Lucentis v léčbě diabetického makulárního edému, dvouleté výsledky

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11150%2F22%3A10443201" target="_blank" >RIV/00216208:11150/22:10443201 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/00179906:_____/22:10443201

Výsledek na webu

<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=8sGNWIsWT5" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=8sGNWIsWT5</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.31348/2022/5" target="_blank" >10.31348/2022/5</a>

Jazyk výsledku

čeština

Název v původním jazyce

Lucentis v léčbě diabetického makulárního edému, dvouleté výsledky

Popis výsledku v původním jazyce

AIM: To evaluate, on the basis of two-year observations, the effectiveness of intravitreal treatment with Ranibizumab in patients with diabetic macular edema (DME) unresponsive to the previous laser treatment. Cohort and Methods: A retrospective study evaluates 29 eyes of 29 patients with diffuse DME unresponsive to their previous laser treatment. The group of the patients consisted of 16 males (55.1%) and 13 females (44.8%); their mean age was 71.3. The mean duration of diabetes mellitus was 13 years (3-20). 19 patients (65.5%) were treated with insulin, 10 patients (34.4%) were treated with peroral antidiabetics (PAD); the mean HbA1c value was 52 mmol/l. The treatment was started with 3 initial doses of intravitreal injections of Ranibizumab 0.5 mg. There was a one- -month interval between the applications. Subsequent evaluations and administrations of the following injections were made in the pro re nata (PRN) mode; the check-ups were carried out every month during the first year and on average every 3 months in the second year. The monitored parameters: the best corrected visual acuity (BCVA) measured on ETRDS (Early Treatment Diabetic Retinopathy Study) optotypes, the central retinal thickness (CRT). These parameters were monitored prior to the treatment and then in the 3rd, 6th, 9th, 12th, 18th and 24th months. RESULTS: A statistically significant improvement in the mean value of BCVA was detected. From the initial 65.4 +-10.61 letters it improved by 11.2 letters (p.

Název v anglickém jazyce

Lucentis In The Treatment Of Diabetic Macular Edema, Two-Year Results

Popis výsledku anglicky

Aim: To evaluate, on the basis of two-year observations, the effectiveness of intravitreal treatment with Ranibizumab in patients with diabetic macular edema (DME) unresponsive to the previous laser treatment. Cohort and Methods: A retrospective study evaluates 29 eyes of 29 patients with diffuse DME unresponsive to their previous laser treatment. The group of the patients consisted of 16 males (55.1%) and 13 females (44.8%); their mean age was 71.3. The mean duration of diabetes mellitus was 13 years (3-20). 19 patients (65.5%) were treated with insulin, 10 patients (34.4%) were treated with peroral antidiabetics (PAD); the mean HbA1c value was 52 mmol/l. The treatment was started with 3 initial doses of intravitreal injections of Ranibizumab 0.5 mg. There was a one-month interval between the applications. Subsequent evaluations and administrations of the following injections were made in the pro re nata (PRN) mode; the check-ups were carried out every month during the first year and on average every 3 months in the second year. The monitored parameters: the best corrected visual acuity (BCVA) measured on ETRDS (Early Treatment Diabetic Retinopathy Study) optotypes, the central retinal thickness (CRT). These parameters were monitored prior to the treatment and then in the 3rd, 6th, 9th, 12th, 18th and 24th months. Results: A statistically significant improvement in the mean value of BCVA was detected. From the initial 65.4 +-10.61 letters it improved by 11.2 letters (p &lt;0.05) at the end of the two-year observations, when the improvement of BCVA by min six letters (compared to the initial VA) was achieved in 19 eyes (65.5%), stabilization (+-5 letters) was detected in 7 eyes (24.1%) and worsening (by more than five letters) occurred in 3 eyes (10.3%). The mean CRT value declined after 2 years from the initial 450.5 +-139.3 μm by 89.5 µm (p = 0,006). The decline in CRT was significant in comparison with the baseline values (the mean of 450.45 µm) in 4 out of the 6 monitored intervals. The mean number of Ranibizumab injections was 5.45 +-1.8 during the first year of treatment, and 3.18 +-1.27 injections in the second year. Conclusions: Intravitreal Ranibizumab injections reduce CRT and improve BCVA in patients with DME who did not show any improvement after laser treatment. The best effect was documented after the three initial applications of Ranibizumab and then at the end of the monitoring period. In two-year time period we detected CRT decline in 79.3% of the patients and BCVA improvement (by 15.3 letters on average) in 65.5% of the patients.

Druh

J_SC - Článek v periodiku v databázi SCOPUS

CEP obor

—

OECD FORD obor

30207 - Ophthalmology

Projekt

—

Návaznosti

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2022

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Česká a slovenská oftalmologie

ISSN

1211-9059

e-ISSN

1805-4447

Svazek periodika

78

Číslo periodika v rámci svazku

1

Stát vydavatele periodika

CZ - Česká republika

Počet stran výsledku

5

Strana od-do

24-28

Kód UT WoS článku

—

EID výsledku v databázi Scopus

2-s2.0-85127729652