| Eligibility |
Inclusion Criteria:
Patients presenting subretinal haematoma linked to AMD
- Occurring at least14 days before the start of therapy
- With the presence of a component overlying the pigmentary epithelium (PE) on the OCT
- And a diameter greater than two pupillary diameters on the retinal photographs
Patients who have provided oral consent
Patients with National Health Insurance cover
Patients available for monthly follow-up
Patient having an effective contraception for the women old enough to procreate during the
treatment and during 6 months which follow his stop.
Exclusion Criteria:
- Subretinal haematoma linked to a cause other than AMD (myopia, angioid streaks…)
- History of subretinal haematoma on the same side
- Cloudy humour making it impossible to photograph the fundus of the eye or carry out
angiography
- Component of the haematoma exclusively underlying the pigmentry epithelium
- Haemorrhage without lifting of the retina
- Patients presenting an INR greater than 4, thus contra-indicating surgery
- Patients requiring cataract surgery in the first 3 months of the study
- Patients presenting a contra-indication relative to injection of the antiangiogenic
(History of AVC bleeding or unknown origin in the last 6 months or MI in the 3
preceding months)
- Pregnant or breast-feeding woman (the patients do not have to breast-feed during at
least 6 months after the administration of the last dose of the antiangiogénique)
- Contraindication in the use of ranibizumab: hypersensitivity in the active ingredient
or in one of the excipients, eye infection or périoculaire active or suspected,
inflammation intraoculaire active severe, treatments anti-VEGF systematic or eye
concomitant,
- Contraindication in the use of bevacizumab: hypersensitivity in the active substance
or in one of the excipients, the hypersensitivity in the products of the ovarian cells
of Chinese hamster (CHO) or in other antibodies human or humanized recombinants, heavy
surgical operation dating less than 28 days, not totally healed surgical wound,
history of lung bleeding or hémoptysie
- Contraindication in the use of alteplase: hypersensitivity in the active substance, in
the gentamicine (a residue of the present manufacturing process in the state of
tracks), or in one of the excipients. As all the thrombolytic agents, contraindication
in every case associated to a high hemorrhagic risk (current significant hemorrhagic
disorder or during the last six months, hemorrhagic known diathesis, concomitant
treatment by oral anticoagulants with effective dose, severe or potentially dangerous,
obvious or recent bleeding, histories or suspicion of intra-cranial bleeding,
suspicion of sub-arachnoid bleeding or history of sub-arachnoid bleeding bound to an
aneurysm, histories of severe lesion of the central nervous system (for example
néoplasie, aneurysm, surgical operation intracerebral or intrathecal), recent
traumatic external cardiac massage (less than 10 days), delivery, recent draining of a
vessel not accessible to the compression (for example draining of the subclavian or
jugular vein),severe uncontrolled high blood pressure, bacterial endocarditis,
pericarditis, acute pancreatitis, gastrointestinal ulcers documented during the last 3
months, esophageal varices, arterial aneurysm, arterial or venous deformations,
neoplasia increasing the hemorrhagic risk, severe hepatic disease, including hepatic
insufficiency, cirrhosis, portal hypertension (esophageal varicose veins) and
evolutionary hepatitis, surgical operation or important traumas during the last 3
months.
- Contraindication in the use of acetazolamide: hypersensitivity in the acetazolamide or
in one of excipients, severe hepatic, renal or suprarenal inadequacies, intolerance in
sulphonamide, histories of renal colic, allergy in the wheat (other than the coeliac
disease).
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