MMHA 6900 Week 5 Postoperative VTE Analysis Example

Healthcare Quality Management Walden University Free custom sample in 24 to 48h

This MMHA 6900 Week 5 postoperative VTE safety analysis example validates flagged blood clot cases at a composite hospital before looking for causes, then examines the real cases through the SEIPS work-system model. Walden MMHA 6900 asks MHA students to analyze a safety signal, and the paper explains surveillance bias using Bilimoria and colleagues: hospitals that look harder for clots find more. Chart review of 31 flagged cases finds only 14 symptomatic postoperative clots, with others present on admission, found on screening or miscoded. The 14 are examined across person, tasks, tools, environment, organization and patient, drawing on Carayon and colleagues and Holden and colleagues, revealing an optional risk assessment, delayed first doses, divided ownership and missing weekend equipment. Four design changes follow, with the indicator reported alongside screening practice.

CourseMMHA 6900 Healthcare Quality Management
WeekWeek 5
Paper typePatient safety analysis
LengthAbout 1,020 words, 6 pages
FormatAPA 7 student paper
SchoolWalden University
ProgramMaster of Healthcare Administration (MHA)
UpdatedOctober 2026

Free sample paper for MMHA 6900 Week 5

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Validate Before You Explain: A Work-System Safety Analysis of Flagged Postoperative Blood Clots

Student Name

Walden University

MMHA 6900: Healthcare Quality Management

Instructor Name

Month Day, Year

What this page is doingThe title states the analysis's first rule, check the flagged cases before looking for causes, which is its main methodological point.
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Validate Before You Explain: A Work-System Safety Analysis of Flagged Postoperative Blood Clots

The Signal

Cobalt Ridge Medical Center, the composite hospital this course follows, received a quarterly report showing that its rate of postoperative pulmonary embolism or deep vein thrombosis, as flagged by a claims-based patient safety indicator, had risen to the top quartile among peer hospitals. The surgical quality committee asked for an analysis. The tempting response is to assume that prophylaxis is being missed and to launch an education campaign. This analysis takes a different first step: it validates the flagged cases, then examines the work system around those that are real, through the lens of the SEIPS work-system model.

What this page is doingThe opening names the tempting shortcut and the analysis's alternative, which sets up the argument for validation.
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Why Validate First

Claims-based venous thromboembolism measures count clots that are coded in discharge data. A hospital that looks harder for clots, for example by ordering more ultrasound scans, will find and code more of them, including small clots that would never have caused symptoms. A study of hospitals in a national surgical quality program found that hospitals with higher rates of imaging for clots had higher reported clot rates, and that the measure was more strongly associated with how often hospitals looked than with how well they prevented clots (Bilimoria et al., 2013). This is surveillance bias, and it means a rising rate can reflect more vigilance rather than worse care.

The analysis therefore reviewed all 31 flagged cases from the past two quarters, an illustrative number, against the medical record.

Screening ultrasound had increased the previous year, after orthopedic surgeons began ordering routine scans before discharge for some patients. That change alone explains much of the rise in the indicator. The 14 symptomatic cases, however, are real events and deserve analysis.

Table 1

Validation of Flagged Cases (Illustrative, Two Quarters)

Finding on chart reviewCases
Clot present on admission, miscoded as postoperative6
Clot found on screening ultrasound, no symptoms9
Symptomatic clot after surgery14
Coding error, no clot documented2
Total flagged31

Fewer than half the flagged cases were symptomatic postoperative clots. Eight were not postoperative clots at all.

What this page is doingReporting validation results in a table makes clear how much of the signal was measurement, which reshapes the rest of the analysis.
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The Work System Around the Real Cases

Carayon et al. (2006) built SEIPS on the idea that harm grows out of how a whole work system fits together, so the model asks about the individuals involved, what they were asked to do, the equipment and software they used, the physical setting and the organization around them, and how all of that shaped the care given. Its later version adds the patient and family as active participants and describes how work systems adapt over time (Holden et al., 2013). The analysis reviewed the 14 symptomatic cases through each component.

The findings point to a system that leaves risk assessment and dose timing to individual memory and divides responsibility between teams without naming an owner. No single person failed. The work system made omissions easy and their detection unlikely.

Table 2

Work-System Findings in 14 Symptomatic Cases

ComponentFindingCases affected
PersonPatients with prior clot history not identified as high risk at preoperative visit4
TasksProphylaxis ordered but first dose delayed more than 24 hours after surgery5
Tools and technologyRisk assessment in the record optional; no prompt when skipped6
EnvironmentMechanical compression devices unavailable on one surgical unit on weekends3
OrganizationNo owner for prophylaxis between surgical team and hospitalist comanagement5
Patient and familyPatients declined injections after discharge teaching was rushed2

Cases often had more than one finding. The most frequent was an optional risk assessment with no prompt, which let high-risk patients go unidentified.

What the Case Reviews Looked Like

Two cases illustrate the pattern. In one, a 71-year-old woman with a prior clot had a hip replacement on a Friday. The preoperative visit did not record her history because the risk assessment screen was optional and the clinic was running late. Her prophylaxis order was written for the following morning, and the weekend nurse could not find compression devices on the unit. She developed a symptomatic clot on day four. In another, a man recovering from bowel surgery was comanaged by the surgical team and a hospitalist. Each assumed the other had ordered prophylaxis, and neither had until the second postoperative day. Neither case involved a single careless act. Both followed from how the work system was arranged: optional steps, divided ownership and equipment gaps that appeared only on weekends.

These reviews also showed what worked. In most surgical cases without clots, the order set had been completed in full by a resident who used it every day. Reliability came from routine use of a well-designed tool, which is the lesson the recommendations build on.

Recommendations

The analysis recommends four changes. First, make the risk assessment a required step in postoperative order sets, with prophylaxis defaulted according to risk. Second, set a standard that the first prophylaxis dose is given within 24 hours of surgery unless a surgeon documents a bleeding concern, and report compliance monthly. Third, assign prophylaxis ownership to the surgical team for the first 48 hours, with hospitalist comanagement after that, written into the comanagement agreement. Fourth, stock compression devices on every surgical unit with a weekend par level.

Separately, the committee should report the indicator with a note on screening practices, and track symptomatic clots confirmed by chart review as an internal measure, since the claims indicator will continue to rise with surveillance.

Limits

Two quarters of cases is a small sample. Chart review depends on documentation, which may miss symptoms. The analysis did not compare Cobalt Ridge's prophylaxis rates with peers. The surveillance finding does not mean screening is wrong; it means the indicator must be read with screening practice in view.

Conclusion

The rise in Cobalt Ridge's postoperative clot indicator was partly a measurement effect: more screening found more clots, and some flags were not postoperative clots at all. Validating the cases first prevented an education campaign aimed at the wrong problem. The real cases revealed a work system with an optional risk assessment, delayed first doses, unclear ownership and missing equipment, each of which can be fixed by design rather than by exhortation.

What this page is doingThe conclusion separates the measurement finding from the safety finding, which is the analysis's main contribution to the committee.
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References

Bilimoria, K. Y., Chung, J., Ju, M. H., Haut, E. R., Bentrem, D. J., Ko, C. Y., & Baker, D. W. (2013). Evaluation of surveillance bias and the validity of the venous thromboembolism quality measure. JAMA, 310(14), 1482-1489. https://doi.org/10.1001/jama.2013.280048

Carayon, P., Schoofs Hundt, A., Karsh, B. T., Gurses, A. P., Alvarado, C. J., Smith, M., & Flatley Brennan, P. (2006). Work system design for patient safety: The SEIPS model. Quality and Safety in Health Care, 15(Suppl 1), i50-i58. https://doi.org/10.1136/qshc.2005.015842

Holden, R. J., Carayon, P., Gurses, A. P., Hoonakker, P., Hundt, A. S., Ozok, A. A., & Rivera-Rodriguez, A. J. (2013). SEIPS 2.0: A human factors framework for studying and improving the work of healthcare professionals and patients. Ergonomics, 56(11), 1669-1686. https://doi.org/10.1080/00140139.2013.838643

What the MMHA 6900 Week 5 instructions ask for

Patient safety analyses ask you to examine a signal and explain the events behind it. Before seeking causes, check whether the signal is accurate: review flagged cases against the record and sort out miscoding, events present on admission and effects of how hard the hospital looks. Then apply a systems framework to the confirmed cases, examining each component of the work system rather than individual blame. Present findings in a table showing how many cases each factor affected. Illustrate the pattern with one or two case narratives. Recommend design changes that make the safe action easier and the omission harder. Address how the measure itself should be reported going forward, and name the limits of a small sample.

Inside the MMHA 6900 Week 5 example

The analysis opens with the rising indicator and the tempting education campaign. A section explains surveillance bias, citing Bilimoria and colleagues, and Table 1 validates 31 flagged cases. A section explains the SEIPS model, citing Carayon and colleagues and Holden and colleagues, and Table 2 sorts findings in 14 symptomatic cases by work-system component. A section describes two cases, one involving a skipped risk assessment and missing devices, the other divided ownership. Recommendations require the risk assessment, set a dose timing standard, assign ownership and stock devices, and advise reporting the indicator with screening context. Limits and a conclusion separate the measurement and safety findings.

MMHA 6900 Week 5 rubric: what earns full marks

Safety analyses are graded on method and fairness. Checking the signal before hunting for causes is rewarded heavily, since it proves the writer knows measures can mislead. Explaining surveillance bias with evidence demonstrates sophistication. Applying a recognized systems framework to every confirmed case, with counts, earns the core share. Avoiding individual blame and locating causes in the work system is expected at the graduate level. Case narratives that illustrate the pattern add depth. Recommendations should change system design rather than rely on education alone. Attention to how the measure is reported going forward shows judgment. Tables should be accurate and labeled illustrative where needed. Limits should be honest, and the reference list must support each methodological claim.

Common MMHA 6900 Week 5 mistakes, and how to avoid them

Safety analyses often accept a rising rate at face value and launch training. Check the flagged cases first; some will not be what the indicator says. Ask whether anyone started looking harder, since screening can inflate rates. Then examine the real cases one by one through a systems model, looking at people, tasks, tools, setting and organization. Count how many cases each factor touched. Tell one or two stories in plain language. Recommend changes that make the right action automatic. Explain how the measure should be read in future. If your unit faces a safety signal that seems wrong, our writers can help you validate the cases and analyze the real ones in a paper your committee will trust.

Get a MMHA 6900 Week 5 example written to your instructions

Which safety event or indicator does the prompt concern? Say so, include any case your section distributes, attach the rubric too, and the analysis is traced through whichever model the course assigns. Nothing is charged for the first request, answered in 24 to 48 hours. No patient chart was read for the flagged cases, which were invented along with the hospital.

More MMHA 6900 papers and MHA samples

MMHA 6900 Week 5 questions, answered

Where can I find a free MMHA 6900 Week 5 sample paper?

The postoperative VTE safety analysis, with both tables, is published here.

Why does the MMHA 6900 Week 5 analysis validate cases first?

Hospitals that screen more find more clots, so a rising indicator can reflect vigilance rather than worse care.

How many flagged cases were real postoperative clots?

Fourteen of 31 were symptomatic postoperative clots; others were present on admission, found on screening or miscoded.

Which work-system factors appeared most?

An optional risk assessment with no prompt, delayed first doses and unclear ownership between surgical and hospitalist teams.

How should the indicator be reported going forward?

Alongside screening practice, with chart-confirmed symptomatic clots tracked as an internal measure.