| Course | NR 361 RN Information Systems in Healthcare |
|---|---|
| Week | 3 |
| Paper type | Technology evaluation paper |
| Length | About 1,110 words, 6 pages |
| Format | APA 7 student paper |
| School | Chamberlain University |
| Program | RN-to-BSN |
| Updated | October 2026 |
Free sample paper for NR 361 Week 3
Continuous Pulse Oximetry Surveillance for Postoperative Patients on Opioids: A Technology Evaluation for a Surgical Ward
Student Name
College of Nursing, Chamberlain University
NR 361: RN Information Systems in Healthcare
Instructor Name
Month Day, Year
Continuous Pulse Oximetry Surveillance for Postoperative Patients on Opioids: A Technology Evaluation for a Surgical Ward
The Problem Before the Product
The problem this technology is meant to affect is a specific, measurable event: unrecognized respiratory depression in adults receiving opioids after surgery on a general ward, leading to a rescue event such as a rapid response call, naloxone, emergency intubation or transfer to intensive care. On a composite 30-bed orthopedic and general surgery ward, patients receive opioids by patient-controlled analgesia or as needed after joint replacement, spine surgery and abdominal procedures, and nurses check vital signs and sedation every four hours, less often overnight. The concern is the gap between checks. In an analysis of malpractice claims for postoperative opioid-induced respiratory depression, most events occurred within the first 24 hours after surgery, many during the night, and reviewers judged nearly all of them preventable with better monitoring and response (Lee et al., 2015).
The unit's own data are small but consistent with that pattern: over the past year, 7 rapid response calls on the ward were for oversedation or low oxygen saturation in postoperative patients receiving opioids, 5 of them between 2300 and 0600, and 2 patients were transferred to intensive care.
The Technology and Its Outputs
The technology evaluated is continuous pulse oximetry surveillance: a finger or ear sensor on each postoperative patient, connected wirelessly to a central system that monitors oxygen saturation and pulse rate continuously and sends an alert to the assigned nurse's phone when values cross set thresholds for a set length of time. What the technology produces is specific. It emits a continuous saturation and pulse value visible at a central station, a time-stamped alert to a named nurse's phone when saturation stays below the threshold, commonly 88 percent, for a delay period, and an escalation to the charge nurse if the first alert is not acknowledged within a set number of minutes. It does not produce a sedation score, a respiratory rate in most configurations or a measure of carbon dioxide. Those outputs matter more than the device's list of features, because the nurse receives outputs, not features.
Sorting the Evidence by What It Measured
The evidence on this technology measured different things, and sorting it by outcome keeps claims honest. The strongest outcome evidence comes from a before-and-after study on an orthopedic unit at an academic medical center, where continuous pulse oximetry surveillance with alerts to nurses' pagers was introduced; rescue events fell from 3.4 to 1.2 per 1,000 patient discharges and transfers to intensive care fell from 5.6 to 2.9 per 1,000 patient days, while comparison units without the system showed no change (Taenzer et al., 2010). That is a meaningful outcome, measured over time with comparison units, but it comes from one hospital, was not randomized and depended on careful alarm settings designed to limit nuisance alarms.
Other evidence addresses process rather than outcome. Professional guidance from pain management nursing recommends continuous monitoring of oxygenation, and of ventilation where possible, for patients at higher risk of opioid-induced respiratory depression, alongside regular sedation assessment by a nurse, and it stresses that monitoring technology supplements rather than replaces nursing assessment (Jungquist et al., 2020). The claims analysis contributes evidence about the problem, not the technology: it shows when and how the harm occurs (Lee et al., 2015). Satisfaction surveys and vendor case studies, which make up much of the remaining material, measure acceptance or marketing rather than patient outcomes and are not weighed here.
What the Technology Costs the Ward
The costs are specific. The first is alarms. Pulse oximetry generates false alarms from sensor displacement and patient movement, and a poorly configured system can add dozens of alerts per nurse per shift, which is exactly the kind of alarm burden that leads to ignored alarms. The system studied by Taenzer et al. (2010) used a low saturation threshold and a delay before alerting to limit this, and the ward would need to copy those settings rather than accept the manufacturer's defaults. The second cost is a blind spot: pulse oximetry detects falling oxygen, but in a patient receiving supplemental oxygen, saturation can stay normal while carbon dioxide rises, so a patient on oxygen could be sedated and hypoventilating without an alert. The third cost is attention: a green central screen can make continuous monitoring feel like continuous assessment, which it is not. The fourth is money for sensors, wireless infrastructure and the central system, which the ward cannot estimate without a vendor quote.
Fit With the Ward's Workflow
The technology fits the ward only if alerts reach a person who can act within minutes. On this ward, the night nurse has six patients and may be in a room with the door closed. Alerts to a phone she carries would reach her; alerts to a central station nobody watches overnight would not. The escalation to the charge nurse matters for the same reason. The ward would also need a rule about which patients are monitored, for example all postoperative patients on patient-controlled analgesia or with known sleep apnea for the first 24 hours, since monitoring every patient multiplies alarms without adding much protection for low-risk patients.
Nurses on the ward raised one more practical point during a staff meeting: patients get up to the bathroom at night, and a finger sensor that falls off generates an alert that looks the same as a real desaturation. The ward would need an agreed response, a quick look at the patient before anything else, and a way to pause monitoring for a few minutes while a patient is up, which most systems allow.
Verdict
The evidence supports adopting continuous pulse oximetry surveillance on this ward for higher-risk postoperative patients receiving opioids, with three conditions. Alarm thresholds and delays must be set to limit nuisance alarms, following the settings in the published study rather than defaults. Alerts must go to the assigned nurse's phone with escalation. And the ward must keep its sedation assessment practice unchanged, because the device cannot see sedation, and must use the lowest oxygen flow that keeps saturation acceptable so that the oximeter can still detect falling oxygen. The ward should measure the same outcome the published study measured, rescue events and intensive care transfers among postoperative opioid patients, for a year before and after adoption, alongside alerts per patient per day as a measure of the burden the technology adds.
References
Jungquist, C. R., Quinlan-Colwell, A., Vallerand, A., Carlisle, H. L., Cooney, M., Dempsey, S. J., Dunwoody, D., Maly, A., Meloche, K., Meyers, A., Sawyer, J., Singh, N., Sullivan, D., Watson, C., & Polomano, R. C. (2020). American Society for Pain Management Nursing guidelines on monitoring for opioid-induced advancing sedation and respiratory depression: Revisions. Pain Management Nursing, 21(1), 7-25. https://doi.org/10.1016/j.pmn.2019.06.007
Lee, L. A., Caplan, R. A., Stephens, L. S., Posner, K. L., Terman, G. W., Voepel-Lewis, T., & Domino, K. B. (2015). Postoperative opioid-induced respiratory depression: A closed claims analysis. Anesthesiology, 122(3), 659-665. https://doi.org/10.1097/ALN.0000000000000564
Taenzer, A. H., Pyke, J. B., McGrath, S. P., & Blike, G. T. (2010). Impact of pulse oximetry surveillance on rescue events and intensive care unit transfers: A before-and-after concurrence study. Anesthesiology, 112(2), 282-287. https://doi.org/10.1097/ALN.0b013e3181ca7a9b
The Chamberlain NR 361 Week 3 instructions
The Week 3 evaluation asks you to assess a health information technology for a specific practice setting. You will likely need the clinical problem, a description of the technology, the evidence on its effectiveness, costs and burdens, fit with workflow and a recommendation, in APA. State the problem as a measurable event before naming the product. Describe what the tool actually sends and to whom, not its brochure features. Sort the evidence by what each source measured, and let only outcome studies support outcome claims. Name the costs specifically, including alarms. Check the fit with your unit's staffing at night. Make the verdict conditional where the evidence requires it.
How this NR 361 Week 3 example is built
The problem section uses Lee and colleagues to show that respiratory depression after surgery is often preceded by sedation and reports seven local rapid response calls over a year. The technology section describes a sensor on each patient, wireless links and alerts to the nurse's phone, and notes what the system does not detect, such as sedation. The evidence section sorts sources: Taenzer and colleagues' orthopedic unit study, with rescue events falling from 3.4 to 1.2 per 1,000 discharges, as outcome evidence, and the pain nursing guideline as process advice. The costs section covers false alarms and oxygen flow that masks falling saturation. The workflow section considers a night nurse with six patients. The verdict sets three conditions.
Where the points sit in the NR 361 Week 3 rubric
Technology evaluation rubrics for this course typically score the problem statement, the description of the technology, the strength and use of evidence, analysis of costs and workflow, the recommendation and APA. Use of evidence decides the most, and the paper earns it by sorting sources by what they measured so outcome claims rest only on outcome data. The problem row is credited for national and local figures. Description scores because the outputs and their recipients are named, including what the device cannot see. The costs and workflow rows are met through alarm burden, oxygen flow and the night staffing check. The verdict earns points for conditions that each answer a cost found earlier, and for naming the outcome to measure.
Common NR 361 Week 3 mistakes, and how to avoid them
The dominant loss on this paper is a capability inventory, a page of what the technology can do with no study, setting or user. A second is mixing evidence types, so a professional recommendation is presented as proof of fewer deaths. Students also skip the costs, or name them only as "alarm fatigue" without saying how the system would be set to limit it. Recommendations without conditions read as sales copy. Evaluating a tool your hospital already uses is fine, and recent sources are preferred but landmark studies still count. A comparison with a second product is not usually required. If you have a technology in mind for your unit, describe the problem and an NR 361 evaluation can be built from the problem forward.
Get a NR 361 Week 3 example written to your instructions
Send the Week 3 instructions and the technology you have been assigned or want to pick, and a custom example is written to your section's required headings and returned inside 24 to 48 hours. The first is free. Tell us the unit you work on and the evidence gets weighed against that setting rather than a generic one.
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NR 361 Week 3 questions, answered
Can I evaluate a tool my hospital already uses?
Usually yes and it produces a sharper paper, because you can describe the outputs you have seen rather than the ones a manual promises. Keep the facility unidentifiable and leave out anything internal your employer would not publish. Your own observations remain yours to include or withhold; the evaluation still works when the evidence section carries the argument and your setting appears only as a type of unit.
How recent do the sources have to be?
Sections set their own window, commonly the last five years, and the window matters more here than in most courses because a device evaluated on its first generation may bear little resemblance to what ships now. Where an older study is the best available on an outcome, say so in a clause rather than hiding it, and note which version of the technology it examined.
Is a comparison against a second product expected?
Not usually, and adding one often thins both. A single technology examined against the clinical problem, with the alternative being the current practice it would replace, is the comparison the assignment is really asking for. If your section does request two, hold the same evidence questions to each so the paper does not turn into a preference for whichever had better marketing.
Where can I find a free NR 361 Week 3 sample paper?
The complete Week 3 evaluation of continuous pulse oximetry for postoperative opioid patients, with the problem, outputs, sorted evidence, costs, workflow fit, verdict and three references, can be read here in full.
What conditions does the NR 361 Week 3 verdict set?
Alarm thresholds and delays set to limit nuisance alarms, alerts sent to the assigned nurse's phone with escalation, and sedation checks kept unchanged with the lowest oxygen flow that keeps saturation acceptable.