Native cardiac valves
Cardiac valves may be received in the laboratory after artificial valve replacement surgery for congenital and acquired conditions that have resulted in valve dysfunction.1-4 See the reference provided (Recommendations for processing cardiovascular surgical pathology specimens)2 for more detail on clinical scenarios associated with cardiac valve surgery.
Record the patient identifying information and any clinical information supplied together with the specimen description as designated on the container. See overview page for more detail on identification principles.
- Non-routine fixation (not formalin), describe.
- Special studies required, describe.
- Ensure samples are taken prior to fixation.
Fresh specimens should be carefully examined for any thrombi or vegetations. If identified, a piece of the material should be submitted for microbiological evaluation.1-3 Note that swabs are not useful for microbiological culture and that molecular biological studies may also be required.2
- Not performed
- Performed, describe type and result
- Frozen section
- Other, describe
See general information for more detail on specimen handling procedures.
Inspect the specimen and dictate a macroscopic description.
Orientate and identify the anatomical features of the specimen.
Record additional orientation or designation provided by operating clinician:
- Method of designation (e.g. suture, incision)
- Featured denoted
Photographs of both inflow and outflow valve surface can be helpful.1
Describe the following features of the specimen:
Record as stated by the clinician.
- Cardiac valve, state whether excision or repair, if known
- Other, describe
- Intact valve cusps
- Incomplete cusps/fragmented material
Anatomical components included (more than one may apply) and specimen dimensions (mm)
- Total specimen, in three dimensions1-4
- Each cusp valve leaflet, in three dimensions, free edge x free edge to cut-edge (valve ring) x thickness1
- Other, specify
Annual tissue/valve ring
- Measurement (circumference in mm)
- Number of cusps involved and size of deposits (maximum dimension in mm)
- Number, location(s) and size (maximum dimension in mm)
- Number of or specific valves involved, if known
- Present, describe
- Shortened or elongated/muscular
- Intact with smooth surgical cut or ruptured
- Attenuated e.g. scarred/hypertrophied
- Number, size (max. dimension in mm) and location of each
Floppy mitral valve is the result of myxoid change which may be evident as thickening and translucency macroscopically.4
A raphe is the area of failed cusp separation present in a congenitally bicuspid valve as a ridge from the base of the cusps at the aortic wall extending toward the free margin of the valve cusps.2 It can be distinguished from the more common acquired cusp fusion where fibrocalcification extends all the way through to the free margin.2
Decalcification of the whole specimen may be necessary prior to sectioning if the valve is calcified.2
Section transversely at 5mm intervals perpendicular to the valve ring and free edge.1
Section all fused commissures and raphes. Section papillary muscle if present.1
Submit all sections of cusp tissue for processing.
Standard protocols for special stains required for cardiac valve specimens should be available. Care should be taken to conserve tissue in case ancillary studies are required.
- Alcian blue Periodic Acid Schiff +/- diastase (AB PAS+/-D) to distinguish neutral from acid mucopolysaccharides
- Elastic Verhoeff Van Gieson (EVG) or Alcian Blue EVG for elastin
Record details of each cassette.
An illustrated block key similar to the one provided may be useful.
Prof Tony Thomas for his contribution in reviewing and editing this protocol.
Block allocation key
No. of pieces
Stone JR, Basso C, Baandrup UT, Bruneval P, et al. Recommendations for processing cardiovascular surgical pathology specimens: a consensus statement from the Standards and Definitions Committee of the Society for Cardiovascular Pathology and the Association for European Cardiovascular Pathology. Cardiovasc Pathol. 2012;21(1):2-16