Ocular perfusion pressure control during pars plana vitrectomy: testing a novel device.
Rossi Tommaso, Querzoli Giorgio, Gelso Aldo, Angelini Giampiero, Rossi Alessandro, Corazza Paolo, Landi Laura, Telani Serena, Ripandelli Guido
AI Summary
A novel device controlling ocular perfusion pressure during vitrectomy effectively lowered intraoperative IOP and maintained higher perfusion, reducing dangerous pressure dips. This could improve surgical safety and outcomes.
Abstract
Purpose
To study the efficacy of a novel device intended to control infusion pressure based on mean ocular perfusion pressure (MOPP) during pars plana vitrectomy (PPV).
Methods
An arm blood pressure cuff connected to a vitrectomy machine calculated mean arterial pressure (MAP), while a pressure sensor close to the infusion trocar measured intraocular pressure (IOP). MOPP was calculated in real time in 36 consecutive patients undergoing PPV, who were divided into two groups. The device lowered IOP every time that calculated MOPP fell below 30 mmHg in the Control ON group (18 patients), while no action was taken in the Control OFF group (18 patients).
Results
Baseline IOP and blood pressure were similar between groups. The Control ON group had significantly lower average intraoperative IOP (30.5 ± 2.1 vs. 35.9 ± 6.9 mmHg; p = 0.002) and higher MOPP (56.4 ± 5.9 vs. 49.7 ± 6.1 mmHg) than the Control OFF group. The Control ON group also spent less time at MOPP < 10 mmHg and < 30 mmHg: 0 vs. 3.40 ± 2.38 min (p < 0.001) and 9.91 ± 7.15 vs. 16.13 ± 8.12 min (p = 0.02), respectively.
Conclusions
The MOPP control device effectively maintained lower IOP and higher MOPP throughout surgery. It also helped avoid dangerous IOP peaks and MOPP dips, allowing patients to spend less time at MOPP of < 10 and < 30 mmHg.
MeSH Terms
Shields Classification
Key Concepts5
The MOPP control device significantly lowered average intraoperative IOP (30.5 2.1 vs. 35.9 6.9 mmHg; p = 0.002) and maintained higher MOPP (56.4 5.9 vs. 49.7 6.1 mmHg) in the Control ON group (18 patients) compared to the Control OFF group (18 patients) during pars plana vitrectomy.
The MOPP control device in the Control ON group (18 patients) resulted in less time spent at MOPP < 10 mmHg (0 vs. 3.40 2.38 min; p < 0.001) and MOPP < 30 mmHg (9.91 7.15 vs. 16.13 8.12 min; p = 0.02) compared to the Control OFF group (18 patients) during pars plana vitrectomy.
The MOPP control device effectively maintained lower intraocular pressure (IOP) and higher mean ocular perfusion pressure (MOPP) throughout pars plana vitrectomy surgery.
The MOPP control device helped avoid dangerous intraocular pressure (IOP) peaks and mean ocular perfusion pressure (MOPP) dips, allowing patients to spend less time at MOPP of < 10 and < 30 mmHg during pars plana vitrectomy.
A novel device intended to control infusion pressure based on mean ocular perfusion pressure (MOPP) during pars plana vitrectomy (PPV) was studied for its efficacy.
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