scholarly journals One‐year results of the Variation of Orthokeratology Lens Treatment Zone (VOLTZ) Study: a prospective randomised clinical trial

Author(s):  
Biyue Guo ◽  
Sin Wan Cheung ◽  
Randy Kojima ◽  
Pauline Cho
Blood ◽  
2007 ◽  
Vol 110 (11) ◽  
pp. 575-575 ◽  
Author(s):  
Aurelio Maggio ◽  
Marcello Capra ◽  
Liana Cuccia ◽  
Francesco Gagliardotto ◽  
Carmelo Magnano ◽  
...  

Abstract Three short-term randomised clinical trials suggested not difference of Deferiprone (L1) vs Deferoxamine (DFO) in term of iron overload efficacy in thalassemia major (TM) patients. To assess whether L1 (75mg/Kg) alone was comparable to a sequential treatment using L1 (75mg/Kg) for 4 days and DFO (50mg/Kg) for 3 days, we carried ahead a large long-term randomised clinical trial. One-hundred and forty consecutive patients with TM and serum ferritin between 1,500 and 3,000 ng/ml were randomly assigned to L1 (n°69) or sequential L1-DFO (n°71) and treated for 5 years. The main measure of efficacy was the reduction of serum ferritin levels. Secondary outcomes were liver and heart iron contents assessed by T2* magnetic resonance. After one year-treatment the mean serum feritin reduction was −105 ± 90.4 in L1 and −409 ± 64.2 in sequential L1-DFO treatment (p <0.01), respectively. The greater mean serum ferritin reduction of sequential L1- DFO treatment was also confirmed all over the study (2° year L1 106 ± 713, L1-DFO -321 ± 92 (p <0.01); 3° year L1 137 ± 137, L1-DFO -292 ± 117 (p <0.05); 4° year L1 216 ± 200, L1-DFO-230 ± 170 (p <0.01); 5° year L1 336 ± 244, L1-DFO -598 ± 203 (p <0.01)). After one-year treatment this sequential group showed greater efficacy in term of serum ferritin levels reduction (−409 ± 64.2) in comparison with the DFO alone arm (−232 ± 619) of a previous randomised multicenter clinical trial in which a comparable cohort of patients were studied (p<0.05). Reversible leukocytopenia was shown in 8 (11.5%) L1 and in 7 (9.8%) sequential L1-DFO treated patients. No agranulocythosis was reported on sequential L1-DFO treated patients during the 5 years study. Hypertransaminasemia developed in 13 (18.8%) L1 and in 5 (7%) sequential L1-DFO treated patients. No other major side effects have been reported. Discontinuation of treatment was necessary in 55.6% L1 and in 57.7% sequential L1-DFO treated patients (chi2 0.03, p=0.86). The failures of treatment were less in sequential L1-DFO arm (n°2) in comparison to L1 alone arm (n°8), although this difference not so far reached the statistical significance (chi2 3.4, p=0.06). These findings suggest that sequential L1-DFO treatment in a long-term study is more effective than L1 alone with milder and reversible side effects. Moreover, its efficacy is also higher in comparison with DFO alone at short-term evaluation. Fig. 1 VARIATIONS OF THE FERRITIN LEVELS DURING FIVE YEARS TREATMENT BETWEEN THE TWO ARMS OF THE TRIAL Fig. 1. VARIATIONS OF THE FERRITIN LEVELS DURING FIVE YEARS TREATMENT BETWEEN THE TWO ARMS OF THE TRIAL


2019 ◽  
Vol 6 (1) ◽  
pp. 43-53
Author(s):  
Patrícia Manarte-Monteiro ◽  
Joana Domingues ◽  
Liliana Teixeira ◽  
Sandra Gavinha ◽  
Maria Conceição Manso

2015 ◽  
Vol 24 (11-12) ◽  
pp. 1611-1621 ◽  
Author(s):  
Olga Kadda ◽  
Anastasia Kotanidou ◽  
Athanasios Manginas ◽  
George Stavridis ◽  
Serafim Nanas ◽  
...  

Author(s):  
Mohammad Pakravan ◽  
Mohammadmehdi Hatami ◽  
Hamed Esfandiari ◽  
Shahin Yazdani ◽  
Azadeh Doozandeh ◽  
...  

Purpose: To compare the efficacy and safety of graft-free short tunnel small flap (STSF) technique with that of scleral patch graft (SPG) in Ahmed glaucoma valve (AGV) implantation. &nbsp;Design: Randomized clinical trial. &nbsp;Participants: Eighty-eyes of eighty patients with medically uncontrolled glaucoma including 41 in STSF and 39 eyes in SPG. Methods: Patients were enrolled and assigned randomly to STSF or SPG. &nbsp;Main Outcome Measures: tube exposure, Intraocular pressure (IOP), number of glaucoma medications, best corrected visual acuity (BCVA), surgical complications, and success rate ( defined as intraocular pressure (IOP) &gt;5 mmHg, &le;21 mmHg, and IOP reduction &ge;20% from baseline at two consecutive visits after three months, no reoperation for glaucoma). &nbsp;Results: only one case in SPG developed tube exposure at 1-year follow-up. The cumulative probability of success during the first year of follow-up was 70% in the STSF and 65% in SPG (P = 0.36). IOP decreased significantly from 29.6 &plusmn; 8.6 mmHg at baseline to 16.4 &plusmn; 3.6 mmHg at the final follow-up in STSF (p = 0.001). The corresponding numbers for SPG were 30.9 &plusmn; 11.2 and 15.8 &plusmn; 4.7, respectively (p = 0.001). The final IOP was comparable between both groups (p = 0.65). Mean &plusmn; standard deviation of the number of glaucoma medications was 1.8 &plusmn; 0.9 in STSF and 1.6 &plusmn; 0.9 in SPG at final follow-up (P = 0.32). Postoperative complications developed in 8 patients (19%) in STSF and 9 patients (23%) in SPG (P = 0.81). &nbsp;Conclusions: STSF and SPG techniques had comparable complication rate at one-year follow-up. Both techniques were comparable in terms of success rate, postoperative IOP, and glaucoma medications.


2020 ◽  
Vol 40 (5) ◽  
pp. 557-566 ◽  
Author(s):  
Qi Tan ◽  
Alex LK Ng ◽  
Bonnie NK Choy ◽  
George PM Cheng ◽  
Victor CP Woo ◽  
...  

BMJ ◽  
1992 ◽  
Vol 304 (6827) ◽  
pp. 601-605 ◽  
Author(s):  
B. W. Koes ◽  
L. M. Bouter ◽  
H. van Mameren ◽  
A. H. Essers ◽  
G. M. Verstegen ◽  
...  

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