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Archive for August 12th, 2011

Patent foramen ovale (PFO) is the new generation hole in the heart for  21st century  cardiologist. Present in about 20% of population  , would correspond to 140 crore  “man holes”  as  on  2012   in this planet. PFOs are embryological remnants across the inter atrial septum.

These minute  holes measuring few mm  are largely a  benign finding .In the recent  decades , it is being increasingly debated these holes  may  not  be innocent after all .Extensive  use of echocardiography in recent times   has contributed to  the awareness  as well as anxiety.

Evidence  is mounting  linking PFO to

  • Migraine,
  • Stroke and
  • Peripheral embolism.

While the above   observation may be true  ,  the  fact that >100 crore people have this entity   , raises  a serious question ,  as labeling  all of  them as heart disease will create chaos among the already health obsessed   population .

So , the main purpose should be ,  to identify the high risk subsets* of PFO population .(This will be a <5 %  at the most). People with PFO may  carry  a mental  stigma because it is referred to as a hole in  the heart by the  general  public .For many  the sense of living with a hole in heart is often more damaging than the hole itself ! (Incidentally , many develop  migraine only after reporting about this hole !)In a strict sense  PFO  is not a hole , rather  it is a communication it may be tunnel  or  slit like .It is argued physician should avoid calling PFO as a hole .

*What is a significant PFO ?

  • Large PFOs >5mm
  • PFOs that shunt blood
  • PFOs with septal aneurysms
  • PFOs with documented stroke or embolism
  • PFOs with atrial chiary network
  • PFO in  persons with systemic pro-coagulant states (Except probably in  pregnancy )

Final message 

PFO is a common residual congenital  atrial septal  anomaly . Usually  benign  . One can  live with it perfect harmony. Only occasional patients  are  at risk.

So the prime job of cardiologists is to not diagnose and create panic about  this entity. rather reassure  them (Is it better do not reveal to them if it is found incidentally ? Patient empowerment group would call  this a  foul !  I do not support blind empowerment  )

At the same time our main  aim is to identify the  high  risk subsets who are prone for events.

Closure of   PFO with device is required in a fraction . (*By the way ,  if   PFO is really dangerous ,  why It is never an indication for surgical closure ?  )

Reference

Your  search for best information  on PFO  would end here .  Here is  land mark   article  in JACC  by  Hara   also contributed by  Renu Virmani . A US  Japan  combines initiative  : A must read by every cardiologists

http://content.onlinejacc.org/cgi/reprint/46/9/1768.pdf

http://www.anesthesia-analgesia.org/content/93/5/1137.full

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Hypertrophic cardiomyopathy(HOCM)  is a relatively common inherited myocardial disease.Since it predominately involves  LV myocardium and we know LV muscle mass is an integral part of  mitral valve apparatus , it is natural HOCM  has a major  impact on   mitral valve function .

The mechanism  of MR in HOCM is attributed to the following .

  • Asymmetric septal hypertrophy (ASH ) related abnormal pap muscle alignment (Geometric distortion  )
  • Exaggerated SAM(AML  is attracted towards LVOT with every systole that tend to  keep the mitral  valve  unguarded and MR results)*
  • Intrinsic abnormalities of mitral valve.
  • Associated MVPS
  • VPDs and Non-sustained VT can result in transient MR
  •  Pacemaker mediated MR (DDD pacemaker was used to induce desynchrony of LVOT vs LV free wall .This  concept  is almost a failed  one now !)
  • End stage HOCM -Left ventricular dilatation

* This mechanism is considered less important ,  as SAM is almost universal in HOCM  but MR occurs in less than 20%  patients with HOCM.

Eccentric MR vs central MR

In HOCM the MR is more often eccentric .This is understandable as the primary mechanism is related to faulty angle of pap ,muscle vs leaflet attachment.

If SAM is primary mechanism jet is directed posterior.

Murmur of MR in  HOCM

Is rarely pansytolic as the mechanism of MR begins to operate well after the systole starts .

Many times it is difficult to differentiate LVOT murmur from MR murmur . Th ever confusing and tentative  maneuvers might help in few shrewd cardiologists.

Issues  during echocardiogram

Very often MR jets are mistaken for LVOT gradient.Ideally two gradients in isolation (or  overlapping each other)  one bell shaped other dagger shaped must be documented.

Please note : LVOT jet is different from MR jet in size, shape, timing and site of maximum signal . Still it is often be confused with one other. Most common reason for this is technical .A careful apical 4 chamber view with well opened LVOT will reduce the error . Never record a HOCM echo without ECG gating . The MR jet may be very trivial in color flow but doppler will still pick the signal well . Realise ,for hemodyanmic reasons MR jet must be always more than LVOT jet.Finally if you get a report a LVOT gradient > 100mmhg in HOCM suspect it to be MR ! More often your suspicion will prove to be right !

Can mitral regurgitation occur in non obstructive HCM ?

Yes , in few . This is due to intrinsic abnormalities of mitral valve .

What happens to MR with surgical correction ? Can medical management  regress the MR ?

It is expected to regress.But many patients don’t. Effect of beta blockers   on MR severity is not studied well.

Management

  • Most cases of MR  do not require specific intervention.Just reassure them.
  • Correction of LVOT obstruction is expected to relieve MR considerably.
  • Intensive beta blocker or calcium blocker can regress the MR.(Negative inotropy)
  • Mitral valve repair may be necessary in few  with re-engineering of pap and chordae .
  • Mitral valve replacement should be a last resort. It  may be highly tempting  .But restraint is warranted. Much  damage has been done by showing undue haste in replacing mitral valve in HOCM

Final message

It needs to be realized whatever we do  for the HOCM patients , the ultimate outcome is determined by the quantum myocardial disarray  the patient has inherited from their parents.The myectomy , the alcohol ablation, mitral valve repair,  DDD pacing , beta blockers all are palliative. Except a few  , most HOCM patients generally live their natural history .

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