Patient-reported outcomes with LASIK - pre-operative panel [Patient reported outcomes with LASIK] 99192-7
LOINC Code
| LOINC code | 99192-7 | ||
|---|---|---|---|
| name | Patient-reported outcomes with LASIK - pre-operative panel [Patient reported outcomes with LASIK] | ||
| description | The 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 36 questions not included in this LOINC panel due to copyright. This LOINC is for the pre-op questionnaire, for the post-op questionnaire, see [LOINC:99745-2] | ||
| status | ACTIVE | ||
Fully-Specified Name | |||
| component | Patient-reported outcomes with LASIK - pre-operative panel | ||
| property | - | ||
| time | Pt = 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 | - | ||
| method | PROWL | ||
Additional Names | |||
| short name | |||
Basic Attributes | |||
| class | PANEL.SURVEY.PROWL | ||
| type | 4 Surveys | ||
| order vs. observation | Order | ||
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 updated | 2.72 | ||
| last change type | ADD - added | ||
Related Names | |||
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