Table 2.
Non-AHT Conditions Related to RH |
Incidence | Timing | Risk Factors/Positive Elements | Mechanism | Morphologic Aspect |
Exclusion Elements |
---|---|---|---|---|---|---|
Birth trauma | Approximately one-third of newborns [38] | First two days of life, 85% of cases heal within 2 weeks [79,80] | Vacuum-assisted delivery [31] | Perinatal hemodynamic changes, ocular compression, prostaglandin release | Often numerous, extended over ora serrata (such as AHT-related) but only intraretinal, with rare retinal folds | RH with numerous, diffuse, extraretinal, duration extended over the first month of life |
Accidental head injury | Less than 4% according to multiple authors; short falls have an RH incidence close to 0% [36,81,82,83] | Same as AHT | Unambiguous and consistent history given by parents, presence of witnesses, other lesions compatible with referred kind and force of impact | Direct impact, Terson’s Syndrome, rapid acceleration and rotational movements of the head | Often confined to posterior pole, few in number, rarely subretinal. Severe accidents or impacts may determine extended lesions [84] | Absence of other lesions, suspicious behavior and history given by parents, absence of witnesses |
Raised ICP | Not estimated | Same as AHT | Severe elevation of ICP | Terson’s Syndrome | Superficial, intraretinal, located on or close to the optic disc [84] | Absence of papilledema (present in only 10% cases of AHT), other different patterns |
Systemic diseases | Variable | Coagulopathy (leukemia, thrombocytopenia, severe anemia, Vitamin K and factors deficiencies, and hemolytic uremic syndrome); raised ICP (glutaric aciduria type 1, meningitis); thrombosis of retinal artery (e.g., endocarditis), damage to the retinal endothelium (e.g., vasculitis) | Related to specific pathology | Deficiency of coagulation mechanisms | Low number and extension | Lack of diagnosis from accurate clinical and laboratory assessments |