scholarly journals Say what? A Guided Virtual Level I Fieldwork for Occupational Therapy Assistant (OTA) Students

2019 ◽  
Vol 5 (4) ◽  
pp. 1-3
Author(s):  
Amy M Wix ◽  

Life experience is what makes us who we are. I started my career in academia as a fieldwork coordinator in fall 2013, so I learned quickly that securing traditional fieldwork sites can be difficult. I am certainly a fan of faculty led fieldwork and have used this approach. In spring 2017, I was excited to find out that I was expecting my first baby however in the summer of 2017, at the 20-week anatomy ultrasound, my excitement turned to tears as we found out our baby had a Neural Tube Defect (NTD) and the most severe type of spina bifida (myelomeningocele). I was then introduced as to what I call the “spina bifida underworld” private pages for moms who were considering fetal surgery, moms who had fetal surgery, moms who had post-natal repair, pages called united by spina bifida, blogs from various individuals with spina bifida etc., I have personally found these pages to be a wealth of knowledge and have made many friends in unexpected places.

2016 ◽  
Vol 214 (1) ◽  
pp. S177-S178 ◽  
Author(s):  
Michael Belfort ◽  
William E. Whitehead ◽  
Alireza A. Shamshirsaz ◽  
Sundeep G. Keswani ◽  
Tim Lee ◽  
...  

Author(s):  
Hary F. Rabarikoto ◽  
Patrick S. Rakotozanany ◽  
Rosa L. Tsifiregna ◽  
Willy Ratovondrainy ◽  
Domoina M. A. Randriambololona

Craniorachischisis is the most severe type of neural tube defect in which almost the entire brain and spinal cord remain open. We report a case in a female fetus born at gestational week 38, with both anencephaly and open spina bifida. It was the second pregnancy of a 26-year-old woman. The first pregnancy had to be interrupted by a medical termination at 18th gestational week because of an anencephaly. We aim to report the first case documented in Madagascar.


2020 ◽  
Vol 15 (1) ◽  
pp. 81-83
Author(s):  
Tripti Shrestha ◽  
Gehanath Baral ◽  
Nesuma Sedhain

An extremely rare case of sirenomelia in dicephalic parapagus twins discordant for anencephaly and spina bifida that was diagnosed after birth is presented. High incidence of congenital anomalies both with sirenomelia and parapagus twins independently make the prognosis much worse, with additional neural tube defect rendering it almost incompatible with life. Termination of pregnancy is advised when diagnosed in utero. Key words: anencephaly, dicephalic parapagus, spina bifida, sirenomelia


2018 ◽  
Vol 4 (1) ◽  
pp. 58-62
Author(s):  
DM Arman ◽  
Sheikh Muhammad Ekramullah ◽  
Sudipta Kumer Mukherjee ◽  
Md Rahimullah Chowdhury ◽  
Md Abdul Quddus Mia ◽  
...  

Encephalocele is defined as protrusion of cranial contents like meninges and cerebral tissue beyond the normal confines of the skull through a defect in the cranium. It is one form of a neural tube defect as are anencephaly and spina bifida. There are 2 main types of encephalomeningocele, frontoethmoidal and occipital, according to the location of the defect. The frontoethmoidal type defect, which is located in the area of the frontal and ethmoidal bones. The authors present a case of frontonasal encephalocele in a very young child.Journal of National Institute of Neurosciences Bangladesh, 2018;4(1): 58-62


Author(s):  
Jennifer A Noyes ◽  
P J Wood

We measured Concanavalin A (Con A) non-binding alphafetoprotein in amniotic fluid from 21 normal pregnancies and 20 abnormal pregnancies (complicated by anencephaly, spina bifida, or exomphalos) using small Con A-sepharose chromatography columns. There was a highly significant difference between percentage non-binding alphafetoprotein levels for pregnancies with a normal outcome (mean result 32%; range 18–47%) and pregnancies complicated by a neural tube defect or exomphalos (mean 14%; range 7–20%). The test is therefore of potential value in cases where there is uncertainty over the interpretation of total amniotic fluid alphafetoprotein levels.


Author(s):  
Jayme Castillo ◽  
Christina Wassef ◽  
Audrey Wassef ◽  
Katie Stormes ◽  
Anna E. Berry

Abstract Objective With the increasing interest in fetal repair of myelomeningoceles (MMCs) over the last decade, it is reasonable to anticipate the need for high quality and accessible educational materials for patients. Patients often look to the internet for details regarding medical topics and specifically to YouTube for informative health-related videos. This study aims to analyze the content and shortcomings of currently available videos on YouTube regarding prenatal repair of MMCs. Study Design A YouTube search was performed on December 15, 2018, using the terms “fetoscopic surgery for neural tube defect” and “fetal surgery for neural tube defect.” The first 50 videos from each search were sorted by relevance and evaluated for video source (i.e., professional, personal, or other), target audience (medical professionals or general public), general descriptive statistics (i.e., video length, number of views, number of comments), and for five areas of content determined by the authors to constitute basic patient information regarding a surgical procedure: (1) procedure details, (2) eligibility criteria, (3) alternatives to surgery, (4) surgical risks, and (5) success rate. Accuracy of videos was not assessed. Results Of the 16 videos that met inclusion criteria, only 1 discussed fetoscopic surgery. The majority (62.5%) of videos were produced by a professional source and 81.3% were targeted toward the general public rather than medical professionals. Of the 16 videos, 10 (62.5%) included details regarding the surgery, 3 (18.8%) discussed eligibility criteria, and 8 (50.0%) mentioned alternatives to surgery. Additionally, seven videos (43.8%) discussed risks of the procedure and six (37.5%) included surgical success rate. Conclusion Only 2 of the 16 videos included all five areas of content that were evaluated, and both were in regard to open fetal repair. This study not only calls attention to the initial shortcomings of YouTube videos regarding fetal surgery for neural tube defects but also demonstrates the need for further investigation and more comprehensive analysis.


Author(s):  
K.K. Otaryan , M.A. Kolyshkina , Y.B. Aninyan et all

The case of prenatal diagnosis of neural tube defect at 11+5 weeks of gestation is presented. Chorion villus sampling performed. Karyotyping revealed double trisomy (48,XXX,+18). Termination of pregnancy was performed at 13 weeks of gestation.


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