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1.
Cell Tissue Bank ; 13(4): 565-7, 2012 Dec.
Article in English | MEDLINE | ID: mdl-21814737

ABSTRACT

Tissue recovery personnel often find themselves in a situation in which, upon donor physical assessment, they discover an unusual or suspicious skin or tissue lesion. Because of the concern about the possibility of recovering tissues from a donor who may have an occult malignancy or infection, the Recovery Team may elect not to recover. Otherwise they may continue with the recovery, documenting their concern on the physical assessment form. At the time of evaluation of donor suitability the Medical Director must determine what the lesion is. This is inherently difficult and sometimes has led to the discard of recovered tissues. In order to optimize the gift of donation and avoid unnecessary deferral or discard of tissues we instituted a recovery biopsy procedure several years ago. Between January, 2005 and March, 2010, 561 biopsies were performed. In 552 donors (98.4%) there was no negative effect on medical suitability. Nine donors (1.6%) were found unsuitable based on the biopsy results. The recovery biopsy has allowed Recovery Teams to better manage their time by quickly identifying and biopsying suspicious lesions without trying to make a determination of donor eligibility and possibly ruling ineligible a qualified donor. The recovery biopsy has allowed the Medical Directors to make suitability decisions to accept or reject based on diagnostic certainty.


Subject(s)
Donor Selection , Tissue Donors , Biopsy , Humans , Infections/diagnosis , Tissue and Organ Procurement
2.
J Periodontol ; 82(2): 281-6, 2011 Feb.
Article in English | MEDLINE | ID: mdl-20731588

ABSTRACT

BACKGROUND: Bisphosphonate-associated osteonecrosis (BON) of the jaw is a growing concern in the dental community, but the possible presence of residual bisphosphonates in demineralized allograft bone from bisphosphonate-using tissue donors and the clinical implications of using such bone are unclear. The objectives of this study are to determine whether alendronate remained in demineralized bone matrix (DBM) procured from donors with a documented history of oral bisphosphonate use and to examine whether the demineralization process removes alendronate from allograft bone. METHODS: A gas chromatography?mass spectrometry method was developed and validated to quantify residual alendronate in allograft bone. Alendronate levels in DBM procured from tissue donors with a history of oral bisphosphonate use were compared to alendronate levels in DBM procured from donors without a history of bisphosphonate use. In addition, mineralized and demineralized bone was soaked in alendronate at concentrations of 0.002, 2.0, and 2,000 ng/mg bone and analyzed to examine the effect of the demineralization process. RESULTS: Residual alendronate was not detected in the DBM from either group, nor was it detected in any of the DBM samples soaked in alendronate solutions. Soaked mineralized bone contained measureable alendronate, but the substance was removed by demineralization. CONCLUSIONS: The demineralization process effectively removed residual alendronate from allograft bone. These results may relieve anxieties regarding the use of DBM in dental patients because it is unlikely to trigger BON of the jaw.


Subject(s)
Alendronate/analysis , Bone Demineralization Technique , Bone Density Conservation Agents/analysis , Bone Matrix/chemistry , Bone Transplantation/adverse effects , Osteonecrosis/prevention & control , Aged , Alendronate/adverse effects , Bone Demineralization Technique/methods , Bone Density Conservation Agents/adverse effects , Bone Matrix/transplantation , Bone Transplantation/methods , Female , Humans , Male , Middle Aged , Osteonecrosis/chemically induced , Tissue Donors
3.
Anat Rec A Discov Mol Cell Evol Biol ; 282(1): 8-12, 2005 Jan.
Article in English | MEDLINE | ID: mdl-15470665

ABSTRACT

The germinal matrix neuroepithelium and the choroidal fissure of the fetal choroid plexus commonly possess microvessels that are often poorly developed. There may be a reduction of type IV collagen that surrounds these fragile microvessels. During the first and second trimester of neural development, these microvessels are friable and can undergo intraventricular hemorrhage under a number of circumstances. Early subtle changes in the integrity of germinal matrix epithelium are not easily visualized by ultrasound. The current investigation employing scanning electron microscopy clearly defines subtle hemorrhagic events and tearing of the germinal matrix neuroepithelium in the brains of human fetuses. A 23-week-old fetus survived for 11 days but died from other causes. The choroid plexus of this fetus was compared with the choroid plexus and germinal matrix epithelium of a 22-week-old fetus that was the product of an elective termination due to severe anhydramnios of unknown origin and a 19-week-old male fetus from an elective termination. All tissues were autopsy material not requiring institutional review board approval.


Subject(s)
Cerebral Hemorrhage/etiology , Choroid Plexus/abnormalities , Fetal Development/physiology , Infant, Premature, Diseases/etiology , Microcirculation/abnormalities , Microscopy, Electron, Scanning/methods , Cerebral Hemorrhage/pathology , Choroid Plexus/blood supply , Choroid Plexus/ultrastructure , Endothelium, Vascular/abnormalities , Endothelium, Vascular/ultrastructure , Extracellular Matrix/ultrastructure , Fetus , Gestational Age , Humans , Infant, Newborn , Infant, Premature , Male , Microcirculation/ultrastructure
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