Uterine autotransplantation in cynomolgus macaques: the first case of pregnancy and delivery

BACKGROUND

For women with congenital uterine infertility, or for those who have undergone hysterectomy, uterine transplantation is one of the potential treatments to regain fertility. In this study, we utilized a primate model of uterine transplantation, and evaluated the patency of our microsurgical anastomoses, and the perfusion of the transplanted uterus.

METHODS

Two female cynomolgus monkeys underwent surgery. We anastomosed two arteries and one vein in Case 1 and two arteries and two veins in Case 2. The arteries used were the uterine arteries and the anastomosis was done to the external iliac artery. We used one of the ovarian veins in both animals, but resected the ovary from the Fallopian tube. Uterine arterial blood flow and uterine size were determined by intraoperative indocyanine green (ICG) angiography and ultrasonography. The biopsy of the uterine cervix was performed after surgery.

RESULTS

ICG angiography showed that the unilateral uterine artery perfused the bilateral uterine bodies and cervix. In Case 1, ICG angiography showed the occlusion of one of the anastomosed arteries during the operation and the uterus appeared atrophied 2 months after operation. In Case 2, the transplanted uterus survived and normal menstruation occurred. The animal achieved a natural pregnancy and was delivered by the Caeserean section due to early separation of the placenta. The newborn suffered fetal distress.

CONCLUSIONS

These results show the anastomosis of at least the bilateral uterine arteries and the unilateral ovarian vein is required for uterus transplantation. This is the first report of a natural pregnancy in a primate following uterine autotransplantation.

Source:
http://humrep.oxfordjournals.org/rss/current.xml

Lesion kinetics in a non-human primate model of endometriosis

BACKGROUND

Endometriosis is a common cause of pelvic pain and infertility in women of reproductive age. It is characterized by the presence of endometrial tissue outside the normal location, predominantly in the pelvic peritoneum causing severe abdominal pain. However, the severity of the symptoms of endometriosis does not always correlate with the anatomic severity of the disease. This lack of correlation may be due to morphological lesion variation during disease progression. This study examined lesion kinetics in a non-human primate model of endometriosis to better understand lesion dynamics.

METHODS

Endometriosis was experimentally induced in nine normal cycling female adult olive baboons (Papio anubis) by i.p. inoculation of autologous menstrual endometrium on Day 2 of menses for two consecutive menstrual cycles. Diagnostic laparoscopies were performed between Day 8–12 post-ovulation at 1, 3, 6, 9 and 12 months, followed by a necropsy at 15 months, after the second inoculation. In two animals, lesions were excised/ablated at 6 months and they were monitored for lesion recurrence and morphological changes by serial laparoscopy. Furthermore, five control animals underwent surgeries conducted at the same time points but without inoculation.

RESULTS

A total of 542 endometriotic lesions were observed. The location, macroscopic (different colours) and microscopic appearance confirmed distinct endometriosis pathology in line with human disease. The majority of the lesions found 1 month after tissue inoculation were red lesions, which frequently changed colour during the disease progression. In contrast, blue lesions remained consistently blue while white lesions were evident at the later stages of the disease process and often regressed. There were significantly lower numbers of powder burn, blister and multicoloured lesions observed per animal in comparison to black and blue lesions (P-value ≤ 0.05). New lesions were continually arising and persisted up to 15 months post-inoculation. Lesions reoccurred as early as 3 months after removal and 69% of lesions excised/ablated had reoccurred 9 months later. Interestingly, endometriotic lesions were also found in the non-inoculated animals, starting at the 6-month time point following multiple surgeries.

CONCLUSIONS

Documentation of lesion turnover in baboons indicated that lesions changed their colour from red to white over time. Different lesion types underwent metamorphosis at different rates. A classification of lesions based on morphological appearance may help disease prognosis and examination of the effect of the lesion on disease symptoms, and provide new opportunities for targeted therapies in order to prevent or treat endometriosis. Surgical removal of endometriotic lesions resulted in a high incidence of recurrence. Spontaneous endometriosis developed in control baboons in the absence of inoculation suggesting that repetitive surgical procedures alone can induce the spontaneous evolution of the chronic disease. Although lesion excision/ablation may have short-term benefits (e.g. prior to an IVF cycle in subfertile women), for long-term relief of symptoms perhaps medical therapy is more effective than surgical therapy.

Source:
http://humrep.oxfordjournals.org/rss/current.xml

The value of MRI in assessing parametrial involvement in endometriosis

STUDY QUESTION

What is the accuracy of magnetic resonance imaging (MRI) in the diagnosis of parametrial endometriosis in comparison with surgicopathological findings?

SUMMARY ANSWER

MRI displayed an accuracy of 96.4% in the preoperative diagnosis of parametrial involvement by deep infiltrating endometriosis (DIE).

WHAT IS KNOWN AND WHAT THIS PAPER ADDS

MRI is the best technique for preoperative mapping of DIE. This preliminary paper shows that T2-weighted MRI is a valuable tool for the preoperative evaluation of parametrial involvement by endometriosis.

DESIGN

A retrospective study of an MRI database was used to identify examinations performed in women, who had a clinical suspicion of pelvic endometriosis (n = 666), between 2005 and 2009 in a university medical centre in France.

PARTICIPANTS AND SETTING

Exclusion criteria were previous surgery for DIE, incomplete surgical evaluation, repeat MRI examinations and incomplete MR protocol. Only symptomatic patients who underwent surgery with a pathological correlation were included (n = 83). An experienced radiologist, blind to the surgical and histological findings, evaluated sagittal, axial and thin-section oblique axial MR images obtained from the 83 patients.

DATA ANALYSIS METHOD

Descriptive statistics and Fisher exact test were used.

MAIN FINDINGS

The prevalence of DIE and parametrial endometriosis was 76/83 (91.6%) and 12/83 (14.5%), respectively. The sensitivity, specificity, positive and negative predictive values, accuracy and positive and negative likelihood ratios for the diagnosis of parametrial endometriosis of low signal intensity on T2-weighted MRI, pelvic wall involvement and ureteral dilatation, were 83.3%, 98.6%, 90.9%, 97.2%, 96.4%, 59.2 and 0.17, 58.3%, 98.6%, 87.5%, 93.3%, 92.8%, 41.4 and 0.42 and 16.7%, 100%, 100%, 87.7%, 88%, infinity and 0.83, respectively, with the patient as the unit of analysis.

BIAS AND LIMITATIONS

The study design was retrospective, and thus prone to bias. Only one experienced reader performed the analysis, so no data are available on intra- or interobserver variability.

GENERALISABILITY

At present, no consensus exists on the optimal MR protocol to be used for the evaluation of DIE, thus limiting the wider implications of this study.

STUDY FUNDING AND COMPETING INTERESTS

No funding was obtained for this study. The authors have no conflict of interest.

Source:
http://humrep.oxfordjournals.org/rss/current.xml

Does this woman have adnexal torsion?

BACKGROUND

No questionnaire is currently available for the presurgical diagnosis of adnexal torsion (AT). Our objective was to develop a predictive model for AT, based on the Self Assessment Questionnaire for Gynecologic Emergencies (SAQ-GE) designed for triaging women with acute pelvic pain.

METHODS

We performed a multicenter prospective trial conducted in five hospitals in France. Four hundred and ninety-six (496) women with acute pelvic pain (Numeric Rating Scale >4), including 31 with AT, were recruited from September 2006 through April 2008. An AT score was built using the SAQ-GE.

RESULTS

Five criteria were independently associated with AT confirmed by surgery: unilateral lumbar or abdominal pain [adjusted diagnostic odds ratio (aDOR), 23.3; 95% confidence interval (95% CI), 3.0–178]; absence of leucorrhea and metrorrhagia (aDOR, 7.0; 95% CI, 2.5–20), ovarian pain (aDOR, 5.5; 95% CI, 1.5–21), unbearable pain (aDOR, 5.0; 95% CI, 1.4–18) and vomiting (aDOR, 3.7; 95% CI, 1.6–9.0). The SAQ-GE torsion score was based on these five criteria and its values range from 0 to 10. The low-risk group (SAQ-GE torsion score <7), based on the score values, has a sensitivity (Se) of 96.7% (95% CI, 90.5–100), a negative predictive value of 99.7% (95% CI, 99.1–100) and a negative likelihood ratio (Lr–) of 0.05, ruling out AT with a probability of AT of 0.3% (95% CI, 0.0–0.9). Cross-validation of the model was performed using the jackknife resampling procedure, retrieving an unbiased Se of 87.1 (95% CI, 75.1–99.1) and a specificity of 74.2% (95% CI, 70.2–78.2).

CONCLUSIONS

The SAQ-GE torsion score may prove useful for screening for AT in patients experiencing acute pelvic pain.

Source:
http://humrep.oxfordjournals.org/rss/current.xml

The use of follicle flushing during oocyte retrieval in assisted reproductive technologies: a systematic review and meta-analysis

STUDY QUESTION

Does follicular flushing during assisted reproductive technologies (ART) improve the number of oocytes retrieved?  

SUMMARY ANSWER

Follicular flushing during ART does not result in a greater number of oocytes in normal responders.

WHAT IS KNOWN ALREADY

Despite limited evidence supporting the use of follicular flushing, it continues to be a common procedure in many ART clinics. Prior studies have provided conflicting results regarding the routine use of flushing during oocyte retrieval.

STUDY DESIGN, SIZE, DURATION

Systematic review and meta-analysis of 518 patients who participated in 6 randomized trials over 20 years.

PARTICIPANTS/MATERIALS, SETTING, METHODS

Literature searches were conducted to retrieve randomized controlled trials on follicle or ovarian flushing in ART. Databases searched included PubMed, EMBASE, Web of Science and the Cochrane Database of Clinical Trials (CENTRAL). Six trials that included 518 subjects matched the inclusion criteria. Studies included were limited to trials that were published, randomized trials comparing oocyte retrieval with a single-lumen pick-up needle versus follicle flushing after direct aspiration with a multi-channel oocyte pick-up needle in ART patients.

MAIN RESULTS AND THE ROLE OF CHANCE

In each of the trials, measures of the oocyte yield (oocytes retrieved divided by follicles aspirated), total oocytes retrieved, fertilization or pregnancy were not different when comparing direct aspiration with follicle flushing. Four trials reported a higher operative time with follicle flushing. Results of the meta-analysis indicated no significant differences in the oocytes retrieved [weighted mean difference: 0.07, 95% confidence interval (CI): –0.13 to 0.29] or the oocyte yield (odds ratio: 1.06, 95% CI: 0.95–1.18) between the non-flushing and flushing groups.

LIMITATIONS, REASONS FOR CAUTION

All trials featured an open label design and the majority of patients in this meta-analysis were normal responders. The applications of these results to poor responders, patients undergoing natural cycle ART or minimal stimulation ART should be made with caution.

WIDER IMPLICATIONS OF THE FINDINGS

Follicle flushing does not improve ART outcomes in normal-responding patients and should not be performed. This meta-analysis should solidify this recommendation as it includes the largest trial published on the subject and is consistent with a recently published Cochrane review.

STUDY FUNDING/COMPETING INTEREST(S)

This work was supported, in part, by the Program in Reproductive and Adult Endocrinology, NICHD, NIH, Bethesda, MD. The authors have no competing interests to declare.

TRIAL REGISTRATION NUMBER

N/A.

Source:
http://humrep.oxfordjournals.org/rss/current.xml

The impact of the new Turkish regulation, imposing single embryo transfer after assisted reproduction technology, on neonatal intensive care unit utilization: a single center experience

OBJECTIVES AND AIM

IVF has become an efficient and widely used treatment for infertile couples, however, it is responsible for an increasing number of multifetal pregnancies and adverse neonatal outcomes. This study aimed to assess a health service utilization in one neonatal intensive care unit (NICU), as a response to the 2010 Turkish reproductive regulation requiring single embryo transfer (SET).

METHODS

All assisted reproductive technology (ART) pregnancies delivered at Zekai Tahir Burak Maternity Teaching Hospital between February 2010 and October 2011 were included in this study. Subjects were divided into two groups: Group 1 consisted of infants conceived before the ART regulation, and born between February 2010 and October 2010, and Group 2 consisted of infants conceived after the ART regulation, and born between November 2010 and October 2011.

RESULTS

Upon comparing the study groups, we observed a significant decrease in the incidence of multiple births in Group 2. The mean gestational age and mean birthweight were significantly higher in Group 2. The rates of prematurity and low birthweight, very low birthweight and extremely low birthweight infants were significantly lower in Group 2. Similarly, the rates of NICU admission, respiratory distress syndrome, necrotizing enterocolitis anemia and pneumonia/sepsis, and the need for respiratory support (mechanical ventilation and nasal continuous positive airway pressure) were significantly lower in Group 2.

CONCLUSIONS

According to our data, NICU utilization was reduced and the early post-natal outcomes of the babies were improved after the new Turkish regulation on ART imposing SET. However, multicenter studies are needed to generalize our results to the whole country.

Source:
http://humrep.oxfordjournals.org/rss/current.xml

The impact of IVF/ICSI on parental well-being and anxiety 1 year after childbirth

BACKGROUND

More couples are delaying childbirth resulting in an increase of age-related subfertility in women. Subfertility and assisted reproductive technology (ART) treatments may affect couples' psychological well-being. The aim of the present study was to investigate whether factors related to IVF/ICSI affect anxiety and mental health in couples 1 year after childbirth.

METHOD

In this cohort study, we included couples with a singleton pregnancy following IVF/ICSI treatment (n = 113) and subfertile couples who naturally conceived (NC; n = 83). Parental trait anxiety (Dutch version of the Spielberger State-Trait Anxiety Inventory) and mental health (Dutch version of General Health Questionnaire) were assessed 1 year after childbirth. The influence of fertility-related factors was analyzed with logistic regression analyses.

RESULTS

One hundred and ninety-six couples participated, 93% of those eligible. Trait anxiety and mental health were similar in IVF/ICSI and NC groups. However, NC fathers had more often mental health scores in the clinical range (21%) than fathers in the IVF/ICSI group (9%). The risk of having a trait anxiety or mental health score in the clinical range was reduced by the presence of one of the following factors: for females a higher number of IVF/ICSI treatment cycles, and a maternal cause of subfertility, for males having been treated by IVF/ICSI and a longer time to pregnancy.

CONCLUSIONS

The present study indicates (i) that IVF/ICSI treatment is not associated with an increase in clinically relevant Spielberger State-Trait Anxiety Inventory and General Health Questionnaire scores in parents 1 year after childbirth and (ii) a higher number of IVF/ICSI treatment cycles and a longer time to pregnancy were associated with less trait anxiety and better mental health. A limitation of the study is the absence of mental health and trait anxiety data at baseline.

Source:
http://humrep.oxfordjournals.org/rss/current.xml

The FAST study: Fertility ASsessment and advice Targeting lifestyle choices and behaviours: a pilot study

BACKGROUND

Lifestyle has been shown to affect fertility in both males and females, with compelling evidence that smoking and being under or overweight impairs natural and assisted fertility, and other factors such as stress and caffeine have also been implicated. The objective of this study was to determine whether providing infertile couples with individualized lifestyle assessments and ongoing support facilitates positive lifestyle changes enhancing healthy fertility.

METHODS

We conducted a prospective cohort pilot study of 23 infertile couples attending an Adelaide-based fertility clinic for advice and treatment relating to infertility. The intervention was a comprehensive assessment interview with the couple, focused on health and lifestyle. Motivational interviewing techniques were used and ongoing support provided. The assessment was repeated after 4 months and included an exit questionnaire. The main outcome measure(s) was self-reported lifestyle changes, including increased exercise, modified diet, reduced caffeine and alcohol consumption, ceased or reduced smoking and decreased psychological stress.

RESULTS

Following the initial lifestyle assessment interview, all participants reported adverse lifestyle behaviour.

CONCLUSIONS

The results suggest that the FAST (Fertility ASsessment and advice Targeting lifestyle choices and behaviours) approach of an individualized assessment of current lifestyle practice followed by ongoing one to two weekly telephone support is effective in promoting healthy lifestyle change. Larger studies using this methodology are now required.

Source:
http://humrep.oxfordjournals.org/rss/current.xml

Childless Canadian men’s and women’s childbearing intentions, attitudes towards and willingness to use assisted human reproduction

STUDY QUESTION

What are the childbearing intentions of currently childless men and women? What is their attitude towards, and willingness to use, assisted human reproduction (AHR) treatments and family-building options should they be faced with fertility challenges in the future?

SUMMARY ANSWER

Men and women expect to become parents significantly later in life than they believe is ideal. If faced with future fertility challenges, respondents were open to using IVF, but were not positively predisposed to third-party family-building options.

WHAT IS KNOWN ALREADY

Delayed childbearing is an increasing worldwide phenomenon that has considerable health and fertility-related implications. Research to date has focused primarily on women, and indicates a lack of knowledge about the fertility life span and the limitations of AHR in fully compensating for age-related fertility declines.

STUDY DESIGN, SIZE, DURATION

Cross-sectional study of 2000 childless women and 599 childless men, conducted between April 2010 and May 2011.

PARTICIPANTS/MATERIALS, SETTING, METHODS

A total of 2599 childless, presumed fertile individuals between the ages of 20 and 50 years. An online questionnaire assessed fertility beliefs and intentions and willingness to use AHR.

MAIN RESULTS AND THE ROLE OF CHANCE

The findings indicate that men and women expect to become parents significantly later in life than they believe is ideal. If faced with fertility challenges in the future, both men and women were open to using IVF. Men were significantly more willing to consider using donated eggs and embryos, gestational surrogacy and fertility preservation. Women were significantly more willing to consider using home fertility testing, IVF, ICSI and donor sperm. Overall, the childless respondents were not positively predisposed to third party-family-building options.

LIMITATIONS

The geographic specificity of the sample, the online format and recruitment methods may limit the generalizability of these findings.

WIDER IMPLICATIONS OF THE FINDINGS

Given the worldwide trend towards delayed childbearing, and the widespread availability of AHR, it is likely that these findings could extend to the wider North American, European and Australasia populations of English- and French-speaking childless men and women. However, it should be noted that international differences exist, especially concerning regulations governing the funding of AHR and payment for gametes and surrogacy. It is significant that women and men in this study indicated a lack of willingness to consider the use of third third-party treatments—the very options they may need to use in building their families, if the increasing trend towards delayed childbearing continues.

STUDY FUNDING/COMPETING INTERESTS

This research was funded by a grant from the Canadian Institutes of Health Research and Assisted Human Reproduction Canada #PAH-103594, 2009/10. No competing interests.

Source:
http://humrep.oxfordjournals.org/rss/current.xml

Spontaneous conceptions following successful ART are not associated with premature referral

STUDY QUESTION

What is the rate of spontaneous live births after successful IVF treatment in a cost-free environment, and were couples who achieved a spontaneous live birth referred prematurely?

SUMMARY ANSWER

Despite unlimited IVF treatments offered free of charge, the spontaneous live birth rate following successful IVF remained unchanged compared with that cited in previous literature. Couples were not referred prematurely to IVF before fully utilizing other less invasive treatments.

WHAT IS KNOWN ALREADY

A significant number of infertile couples, who achieve their first live birth through assisted reproductive technology (ART), subsequently achieve a second live birth spontaneously. As IVF has become more widely available, it is used in less severe cases of infertility, perhaps explaining a rise in the subsequent spontaneous live birth rate after successful treatments.

STUDY DESIGN, SIZE, DURATION

This retrospective cohort study was performed at a university-based tertiary medical center. The study population included women aged <35 years, with primary infertility, referred for their first IVF treatment to the Sheba Medical Center IVF unit between 2001 and 2002 and followed up for 7 years. The primary outcome was spontaneous live birth rate following successful ART. Relevant data were obtained from the patient files and supplemented by a standardized telephone questionnaire.

PARTICIPANTS/MATERIALS, SETTING, METHODS

Of the 171 couples who met the study inclusion criteria, 6 refused to participate in the questionnaire and 31 couples were lost to follow-up. Of the 134 couples who participated, 109 achieved a first live birth with ART. After achieving their first live birth with ART, seven couples who began using contraception or separated or divorced were excluded.

MAIN RESULTS AND THE ROLE OF CHANCE

Of 102 couples who continued unprotected intercourse after successful ART, 22 subsequently achieved their second live birth spontaneously (21.6%). The women who achieved a second birth spontaneously were not referred earlier to IVF, and actually performed a higher number of ovulation induction cycles before initiating IVF, compared with women who did not conceive spontaneously.

LIMITATIONS, REASONS FOR CAUTION

This is a retrospective cohort study, and findings should be reaffirmed with a larger prospective randomized study comparing retreatment to achieve a second pregnancy with attempting to conceive spontaneously.

WIDER IMPLICATIONS OF THE FINDINGS

Our data suggests that young patients (<35 years), who previously conceived with IVF, without utilizing ICSI and with no known tubal pathology, should consider attempting to conceive spontaneously.

STUDY FUNDING AND COMPETING INTEREST(S)

No funding was obtained for this study and the authors have no competing interests.

Source:
http://humrep.oxfordjournals.org/rss/current.xml

Digital Pathology FAQs

Courtesy of the Digital Pathology Association.

Answers to many key questions you may have been afraid of asking.

1. Q: Is digital pathology FDA approved for primary diagnosis?  

A: No, digital pathology is not FDA approved for primary diagnosis.  However, several manufacturers have received 510(k) clearances or specific uses.  Please refer to theregulatory page for more information.  

2. Q: What CPT codes can apply to digital pathology?

 A: (Reference chart below) 

CPT CODE(S)DESCRIPTIONDIGITAL PATHOLOGY APPLICATION
88300-88309Accession, examination, and reporting of gross and microscopicPrimary Diagnosis preformed on whole slide images*
88321Consultation and report on referred slides prepared elsewhereSecond opinion consultations preformed on whole slide images
88323Consultation and report on referred material requiring preparation of slidesSecond opinion consultations on whole slide images
88329, 88331, 88332Pathology consultation during surgery, frozen sectionFrozen section consultation preformed via live telepathology or on whole slide images
88360, 88361Morphometric analysis, tumor immunohistochemistry (eg. Her-2/neu, ER/PR), quantitative or semiquantitative, each antibody, manual or using computer assisted technologyManual or computer- assisted analysis of HER2, ER/PR, Ki-67, p53, etc**
88365, 88367, 88368In situ hybridization (eg. FISH), morphometric analysis (quantitative or semi-quantitative), manual or using computer assisted technology for each probeManual or computer assisted analysis of FISH*

*No manufacturers at this time are FDA approved for primary diagnosis. Refer to the Regulatory page for more information.  
** Some manufacturers have obtained 510(k) clearances for manual and/or quantitative analysis of Immunohistochemistry and/or FISH.  Please refer to the 510(k) clearance list [link to page] and the Regulatory page for more information.

3. Q: Do I need to validate my digital pathology system for clinical use? 
A: It is recommended by the College of American Pathologists (CAP), a CLIA accredited organization, that all institutions or practices considering the implementation of digital pathology for clinical diagnostic purposes must carry out their own validation.  For more information please refer to the Regulatory page.

 4. Q: Do I need to preform a validation if I am only doing the professional component (PC) of the diagnosis? 

A: It is recommended by the College of American Pathologists (CAP), a CLIA accredited organization, that all institutions or practices considering the implementation of digital pathology for clinical diagnostic purposes must carry out their own validation. However, it is up to the institution or practice who has implemented the digital pathology system to determine the scope of the validation study; specifically what will and will not be included as an intended use. Refer to the institution preforming the technical component (TC) for information on their validation of the digital pathology system and weather it is validated for the professional component (PC) of a primary or secondary diagnosis.

5. Q: How can digital pathology benefit patients? 
A: Often pathologists do not meet the patients they serve.  However, digital pathology provides the tools and innovation necessary to bridge the gap between a patient, their diagnosis, and their pathologist.  Digital pathology can illustrate and document key findings within a patient diagnosis to promote better communication between pathologists, other physicians, and patients.  Examples include a digital image imbedded into the pathology report, the delivery of a prognostic score based on computer assisted quantitative analysis, whole slide images of a patient case being discussed at a tumor board, or simply improving the turnaround time of a patient diagnosis.

6. Q: Is viewing a whole slide image on a computer monitor the same as viewing a glass slide under a microscope?  
A: Many pathologists believe the viewing experience of a whole slide image is better then a microscope.  When you look through the eye pieces of a microscope you have a limited field of view and can only view one slide. With digital pathology you can see more slides and more of the tissue all at once. In addition you can move the slide around, change objectives, and even focus up and down through the tissue - just like a microscope!

7. Q: What is the file size of a whole slide image and how should they be managed? 
A: Most scanners support capture resolutions of 0.5 microns/pixel (effective viewing magnification: 20X) or 0.275 microns per pixel (effective viewing magnification: 40X). The image file associated with a 20X scan of a 15mmx20mm tissue specimen is as large as 3.6GB and a 40X scanned image can be as large as 14.5GB. The images are compressed to more manageable sizes (25:1 compression or greater) such that there is an optimization between image quality, image file size, network bandwidth usage, and server and client resource utilization. For example, the 20X scan could be stored in a JPEG2000-compression file of size 144MB. The 40X image described above could be stored in a JPEG2000-compressed file of size 576MB. Digital Pathology images are about 10X that of Radiology images and will require more storage management through their useful life cycle.  For more information on how they should be managed please refer to the DPA white paper “Archival and Retrieval in Digital Pathology Systems.” 

8. Q: Is cloud (SaaS) storage secure and fast for digital pathology? 
A: Yes, cloud technology or Storage as a Service (SaaS) is growing in popularity and offers some significant benefits for primary storage and for replication of data.  Cloud based storage can lower storage costs, maintain or improve security and data integrity including HIPPA compliance, improve flexibility, and expand capacity when capacity resources are strained.  More information on cloud replication of data is provided in the DPA white paper “Archival and Retrieval in Digital Pathology Systems.”

9. Q: Are whole slide images DICOM compatible? 
A: Yes, however digital pathology solution manufacturers must support DICOM Supplement 145: Whole Slide Microscopic Image IOD and SOP Classes, finalized by the DICOM Standards Committee, and Working Group 26 for Pathology in 2010.

10. Q: Is digital pathology HIPAA compliant? 
A: The metadata associated with a whole slide image, but not the whole slide image itself, can contain protected health information (PHI) which is at the center of HIPAA compliancy.  However, most digital pathology manufacturers can support a HIPAA compliant solution by encrypting PHI sensitive metadata such as slide labels, hospital / patient / case / specimen information, etc.  Furthermore, procedures must be in place to protect PHI within the digital pathology system to reduce the risk of unauthorized access to the computer system.

11. Q: How long does it take to scan a glass slide? 
A: Scan time is calculated by the time it takes to acquire the high resolution whole slide image of the tissue represented on the glass slide; most manufacturers have scan times  under 3 minutes a slide.  Scan time will typically include the overview image, focus, and acquisition of the whole slide image at either 0.5 microns/pixel (effective viewing magnification: 20X) or 0.275 microns per pixel (effective viewing magnification: 40X).  Scan time does not take into account post processing time, which is the time it may take to compress the image and transfer the image to a data management solution for viewing of the whole slide image remotely.  Other variables that contribute to variation in scan time include tissue size, capture resolution, if z-plane scanning is added, brightfield versus fluorescence, and the manufacturers specification since scan time will vary from scanner to scanner.

12. Q: Can whole slide images be integrated with my Laboratory Information System (LIS) or a snapshot put into my pathology report? 
A: Yes, the current state of integration between digital pathology systems (DPS) and anatomic pathology laboratory information systems (APLIS) provide pathologists with access to images and image analysis data from within the APLIS or the DPS. This information is then available to the Patient Report. More detailed information on this topic can be found in the DPA white paper “Interoperability between Anatomic Pathology Laboratory Information Systems and Digital Pathology Systems.”

 

Source:
http://feeds.feedburner.com/DigitalPathologyBlog

Telemedicine bill enables VA providers to practice across state lines

Courtesy of FierceHealthIT

By Dan Bowman  Comment |  Forward | Twitter | Facebook | LinkedIn

Telemedicine services for veterans get a shot in the arm in a new bipartisan supported bill introduced in the House last week.

The bill--the Veterans E-Health & Telemedicine Support (VETS) Act of 2012 (H.R. 6107)--would remove restrictions that currently prevent providers with the Department of Veterans Affairs from practicing across state lines if they aren't licensed in the same state as the patients they are treating. According to Glenn Thompson (R-Pa.), who introduced the bill along with Charles Rangel (D-N.Y.), veterans with mental health issues will benefit greatly from such a change.

"This bill enables the VA to expand key treatment services, including behavioral health, which is critical considering the department is facing increasing care demand and mounting provider shortages," Thompson said in a statement.

According to an announcement by Rangel, 11 other representatives have joined as co-sponsors of the bill, which also was endorsed by the American Telemedicine Association, the American Foundation for Suicide Prevention and Veterans of Foreign Wars.

The bill was proposed on the heels of the VA's announcement last week that it was launching a three-year, $15 million pilot to test the potential of providing long-distance specialty training and support to rural primary care providers who treat veterans, a program dubbed Specialty Care Access Network-Extension for Community Healthcare Outcomes (SCAN-ECHO).

Last month, the VA announced that it has set a goal of providing 200,000 remote consultations in 2012 through videoconferencing. And earlier in the year, the VA announced that it no longer would charge veterans a co-payment for any telehealth services.

To learn more:
- read the proposed bill (.pdf)
- here's Thompson's announcement
- here's Rangel's announcement

Related Articles:
VA telemedicine pilot has specialists training rural primary care docs
VA to boost remote mental health services
VA set to waive co-pays on telehealth visits
Telehealth helps single VA division save $742K

Read more about: Department of Veterans Affairstelemedicine

 

Source:
http://feeds.feedburner.com/DigitalPathologyBlog

Going glass to digital: virtual microscopy as a simulation-based revolution in pathology and laboratory science

Recent review article on whole slide imaging/virtual microscopy for use in education.

    Abstract

    The recent technological advance of digital high resolution imaging has allowed the field of pathology and medical laboratory science to undergo a dramatic transformation with the incorporation of virtual microscopy as a simulation-based educational and diagnostic tool. This transformation has correlated with an overall increase in the use of simulation in medicine in an effort to address dwindling clinical resource availability and patient safety issues currently facing the modern healthcare system. Virtual microscopy represents one such simulation-based technology that has the potential to enhance student learning and readiness to practice while revolutionising the ability to clinically diagnose pathology collaboratively across the world. While understanding that a substantial amount of literature already exists on virtual microscopy, much more research is still required to elucidate the full capabilities of this technology. This review explores the use of virtual microscopy in medical education and disease diagnosis with a unique focus on key requirements needed to take this technology to the next level in its use in medical education and clinical practice.

    J Clin Pathol doi:10.1136/jclinpath-2012-200665
    1. Danielle Nelson1
    2. Amitai Ziv2,3
    3. Karim S Bandali1

    1. 1The Michener Institute for Applied Health Sciences, Toronto, Ontario, Canada

    2. 2The Israel Center for Medical Simulation, Sheba Medical Center, Tel-Hashomer, Israel

    3. 3Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel
    1. Correspondence to: Dr Karim S Bandali, The Michener Institute for Applied Health Sciences, 222 St Patrick Street, Toronto, Ontario M5T 1V4, Canada; kbandali@michener.ca
    • Accepted 24 April 2012
    • Published Online First 12 July 2012

     

    Source:
    http://feeds.feedburner.com/DigitalPathologyBlog

    Seldom wrong, never in doubt

    MclogoThe need, impact, importance and disagreement rate for second opinion pathology referrals has been a constant topic of discussion for many years.  These second opinions generally come in two flavors.  The first is a consultation of a particularly challenging case by a pathologist or clinician.  Patients can also initiate these consults if they are uncomfortable with a diagnosis.  The second flavor is the review of pathology diagnoses of patients now seeking treatment at a new institution who were originally diagnosed by an outside pathologist from the referring institution.  The popular press contains many stories about misdiagnoses in patients and mismanagement until second opinion/expert review identified a problem with the original pathology review.  The pathology literature contains dozens of studies and meta-analyses looking at disagreement rates from referral centers looking at "us versus them", working off the notion that the second opinion/referral/expert diagnosis is "the right one", "the gold standard" or represents "the absolute truth" for treatment, management, outcomes measurements and classification for subsequent tissue/molecular studies.  In a similar, but distinctly different scenario, pathologists, clinicians and patients can each seek a "second opinion" or consultation on challenging cases or diagnoses they are uncomfortable with.

    Here is the typical scenario and how this works:

    SecondOpinion2"Most people never consider the possibility of getting a second opinion on the pathology report from which the diagnosis was made, but the entire plan of treatment depends on what kind of cancer you have and how far it has spread, both of which usually depend in part or whole on the pathologists interpretation of the biopsy or surgical specimen. Changes in the interpretation of the pathology can dramatically change both the treatment and the prognosis.

    At the same time, most patients probably do not need a second pathology opinion. There are some common sense cues that can let you know if it might make sense. I think that if you have a really rare cancer, it is always advisable to get a second pathology opinion.

    If your pathology report doesn't give a definite diagnosis, a second opinion is probably in order.

    Your hospital/group name here Pathology Department has the expertise to diagnose and classify all types of cancer, which helps oncologists choose the most effective treatment method for their patients. We provide second opinion evaluation of tissue samples submitted by physicians and pathologists for patients outside Your health care system name here.

    We have experts in a wide range of cancer subspecialties, including:

    • Breast
    • Dermatopathology
    • Gastrointestinal
    • Genitourinary
    • Gynecological
    • Head and neck
    • Neuropathology
    • Bone and soft tissue
    • Thoracic

    SecondopinionFees must be paid at time of the review. Many insurance carriers will reimburse the costs of second opinion consultations. If payment is a problem, we can work with you. Follow-up reviews are payable separately. Please remember that our service is for pathology second opinions only. We cannot discuss or recommend treatment options."

    Consultations in pathology are an integral and routine part of daily practice.  Except for the pathologist or the group that claims "I/we don't send anything out".  That person/group may not but informed patients/clinicians will.  As a resident I was warned if you don't show cases to others or get consults from external sources you are doing your patients and yourself a disservice.  

    Institutions/individuals who provide second opinion reads as part of or exclusively as their practice of pathology have from time to time, in many subspecialties made claims about disagreement rates that justify the practice for risk management and appropriate patient management with published disagreement rates from 2-5%, depending on the specimen tissue source or part type.  There is also the issue of defining what constitutes a "disagreement", although most studies cite a difference that would alter prognosis or treatment.

    Teleconsultations using whole slide imaging, as frequent readers know, I think are one of the many use cases/applications for digital pathology.  Mitigating slide handling issues, improving turn around time, retaining original glass slides onsite, reviewing cases with your consultant in real-time and education/training from external review at another site.

    A recent paper shows that, in general, there is a very high level of agreement among pathologists for secondary review of pathology for referral patients, in this study, a rate of 99.4% agreeement.  While small (0.6%), the diagnostic differences may be highly clinically significant, arguing that secondary review of pathology materials should be standard of care.  This high agreement rate should allay concerns of patients and clinicians (and perhaps some pathologists) alike regarding the value and consistency of diagnoses rendered by the pathology community at large.

    With such high agreement, why not digital pathology for second opinions/specimen review for patient referrals/slide review prior to additional surgery/treatment?

    And in some cases, with follow up case sharing, even outsmart the consultant?

    Ryan Swapp, M.D., Marie Christine Aubry, M.D., Diva Salomao, M.D., and John Cheville, M.D., all of Mayo Clinic’s Division of Anatomic Pathology, recently released a study, “Outside Case Review of Surgical Pathology for Referred Patients: The Impact on Patient Care,” that can now be found as an early online release in CAP Archives of Pathology & Laboratory Medicine.

    ChickenThe Division of Anatomic Pathology reviewed the pathology of nearly all patients that were referredto Mayo Clinic for treatment from 2005-2010. The objective was to identify the rate of major disagreements with diagnoses from external institutions and to characterize the nature and impact of discordant diagnoses on patient care.

    Interestingly, they also concede that that their review diagnosis was not always the correct one.

    Summary:  Major disagreements occurred only 0.6% of the time (457 of 71,811 cases) from 2005-2010.  The most frequent areas of disagreement were gastrointestinal (80 cases; 17.5%), lymph node (73;16.0%), bone/soft tissue (47; 10.3%), and genitourinary(43; 9.4%).  The disagreeing diagnosis was not always the correct one.  In a subset of these cases for which additional tissue was taken (n=86 disagreements from July 2009 – Dec 2010), this subsequent tissue showed that the original diagnosis was correct 15.1% of the time (13 of 86 cases).

    View Full Study

     

    Source:
    http://feeds.feedburner.com/DigitalPathologyBlog

    Detection and Segmentation of Cell Nuclei in Virtual Microscopy Images: A Minimum-Model Approach

    Automated image analysis of cells and tissues has been an active research field in medical informatics for decades but has recently attracted increased attention due to developments in computer and microscopy hardware and the awareness that scientific and diagnostic pathology require novel approaches to perform objective quantitative analyses of cellular and tissue specimens. Model-based approaches use a priori information on cell shape features to obtain the segmentation, which may introduce a bias favouring the detection of cell nuclei only with certain properties. In this study we present a novel contour-based “minimum-model” cell detection and segmentation approach that uses minimal a priori information and detects contours independent of their shape. This approach avoids a segmentation bias with respect to shape features and allows for an accurate segmentation (precision = 0.908; recall = 0.859; validation based on ?8000 manually-labeled cells) of a broad spectrum of normal and disease-related morphological features without the requirement of prior training.

    Full article


     

    Source:
    http://feeds.feedburner.com/DigitalPathologyBlog

    Digital Pathology Association Regulatory Committee Offerings

    The Digital Pathology Association has established a regulatory committee; the committee goal is to create a sense of urgency within regulatory agencies and to bring clarity to the digital pathology clearance and approval process. 

    At Pathology Visions 2011 a Regulatory Panel of experts convened with representatives from the U.S. Food and Drug Administration (FDA), the Centers for Medicaid and Medicare Services (CMS), and the College of American Pathologists (CAP).  The DPA regulatory committee presented a series of questions for the panel to address.  DPA members can view the panel experts presentations and the panel recording “Navigating Digital Pathology’s Path to Patients” within the Member Community.

    Choose one of categories below:

    FDA

    CMS/CLIA

    CAP

    FDA

    In the United States, technology manufactured for digital pathology (i.e. scanners, software) are considered medical devices and are regulated by the U.S. Food and Drug Administration (FDA). Manufacturers may market their digital pathology technology for Research Use Only (RUO) unless the FDA has issued a clearance or approval to a specific manufacturer and for an intended use of the digital pathology hardware and software.  Several manufacturers have received one or more FDA 510(k) clearances, however no manufacturer has yet received an FDA approval of their technology for primary diagnosis.
     
    The FDA remains focused on the safety and the effectiveness of digital pathology.  Safety is defined in 21 CFR 860.7(d)(1) as the “Reasonable assurance, based on valid scientific evidence, that the probable benefits to health from use of the device for its intended uses and conditions of use, when accompanied by adequate directions and warnings against unsafe use, outweigh any probable risks.”   Effectiveness is defined in 21 CFR 860.7(e)(1) as “Reasonable assurance, based on valid scientific evidence, that in a significant portion of the target population, the use of the device for its intended use and conditions of use, when accompanied by adequate directions for use and warning against unsafe use, will provide clinically significant results.”

    In October 2009 the FDA Hematology and Pathology Devices Panel held a meeting to gain expert opinion and industry feedback on the replacement of H&E glass slides and conventional microscopy by whole slide images (WSI), specifically for rendering a routine surgical pathology diagnosis of a disease or condition.  No formal guidance document has been issued by the FDA for digital pathology, however one is expected soon.  In the meantime the FDA has provided two guidance documents, IVD 
    Diagnostic products Labeled for Research Use Only and Mobile Medical Applications, that are relevant to digital pathology. 

    Pathology Visions 2011 Presentations (Members Only)
    - Regulatory Panel | Navigating Digital Pathology’s Path to Patients (Members Only)
    Digital Pathology 510(k) Clearances
    FDA October 2009 meeting materials and transcriptions
    - FDA issued guidance documents relevant to digital pathology
        1. IVD Diagnostic Products Labeled for RUO/IUO
        2. Mobile Medical Applications

    CMS/CLIA

    Centers for Medicare and Medicaid Services (CMS) oversees the Clinical Laboratory Improvement Amendments (CLIA) which regulate all non research, laboratory tests preformed on humans in the U.S. The goal of CLIA is to insure quality laboratory testing, and therefore quality control (QC) portions of CLIA will apply to digital pathology;  including the analytic phase of testing which requires monitoring the testing personnel, the test system, and the laboratory environment. Other requirements that apply to all testing include calibrations, establishing or verifying performance specifications, test system or equipment maintenance, test results comparisons, corrective actions, having a back-up plan for instrument failure, and a procedure manual.  Validation of a digital pathology system is also necessary, and labs should follow CLIA requirements for test reports. 

    In February 2012 Clinical Laboratory Improvement Advisory Committee (CLIAC) held a meeting which discussed emerging issues in digital pathology. CLIAC provides scientific and technical advice and guidance to the Secretary of Department of Health and Human Services (HHS); the Assistant Secretary for Health; the Director of Centers for Disease Control and Prevention (CDC); the Commissioner of the Food and Drug Administration (FDA); and the Administrator of the Centers for Medicare and Medicaid Services (CMS). The advice and guidance pertain to general issues related to improvement in clinical laboratory quality and laboratory medicine.  CLIAC may also provide advice and guidance on specific questions related to a possible revision of CLIA standards. 

    Validation of Digital Pathology in a Healthcare Environment
    Pathology Visions 2011 Presentations (Members Only)
    - Regulatory Panel | Navigating Digital Pathology’s Path to Patients (Members Only)
    Current CLIA Regulations
    Summary of CLIAC February 2012 Meeting

    CAP

    The College of American Pathologists (CAP) is a CLIA accredited organization composed of board-certified pathologists with a mission to serve patients, pathologists, and the public through the advocation of excellence in pathology and laboratory medicine worldwide. 

    CAP issues laboratory accreditation checklists which support the accreditation process.  The checklists align with the CLIA mandate of high quality laboratory testing by providing a solid foundation for excellence in patient safety, and compliance with policies, procedures, and laboratory processes.  The Anatomic Pathology, Laboratory General, and Cytopathology checklists have items that can apply to digital pathology systems.  

    In 2011 a CAP Center working group was formed to create guidelines for digital pathology.  Thirteen guidelines were developed to assist the pathology community with validating WSI for clinical diagnostic use.  The thirteen guidelines, which are still under development, were presented at Pathology Visions 2011.  The final version of the guidelines has not been issued but is expected soon.  

    Download the DPA white paper, Validation of Digital Pathology in a Healthcare Environment, for more specific information about the CAP checklist items and the draft guidelines. 

    Validation of Digital Pathology in a Healthcare Environment
    Pathology Visions 2011 Presentations (Members Only)
    - Regulatory Panel | Navigating Digital Pathology’s Path to Patients (Members Only)
    The College of American Pathologists' Laboratory Accreditation Program (CAP-LAP) Practical World View on Digital Pathology from a CLIA Accreditation Provider (Members Only)
    - Recommendations for Validating Whole Slide Imaging in Pathology: College of American Pathologists (CAP) Pathology and Laboratory Quality Center (Members Only)
    CAP Checklists

     

    Source:
    http://feeds.feedburner.com/DigitalPathologyBlog

    "Dissection on Display: Cadavers, Anatomists and Public Spectacle" by Christine Quigley, Book Review by Bess Lovejoy

    I am very excited to read the new and wonderful looking book Dissection on Display: Cadavers, Anatomists and Public Spectacle by Christine Quigley, who many of you might best know as editor of the wide-ranging blog Quigley's Cabinet. I have not yet had a chance to read the book, but we are all in luck, as friend of Morbid Anatomy Bess Lovejoy--author of the forthcoming Rest in Pieces: The Curious Fates of Famous Corpses--has kindly offered up a very detailed and thoughful review of the book special for the Morbid Anatomy blog.

    Lovejoy's review follows; you can also find out more about the book--or purchase a copy of your very own--by clicking here.

    Dissection on Display: Cadavers, Anatomists and Public Spectacle
    By Christine Quigley
    Mcfarland, February 24, 2012

    Most of us have never seen a dead body, let alone witnessed the dissection of a cadaver. But for centuries in Europe, Britain, and America, public dissections were highly social occasions. In the candlelit, damask-draped anatomy theatre of 18th century Bologna, townspeople jostled medical students and high-ranking officials during a two-week-long dissection that took place as part of the annual carnival. In 16th century Britain, hundreds crowded around to watch the dissections of executed criminals. And in early 19th century America, the most fashionable strata of society (men and women alike) attended public dissections for a chance to “see and be seen.”

    In her new book, Dissection on Display: Cadavers, Anatomists and Public Spectacle, scholar, author, and blogger Christine Quigley traces the hidden history of anatomists who perform for the public. Not all of the men she profiles are known just for their dissections: some, like 17th and 18th century Europeans Frederik Ruysch and Honoré Fragonard, did the dirty work in private, then displayed the exquisitely-crafted results to the public in the form of art and illustration. Many of the names Quigley profiles will be familiar to Morbid Anatomy readers, though others -- like Thomas “Mummy” Pettigrew, the 19th century London antiquarian who unrolled mummies to entertain his guests – may be fresh discoveries.

    Using a series of thematically-grouped vignettes, Quigley explores anatomists as demonstrators, educators, collectors, showmen, and more. Some of the book’s most intriguing passages deal with the lessons that public dissections were supposed to impart: not just about the workings of the body, but the workings of God, and of justice. Even more than a chance to gain medical wisdom, public dissections were often promoted as an opportunity to witness the glory of God in the functioning of a corpse’s entrails. Sometimes they were also seen as a chance to exult in the final stage of  punishment meted out to a criminal. The mutilation of the corpse was thought to deny the deceased a chance at Resurrection -- thus condemning him or her both in life and afterlife.

    Quigley also touches on the racial and sexual undertones that have long troubled the study of anatomy. One of the book’s most disturbing sections profiles French naturalist and zoologist Georges Cuvier and his quest to uncover (literally) the mysteries that lay between the legs of Saartjie Bjartmaan, also known as the “Hottentot Venus.” Bjartmaan – a young Khoisan woman from South Africa -- entertained audiences in early 19th century London and Paris with the enormous size of her buttocks. Some whispered that Bjartmaan was also blessed with a similarly enormous labia minora, and like other scientists of the time, Cuvier was fascinated by such rumors. After Bjartmaan’s death, he detailed her dissection in a medical journal and preserved both her brain and genitals in greenish glass bottles outside his office. Thus the last shred of modesty that Bjartmaan had protected in life was unceremoniously stripped from her in death, in a way that calls to mind the brutally frank autopsy reports of modern dead celebrities.

    Today, human dissection is usually hidden from the public. This cloaking began in the 19th century, when, as Quigley writes, “The anatomists withdrew behind the doors of educational institutions, and the townspeople were not invited to join them.” These days dissections occur exclusively in a medical or forensic context, and the only corpses we see are on television. No longer is the public treated to theatrical displays of their own inner-workings, as they were in the days when Andreas Vesalius kept Renaissance audiences glued to their seats.

    But there have been exceptions. In 2002, the controversial Gunter von Hagens – he of the plastinated corpses and Body Worlds exhibits – staged a ticketed dissection of the body of a 72-year-old man in London. The event drew considerable attention, and Hagens faced the threat of arrest even while wielding the scalpel. Yet the room was packed, proving that our appetites for dissection haven’t waned. Quigley includes an excellent photograph of the event, notable not for the pale cadaver about to be sliced apart, but for the front row of the audience, their faces horrified, bemused, and fascinated in turn. One woman crosses her hands over her chest in protection, clutching her check and beginning to grimace. Next to her, an older gentleman folds his wrists behind his elbows and leans back as if to say “show me what you got.” Von Hagens himself is at the forefront of the image, clad in a black fedora -- his nod to Rembrandt’s “The Anatomy Lesson of Dr. Nicolaes Tulp,” which hangs on the wall above him.

    In fact, Quigley takes pains to show us how conscious Von Hagens – the most famous modern anatomist -- is of his historical lineage. (Many of his most famous pieces, such as his flayed horse and rider, quote directly from the work of earlier anatomists such as Fragonard.) This is where the book shines: Quigley has stitched together a family tree of public anatomists who contributed to our understanding of the body, but whose work often remains hidden like the organs beneath our skin. Dissection on Display is recommended reading for anyone with a healthy sense of curiosity, morbid or otherwise, about what used to happen when we were allowed to watch.

    The writer of this post, Bess Lovejoy, is a writer, editor, and researcher based in Seattle. Her book Rest in Pieces: The Curious Fates of Famous Corpsesis coming out March 2013. You can find out more about her at her website besslovejoy.com." To find out more--or to purchase a copy of this book--click here.

    Image: The Anatomy lesson of Dr Nicolaes Tulp, Remrandt van Rijn, 1632; found on Wikipedia. According to Quigley, the dissection was performed in Leiden’s anatomical theatre, and included an audience of townspeople that were left out of the painting. Instead, Rembrandt was paid to include surgeons who may or may not have actually been there.

    Source:
    http://morbidanatomy.blogspot.com/feeds/posts/default?alt=rss

    "Dissection as Studio Practice with Real Anatomical Specimens," Class with Laura Splan, Observatory, Next Monday, July 23

    I am very excited about "Dissection as Studio Practice," a class taking place next Monday, July 23, at Observatory. Taught by artist Laura Splan, the class will begin with an illustrated survey of the use of notions of "dissection" in contemporary art practice; these principles will then be applied to in-class projects which include the dissection of your very own anatomical specimens (i.e. frog, sheep brain, cow eye). This class is open to all expernience levels, and participants are invited to bring additional materials, objects and artifacts that will inspire their “dissective” inclinations.

    We had a wonderful time in the last iteration of this class, as you can see from the photos above. Full description of the class follows. Class size is limited; if interested, be sure to RSVP via email to morbidanatomy[at]gmail.com. You can see more of Laura Splan's work by clicking here. Hope very much to see you there!

    Lecture and Studio Art and Dissection Class with artist Laura Splan
    Date: Monday, July 23
    Time: 7-10 PM
    Fee: $75
    *** Class size is limited to 16; please RSVP to morbidanatomy[at]gmail.com

    This class is part of the
    Morbid Anatomy Art Academy

    This class will survey the use of dissection in contemporary art practice through an illustrated lecture, specimen dissections, and studio time for individual and collaborative projects. We will examine the conceptual and cultural significance of cutting, excavating, disassembling, labeling, observing and displaying “bodies.” The lecture will present a brief history of dissection as well as work by contemporary artists exploring imagery, tropes and methods of dissection. The collaborative and individual art projects will be fun and lively hands on explorations of the meaning of dissection in a work of art. Each student will receive a complete specimen dissection kit (i.e. frog, sheep brain, cow eye) to create a self-directed dissection project with. Participants should bring additional materials, objects and artifacts that will inspire their “dissective” inclinations. Additional supplies will be provided by the instructor to stimulate your creativity. No prior art training is required. Everyone is welcome.

    Laura Splanis a Brooklyn based visual artist. Her mixed media work explores historical and cultural ambivalence towards the human body. She was a Visiting Lecturer at Stanford University where she taught “Art and Biology”. She has been a Visiting Artist at the New York Academy of Sciences, California College of Art, San Francisco Art Institute, Maryland Institute College of Art, and Cal Arts. Her artwork was recently commissioned by the CDC Foundation. She curates the visual portal DomesticatedViscera.com. Images of her artwork can be found on her website: LauraSplan.com. You can find out more here. Feel free to contact Laura through her website with any questions about the class by clicking here. You can see photos from the last class by clicking here.

    You can find out more here, and RSVP with an email to morbidanatomy[at]gmail.com.

    Source:
    http://morbidanatomy.blogspot.com/feeds/posts/default?alt=rss

    Constructing Words From Bones

    Teagan White Bone Type You're Already Dead

    Teagan White Bone Type You're Already Dead

    Freelance designer and illustrator Teagan White first came to our attention because A, she created an amazing anatomically-themed typography print,  The Person You Love Is 72.8% Water and B, she’s from Chicago.

    Teagan’s work ”encompasses intricate renderings of flora and fauna, playful depictions of cute anthropomorphic critters, illustrative typography, and everything in between.”  The pieces above are an exploration into skeletal typography.

    View all of Teagan’s work at teaganwhite.com.

     

    [Spotted by our lovely friend from the Mütter Museum, Evi Numen]

     

    Source:
    http://feeds.feedburner.com/streetanatomy/OQuC

    Real life shooting imitates training exercise at Parker medical school

    The tragedy that played out in an Aurora movie theater Friday was ironically paralleled as a classroom learning experience in a medical school in Parker the same day.

    Rocky Vista University College of Osteopathic Medicine is in the middle of holding specialized classes in disaster life support for 150 second-year medical students. Along with response to natural disasters like hurricanes and floods and terrorist attacks, one of the scenarios being used to train the students is how to respond if a shooter fires at people in a movie theater and also uses a bomb in the attack.

    "The irony is amazing, just amazing," said Rocky Vista Dean Dr. Bruce Dubin.

    He said emergency specialist physicians from Parkland Hospital in Dallas as well as from several other emergency programs around the country are teaching the Advanced Disaster Life Support Training. Rocky Vista is the only medical school in the nation to make that training a part of the curriculum.

    "They are trained to respond in every type of disaster," Dubin said.

    The shootings in Aurora were incorporated into the teaching Friday, Dubin said.

    "It made these medical students very aware that these kinds of things can happen anywhere," he said. "The events of this tragedy have helped to drive that home."

    Nancy Lofholm: 970-256-1957, nlofholm@denverpost.com or twitter.com/nlofholm

    Continued here:
    Real life shooting imitates training exercise at Parker medical school