Accreditation

2012-2013 Psychiatric Pharmacy Review Course - ACPE Credit Only

The Psychiatric Pharmacy Review Course (Review Course) is an excellent course of study and resource for those seeking a review of psychopharmacology and current standards of care.

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2012-2013 APNA Endorsed CPNP Psychiatric Pharmacotherapy Review Course

In cooperation with the American Psychiatric Nurses Association (APNA), the College of Psychiatric and Neurologic Pharmacists (CPNP) is pleased to offer the APNA endorsed CPNP Psychiatric Pharmacotherapy Review Course at CPNP member rates. This course is structured to provide knowledge- based education as defined in Accreditation Council for Pharmacy Education (ACPE) guidelines. The course examinations must be submitted by December 31, 2013.

APNA members can access this Accreditation Council for Pharmacy Education (ACPE) approved distance education course at CPNP member prices. Both a for-credit and no-credit (resource only) purchase option is being provided at a cost of $320 and $150 respectively. Non members of APNA can purchase the product for $480 (for-credit) and $150 (no-credit). The 20.0 contact hours of ACPE credit are accepted for American Nurses Credentialing Center Certification Renewal. You can preview a segment of a curriculum module and speaker presentation. Read on to learn more about this great APNA offer and register now.

Registration

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2012-2013 APNA Endorsed CPNP Psychiatric Pharmacotherapy Review CourseMembersNon-members
Psychiatric Pharmacotherapy Review Course - For Credit$320$480
Psychiatric Pharmacotherapy Review Course - No Credit$150$150

Download the printable registration form to register via mail or fax.

Accreditation (for-credit version only)

The College of Psychiatric and Neurologic Pharmacists is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education. The 2012-2013 APNA Endorsed Psychiatric Pharmacotherapy Review Course is a knowledge-based course and will provide up to 20 contact hours (2.0 CEUs) of continuing education credit.

Statements of Credit (for-credit version only)

Registrants can obtain up to 20.0 contact hours of ACPE credit by successfully completing the CPNP Psychiatric Pharmacotherapy Review Course online examinations for each of the 14 topic areas included in the course. The course expires December 31, 2013.

ACPE Statements of Credit will be available online at cpnp.org upon successful completion of each examination for the 14 topic areas contained in the course. Successful completion is defined as achieving a score of 60% or higher on each examination. Notification of statement availability will be provided upon successful completion of the examination.

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Medico-Legal Considerations in the Management of Behavioral Disturbances in the Elderly

This presentation will provide participants an overview of the medico-legal considerations regarding treatment of neuropsychiatric symptoms in patients with dementia. Read more about this session.

Pharmacological Management of Behavioral Disturbances in the Elderly

This presentation will provide participants an overview of the current evidence regarding treatment of neuropsychiatric symptoms in patients with dementia. The presentation will follow the recommendations from the American College of Neuropsychopharmacology (ACNP) white paper. Before initiating treatment for behavioral symptoms in patients with dementia, differential diagnosis is necessary. Once other causes of the behavior are ruled out, nonpharmacologic treatments should be initiated before starting pharmacologic treatment. Several nonpharmacologic treatments and literature supporting efficacy will be discussed. Finally drug therapy will be discussed focusing on antipsychotic medications, adverse effects, and the results of the CATIE-AD trial. During this presentation  the audience will have several opportunities to interact and participate in discussions of case presentations using Poll Everywhere technology. Read more about this session.

Putting the Action in Long-Acting Antipsychotic Injections

Since the development and introduction of the long-acting antipsychotic medications in the 1960’s, clinical debates have occurred among health-care providers as to when these medications are appropriate to use.  The impact of poor medication adherence among patients with psychiatric disorders has a great impact on their clinical outcomes.  Long-acting injectable antipsychotics have been shown to reduce hospitalizations and to improve medication adherence.  The clinical pharmacologic properties, safety and tolerability profiles of these medications vary between agents. Read more about this session.

Fibromyalgia:
Pain and the Brain

This presentation will discuss the prevalence, clinical presentation, pathophysiology diagnosis and treatment of fibromyalgia syndrome (FMS). While not completely understood, disordered central pain processing likely plays a role in the pathogenesis of FMS and treatment strategies primarily focus on alleviating pain and addressing associated symptoms and comorbid conditions. Read more about this session.

The Role of Antidepressants in Bipolar Disorder:
Myth vs. Reality

The safety and efficacy of antidepressants for patients with bipolar disorder continues to remain a source of tremendous controversy.  Initial reports of antidepressant-induced mania or hypomania led to marked concern among practitioners that antidepressants were highly likely to destabilize mood and worsen the course of illness in most people with bipolar disorder.  More recent investigations indicate that the potential for antidepressants to cause mania or hypomania is a rarer phenomenon than originally thought, occurring in about 10-15% of bipolar disorder patients.  Moreover, studies from the past two decades identify patient-specific risk factors for the emergence of antidepressant-associated mania or hypomania, suggesting its potential significance as an illness endophenotype.  Clinical studies suggest that the risk for mood destabilization from antidepressants appears higher in individuals with bipolar I (rather than bipolar II) disorder, as well as those with concomitant manic/hypomanic symptoms during depressive illness phases, recent manic or hypomanic episodes, comorbid alcohol or drug abuse, and past histories of antidepressant-induced mood destabilization.  Furthermore, risk may be somewhat higher with noradrenergic antidepressants (such as tricyclics or serotonin/norepinephrine reuptake inhibitors) than with purely serotonergic or primarily dopaminergic agents.  Co-therapy with antimanic drugs such as lithium may not reliably mitigate the risk for antidepressant-induced mania or hypomania. Read more about this session.

The FDA:
Inside the Black Box-A Discussion of Regulations and Recent Decisions

The Federal Food Drug and Cosmetic act states that approval of a drug requires “substantial evidence” from “adequate and well-controlled investigations”. The Code of Federal Regulations (CFR) codifies the FD&C Act and provides more details regarding what are considered to be adequate and well-controlled investigations. Guidance documents were developed to provide more detailed information, many times specific to the indications being studied, on various topics including clinical trial designs. Read more about this session.