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๐™’๐™๐™ฎ ๐˜ฝ๐™ค๐™ฃ๐™š ๐™ˆ๐™–๐™ง๐™ง๐™ค๐™ฌ ๐˜ผ๐™จ๐™ฅ๐™ž๐™ง๐™–๐™ฉ๐™š๐™จ ๐˜ฝ๐™š๐™˜๐™ค๐™ข๐™š ๐˜ฟ๐™ž๐™ก๐™ช๐™ฉ๐™š๐™™: ๐˜ผ ๐™ƒ๐™š๐™ข๐™ค๐™™๐™ฎ๐™ฃ๐™–๐™ข๐™ž๐™˜ ๐™€๐™ญ๐™ฅ๐™ก๐™–๐™ฃ๐™–๐™ฉ๐™ž๐™ค๐™ฃ ๐™›๐™ค๐™ง ๐˜พ๐™ก๐™ž๐™ฃ๐™ž๐™˜๐™ž๐™–๐™ฃ๐™จ

  • kparmstrong1
  • Jan 8
  • 2 min read

Every surgeon has seen it: the first 1โ€“2 mL of aspirate is thick and cellular... and everything after that becomes progressively thinner until it looks like pure venous blood.



If the marrow cavity is โ€œfull of marrow,โ€ why does peripheral blood replace it so quickly?



The answer lies in marrow structure, pressure physiology, and fluid dynamics.



๐— ๐—ฎ๐—ฟ๐—ฟ๐—ผ๐˜„ ๐—ฆ๐˜๐—ฟ๐—ผ๐—บ๐—ฎ ๐—œ๐˜€ ๐—ฎ ๐—ฆ๐˜๐—ฟ๐˜‚๐—ฐ๐˜๐˜‚๐—ฟ๐—ฒ, ๐—ก๐—ผ๐˜ ๐—ฎ ๐—Ÿ๐—ถ๐—พ๐˜‚๐—ถ๐—ฑ



The marrow cavity is not a fluid-filled spaceโ€”itโ€™s a semi-solid, thixotropic, reticular tissue made of:



Mesenchymal stromal cells and fibroblasts


Adipocytes and macrophages


Extracellular matrix (collagen, laminin, fibronectin)


A dense network of venous sinusoids



Stroma is high-viscosity and mechanically resistant, meaning it moves slowly when suction is applied.ย 



This sets up a competition:



Marrow stroma: high viscosity, high resistance


Peripheral blood: low viscosity, low resistance



Once a low-resistance pathway opens, the thinner fluid always wins.



๐—ง๐—ต๐—ฒ ๐——๐—ฒ๐—น๐—ถ๐—ฐ๐—ฎ๐˜๐—ฒ ๐—ฃ๐—ฟ๐—ฒ๐˜€๐˜€๐˜‚๐—ฟ๐—ฒ ๐—˜๐—พ๐˜‚๐—ถ๐—น๐—ถ๐—ฏ๐—ฟ๐—ถ๐˜‚๐—บ



Inside trabecular bone, three pressures are normally balanced:



Marrow interstitial pressure


Sinusoidal venous pressure


Intraosseous venous pressure



Bone marrow sinusoids are fenestrated, discontinuous, extremely thin-walled, and compliant.


They are perfect for cell traffickingโ€”but extremely vulnerable to shear stress and rapid pressure drops.



๐—›๐—ผ๐˜„ ๐——๐—ถ๐—น๐˜‚๐˜๐—ถ๐—ผ๐—ป ๐—›๐—ฎ๐—ฝ๐—ฝ๐—ฒ๐—ป๐˜€: ๐—ง๐—ต๐—ฒ โ€œ๐—–๐—ต๐—ฎ๐—ป๐—ป๐—ฒ๐—น๐—ถ๐—ป๐—ดโ€ ๐— ๐—ฒ๐—ฐ๐—ต๐—ฎ๐—ป๐—ถ๐˜€๐—บ



Aspiration creates a localized low-pressure zone at the needle tip.



Phase 1: Harvest (0โ€“2 mL)



You draw true marrow because you are sampling the tissue immediately adjacent to the needle ports.



Phase 2: Rupture (>2 mL)



As you keep pulling:



Thick stroma cannot move fast enough;


Local negative pressure spikes;


The path through the stroma has high resistance;


The path through sinusoids has low resistance;



The result: sinusoidal endothelial rupture.



Phase 3: Flood



Once a sinusoid breaks:



Low-viscosity venous blood accelerates toward low-pressure zones


Blood outpaces stromal flow by orders of magnitude


The aspirate rapidly transitions from marrow to blood



This is classic "channeling"โ€”fluid choosing the pathway of least resistance.



๐—ฆ๐˜‚๐—บ๐—บ๐—ฎ๐—ฟ๐˜†



Peripheral blood contamination isnโ€™t necessarily a technique failure (although that certainly contributes)โ€”itโ€™s physics:



Anatomy: Marrow is semi-solid; blood is liquid.


Physiology: Sinusoids rupture when exposed to high shear or suction.


Fluid Dynamics: Low-viscosity blood overwhelms high-viscosity stroma once a channel opens.


Engineering: Reducing point-source suction and distributing negative pressure prevents rupture and preserves true marrow content.



The most current best practices can help reduce peripheral blood. This will be a future topic or DM me for the advanced copy.

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