Visual performance, safety and patient satisfaction after bilateral implantation of a trifocal intraocular lens in presbyopic patients without cataract

Evidence database / Studies / fernandez-2022-at-lisa-tri-rle

36enrolled patients*

72enrolled eyes*

1structured arms

365maximum standardized days follow-up

* Descriptive sum of reported arm counts. “≥” indicates that one or more arm counts were not reported; missing values are not treated as zero.

Study arm

Bilateral AT LISA tri RLE

RLEAT LISA tri 839MP

Inclusion
Presbyopic patients without cataract receiving bilateral RLE with AT LISA tri 839MP.

Exclusion
Not structured

Outcome	Follow-up	Follow-up sample	Result	Reported fraction	Provenance
MRSE within ±0.50 D predictability	Postoperative assessment	72 eyes	82.4%	denominator: 72 eyes	VERIFIED Source
Refraction within ±1.00 D efficacy	Postoperative assessment	72 eyes	97.1%	denominator: 72 eyes	VERIFIED Source
Mean postoperative spherical equivalent refractive	Postoperative assessment	72 eyes	-0.10 D	Not reported	VERIFIED Source
Distance spectacle independence patient_reported	Postoperative assessment	72 eyes	87.5%	denominator: 36 patients	VERIFIED Source
Intermediate spectacle independence patient_reported	Postoperative assessment	72 eyes	84.4%	denominator: 36 patients	VERIFIED Source
Near spectacle independence patient_reported	Postoperative assessment	72 eyes	78.1%	denominator: 36 patients	VERIFIED Source
Patient satisfaction patient_reported	Postoperative assessment	72 eyes	78.1%	denominator: 36 patients	VERIFIED Source

No structured complication observations are available for this arm. This means “not reported in this dataset,” not zero complications.