Patient reported outcomes with LASIK - post-operative panel [Patient reported outcomes with LASIK]   99745-2

LOINC Code


LOINC code99745-2
namePatient reported outcomes with LASIK - post-operative panel [Patient reported outcomes with LASIK]
descriptionThe Patient-reported outcomes with LASIK (PROWL) survey instrument is used to assess visual symptoms both before and after LASIK eye surgery to identify changes over time and to measure the impact symptoms directly had on performing usual activities. The URL is https://www.fda.gov/medical-devices/lasik/lasik-quality-life-collaboration-project#presentations. The full PROWL pre-op questionnaire contains an additional 8 questions not included in this LOINC panel due to copyright. This LOINC is for the post-op questionnaire, for the pre-op questionnaire, see [LOINC:99192-7]
statusACTIVE

Fully-Specified Name

componentPatient reported outcomes with LASIK - post-operative panel
property-
timePt  =  Point in time:  To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements.
system^Patient
scale-
methodPROWL

Additional Names

short name

Basic Attributes

classPANEL.SURVEY.PROWL
type4  Surveys
order vs. observationBoth

Associated Observations

LOINC codes that represent optional associated observation(s) for a clinical observation or laboratory test. A LOINC term may represent a single associated observation or panel containing several associated observations.

History/Usage

first released
last updated2.72
last change typeADD  - added

Related Names

After
Pan
Panl
Pnl
Point in time
PROWL post-op
PST
Random
Survey

Copyright © 2023 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2023, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://loinc.org/license for the full LOINC copyright and license.

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