Germinal matrix hemorrhage-intraventricular hemorrhage (GMH-IVH) commonly affects premature neonates. The gravity of the consequences associated with GMH-IVH makes it a major concern in their care. GMH-IVH begins in the germinal matrix tissue and is, most commonly, the result of venous rupture. Arteriole-to-venous precapillary shunts in the cerebrum of premature neonates could, if present, lead to elevated venous pressure in the germinal matrix and, thus, would be an important etiological factor. We report an autopsy study, involving 33 cases of premature neonates, designed to determine whether precapillary arteriole-to-venous shunts are present in the cerebral vasculature. Brain tissue was embedded in celloidin, sectioned into 100-m-thick slices and stained using alkaline phosphatase enzyme histochemistry, a method that distinguishes afferent from efferent vessels. Our sections, which are ideal for tracing vessels over long distances and for displaying patterns of branching and connections with other vessels, indicate that precapillary arteriole-to-venous shunts are not a major influence on cerebral blood flow in babies born at 23 wk gestation or later. The cerebral vasculature in one baby, who died at 24 wk postconception, included shunt-like connections, whereas in 34 babies shunts were not identified. We conclude that precapillary arteriole-to-venous shunts are not a significant factor leading to GMH. GMH-IVH is the most common intracranial hemorrhage afflicting premature neonates (1). The incidence, though declining, is about 1.45% of live births or about 58,000 cases per year. However, the incidence is highest in the smallest premature babies and, with survival rates increasing for this group, GMH-IVH remains, and will remain, a major focus of concern in neonatal intensive care units. In addition to the high number of cases, the gravity of the consequences associated with hemorrhagic damage make GMH-IVH a major concern in the care of premature neonates. Understanding the etiology and neuropathology of GMH-IVH is a necessary prerequisite for maximizing the benefits of current care and for discovering preventive measures (1, 2).It is widely accepted that GMH-IVH begins in the germinal matrix tissue (1). However, descriptions of GMH-IVH neuropathology vary considerably, especially in reference to the identity of the ruptured vascular element. The vascular origin of a hemorrhage is difficult to identify in histologic preparations because of the unusual structural qualities and high concentration of vessels within the germinal matrix tissue. Thus, even when a ruptured vessel is identified, designating it as an arteriole, capillary, or vein can be problematic and, in fact, all three vascular components have been implicated as sites of hemorrhagic origin (1, 3-10).Ghazi-Birry et al. (10) studied a series of neonatal brains that contained hemorrhagic foci. In this study, they used a specialized histochemical technique that distinguishes veins from arteries and capillaries and demonstrated that the overwhelming maj...