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1.
Am J Transplant ; 6(11): 2765-73, 2006 Nov.
Article in English | MEDLINE | ID: mdl-17049064

ABSTRACT

Lung transplant recipients exhibit a high incidence of invasive aspergillosis. The inhalation of lipid complex amphotericin-B (Abelcet; ABLC) offers a possible prophylactic strategy. The goals of this study were to select the optimal nebulizer delivery system for ABLC and to measure deposited aerosol dose in 12 lung transplant recipients. In vitro testing was performed to select a nebulizer delivery system, and an empirical model was used to estimate lung deposition. Estimated pulmonary doses varied by as much as 2-fold between different nebulizers. Aerosol deposition testing was performed in six single and six double lung recipients, each of whom received one 7 mL (35 mg) nebulized dose of Technetium-labeled ABLC using the selected nebulizer. In single lung recipients, the average deposited doses were 3.9 +/- 1.6 mg (mean +/- S.D.) in the allograft versus 2.1 +/- 1.1 mg in the native lung. Double lung recipients deposited on average 2.8 +/- 0.8 mg (left lung) and 4.0 +/- 1.3 mg (right lung). The drug was well distributed throughout the lungs, but delivery to the native lung was in some cases suboptimal. These studies provide an important precursor to studies of the efficacy of inhaled ABLC as a prophylaxis of invasive aspergillosis after lung transplant.


Subject(s)
Amphotericin B/pharmacokinetics , Antifungal Agents/pharmacokinetics , Lung Transplantation , Phosphatidylcholines/pharmacokinetics , Phosphatidylglycerols/pharmacokinetics , Aerosols , Amphotericin B/administration & dosage , Antifungal Agents/administration & dosage , Drug Combinations , Humans , Lung/diagnostic imaging , Metabolic Clearance Rate , Nebulizers and Vaporizers , Phosphatidylcholines/administration & dosage , Phosphatidylglycerols/administration & dosage , Radiography , Radioisotopes , Technetium
2.
Clin Nucl Med ; 17(6): 431-8, 1992 Jun.
Article in English | MEDLINE | ID: mdl-1319860

ABSTRACT

Thirty-three patients with biopsy-proven lung cancer and a total of 150 lesions diagnosed by conventional staging procedures were imaged using a Tc-99m labeled monoclonal Fab fragment of an IgG2B murine monoclonal antibody (MoAb) (NR-LU-10, NeoRx Corporation). Immunoscintigraphy demonstrated 100% of primary and 78% of metastatic lesions. MoAb imaging detected 88% of lesions in 12 small cell lung cancer (SCLC) patients and 77% of lesions in 21 non-small cell lung cancer (NSCLC) patients. Based on initial evaluation by other methods, 29 sites of MoAb activity were not associated with evidence of disease. Eleven of these were subsequently shown to represent sites of metastases; 18 remain unconfirmed. Four of ten patients studied with limited NSCLC had eight unsuspected lesions on MoAb imaging. Confirmation of unsuspected lesions in two patients altered initial clinical staging, and surgical therapy was abandoned. This study demonstrates that Tc-99m labeled NR-LU-10 can accurately stage patients with lung cancer.


Subject(s)
Carcinoma, Non-Small-Cell Lung/diagnostic imaging , Carcinoma, Small Cell/diagnostic imaging , Lung Neoplasms/diagnostic imaging , Radioimmunodetection , Carcinoma, Non-Small-Cell Lung/pathology , Carcinoma, Non-Small-Cell Lung/secondary , Carcinoma, Small Cell/pathology , Carcinoma, Small Cell/secondary , Female , Humans , Lung Neoplasms/pathology , Male , Middle Aged , Neoplasm Staging , Technetium , Tomography, Emission-Computed, Single-Photon
3.
Baillieres Clin Endocrinol Metab ; 3(1): 89-119, 1989 May.
Article in English | MEDLINE | ID: mdl-2679526

ABSTRACT

The continued development of high technology in the rapidly expanding field of computer-based imaging has had a significant impact on many areas of diagnostic imaging. The problem of rising medical costs emphasizes the importance of reaching a diagnosis by the most straightforward and cost-effective method while providing minimal patient discomfort. This responsibility to the patient and the medical care system rests with the physician. It is therefore essential that both imaging and referring physicians have a broad background of information regarding the potential limitations and relative merits of both old and new technologies available to patients with thyroid disorders. The appropriate utilization and relative roles of these imaging modalities have been discussed with respect to the individual clinical problem in this chapter.


Subject(s)
Diagnostic Imaging , Thyroid Diseases/diagnosis , Humans , Magnetic Resonance Imaging , Radiography , Radionuclide Imaging , Thyroid Diseases/diagnostic imaging , Thyroid Diseases/pathology , Thyroid Gland/pathology , Thyroid Neoplasms/diagnosis , Thyroid Neoplasms/pathology , Ultrasonography
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