NU675 Unit 2 Antipsychotic Continuation Decision Example

Reviewed by Elspeth Marlowe, MSN, RN PMHNP Diagnosis and Management Across the Lifespan II Purdue University Global Free custom sample in 24 to 48h

This NU675 Unit 2 sample is a continuation decision paper for a composite 22-year-old bicycle mechanic who wants to stop aripiprazole fourteen months after a first psychotic episode that ended in a sixteen-day admission. It was written for Purdue Global NU 675, PMHNP Diagnosis and Management Across the Lifespan II, in the MSN psychiatric mental health nurse practitioner program. The paper weighs the severity of his episode against his rapid recovery, then sets the Zipursky review and the Tiihonen cohort beside the Wunderink trial of guided dose reduction. Three options are discussed with him and his mother, and they choose a slow reduction with named warning signs, a return-to-dose rule and monthly visits.

CourseNU675 PMHNP Diagnosis and Management Across the Lifespan II
UnitUnit 2
Paper typeContinuation decision paper
LengthAbout 1,090 words, 6 pages double-spaced
FormatAPA 7 student paper
SchoolPurdue University Global
ProgramMSN
UpdatedSeptember 2026

Free sample paper for NU675 Unit 2

1

Flattened but Well: A Continuation Decision Paper for a 22-Year-Old Bicycle Mechanic Who Wants to Stop His Antipsychotic Fourteen Months After a First Episode

[Student Name]

Purdue University Global

NU675: PMHNP Diagnosis and Management Across the Lifespan II

Unit 2 Continuation Decision Paper

[Instructor Name]

[Date]

The patient is composite; doses, dates and details are bracketed.

What this part is doingThe paper states its conclusion early, a middle path, and then shows the evidence that leads there.
2

The Patient and His Request

Mr. [B.] is a [22]-year-old bicycle mechanic who had his first episode of psychosis [fourteen] months ago. Over [six] weeks he became convinced that his coworkers were sabotaging bikes to frame him, heard a voice commenting on his work and stopped sleeping. He was admitted for [16] days and treated with aripiprazole, now [15] mg daily. His positive symptoms resolved within [eight] weeks. He returned to work at [four] months and has had no psychotic symptoms for [eleven] months.

He now says the medication makes him feel "flat, like the color's turned down," and that he has gained [6] kg. He wants to stop. He has taken it regularly, confirmed by pharmacy refills, and has used no cannabis since his admission, confirmed by urine screens at two visits. His mother, who lives with him, is worried about relapse.

What Makes His Episode More or Less Serious

Features that raise concern: a hospitalization, a period of [six] weeks of untreated psychosis before admission, and paranoid ideas directed at his workplace, where a relapse would cost him his job. Features that are more reassuring: a rapid and complete response to medication, good premorbid function, no substance use now, stable work and housing, a supportive family, and good insight; he recognizes the voice as part of the illness. He has had no depressive or manic features, and the diagnosis at [six] months was schizophreniform disorder that has not yet met the duration for schizophrenia because he recovered quickly.

What the Evidence Says About Stopping

A systematic review of first-episode psychosis studies found that the risk of symptom recurrence after medication discontinuation was high, with most patients relapsing within a year or two of stopping (Zipursky et al., 2014). A 20-year Finnish nationwide cohort of patients with first-episode schizophrenia found that the risk of treatment failure or relapse after stopping antipsychotics did not decline over the first eight years, and that long-term antipsychotic use was associated with lower mortality (Tiihonen et al., 2018).

Against this, the Dutch trial by Wunderink and colleagues randomized patients in remission from a first episode to guided dose reduction and discontinuation or to maintenance treatment. In the short term, relapse was more common in the reduction group, but at seven years the reduction group had twice the rate of functional recovery, [40.4] percent against [17.6] percent (Wunderink et al., 2013). The authors called for further studies before the finding changes practice.

The evidence says stopping raises the risk of relapse in the next year or two, and one trial suggests a guided reduction may still leave people better off in the long run; both findings apply to him.

What this part is doingThe two bodies of evidence are placed side by side, since the decision depends on weighing them rather than choosing one.
3

Weighing the Options With Him

Three options were discussed with Mr. [B.] and his mother.

1. Continue at [15] mg. Lowest short-term risk of relapse, but his side effects continue, and people who stop on their own, without a plan, often do so abruptly.

2. Stop now. Highest risk of relapse, and abrupt stopping of an antipsychotic can itself cause rebound symptoms.

3. Reduce gradually, with monitoring. A middle path: lower the dose by small steps over several months, watch for early warning signs, and stop only if he remains well, with an agreement to return to the previous dose at the first sign of relapse.

He and his mother chose option three. His reasons: he values his work and does not want a relapse, but he also wants to feel "like myself" and believes the side effects affect his work and relationships. His mother agreed on condition that she can call the clinic if she notices warning signs.

The Plan

1. Reduce aripiprazole from [15] mg to [10] mg for [eight] weeks, then to [5] mg for [eight] weeks, then review whether to stop.

2. Early warning signs, identified with him and his mother from the first episode: sleeping less than [five] hours, feeling that coworkers are talking about him, and withdrawing to his room. Any one of these triggers a call to the clinic within [48] hours and a return to the previous dose.

3. Monthly visits during the reduction, with a brief symptom rating and a check on sleep.

4. Continued abstinence from cannabis, since use would raise his risk sharply.

5. Weight and metabolic check at each dose step.

6. Coordinated specialty care team involvement for family education and supported employment.

His Mother's Concerns

His mother asked two questions. The first was whether the first episode might have been a one-time event caused by stress and lack of sleep. The answer given was that it is possible, since some people have a single episode, but that no test can tell in advance who will stay well, which is why the reduction is gradual and monitored. The second was what she should do if she noticed a warning sign and he disagreed. The plan answers this: she can call the clinic herself, and he agreed in writing that she may do so and that the team may speak with her about his early warning signs, though not about everything he discusses in his visits. She said this made the plan acceptable to her. Including her in this way also reflects the role families play in noticing early relapse, which patients themselves may be the last to recognize.

What the Decision Respects

The decision gives weight to his experience of side effects, which is a legitimate reason to adjust treatment, while keeping the risk of relapse visible and planned for. It avoids the worst outcome, an abrupt unplanned stop, which is what often happens when a patient's wish to stop is refused. It also treats the reduction as an experiment with a clear rule for ending it early, so neither he nor the team has to argue about whether a warning sign counts once it actually appears.

Limitations

The Wunderink trial was a single study in one country; its long-term finding has not been replicated widely, and later trials are under way. The Finnish cohort was observational, so people who stopped may have differed in ways that affected their outcomes. His own course may differ from the averages in either.

What this part is doingThe limitations section keeps the decision honest about how uncertain the evidence remains.
4

References

Tiihonen, J., Tanskanen, A., & Taipale, H. (2018). 20-year nationwide follow-up study on discontinuation of antipsychotic treatment in first-episode schizophrenia. American Journal of Psychiatry, 175(8), 765-773. https://doi.org/10.1176/appi.ajp.2018.17091001

Wunderink, L., Nieboer, R. M., Wiersma, D., Sytema, S., & Nienhuis, F. J. (2013). Recovery in remitted first-episode psychosis at 7 years of follow-up of an early dose reduction/discontinuation or maintenance treatment strategy: Long-term follow-up of a 2-year randomized clinical trial. JAMA Psychiatry, 70(9), 913-920. https://doi.org/10.1001/jamapsychiatry.2013.19

Zipursky, R. B., Menezes, N. M., & Streiner, D. L. (2014). Risk of symptom recurrence with medication discontinuation in first-episode psychosis: A systematic review. Schizophrenia Research, 152(2-3), 408-414. https://doi.org/10.1016/j.schres.2013.08.001

NU675 Unit 2 instructions, in plain terms

For Unit 2 you write a decision paper about whether a patient should continue a long-term medication after an episode has resolved. Prompts usually ask you to describe the episode and the patient's current state, weigh features that raise or lower the risk of recurrence, review the evidence on continuing and stopping, present the options to the patient and family, and document the decision with a monitoring plan. Four to six pages is a common length. Instructors reward papers that present conflicting evidence fairly, respect the patient's reasons for wanting to change treatment, and turn the decision into specific steps. Including family concerns and how they were addressed shows the decision was genuinely shared.

Inside the NU675 Unit 2 example

The paper opens with his episode, his recovery and his reasons for wanting to stop, including feeling flattened and weight gain. A section sorts the features of his illness into those that raise concern and those that reassure. The evidence section reports the Zipursky review, the Finnish cohort and the Wunderink trial, with a highlighted sentence explaining that both findings apply to him. Three options are laid out with their risks, and his reasons for choosing gradual reduction are recorded. A six-step plan follows, including early warning signs from his first episode. A section records his mother's two questions and the consent for her to call, and a limitations section closes the paper.

Reading the NU675 Unit 2 grading rubric

Continuation decision papers are generally graded on assessment of risk, use of evidence, shared decision making, the plan and critical appraisal. Risk assessment earns full points when features of the episode and the person are weighed separately. Evidence points reward presenting studies that point in different directions, with their designs, rather than citing only one side. Shared decision making is judged on whether the patient's reasons and the family's concerns shape the outcome. The plan row looks for dose steps with dates, warning signs drawn from his own history and a clear rule for returning to the previous dose. Appraisal credit goes to an honest account of the evidence's limits and uncertainty.

NU675 Unit 2 help: mistakes that cost points

Students often cite only the relapse data, which makes stopping look reckless, or only the long-term recovery trial, which makes it look easy. Another frequent error is refusing the patient's request without offering a monitored alternative, which can lead to an abrupt unplanned stop. Some papers list warning signs that are generic rather than drawn from the patient's own first episode. Others leave the family out, even when they live together. Many forget substance use, which sharply changes the risk. And a plan without a rule for returning to the previous dose leaves everyone arguing about whether a warning sign counts.

Get an NU675 Unit 2 example written to your instructions

Include the case from your NU675 Unit 2 prompt with every prior episode, admission and side effect it lists, plus the rubric; a continuation decision rests on that history. Your first custom paper is free, weighs each factor openly and fixes the next decision date, and it arrives within 24-48h. The paper above is an original model document written by our desk, not a submitted student paper and not an official Purdue University Global document.

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NU675 Unit 2 questions, answered

Is a first episode always a reason to stop treatment sooner?

Not always. A single episode lowers one risk factor but says nothing about severity, insight, substance use or family history, each of which can argue for longer maintenance. Guidelines commonly recommend continuing antipsychotic treatment for a year or more after a first episode. Weigh the factors visibly and cite the guideline you rely on, with its year.

How should the paper use studies with conflicting results?

Describe each study's population and design before its result, then explain why their findings differ. Here a registry cohort, a trial with long follow-up and a recent multi-episode trial point in different directions partly because they asked different questions. Say which study resembles the patient most, and let that comparison, rather than the most convenient result, carry the argument.

Can a continuation paper recommend reducing the dose instead of stopping?

Yes, and many strong papers do, provided the reduction is gradual, monitored and tied to criteria. Say how the lowest effective dose would be approached, which early signs would halt it and who would notice them. Keep any figures bracketed as composite. A reduction written as a vague intention to lower the dose later earns little.

Where can I find a free NU675 Unit 2 sample paper?

Read the NU675 Unit 2 continuation decision paper in full above, including the risk assessment, the conflicting evidence, three options, the chosen reduction plan, his mother's questions and the limitations, plus three references. A decision paper for your own case can be requested.

What did the Wunderink trial find in NU675 Unit 2?

Patients in remission from a first episode who were randomized to guided dose reduction had more relapses in the short term, but at seven years their rate of functional recovery was about twice that of the maintenance group, 40.4 percent against 17.6 percent.