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1.
Clin Radiol ; 78(2): 115-122, 2023 02.
Article in English | MEDLINE | ID: mdl-36180271

ABSTRACT

Artificial intelligence (AI) is becoming more widespread within radiology. Capabilities that AI algorithms currently provide include detection, segmentation, classification, and quantification of pathological findings. Artificial intelligence software have created challenges for the traditional United States Food and Drug Administration (FDA) approval process for medical devices given their abilities to evolve over time with incremental data input. Currently, there are 190 FDA-approved radiology AI-based software devices, 42 of which pertain specifically to thoracic radiology. The majority of these algorithms are approved for the detection and/or analysis of pulmonary nodules, for monitoring placement of endotracheal tubes and indwelling catheters, for detection of emergent findings, and for assessment of pulmonary parenchyma; however, as technology evolves, there are many other potential applications that can be explored. For example, evaluation of non-idiopathic pulmonary fibrosis interstitial lung diseases, synthesis of imaging, clinical and/or laboratory data to yield comprehensive diagnoses, and survival or prognosis prediction of certain pathologies. With increasing physician and developer engagement, transparency and frequent communication between developers and regulatory agencies, such as the FDA, AI medical devices will be able to provide a critical supplement to patient management and ultimately enhance physicians' ability to improve patient care.


Subject(s)
Artificial Intelligence , Radiology , Humans , United States , United States Food and Drug Administration , Algorithms , Radiology/methods , Radiography, Thoracic
2.
Int J Gynecol Cancer ; 18(2): 329-38, 2008.
Article in English | MEDLINE | ID: mdl-18334011

ABSTRACT

PTEN mutations have been implicated in the development of endometrial hyperplasia and subsequent cancer. Peroxisome proliferator-activated receptor gamma (PPAR-gamma) agonists have demonstrated antineoplastic and chemopreventive effects. The purpose of this study was to evaluate the effects of the PPAR-gamma agonist rosiglitazone on both PTEN wild type and PTEN null cell lines and in the PTEN heterozygote((+/-)) murine model. Hec-1-A (PTEN wild type) and Ishikawa (PTEN null) cells were treated with rosiglitazone. Thirty-five female PTEN(+/-) mice were genotyped and placed into one of four groups for treatment for 18 weeks: A) PTEN wild type with 4 mg/kg rosiglitazone, B) PTEN(+/-) mice with vehicle, C) PTEN(+/-) mice with 4 mg/kg rosiglitazone, and D) PTEN(+/-) mice with 8 mg/kg rosiglitazone. Proliferation and apoptosis were measured by bromodeoxyuridine (BrdU) and terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labeling of DNA fragmentation sites assay. Rosiglitazone caused cell growth inhibition in both Hec-1-A and Ishikawa in a dose-dependent manner (P < 0.02 and P < 0.03, respectively). Rosiglitazone also induced apoptosis in both Hec-1-A (P < .001) and Ishikawa (P < .001) cells in a dose-dependent manner. In the murine model, rosiglitazone decreased proliferation of the endometrial hyperplastic lesions (B vs C; 39.7% vs 9.3% and B vs D; 39.7% vs 4.2%; P < 0.0001) and increased apoptosis of glandular endometrial epithelial cells (B vs C; 2.8% vs 22.4%; P < 0.0001 and B vs D; 2.8% vs 30.2%; P = 0.003). PPAR-gamma agonist rosiglitazone inhibits proliferation and induces apoptosis in both PTEN intact and PTEN null cancer cell lines and in hyperplastic endometrial lesions in the PTEN(+/)(-)murine model.


Subject(s)
Anticarcinogenic Agents/pharmacology , Endometrial Hyperplasia/prevention & control , PPAR gamma/agonists , Thiazolidinediones/pharmacology , Animals , Anticarcinogenic Agents/therapeutic use , Apoptosis/drug effects , Cell Proliferation/drug effects , Cell Survival/drug effects , Chemoprevention , Disease Models, Animal , Female , Heterozygote , Mice , Mutation , PTEN Phosphohydrolase/genetics , Rosiglitazone , Thiazolidinediones/therapeutic use
3.
Int J Gynecol Cancer ; 18(3): 571-5, 2008.
Article in English | MEDLINE | ID: mdl-17692091

ABSTRACT

At present, there is no standard technique that allows surgeons performing total laparoscopic radical hysterectomy to complete the colpotomy and remove an adequate (2-cm) margin of upper vaginal tissue while maintaining adequate pneumoperitoneum. We evaluated the feasibility and safety of using a modified uterine manipulator for total laparoscopic radical hysterectomy in patients with cervical or endometrial cancer. A retrospective review was performed in all patients who underwent total laparoscopic radical hysterectomy using a modified uterine manipulator at our institution during the period April 2004 to December 2006. This analysis included 30 patients who underwent surgery with the modified uterine manipulator. There were no reports of difficulty with placement of the instrument, multiple attempts at placement, difficulty with uterine manipulation, or uterine perforation. In no patient was a vaginal incision or episiotomy required to fit the instrument through the introitus. In no case was there loss of pneumoperitoneum during colpotomy. Additional upper vaginal tissue had to be removed after intraoperative assessment of the adequacy of the surgical specimen in five (16.7%) of 30 patients. Use of the modified uterine manipulator according to our technique is safe and feasible, allowing for adequate vaginal resection and maintenance of pneumoperitoneum.


Subject(s)
Hysterectomy, Vaginal/instrumentation , Hysterectomy, Vaginal/methods , Hysteroscopy/methods , Uterine Cervical Neoplasms/surgery , Adult , Aged , Cohort Studies , Contraceptive Devices, Female , Equipment Design , Equipment Safety , Female , Follow-Up Studies , Humans , Laparoscopy/methods , Middle Aged , Neoplasm Staging , Retrospective Studies , Risk Assessment , Survival Analysis , Treatment Outcome , Uterine Cervical Neoplasms/mortality , Uterine Cervical Neoplasms/pathology
4.
Int J Gynecol Cancer ; 18(1): 146-51, 2008.
Article in English | MEDLINE | ID: mdl-17466036

ABSTRACT

The objective of our study was to evaluate the phosphatase and tensin homologue deleted on chromosome 10 (PTEN), p27, and mammalian target of rapamycin (mTOR) expressions in women with progesterone-responsive and refractory endometrial hyperplasia (EH) samples and to determine if these markers could be associated with response or used as potential targets for treatment. Thirty-eight matched pre- and posttreatment pairs of paraffin-embedded endometrial biopsies were obtained from patients with EH. Immunohistochemical analysis for PTEN, p27, and phospho-mTOR were performed on all samples. Median age at diagnosis was 49 years (20-79 years). Median treatment interval was 3 months (1-12 months). Sixteen patients (42.1%) had complete resolution of their hyperplasia (responders), and 22 (57.9%) had persistent hyperplasia (nonresponders) after treatment with progesterone. In the pretreatment samples, no markers were found to predict nonresponders. In posttreatment samples, loss of PTEN expression with phospho-mTOR expression was observed in more nonresponders than responders (40.9% vs 6.3%; P= 0.03). Phospho-mTOR overexpression was found in 63.6% of nonresponders. We found that persistent hyperplasia refractory to progesterone therapy was associated both with the loss of PTEN and with the loss of phosphorylation of mTOR. In select cases of non-responsive progesterone refractory EH, a rational target for treatment may involve the mTOR pathway.


Subject(s)
Chromosomes, Human, Pair 10/genetics , Cyclin-Dependent Kinase Inhibitor p27/metabolism , Endometrial Hyperplasia/drug therapy , Gene Deletion , PTEN Phosphohydrolase/genetics , Progesterone/therapeutic use , Progestins/therapeutic use , Protein Kinases/metabolism , Adult , Aged , Endometrial Hyperplasia/genetics , Endometrial Hyperplasia/pathology , Female , Humans , Immunoenzyme Techniques , Middle Aged , Neoplasm Recurrence, Local/drug therapy , Neoplasm Recurrence, Local/metabolism , Neoplasm Recurrence, Local/pathology , Phosphorylation/drug effects , TOR Serine-Threonine Kinases
5.
Int J Gynecol Cancer ; 18(4): 660-9, 2008.
Article in English | MEDLINE | ID: mdl-17892451

ABSTRACT

The purpose of the study was to determine the ethnic disparities in socioeconomic status (SES) and in receiving definitive surgical treatment and adjuvant chemotherapy and to examine if these differences contribute to ethnic disparities in survival. We studied a population-based cohort of 5131 women diagnosed with epithelial ovarian cancer at age >or=65 between 1992 and 1999, identified from the Surveillance, Epidemiology and End Results-Medicare linked databases with up to 11 years of follow-up. The percentage of women diagnosed with epithelial ovarian cancer at advanced stage (stage III or IV) was 71.6% in Caucasians and 69.7% in African-Americans. Of these 4264 with stage IC-IV disease who are recommended for chemotherapy, fewer African-Americans received chemotherapy compared to Caucasians (50.2% versus 64.7%, P < 0.001). The risk of all-cause mortality in African-Americans was not significantly different from Caucasians (hazard ratio [HR] = 1.00, 95% CI = 0.88-1.13) after controlling for patient demographics, tumor characteristics, and comorbidity. The HR remained not significant in African-Americans compared to Caucasians after additionally adjusting for treatments (0.93, 0.82-1.06) or SES (0.94, 0.82-1.08) or both (0.88, 0.77-1.01). Women who underwent cancer-directed surgery and received adjuvant chemotherapy were 50% less likely to die than those who did not. The survival benefits from these therapies were similar in Caucasian and African-American women with ovarian cancer. There was no significant difference in survival between African-American and Caucasian women with ovarian cancer after adjusting for tumor characteristics, treatment, and sociodemographic factors. Although adjuvant chemotherapy was effective in prolonging survival, substantial numbers of women with ovarian cancer still did not receive chemotherapy.


Subject(s)
Neoplasms, Glandular and Epithelial/ethnology , Neoplasms, Glandular and Epithelial/mortality , Neoplasms, Glandular and Epithelial/therapy , Ovarian Neoplasms/ethnology , Ovarian Neoplasms/mortality , Ovarian Neoplasms/therapy , Social Class , Black or African American/statistics & numerical data , Age Factors , Aged , Aged, 80 and over , Female , Humans , Neoplasms, Glandular and Epithelial/diagnosis , Ovarian Neoplasms/diagnosis , Survival Analysis , United States/epidemiology , White People/statistics & numerical data
6.
Int J Gynecol Cancer ; 16(4): 1668-72, 2006.
Article in English | MEDLINE | ID: mdl-16884382

ABSTRACT

Cyclins D1 and D3 play key roles in cell cycle progression. The downregulation of cyclin D3 was associated with phosphatase and tensin homolog deleted on chromosome ten-(PTEN)-induced cell cycle arrest. We attempted to determine whether cyclin D1 and D3 overexpression is correlated with PTEN inactivation in endometrioid endometrial cancer (EEC). The expression of PTEN, cyclin D1, and cyclin D3 were determined by immunohistochemical analysis in 105 EEC specimens. Forty-three percent of the EEC demonstrated loss of PTEN expression. Cyclin D3 was overexpressed in only 18% of the EEC specimens and was not associated with tumor grade. Cyclin D1 was overexpressed in 64% of the specimens and was more common in moderate or high-grade tumors (P = 0.002 and P = 0.02, respectively). The overexpression of cyclin D3 was not correlated with loss of PTEN in the EEC. The overexpression of cyclin D1 was much higher in grade 1 tumors with negative PTEN than tumors with positive PTEN expression (67% vs 26%). The overexpression of cyclin D3 was neither frequent nor correlated with the loss of PTEN expression. The overexpression of cyclin D1 was higher in the low-grade tumors with negative PTEN expression than tumors with positive PTEN expression. Overexpression of cyclin D1 is frequent in moderate or high-grade EECs and likely results from multiple mechanisms.


Subject(s)
Carcinoma, Endometrioid/metabolism , Cyclin D1/metabolism , Cyclins/metabolism , Endometrial Neoplasms/metabolism , Gene Expression Regulation, Neoplastic , PTEN Phosphohydrolase/metabolism , Carcinoma, Endometrioid/pathology , Cyclin D3 , Endometrial Neoplasms/pathology , Female , Humans , Immunoenzyme Techniques
7.
Int J Pediatr Otorhinolaryngol ; 59(1): 63-8, 2001 May 31.
Article in English | MEDLINE | ID: mdl-11376820

ABSTRACT

Tracheal agenesis (TA) is a rare congenital anomaly that typically has fatal consequences. Its rarity, lack of prenatal symptoms, and emergent presentation usually lead to a failure to arrive at the correct diagnosis and manage the airway properly before the onset of irreversible cerebral anoxia. We report the case history of an infant born with immediate respiratory failure who was diagnosed with tracheal agenesis. The clinical features, embryology, classification schemes and surgical management are discussed with the hope that increased awareness and earlier diagnosis may lead to better chances of survival for affected individuals.


Subject(s)
Trachea/abnormalities , Tracheal Diseases/diagnosis , Tracheal Diseases/surgery , Fatal Outcome , Humans , Infant, Newborn , Radiography , Trachea/diagnostic imaging
8.
Infect Control Hosp Epidemiol ; 22(10): 653-5, 2001 Oct.
Article in English | MEDLINE | ID: mdl-11776355

ABSTRACT

To determine if fabric stethoscope covers pose an infection control problem, we studied how they are cared for by our healthcare workers and performed microbiological investigations on 22 covers collected over a 3-week period. Our study suggests that fabric stethoscope covers represent a potential infection control problem because they are used for prolonged periods, are infrequently laundered, and are contaminated with bacteria.


Subject(s)
Bacteria/isolation & purification , Equipment Contamination , Stethoscopes/microbiology , Textiles/microbiology , Equipment and Supplies, Hospital/microbiology , Humans , Infection Control/methods , Personnel, Hospital , Species Specificity , United States
9.
Laryngoscope ; 110(12): 2123-7, 2000 Dec.
Article in English | MEDLINE | ID: mdl-11129034

ABSTRACT

OBJECTIVE: To determine whether age-related mitochondrial DNA mutations occur in the human larynx. STUDY DESIGN: Genetic study of cadaveric larynx specimens. METHODS: Vocal fold mucosa, thyroarytenoid muscle, and cricoarytenoidjoint tissue were harvested from 13 fresh postmortem larynges (age range, 2 d-82 y). DNA was extracted from each sample, and the polymerase chain reaction (PCR) was used to amplify a target DNA sequence resulting from the common age-associated, 4977-base-pair (bp) mitochondrial DNA deletion. PCR products were visualized by agarose gel electrophoresis. Automated sequencing determined the sequence of identified PCR products. SUBJECTS: Thirteen cadaveric larynges were obtained through the University of Kentucky Medical Center (Lexington, KY). Specimens from patients with a history of head and neck cancer, previous laryngeal trauma, or surgery were excluded. RESULTS: Strongly positive bands were identified in samples from three individuals. Weaker bands were seen in samples from four other samples. No band was noted from the two pediatric larynges. Different band patterns were seen among the three different tissue sites in the larynges with positive PCR products, but no consistent pattern was seen. Sequencing of the identified PCR products from selected samples confirmed that they were products of the age-associated, 4977-bp mitochondrial DNA deletion. CONCLUSIONS: An age-associated mitochondrial DNA deletion was detected in several post-mortem human larynges. Its presence seemed to increase in appearance with age. In the larynges in which the deletion occurred, there were individual regional differences in the occurrence of the deletion, but no consistent pattern was noted across all individuals who carried the deletion.


Subject(s)
DNA, Mitochondrial/genetics , Larynx/physiology , Mutation , Adult , Age Factors , Aged , Aging/genetics , Chromosome Deletion , Humans , Infant , Infant, Newborn , Middle Aged , Polymerase Chain Reaction , Sequence Analysis, DNA
10.
J Nematol ; 24(4S): 779-82, 1992 Dec.
Article in English | MEDLINE | ID: mdl-19283062

ABSTRACT

During September 1990, 30 cotton fields in each of three Missouri counties were surveyed for plant-parasitic nematodes. Soil samples for nematode analysis consisted of a composite of 20 cores collected in a zig-zag pattern within a 1-ha block in each field. Cores were taken from within weed-free cotton rows. Nine genera of plant-parasitic nematodes were found (Rotylenchulus, Helicotylenchus, Hoplolaimus, Meloidogyne, Paratylenchus, Pratylenchus, Tylenchorhynchus, Heterodera, and Trichodorus), and five species were identified: Meloidogyne incognita, Rotylenchulus reniformis, Hoplolaimus galeatus, Pratylenchus vulnus, and P. scribneri. This is the first report of R. reniformis, H. galeatus, P. vulnus, and P. scribneri in Missouri cotton fields and the first report of R. reniformis and P. vulnus in Missouri. The known cotton pathogens M. incognita, R. reniformis, and H. galeatus were found in 30%, 3%, and 2% of the fields sampled, respectively. The correlation between sand content of the soil sample and the number of vermiform M. incognita in the sample was not significant, with r(2) = 0.13. Select fields where H. galeatus and R. reniformis were found in 1990 were sampled more intensely in 1991. The 1-ha block sampled in 1990 was sampled in 1991, along with three other 1-ha blocks uniformly distributed within the field. In addition, a 1-ha block was sampled in each of eight nearby fields, within 2 km of the first field. The nine plant-parasitic nematode genera identified in the 1990 survey were observed again in 1991. Within-field distribution of M. incognita, R. reniformis, and H. galeatus was not uniform. When M. incognita, R. reniformis, or H. galeatus were present in a field, the same species was found in 38%, 25%, or 50% of nearby fields, respectively.

12.
Am J Respir Cell Mol Biol ; 2(3): 257-61, 1990 Mar.
Article in English | MEDLINE | ID: mdl-2138022

ABSTRACT

The contribution of lung glucose-6-phosphate dehydrogenase (G-6-PD) activity to pulmonary antioxidant defenses was investigated in the isolated perfused rabbit lung using dehydroepiandrosterone (DHEA), a specific steroidal inhibitor of G-6-PD. Infusion of xanthine oxidase (0.002 U/ml) generated moderate lung edema as measured by increased lung weight and lung lavage albumin content. Infusion of DHEA caused an augmentation of xanthine oxidase-induced lung edema. Hydrostatic factors did not participate in the worsened lung edema because mean pulmonary artery pressures were similar in both experimental groups. Incubation of lung tissue in vitro with DHEA demonstrated ablation of tissue G-6-PD activity without decreasing catalase, glutathione peroxidase, or superoxide dismutase activity. It was concluded that DHEA is a specific inhibitor of lung G-6-PD, and that G-6-PD provides an important antioxidant defense mechanism in preventing oxidant-induced lung injury.


Subject(s)
Dehydroepiandrosterone/pharmacology , Guanine Nucleotides/antagonists & inhibitors , Guanosine Diphosphate/antagonists & inhibitors , Lung/enzymology , Pulmonary Edema/metabolism , Animals , Organ Size , Oxidation-Reduction , Rabbits , Xanthine Oxidase/pharmacology
14.
Chest ; 96(3): 477-9, 1989 Sep.
Article in English | MEDLINE | ID: mdl-2766807

ABSTRACT

It is a common practice for some clinicians to obtain a chest roentgenogram immediately following FOB in an attempt to detect complications of the procedure, particularly pneumothorax; however, the roentgenogram adds substantially to the cost of FOB. It was our clinical impression that the diagnostic and therapeutic value of immediate chest roentgenography was minimal. Therefore, we reviewed 130 chest roentgenograms taken immediately after bronchoscopy that were obtained over 36 months. One hundred fourteen (88 percent) were unchanged from the most recent roentgenogram before bronchoscopy. Ten (8 percent) showed an increase in alveolar infiltrate due to bronchoalveolar lavage or hemorrhage. Five (4 percent) had changes presumably unrelated to the procedure. Only one patient had a pneumothorax on the roentgenogram taken immediately after bronchoscopy; however, the patient was symptomatic, and the pneumothorax was detected by fluoroscopy prior to the chest roentgenogram. Management of the patient's condition was not altered in a single case based upon findings on the chest roentgenogram. We conclude that the immediately postbronchoscopic chest roentgenogram rarely provides clinically useful information or detects a complication that is not suspected clinically; furthermore, it appears to have minimal impact, if any, on the management of a patient's condition.


Subject(s)
Bronchoscopy , Pneumothorax/diagnostic imaging , Radiography, Thoracic , Bronchoscopy/adverse effects , Costs and Cost Analysis , Humans , Pneumothorax/etiology , Time Factors
15.
Chest ; 94(5): 1093-4, 1988 Nov.
Article in English | MEDLINE | ID: mdl-3053061

ABSTRACT

We report the findings in a patient who developed Horner's syndrome as the first manifestation of mediastinal migration of a central venous catheter that resulted in hydromediastinum and hydrothorax. The pathogenesis of this complication of central venous catheterization is discussed.


Subject(s)
Catheterization, Central Venous/adverse effects , Foreign Bodies/complications , Foreign-Body Migration/complications , Horner Syndrome/etiology , Mediastinal Diseases/etiology , Humans , Hydrothorax/etiology , Male , Middle Aged
17.
Cancer ; 60(7): 1545-7, 1987 Oct 01.
Article in English | MEDLINE | ID: mdl-2441844

ABSTRACT

Previous reports indicate that enlarged hilar and mediastinal lymph nodes due to sarcoid-like reactions may develop after curative resection of testicular cancer, and their presence does not necessarily denote neoplastic recurrence. Reports further suggest that coexisting pulmonary nodules in this setting may be related to nodular sarcoidosis. A patient developed progressive hilar and mediastinal adenopathy associated with multiple pulmonary nodules after apparent curative resection of a testicular embryonal cell cancer. Biopsy specimens from the mediastinal lymph nodes demonstrated granulomas, suggesting the diagnosis of nodular sarcoidosis. Needle aspiration of the pulmonary nodules, however, revealed metastatic testis cancer. Sarcoid-like mediastinal reactions occur after resection of testis cancer, but biopsies should be performed on coexisting pulmonary nodules to exclude pulmonary metastases.


Subject(s)
Lymph Nodes/pathology , Lymphoma/complications , Testicular Neoplasms/complications , Adult , Biopsy, Needle , Bleomycin/therapeutic use , Cisplatin/therapeutic use , Diagnosis, Differential , Granuloma/pathology , Humans , Lung Neoplasms/secondary , Lymphoma/drug therapy , Lymphoma/pathology , Male , Orchiectomy , Podophyllotoxin/therapeutic use , Sarcoidosis/diagnosis , Teratoma/complications , Teratoma/pathology , Testicular Neoplasms/diagnosis , Testicular Neoplasms/pathology
20.
J Cell Biol ; 56(3): 659-65, 1973 Mar.
Article in English | MEDLINE | ID: mdl-4734569

ABSTRACT

Normal and transformed baby hamster kidney (BHK) cells attach to Falcon polystyrene with the same first order rate constant. The longer the cells are attached to the bottles, the more difficult they are to remove. Sulfhydryl (-SH) binding reagents inhibit both the attachment of BHK cells and the increase in adhesive strength of attached cells. Attached BHK cells bind fewer molecules of [1-(14)C]N-ethylamleimide (an -SH binding reagent) than do suspended cells. Incubation of cells with high concentrations of trypsin results in a reversible loss of cell adhesiveness. The recovery of adhesiveness of trypsin-treated cells is inhibited by cycloheximide.


Subject(s)
Cell Adhesion , Cell Line , Animals , Cell Adhesion/drug effects , Cricetinae , Cycloheximide/pharmacology , Dithiothreitol/pharmacology , Ethylmaleimide/pharmacology , Kidney , Polystyrenes , Sulfhydryl Reagents/pharmacology , Trypsin/pharmacology
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