Patent ductus arteriosus pathophysiology: Difference between revisions
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{{CMG}}; '''Associate Editor-In-Chief:''' [[Priyamvada Singh|Priyamvada Singh, M.B.B.S.]] [mailto:psingh@perfuse.org], {{CZ}}, '''Assistant Editor-In-Chief:''' [[Kristin Feeney|Kristin Feeney, B.S.]] [mailto:kfeeney@perfuse.org] | {{CMG}}; '''Associate Editor-In-Chief:''' [[Priyamvada Singh|Priyamvada Singh, M.B.B.S.]] [mailto:psingh@perfuse.org], {{CZ}}, '''Assistant Editor-In-Chief:''' [[Kristin Feeney|Kristin Feeney, B.S.]] [mailto:kfeeney@perfuse.org] | ||
==Overview== | ==Overview== | ||
The pathophysiological findings depend on the size of defect and the pulmonary vascular resistance | |||
==Pathophysiology== | ==Pathophysiology== | ||
Consequences depend on the size of the defect and the [[pulmonary vascular resistance]] ([[PVR]]). <ref>Giuliani et al, Cardiology: Fundamentals and Practice, Second Edition, Mosby Year Book, Boston, 1991, pp. 1653-1663.</ref> | Consequences depend on the size of the defect and the [[pulmonary vascular resistance]] ([[PVR]]). <ref>Giuliani et al, Cardiology: Fundamentals and Practice, Second Edition, Mosby Year Book, Boston, 1991, pp. 1653-1663.</ref> | ||
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==[[Patent ductus arteriosus pathologic findings|Pathological Findings]]== | ==[[Patent ductus arteriosus pathologic findings|Pathological Findings]]== | ||
==References== | ==References== | ||
{{reflist}} | {{reflist}} | ||
[[Category: | ==External links== | ||
* [http://www.schneiderchildrenshospital.org/peds_html_fixed/peds/hrnewborn/pda.htm High-Risk Newborn - Patent Ductus Arteriosus (PDA)] | |||
* [http://www.merck.com/mmhe/sec23/ch265/ch265b.html#sec23-ch265-ch265b-293 Patent Ductus Arteriosus from Merck] | |||
* [http://mcb.berkeley.edu/courses/mcb135e/fetal.html Fetal Circulation at berkeley.edu] | |||
* [http://goldminer.arrs.org/search.php?query=Patent%20ductus%20arteriosus Goldminer: Patent ductus arteriosus] | |||
[[Category:Disease state]] | |||
[[Category:Cardiology]] | [[Category:Cardiology]] | ||
[[Category:Congenital heart disease]] | [[Category:Congenital heart disease]] |
Revision as of 01:29, 16 August 2011
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor-In-Chief: Priyamvada Singh, M.B.B.S. [2], Cafer Zorkun, M.D., Ph.D. [3], Assistant Editor-In-Chief: Kristin Feeney, B.S. [4]
Overview
The pathophysiological findings depend on the size of defect and the pulmonary vascular resistance
Pathophysiology
Consequences depend on the size of the defect and the pulmonary vascular resistance (PVR). [1]
Small PDA
- Small left-to-right shunt (Qp/Qs < 1.5).
- Normal ratio of pulmonary artery (PA) to systemic pressure.
- Shunt throughout the cardiac cycle, continuous murmur.
Medium-sized PDA
- Qp/Qs 1.5 to 2.0 yet small enough to offer some resistance to flow.
- PA systolic to systemic pressures are < 0.5.
- Unusual for this group to have markedly increased PVR.
- Due to increased return to the left heart, there is volume overload of the left atrium (LA) and the left ventricle (LV).
Large PDA
- Defect does not restrict flow.
- There is pulmonary hypertension at near systemic pressures (PA systolic/systolic pressure is >0.5).
- Because of the physiologic decrease in the PVR over the first three months of life there is a large left-to-right shunt with Qp/Qs > 2.
- The large volume overload of the left ventricle may result in LV failure.
- There is pulmonary hypertension.
- There may be two courses:
- A decrease in the relative size of the ductus compared with other cardiovascular structures. This results in a medium-sized defect compared with the course expected for a medium-sized defect.
- The development of severe pulmonary vascular obstructive disease, can occur at any time from age 3 until early adulthood. The left-to-right shunt converts to a right-to-left shunt with cyanosis and disappearance of the continuous murmur.
Pathological Findings
References
- ↑ Giuliani et al, Cardiology: Fundamentals and Practice, Second Edition, Mosby Year Book, Boston, 1991, pp. 1653-1663.