RESULTS OF TREATMENT OF CARCINOMA OF THE ESOPHAGUS BY THE COMBINED USE OF RADIUM EMANATIONS AND THE DEEP ROENTGEN RAY: REPORT OF SIXTEEN PATIENTS TREATED AT THE MASSACHUSETTS GENERAL HOSPITAL AND THE HUNTINGTON MEMORIAL HOSPITAL

Author(s):  
D. C. GREENE
PEDIATRICS ◽  
1953 ◽  
Vol 11 (3) ◽  
pp. 304-305

Announcement is made of a 2 Week Postgraduate Course in General Pediatrics, Burnham Memorial Hospital for Children, Massachusetts General Hospital, Boston, under the auspices of the Harvard Medical School, June 8 through June 20, 1953. Clinics providing a broad review of pediatrics emphasizing the new advances will be given daily from 9:00 A.M. to 4:30 P.M. by selected authorities from the Pediatric and Specialty Services of the Massachusetts General Hospital and the Children's Medical Center, Boston.


Author(s):  
Adam Yala ◽  
Peter G. Mikhael ◽  
Fredrik Strand ◽  
Gigin Lin ◽  
Siddharth Satuluru ◽  
...  

PURPOSE Accurate risk assessment is essential for the success of population screening programs in breast cancer. Models with high sensitivity and specificity would enable programs to target more elaborate screening efforts to high-risk populations, while minimizing overtreatment for the rest. Artificial intelligence (AI)-based risk models have demonstrated a significant advance over risk models used today in clinical practice. However, the responsible deployment of novel AI requires careful validation across diverse populations. To this end, we validate our AI-based model, Mirai, across globally diverse screening populations. METHODS We collected screening mammograms and pathology-confirmed breast cancer outcomes from Massachusetts General Hospital, USA; Novant, USA; Emory, USA; Maccabi-Assuta, Israel; Karolinska, Sweden; Chang Gung Memorial Hospital, Taiwan; and Barretos, Brazil. We evaluated Uno's concordance-index for Mirai in predicting risk of breast cancer at one to five years from the mammogram. RESULTS A total of 128,793 mammograms from 62,185 patients were collected across the seven sites, of which 3,815 were followed by a cancer diagnosis within 5 years. Mirai obtained concordance indices of 0.75 (95% CI, 0.72 to 0.78), 0.75 (95% CI, 0.70 to 0.80), 0.77 (95% CI, 0.75 to 0.79), 0.77 (95% CI, 0.73 to 0.81), 0.81 (95% CI, 0.79 to 0.82), 0.79 (95% CI, 0.76 to 0.83), and 0.84 (95% CI, 0.81 to 0.88) at Massachusetts General Hospital, Novant, Emory, Maccabi-Assuta, Karolinska, Chang Gung Memorial Hospital, and Barretos, respectively. CONCLUSION Mirai, a mammography-based risk model, maintained its accuracy across globally diverse test sets from seven hospitals across five countries. This is the broadest validation to date of an AI-based breast cancer model and suggests that the technology can offer broad and equitable improvements in care.


PEDIATRICS ◽  
1952 ◽  
Vol 9 (5) ◽  
pp. 656-657

Pediatric Postgraduate Course, Burnham Memorial Hospital for Children, Massachusetts General Hospital, Boston, June 9 through June 21, 1952. Daily from 9:00 A.M. to 4:30 P.M. under the auspices of the Harvard Medical School. Clinics providing a broad review of pediatrics emphasizing the new advances will be given by selected authorities from the Children's Medical, Endocrine, Cardiac, Neuro-Surgical, Thoracic Surgical, General Surgical, Orthopedic, Allergy, Child Psychiatry, Tumor and Rheumatic Services of the Massachusetts General Hospital, from the Ophthalmological and Otolaryngological Services of the Massachusetts Eye and Ear Infirmary and from the Children's Medical Center, Boston.


Author(s):  
Ronald S. Weinstein ◽  
N. Scott McNutt

The Type I simple cold block device was described by Bullivant and Ames in 1966 and represented the product of the first successful effort to simplify the equipment required to do sophisticated freeze-cleave techniques. Bullivant, Weinstein and Someda described the Type II device which is a modification of the Type I device and was developed as a collaborative effort at the Massachusetts General Hospital and the University of Auckland, New Zealand. The modifications reduced specimen contamination and provided controlled specimen warming for heat-etching of fracture faces. We have now tested the Mass. General Hospital version of the Type II device (called the “Type II-MGH device”) on a wide variety of biological specimens and have established temperature and pressure curves for routine heat-etching with the device.


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