TY - JOUR
T1 - A design thinking approach to primary ovarian insufficiency
AU - Rachel's Well Primary Ovarian Insufficiency Community of Practice Group
AU - Martin, Lisa Arndt
AU - Porter, Alison Gatewood
AU - Pelligrini, Vincent A.
AU - Schnatz, Peter F.
AU - Jiang, Xuezhi
AU - Kleinstreuer, Nicole
AU - Hall, Janet E.
AU - Verbiest, Sarah
AU - Olmstead, Jill
AU - Fair, Ryan
AU - Falorni, Alberto
AU - Persani, Luca
AU - Rajkovic, Aleksandar
AU - Mehta, Khanjan
AU - Nelson, Lawrence M.
N1 - Funding Information:
This work was supported by the Mary Elizabeth Conover Foundation, McLean, VA, USA; Oceti Wakan, Pine Ridge, SD, USA; the National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, NC, USA, and the Intramural Research Program, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA.
Publisher Copyright:
© 2016 Edizioni Minerva Medica.
PY - 2017/3
Y1 - 2017/3
N2 - Most clinicians are not prepared to provide integrated personal care to address all the clinical needs of women with primary ovarian insufficiency. Design thinking is an engineering methodology used to develop and evaluate novel concepts for systems operation. Here we articulate the need for a seamlessly integrated mobile health system to support genomic research as well as patient care. We also review the pathophysiology and management of primary ovarian insufficiency. Molecular understanding regarding the pathogenesis is essential to developing strategies for prevention, earlier diagnosis, and appropriate management of the disorder. The syndrome is a chronic disorder characterized by oligo/amenorrhea and hypergonadotropic hypogonadism before age 40 years. There may be significant morbidity due to: 1) depression and anxiety related to the loss of reproductive hormones and infertility; 2) associated autoimmune adrenal insufficiency or hypothyroidism; and 3) reduced bone mineral density and increased risk of cardiovascular disease related to estrogen deficiency. Approximately 5% to 10% of women with primary ovarian insufficiency conceive and have a child. Women who develop primary ovarian insufficiency related to a premutation in FMR1 are at risk of having a child with fragile X syndrome, the most common cause of inherited intellectual disability. In most cases of spontaneous primary ovarian insufficiency no environmental exposure or genetic mechanism can be identified. As a rare disease, the diagnosis of primary ovarian insufficiency presents special challenges. Connecting patients and community health providers in real time with investigators who have the requisite knowledge and expertise would help solve this dilemma.
AB - Most clinicians are not prepared to provide integrated personal care to address all the clinical needs of women with primary ovarian insufficiency. Design thinking is an engineering methodology used to develop and evaluate novel concepts for systems operation. Here we articulate the need for a seamlessly integrated mobile health system to support genomic research as well as patient care. We also review the pathophysiology and management of primary ovarian insufficiency. Molecular understanding regarding the pathogenesis is essential to developing strategies for prevention, earlier diagnosis, and appropriate management of the disorder. The syndrome is a chronic disorder characterized by oligo/amenorrhea and hypergonadotropic hypogonadism before age 40 years. There may be significant morbidity due to: 1) depression and anxiety related to the loss of reproductive hormones and infertility; 2) associated autoimmune adrenal insufficiency or hypothyroidism; and 3) reduced bone mineral density and increased risk of cardiovascular disease related to estrogen deficiency. Approximately 5% to 10% of women with primary ovarian insufficiency conceive and have a child. Women who develop primary ovarian insufficiency related to a premutation in FMR1 are at risk of having a child with fragile X syndrome, the most common cause of inherited intellectual disability. In most cases of spontaneous primary ovarian insufficiency no environmental exposure or genetic mechanism can be identified. As a rare disease, the diagnosis of primary ovarian insufficiency presents special challenges. Connecting patients and community health providers in real time with investigators who have the requisite knowledge and expertise would help solve this dilemma.
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U2 - 10.23736/S0031-0808.16.03259-6
DO - 10.23736/S0031-0808.16.03259-6
M3 - Review article
C2 - 27827529
AN - SCOPUS:85014152598
SN - 0031-0808
VL - 59
SP - 15
EP - 32
JO - Panminerva Medica
JF - Panminerva Medica
IS - 1
ER -