99745 (99745)    LAB LOINC (95.3)

Name Value
CODE 99745
COMPONENT PATIENT REPORTED OUTCOMES WITH LASIK - POST-OPERATIVE PANEL
CHECK DIGIT 2
PROPERTY DASH
DATE LAST CHANGED 2022-02-16 00:00:00
CHANGE TYPE ADD
TIME ASPECT POINT
SYSTEM ~PATIENT
SCALE TYPE DASH
METHOD TYPE PROWL
CLASS PANEL.SURVEY.PROWL
FULLY SPECIFIED NAME PATIENT REPORTED OUTCOMES WITH LASIK - POST-OPERATIVE PANEL:-:PT:~PATIENT:-:PROWL
LONG COMMON NAME PATIENT REPORTED OUTCOMES WITH LASIK - POST-OPERATIVE PANEL [PATIENT REPORTED OUTCOMES WITH LASIK]
COMMENTS
The Patient-reported outcomes with LASIK (PROWL) survey instrument is used to as
sess 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 a
ctivities. The URL is https://www.fda.gov/medical-devices/lasik/lasik-quality-li
fe-collaboration-project#presentations. The full PROWL pre-op questionnaire cont
ains 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]
MASTER ENTRY FOR VUID YES
VUID 5342429
EFFECTIVE DATE/TIME
  • 2022-04-11 00:00:00
    STATUS:   ACTIVE