About Guidelines
Guidelines
Clinical practice guidelines are statements that include recommendations intended to optimize patient care. They are informed by a systematic review of evidence and an assessment of the benefits and harms of alternative care options.
Learn about the Guideline Development Process
AAN clinical practice guidelines are developed using a rigorous process rooted in evidence-based medicine methodology. The current guideline development process is described in the latest edition of the AAN Clinical Practice Guideline Process Manual, which was approved by the AAN Institute Board of Directors in 2017.
PREVIOUS GUIDELINE DEVELOPMENT MANUALS
Access previous AAN development process manual editions.
Topic Nominations
To submit an idea for a future guideline, complete the topic nomination form linked below. Before you submit a topic, preview the list of questions on the form and gather the required information for your nomination. All topics are reviewed by the AAN Guidelines Subcommittee annually in January or February. To ask questions or for more information, reach out to guidelines@aan.com.
Permission for use
Requests for permission to reproduce AAN guidelines should be directed to the publisher.
For permission to reproduce AAN guideline derivative content (e.g., clinician tools and patient tools), email guidelines@aan.com.
Request An Affirmation of Value
The AAN acknowledges that many organizations and independent developers create high-quality guidelines and other evidence-based documents that may be of value to AAN members. We recognize these documents by granting the AAN's Affirmation of Value and listing affirmed documents on AAN.com. To submit a document for consideration, email your request to guidelines@aan.com. Before submitting a document for consideration, please read our full Policy on Affirmation of Value for External Publications.
1 | Select topic |
The Guidelines Subcommittee reviews topics submitted by committee members, AAN members, AAN sections, and others. Topics are prioritized by board-approved criteria (see FAQ) |
2 | Form development panel | Panel members include Subcommittee members, a methodology expert, neurologist subject matter experts, organization representatives, and patient representatives. All panel members must disclose all potential conflicts of interest. The AAN requires the lead author and over half of the panel members to have no conflicts of interest related to the guideline topic. |
3 | Develop clinical questions and protocol | Each clinical question must have the following four elements: Population, Intervention, Co-Intervention, and Outcome. Questions drive the research and are included in the guideline protocol. The questions should address an area of quality concern, controversy, confusion, or practice variation. |
4 | Post protocol for public comment | The protocol is a document that includes the clinical questions and the plan for the research strategy. The AAN posts the protocol on the AAN website for a 30-day public comment period to get feedback from members, organizations, and others affected by the disease to make sure the right questions are being asked. |
5 | Review and analyze evidence |
A literature search is performed by a medical librarian, and then studies are reviewed by members of the development panel to determine if they meet inclusion criteria. Each study is reviewed by two independent reviewers. Developers then create an evidence table and populate with the essential characteristics of the included studies. Risk of bias is measured for each study using a four-tiered classification scheme. A modified version of the Grading of Recommendations Assessment, Development and Evaluation (GRADE) process is used to determine whether the developer's confidence in the evidence is sufficient to support practice recommendations. |
6 | Synthesize evidence and develop conclusions | Data from the included studies is synthesized into conclusions. Conclusions are succinct statements that summarize the evidence in answer to a specific clinical question. Conclusions inform recommendations. |
7 | Develop recommendation statements | Actionable practice recommendations are based on evidence and also consider the following elements (see FAQ or Guideline Process Manual for full list): patient preferences, cost, and value of benefit relative to the risk.
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8 | Post draft guideline for public comment | The AAN posts the draft guideline on the AAN website for a 30-day public comment period to get feedback from members, organizations, and others affected by the disease, on the comprehensiveness and clarity of the document. |
9 | Journal peer-review | The Neurology® journal solicits reviewers from its network to review and comment on the manuscript. |
10 | AAN approvals | After public comment, the draft guideline must receive approval from the AAN Guidelines Subcommittee, the AAN Quality Committee, and the AAN Institute Board of Directors before publishing |
11 | Develop derivative products | AAN guideline staff may develop tools for clinical and patient audiences, including the following: slide presentation, clinician summary, patient summary, guideline or case definition for clinicians, and algorithms. |
12 | Publish in Neurology® and disseminate | Guidelines are published in the AAN's journal, Neurology®, and posted on the AAN website. AAN communications staff may launch a media publicity campaign which may include tactics such as social media posting and issuing a press release. |
13 | Review for currency | At least every three years, published guidelines are reviewed by the Guidelines Subcommittee for currency. Reviewed guidelines are reaffirmed as current, updated, or retired. |