed 12 Feb 2018, Singapore). Alex Sia Tiong Heng has intellectual property ownership and is the founding scientific director of Innovfusion Pte Ltd. All other authors reports no conflicts of interest in this work.
Funding
This work was supported by the funding from the National Health Innovation Centre Innovation to Develop (I2D) grant (Grant no. NHIC-I2D-1409017). The aforementioned sponsor had no involvement in the study activities.
Authors’ contributions
All authors (BLS, DJT, CWT, NLRH, RS, ATHS) contributed to the study design, data analysis and discussion, drafting and/or revising the manuscript. All authors approved the final version of the manuscript, and agree to be accountable for all aspects of this work.
Acknowledgments
We would like to thank Miss Agnes Teo (Senior Clinical Research Coordinator) and Miss Denise Anne (Clinical Research Coordinator) for their administrative support in this work. The design and layout of the algorithm was performed by Innovfusion Pte Ltd, Singapore.
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Table 1 Baseline and demographic characteristics of recruited subjects
|
Parameters |
No. of patients |
Mean (SD)/ Percentage |
|
Age; years |
19 |
51.5 (8.8) |
|
Race |
19 |
|
|
Chinese |
13 |
68.4% |
|
Indian |
3 |
15.8% |
|
Malay |
2 |
10.5% |
|
Others |
1 |
5.3% |
|
Weight; kg |
19 |
62.0 (9.9) |
|
BMI; kg/m2 |
19 |
24.7 (4.4) |
|
ASA Status |
19 |
|
|
I |
5 |
26.3% |
|
II |
14 |
73.7% |
|
Intraoperative morphine (mg) |
19 |
8.7 (1.3) |
|
Intraoperative fentanyl (mcg) |
19 |
102.0 (35.3) |
SD: Standard deviation.
Table 2 Pain characteristics during Post Anesthesia Care Unit (PACU) and ward stay
|
Parameters |
No. of patients |
Mean (SD) / Median [range] / Percentage |
|
During PACU stay |
19 |
|
|
Morphine (mg) |
19 |
3.6 (3.0) |
|
Last pain score before discharge (0-10) |
19 |
3[0-6] |
|
Last sedation score before discharge (0-3) |
19 |
1[0-2] |
|
Nausea/vomiting before discharge (0-3) |
19 |
0[0-1] |
|
During Ward stay |
|
|
|
12 hours Post-op |
19 |
|
|
Pain score (at rest) (0-10) |
19 |
2[0-6] |
|
Pain score (movement) (0-10) |
19 |
5[0-10] |
|
Sedation score (0-3) |
19 |
0[0-1] |
|
Nausea/vomiting (0-3) |
18 |
0[0-3] |
|
24 hours Post-op |
19 |
|
|
Pain score (at rest) (0-10) |
19 |
0[0-7] |
|
Pain score (movement) (0-10) |
19 |
3[0-8] |
|
Sedation score (0-3) |
19 |
0[0-1] |
|
Nausea/vomiting (0-3) |
19 |
0[0-1] |
|
Morphine consumption (24 hours; mg) |
19 |
12.5 (7.1) |
|
Side effect |
|
|
|
Nausea / vomiting |
6 |
31.6% |
|
Pruritus |
1 |
5.3% |
Table 3 Post-operative feedback (n=19) on the VPIA analgesic infusion pump
|
Parameters |
Values [range] |
|
Feedback (1-5; 1: Strongly disagree; 5: strongly agree) |
|
|
Patient handset button |
4 [4-5] |
|
Mobility of pole with mounted pump |
3[3-4] |
|
No interference of vital signs monitoring with treatment |
4[1-5] |
|
Pump safety |
4[3-5] |
|
Pump effectiveness |
4[3-5] |
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A preliminary assessment of vital-signs-integrated patient-assisted intravenous opioid analgesia (VPIA) for postsurgical pain: a case series
Ban Leong SNG
KK Women's and Children's Hospital
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ORCiD: https://orcid.org/0000-0001-5374-4271
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Background We developed a Vital-signs-integrated Patient-assisted Intravenous opioid Analgesia (VPIA) analgesic infusion pump, a closed-loop vital signs monitoring and drug delivery system which embodied in a novel algorithm that took into account patients’ vital signs (oxygen saturation, heart rate). The system aimed to allow responsive titration of personalized pain relief to optimize pain relief and reduce the risk of respiratory depression. Moreover, the system would be important to enable continuous monitoring of patients during delivery of opioid analgesia.
Methods Nineteen patients who underwent elective gynecological surgery with postoperative patient controlled analgesia (PCA) with morphine were recruited. The subjects were followed up from their admission to the recovery room/ ward for at least 24 hours until assessment of patient satisfaction on the VPIA analgesic infusion pump.
Results The primary outcome measure of incidence of oxygen desaturation showed all patients had at least one episode of oxygen desaturation (<95%) during the study period. Only 6 (31.6%) patients had oxygen desaturation that persisted for more than 5 minutes. The median percentage time during treatment that oxygen saturation fell below 95% was 1.9%. Fourteen (73.7%) out of 19 patients encountered safety pause, due to transient oxygen desaturation or bradycardia. The patients’ median [IQR] pain scores at rest and at movement after post-op 24 hours were 0.0 [2.0] and 3.0 [2.0], respectively. The average morphine consumption in the first 24 hours was 12.5 ± 7.1mg. All patients were satisfied with their experience with the VPIA analgesic infusion pump.
Conclusions The use of VPIA analgesic infusion pump, when integrated with continuous vital sign monitor and variable lockout algorithm, was able to provide pain relief with good patient satisfaction.
Figure 1
Figure 2
Figure 3
Figure 4
More than 230 million major surgeries are performed annually in the world that could result in moderate to severe post-surgical pain [1]. Patient-controlled analgesia (PCA) with an opioid pump is often the commonly used technique, as it allows greater autonomy in managing pain, potentially leading to less analgesic consumption, greater pain relief efficacy and improved patient’s satisfaction [2-4]. However, 10% of patients who received PCA still experienced severe pain [5]. Inadequate postoperative pain management accounted for unwanted physiological and psychological effect such as increased postoperative morbidity, delayed recovery to normal daily living, and reduced patient satisfaction. Importantly, it led to persistent pain after surgery, increased the use of healthcare resources and healthcare costs [6].
Opioids adverse effects such as nausea, vomiting, sedation and respiratory depression may occur especially in high risk patients. The risk of opioid-induced respiratory depression was significantly increased in patients with advanced age, respiratory disease and obstructive sleep apnoea [7, 8], leading to the increased length of stay and overall costs [9]. Intermittent monitoring measures were highly labor intensive, yet not reliably recognized opioid-induced respiratory depression in the postoperative period [5]. According to Anaesthesia Patient Safety Foundation, patients having vital signs charted every 4 hours were usually left unmonitored >90% of the time. Since these patients were commonly administered with supplemental oxygen, this might eventually complicate the monitoring by masking hypoventilation, causing the signs of respiratory depression to be recognized only in its later stage [10].
Our overall aim was to develop a Vital-signs-integrated Patient-assisted Intravenous opioid Analgesia (VPIA) analgesic infusion pump with closed-loop vital signs monitoring and drug delivery system which embodied a novel algorithm that accounted for patients’ vital signs (oxygen saturation, heart rate). In this preliminary study, our primary aim was to investigate the incidence of oxygen desaturation (defined as oxygen saturation <95% in a patient for more than 60 seconds) in post-operative patients using our VPIA analgesic infusion pump. The side effects of opioid administration (nausea, vomiting and sedation), patients’ satisfaction and vital signs monitoring data were also evaluated.
This study was approved by the SingHealth Centralized Institutional Review Board, Singapore (SingHealth CIRB Ref: 2015/3062), and registered on Clinicaltrials.gov (NCT02804022). Written informed consent was obtained from every patient before any study procedure. The study period was between January 2017 and June 2017 and was conducted at KK Women’s and Children’s Hospital, Singapore
We recruited female patients aged 21 to 70 years old with American Society of Anesthesiologists (ASA) status I or II, undergoing elective surgery and intending to use postoperative PCA with morphine for postoperative analgesia. The exclusion criteria were patients with allergies to morphine, history of significant respiratory disease or obstructive sleep apnea, unwilling to wear oxygen saturation monitoring devices throughout the study duration, pregnancy and unable to comprehend the use of PCA. Recruitment was performed either in the pre-operative assessment clinic or on the same day of surgery if they had not attended pre-operative assessment clinic. An information brochure describing the use of VPIA analgesic infusion pump for post-operative analgesia, including potential side effects and complications was provided to patients.
Setting up of Infusion Pump
The algorithm and the VPIA analgesic infusion pump (“Intellifuse pump”; Model: Opiva) was designed by Innovfusion Pte Ltd, Singapore (Figure 1). Intravenous morphine used in the VPIA analgesic infusion pump was administered according to institutional guidelines: morphine diluted in normal saline to a concentration of 1 mg/ml, with bolus doses of 1 mg morphine delivered as per patient demand. In the VPIA analgesic infusion pump, vital signs monitoring (oxygen saturation, pulse rate) was programmed into the VPIA variable lockout algorithm, in which a temporary pause to the pump was triggered when vital signs safety threshold was breached; and subsequently the lockout interval was increased upon re-starting thereby improving the safety of intravenous morphine administration. That means when the vital signs were within normal range, the system was able to increase or decrease the lockout interval according to the analgesic needs of the patient. This lockout interval was a safety mechanism that limited the frequency of demands. By allowing an adequately long interval between each dose, patients were given sufficient time to achieve the opioid’s effects before the next dose. However, if the interval were prolonged, the effectiveness of patient controlled analgesia would be reduced.
The detailed VPIA variable lockout algorithm was illustrated in Figure 2. The bolus lockout interval was empirically set at 7 minutes, and was adjusted automatically according to the patient successful demands and the patient safety in the event of abnormal vital signs monitoring. The monitoring data was performed by taking average epochs of 15 seconds to summarize the vital signs. Missing vital signs were dropped from the analysis. However, if there was no available vital sign for the whole duration of each epoch, a safety pause would be triggered. The VPIA variable lockout algorithm reassessed for the recovery of the patient’s’ vital signs at the end of the safety lockout period. If the patient’s vital signs did not recover to safe levels, the pump automatically raised the on-board alarm. Conversely, if the patient’s vital signs recovered beyond the threshold limits by the end of the safety lockout period, the lockout interval would be prolonged. If at any time, there were critically abnormal vital sign parameters, the system would trigger the “emergency safety stop” function to cease the patient’s boluses. The system would be manually restarted by the clinician or the nurse after reviewing the patient.
All patients had established intravenous access before surgery. The patients were instructed on the use of the VPIA analgesic infusion pump prior to the study and educated to press the demand button whenever they needed pain relief. While in the recovery room after surgery, the VPIA analgesic infusion pump was secured with a 50 ml syringe filled with1 mg/ml morphine that was connected to the patient’s intravenous line for analgesia. The patient’s oxygen saturation and heart rate was continuously monitored by the VPIA analgesic system at least for 24 hours after surgery.
Data Collection
We collected and analyzed three sets of data: (1) patient demographic, surgical and anesthetic characteristics; (2) VPIA analgesic infusion pump data including opioid consumption, patient demands, successful demands, pattern of demands, oxygen saturation and heart rate; and (3) VPIA analgesic infusion pump user feedback survey that was conducted at the end of the study.
Following the initiation of VPIA analgesic infusion pump, attending nurses who were educated on the usage and side effects of morphine therapy would monitor the patient at regular intervals and document pain scores (0-10 numeric rating scale), blood pressure, heart rate, oxygen saturation and sedation score (0 for “awake, alert”, 1 for “occasionally drowsy, easy to rouse, responds to calling”, 2 for “occasionally drowsy, difficult to rouse, responds to shaking only”; 3 for “unresponsive and unarousable-- defined as no response to voice or physical stimulation”; D for “distressed -- defined as awake and in great pain”). Side effects such as nausea and vomiting were also recorded.
An independent observer would assess the patient during the period she was placed on the VPIA analgesic infusion pump. The patient’s overall satisfaction (numerical score between 0-100%) with the postoperative analgesia provided, the feedback on pain relief effectiveness and any side effect from the therapy were also gathered. Once the indications for PCA opioid for pain management were deemed unnecessary by the patient’s primary care team, the VPIA analgesic infusion pump was disconnected.
Sample size calculation and statistical analysis
The primary outcome measure of the study was the incidence of oxygen desaturation (defined as oxygen saturation < 95% in a patient for more than 60 seconds) in patients using the VPIA analgesic infusion pump. The secondary outcome measures were bradycardia, sedation, nausea/vomiting, pain scores, total consumption of morphine, patient’s satisfaction score. Patient’s oxygen saturation and heart rate were measured every minute for at least 24 hours. Assuming that a patient had < 3% oxygen desaturation, 0.005 width of interval and 95% confidence interval, we would require 18,000 oxygen saturation readings. Each patient would provide at least 1200 readings. Therefore, the study was adequately powered for 18 patients with 1200 readings (= 18 X 1200 ~ 21,600) for both primary and secondary aims.
Patient demographics, surgical and anesthetic characteristics were summarized as frequency with corresponding proportion, as mean ± standard deviation (SD) or median [range], whichever applicable. The incidence rate and 95% confidence intervals (CI) of binary outcomes (such as desaturation, bradycardia) were estimated based on the exact method by Wilson [11], which demonstrated to have good statistical properties even for small number of subjects and/or extreme probabilities [12, 13]. Significance level was set at 0.05 and all tests were two-tailed. SAS version 9.3 software (SAS Institute; Cary, North Carolina, USA) was used for the analysis.
Nineteen patients were recruited for this study over a 6-month period (January 2017 to June 2017), with their baseline and demographic characteristics shown in Table 1. The mean age of patients was 51.5 ± 8.8 years (range 36 - 66 years), the average body mass index (BMI) was 24.7 ± 4.4 kg/m2. All patients recruited went through scheduled open surgery, with the majority (n=15) under total abdominal hysterectomy and bilateral salpingo-oophorectomy (TAHBSO). The rest were open myomectomy (n=2) and salpingo-oophorectomy (n=2). Intraoperative morphine and fentanyl was administered with a meandosage of 8.7 ± 1.3 mg and 102.0 ± 35.3mcg respectively.
The patients were offered pain relief via VPIA analgesic infusion pump once they were transferred to the Post-Anesthesia Care Unit (PACU; Table 2). The average morphine consumption during the stay was 3.6 ± 3.0 mg, whereas the last pain score before sending to ward was 3 [0 - 6]. Minimal to moderate sedation was observed in 15 patients, whereas 4 other patients exhibited no sedation, having an median of overall sedation scoring of 1 [0 - 2]. Only one patient showed nausea or vomiting during this period.
At 12 hours post-surgery, the pain score at rest and movement in 19 patients was 2 [0 - 6] and 5 [0 -10], respectively (Table 2). At 24 hours post-surgery, patients had pain scores of 0 [0 - 7] and 3 [0 - 8] at rest and movement, respectively. The average morphine consumption in the first 24 hours was 12.5 ± 7.1 mg.
The primary outcome measure of incidence of oxygen desaturation (Figure 3) showed that all patients had at least one episode of oxygen saturation (SpO2) below 95% transiently during the study period. Only 13 (68.4%, 95%CI 46.0% - 84.6%) patients had oxygen desaturations that persisted for more than 60 seconds. However, only 8 (42.1%, 95%CI 23.1% - 63.7%) and 6 (31.6%, 95%CI 15.4% - 54.0%) patients had persisted oxygen desaturation for 3 and 5 minutes, respectively. The median total time spent and percentage of time that SpO2 fell below 95% was 35.3 minutes and 1.9%, respectively. During the 1st 4 hours post-surgery, the median time period and percentage of time that SpO2 fell below 95% was 2.08 minutes and 0.87%, respectively; whereas the median time period and percentage of time that SpO2 fell below 95% was 26.8 min and 1.4%, respectively after 4 hours until the removal of VPIA infusion pump.
All patients had at least one episode of heart rate (HR) <60/min with 3 (15.8%, 95%CI 5.5% - 37.6%) patients experiencing their HR < 60/min for longer than 60 seconds duration (Figure 4). The median time period and percentage of time that HR fell below 60/min was 1.2 minutes and 0.13%, respectively. Only 1 (5.3%, 95%CI 1.0% - 24.6%) patient had HR <60 for both 3 and 5 minutes. There was no clinically significant respiratory event of note.
Fourteen out of 19 (73.7%) patients encountered safety pause, whereas ten (52.6%) patients had experienced emergency safety stop during the study period. Median [range] number of safety pause was 5 [1 - 21]. Reasons for safety pause included either occurrence of oxygen desaturation or bradycardia. Eleven (57.9%) patients had safety pause due to SpO2 < 95% but all had HR > 60/min during the episode. Six (31.6%) patients had HR < 60/min but all had SpO2 > 95% during the episode. There were 2 (10.6%) patients experiencing oxygen desaturation <90% for more than one minute. Post-operative side effects included nausea / vomiting (6/19) and pruritus (1/19).
The median number of demands of bolus was 21 per patient. User feedback received on VPIA analgesic infusion pump showed that all patients agreed that the pump was safe and effective to use, although they remained neutral on the mobility of the pole where the pump was mounted onto (Table 3).
We presented a case series on a novel drug delivery system with a novel reactive clinical algorithm that integrated with continuous physiological monitoring. This system was able to provide appropriate response to any breach in continuous vital signs monitoring during post-operative pain management. VPIA analgesic infusion pump comprised in-built vital signs monitors and an adaptive algorithm that modulated the patient’s consumption of analgesic by varying the lockout time of patient’s bolus (and therefore the dose of analgesic). The results of the present study suggested that the use of VPIA analgesic infusion pump, when integrated with a VPIA variable lockout algorithm, was able to provide pain relief with good patient satisfaction in post-operative acute pain management. No significant adverse event was observed in this study.
Several studies have evaluated the incidence of oxygen desaturation after different types of analgesia, but few has analyzed the oxygen saturation continuously for 24-60 hours after surgery [14]. Our results showed that all patients had at least one episode of oxygen desaturation (SpO2 < 95%) transiently, whereas only 13 (68.4%) patients had persistent oxygen desaturations more than 60 seconds. Moreover, only 8 (42.1%) and 6 (31.6%) patients had persisted oxygen desaturation for 3 and 5 minutes, respectively. It was important to understand the percentage of time spent with oxygen desaturation. Motamed et al [15] demonstrated that the time spent with SpO2 <95% was about 65% and 40% during 1st and 2nd postoperative night, respectively. This was much higher than our results that showed the median time period and percentage of time that SpO2 fell below 95% was 35.3 minutes and 1.9%, respectively. The reason behind this might due to our novel VPIA analgesic infusion system that integrated with continuous vital sign monitor and variable lockout algorithm.
Respiratory depression was reported in up to 5% patients with the use of PCA opioids [5, 16]. A retrospective study on Chinese patients receiving PCA intravenous morphine showed that the incidence of respiratory depression (as defined by oxygen desaturation < 90% for longer than one minute) was 1.62% (20/1233). This study showed a higher incidence due to differences in definition of oxygen desaturation and continuous monitoring system, because conventional intermittent routine monitoring could under-diagnose the events of oxygen desaturation [17].
We used a closed-loop system with safety pause to lock out patient demands when vital signs safety threshold was breached. These vital signs safety thresholds could be adjusted by the healthcare provider for high risk populations (elderly patients with respiratory disease or morbidly obese). While optimizing the size of bolus dose appeared to provide good pain relief with minimal side effects, there were limited data available concerning the effects of various doses. Owen et al. examined the effects of different demand morphine bolus and found that the patients who were prescribed 0.5 mg demand dose were unable to achieve adequate analgesia, whereas a high incidence of respiratory depression was reported in those who received 2 mg. Hence, an optimal PCA bolus dose for morphine of 1 mg was proposed [18]. This study concentrated on varying the duration of the lockout interval as a safety mechanism. This safety of margin allowed an interval to be long enough for patient to receive the drug effect from the bolus dose before the next bolus was delivered. There was no recommended optimal lockout interval, hence this would need to be individualized to the patient’s pain relief and safety requirements [19]. We also gathered patient centric outcomes through patient’s feedback on device setup (patient handset, pole stand) and overall treatment experiences (interference with treatment, safety and effectiveness). The overall feedback was positive, but patients remained neutral on the reduced mobility of the pump due to vital signs monitor integration. Future design of a more portable setup would be desirable.
Hospital practice of intermittent vital signs monitoring with opioid delivery became an increasing concern. More than 75% of patients with moderate to severe sleep apnea are undiagnosed, and conventional risk stratification for heightened post-op monitoring could potentially miss patients at increased risk of respiratory depression [20]. This could result in increased length of stay, risk of hospital-acquired infections and increased costs [21]. Furthermore, the medical legal implications associated with respiratory depression are huge. Opioid related respiratory depression reportedly had payment to the plaintiff in 45% of claims, with a median payment of USD$216,750 [22].
Our results also showed that the morphine consumption was lower than other groups. Chou et al. found that 80 patients that underwent total abdominal hysterectomy and later given acute postoperative morphine analgesia (1-mg bolus of morphine solution with lockout time of 5 min and a maximum dosage of 15 mg within a 4-hour period in the absence of background infusion) had an average pain score (visual analogue scale VAS; at rest) of 3.75 and 2.8 at 6 hour and 24 hour post-operatively, scorings of 0.9 and 0.5 in nausea and sedation respectively, and a further 15% (12/80) in vomiting [23]. The same study also found an average morphine consumption of 40mg in 48 hours, which was higher than our present data. Another study on patients after total knee arthroplasty showed an approximate VAS pain score of 2 and 1.5 at 12 and 24 hours, respectively as well as an average morphine consumption of 27 mg in 48 hours, indicating the different opioid consumption and pain scores across various surgical procedures [24].
The limitations of the study would be the small sample size as this study was conducted in gynecological surgeries. Patients with different gender and surgical procedures would need to be investigated in future larger trials that may require different predefined critical values. More details on the episodes of oxygen desaturation, such as the when and where the events happen should be included in the future studies. The present system might have artifacts interfering with the algorithms and led to false alert to the users. Future study plans will also include refining new vital signs sensors, incorporating respirator rate monitoring and better integration with the delivery system to ensure better data capture.
In conclusion, this VPIA analgesic infusion pump system was able to detect and automatically respond to oxygen desaturation and bradycardia by instituting safety pause. This pilot study pump had positive user feedback. Future research and development would be needed to assess the cost-effective value of the system in providing safe and effective opioid delivery during postoperative pain management.
ASA: American Society of Anesthesiologists; BMI: Body mass index; CI: Confidence intervals; IQR: Interquartile range; PACU: Post-Anesthesia Care Unit; PCA: Patient controlled analgesia; SD: Standard deviation; SpO2: Oxygen saturation; TAHBSO: Total Abdominal Hysterectomy and Bilateral Salpingo-oophorectomy; VAS: Visual analogue scale; VPIA: Vital-signs-integrated Patient-assisted Intravenous opioid Analgesia.
Ethical approval and consent to participate
This study was approved by the SingHealth Centralized Institutional Review Board, Singapore (SingHealth CIRB Ref: 2015/3062), and registered on Clinicaltrials.gov (NCT02804022). Written informed consent was obtained from all participants prior to start of the study. This work was conducted in accordance with the Declaration of Helsinki.
Consent to publish
Not applicable.
Availability of data and materials
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
Competing interests
Ban Leong Sng is an associate editor of BMC Anesthesiology. Ban Leong Sng and Alex Sia Tiong Heng have filed a patent related to this work (SG 10201801161P, filed 12 Feb 2018, Singapore). Alex Sia Tiong Heng has intellectual property ownership and is the founding scientific director of Innovfusion Pte Ltd. All other authors reports no conflicts of interest in this work.
Funding
This work was supported by the funding from the National Health Innovation Centre Innovation to Develop (I2D) grant (Grant no. NHIC-I2D-1409017). The aforementioned sponsor had no involvement in the study activities.
Authors’ contributions
All authors (BLS, DJT, CWT, NLRH, RS, ATHS) contributed to the study design, data analysis and discussion, drafting and/or revising the manuscript. All authors approved the final version of the manuscript, and agree to be accountable for all aspects of this work.
Acknowledgments
We would like to thank Miss Agnes Teo (Senior Clinical Research Coordinator) and Miss Denise Anne (Clinical Research Coordinator) for their administrative support in this work. The design and layout of the algorithm was performed by Innovfusion Pte Ltd, Singapore.
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Table 1 Baseline and demographic characteristics of recruited subjects
|
Parameters |
No. of patients |
Mean (SD)/ Percentage |
|
Age; years |
19 |
51.5 (8.8) |
|
Race |
19 |
|
|
Chinese |
13 |
68.4% |
|
Indian |
3 |
15.8% |
|
Malay |
2 |
10.5% |
|
Others |
1 |
5.3% |
|
Weight; kg |
19 |
62.0 (9.9) |
|
BMI; kg/m2 |
19 |
24.7 (4.4) |
|
ASA Status |
19 |
|
|
I |
5 |
26.3% |
|
II |
14 |
73.7% |
|
Intraoperative morphine (mg) |
19 |
8.7 (1.3) |
|
Intraoperative fentanyl (mcg) |
19 |
102.0 (35.3) |
SD: Standard deviation.
Table 2 Pain characteristics during Post Anesthesia Care Unit (PACU) and ward stay
|
Parameters |
No. of patients |
Mean (SD) / Median [range] / Percentage |
|
During PACU stay |
19 |
|
|
Morphine (mg) |
19 |
3.6 (3.0) |
|
Last pain score before discharge (0-10) |
19 |
3[0-6] |
|
Last sedation score before discharge (0-3) |
19 |
1[0-2] |
|
Nausea/vomiting before discharge (0-3) |
19 |
0[0-1] |
|
During Ward stay |
|
|
|
12 hours Post-op |
19 |
|
|
Pain score (at rest) (0-10) |
19 |
2[0-6] |
|
Pain score (movement) (0-10) |
19 |
5[0-10] |
|
Sedation score (0-3) |
19 |
0[0-1] |
|
Nausea/vomiting (0-3) |
18 |
0[0-3] |
|
24 hours Post-op |
19 |
|
|
Pain score (at rest) (0-10) |
19 |
0[0-7] |
|
Pain score (movement) (0-10) |
19 |
3[0-8] |
|
Sedation score (0-3) |
19 |
0[0-1] |
|
Nausea/vomiting (0-3) |
19 |
0[0-1] |
|
Morphine consumption (24 hours; mg) |
19 |
12.5 (7.1) |
|
Side effect |
|
|
|
Nausea / vomiting |
6 |
31.6% |
|
Pruritus |
1 |
5.3% |
Table 3 Post-operative feedback (n=19) on the VPIA analgesic infusion pump
|
Parameters |
Values [range] |
|
Feedback (1-5; 1: Strongly disagree; 5: strongly agree) |
|
|
Patient handset button |
4 [4-5] |
|
Mobility of pole with mounted pump |
3[3-4] |
|
No interference of vital signs monitoring with treatment |
4[1-5] |
|
Pump safety |
4[3-5] |
|
Pump effectiveness |
4[3-5] |