After clinical use survey

Please complete the After Clinical Use Survey below based on how acceptable, useful, and effective SimulConsult was for you, and how SimulConsult has changed the resources or time you need to evaluate genetic cases or CV.

1.What is your role?(Required.)

Other (please specify)

2.Now that you are using SimulConsult, please comment on the typical time you spend on each task for a given patient. (Note: Please enter the average minutes you spend on each. Enter 0 if you do not do the task.)(Required.)

Manual review of the chart before the first visit

First patient visit to collect history and findings

Documenting the findings from the first visit

Figuring out what test to order first

Completing an order for a single gene test or small panel

Interpreting the results for a single gene test or small panel

Completing an order for an exome

Exome/genome variant analysis

Interpreting the results of an exome

Preparing for case conferences

Attending case conferences

Drafting the return of results

Sharing and explaining the results with patient families

3.If any of the averages above have significant variation in the time required, please explain.

5.How do you think use of SimulConsult affects the patient experience?(Required.)

6.Would you recommend SimulConsult?(Required.)

Yes

No

7.Now that you are using SimulConsult, any feedback about the process or the tool?

8.Are there any additional outputs you would value?