AutoICD API

99192-7

Surveys

Patient-reported outcomes with LASIK - pre-operative panel [Patient reported outcomes with LASIK]

Definition

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]

LOINC 6-Axis Classification

Component

Patient-reported outcomes with LASIK - pre-operative panel

Property

-

Time Aspect

Pt

System

^Patient

Scale Type

-

Method Type

PROWL

Details

Class

PANEL.SURVEY.PROWL

Order/Observation

Order

Related Names

BeforePanPanlPnlPoint in timePROWLPROWL pre-opRandomSurvey

Frequently Asked Questions

What is LOINC code 99192-7?

LOINC code 99192-7 identifies "Patient-reported outcomes with LASIK - pre-operative panel [Patient reported outcomes with LASIK]". 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]

What does 99192-7 measure?

This code measures Patient-reported outcomes with LASIK - pre-operative panel in ^Patient. It belongs to the PANEL.SURVEY.PROWL class in the LOINC classification.

What is LOINC?

LOINC (Logical Observation Identifiers Names and Codes) is a universal standard for identifying laboratory and clinical observations. It is maintained by the Regenstrief Institute and used worldwide for health data exchange.