DMVD in 9 y old CHH

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DMVD in 9 y old CHH

HI, I wonder if you could help me with this echo.

This is Ash, 9y old MN chihuahua. Has had an episode of CHF a few months ago but I am not certain about the treatment back then. My colleague has seen it recently when cough was getting worse and has started furosemide 1mg-kg.

Here is some info from the echo:

-M-mode measurements of LV and IVS dont quite match my Bmode measurements. I think I trust the bmode more (see pics)

-MReg max vel 4.86m/s, La/Ao ratio: 2.27

HI, I wonder if you could help me with this echo.

This is Ash, 9y old MN chihuahua. Has had an episode of CHF a few months ago but I am not certain about the treatment back then. My colleague has seen it recently when cough was getting worse and has started furosemide 1mg-kg.

Here is some info from the echo:

-M-mode measurements of LV and IVS dont quite match my Bmode measurements. I think I trust the bmode more (see pics)

-MReg max vel 4.86m/s, La/Ao ratio: 2.27

-LV appears quite dilated in diastole and IVS a bit thinner than normal or just normal (compensatory eccentric hypertrophy ?)

– I didnt see tricuspid insuficiency nor PA dilation or turbulent flow.

-RV and RA appear normal.

Questions:

-Initially, I thought there could be chrodae tendineae rupture. Now I think there is not (after seeing more views). What do you think?

-Staging…: I think this dog has moderate cardiac remodeling and has symptoms of left sided CHF (which are improving since furosemide started) so stage C chronic… I think treatment should include furosemide at least 2m/kg and fortekor. My question is…when to start pimobendan? I would start it now but I am basing this on subjective Bmode assessment.

-I have adviced this dog to start SRR (sleeping or resting resp rate) monitoring, BP monitoring and review xrays if dog not well as well as echo in 3 months. including full biochemistry, too.

-Any comments on the clips are welcome.

Comments

Anonymous

Oh… Not why the images
Oh… Not why the images where not loaded:(…

EL

There is a clear prolapse of

There is a clear prolapse of th eanterior mv leaflet in video one but not visible in vodeo 2 and its just an angle thing… 2 dimansional modality for a 3 dimensional degenerative defect. Just one view of prolapse = prolapse. Rutpured chordae is cause of prolapse especially that degree. Volume overload for sure and clinical signs are cardiogenic at least to some extent. I would triple therapy this dog (ace-i, lasix, pimobendan), check bp, watch renal values and reecho in 7-10 days wiht rads. This fits stage B2 or even C1 valve disease dpeending if wet lung or not.

There is no consensus on B2 treatment pimo vs no pimo but I am one of those that starts pimo in B2/C1 (FYI C1 is under discussion right now on how its defined) especially with a prolapse like this one and clearly tachycardic the heart isnt having a good time with that volume. In europe they may exclude the ace-i and just go lasix pimo but my guess is if ace-i were cheap in europe they would triple tx:)

 

Heres the mv disease consensuse excerpt from the Curbside Guide out next month from sonopath. The book is in final editing thank goodness:)

Treatment:The following treatment options are based on the ACVIM consensus statement regarding MVD.

 

Stage A: There is a high risk of cardiac disease, but as there are no clinical signs, no specific therapy—medical or dietary—is indicated. A radiograph and an echocardiogram should be conducted in one year or earlier if the patient is a large-breed dog as MVD may progress faster.

 

Stage B: Heart disease is present.

 

B1: There is a murmur, but no chamber enlargement. Treatment is the same as for stage A.

 

B2: There is a murmur with left atrial and left ventricular enlargement, but the patient is asymptomatic. Start angiotensin-converting enzyme (ACE) inhibitors (enalapril at 0.5 mg/kg PO Q12-24hr or benazepril0.250.5 mg/kg PO Q24hr). Consider beta blockers and mild sodium restriction.

 

Stage C: There are past or current clinical signs of heart failure.

 

Acute CHF:

  • Lasix 2 mg/kg IV or IM hourly to a total dose of 8 mg/kg until the respiratory rate has normalized. Alternatively, for cases of life-threatening pulmonary edema, administer as a CRI (1mg/kg/hour).
  • Oxygen supplementation.
  • Continue with the ACE inhibitor and add pimobendan at 0.25-0.3 mg/kg PO BID.

 

            Chronic therapy:

  • Lasix at 2 mg/kg PO BID and increase incrementally as needed.
  • Continue with the ACE inhibitor.
  • Pimobendan at 0.25-0.3 mg/kg PO BID.
  • Consider adding spironolactone at 0.25-2 mg/kg PO BID to control congestion.
  • A sodium-restricted diet is recommended, although some dogs will not eat it.
  • Consider administering omega-3 fatty acids, digoxin, theophylline, and cough suppressants.
  • If the dog is not already on beta blockers, then do not commence.

 

Stage D: This is the end-stage of the disease. Continue with the standard therapy of diuretics, ACE inhibitors, and pimobendan, and consider the following:

  • Abdominocentesis when applicable to decrease discomfort if the patient is undergoing respiratory distress.
  • Anti-anxiety medications for sedative purposes.
  • Sodium nitroprusside and dobutamine (in a critical care facility).
  • Nitroglycerin.

 

We recommend monitoring serum urea, creatinine, electrolytes, urine specific gravity, and possibly blood pressure for 5-7 days after therapy has commenced. A repeat ECG is warranted if an arrhythmia was present during the original assessment.

 

References:

Atkins C, Bonagura J, Ettinger S, et al. Guidelines for the diagnosis and treatment of canine chronic valvular heart disease. J Vet Int Med 2009; 23(6):1142-50.

Borgarelli M, Buchanan J. Historical review, epidemiology and natural history of degenerative mitral valve disease. J Vet Cardiol 2012;14:93-101.

Chetboul V, Tissier R. Echocardiographic assessment of canine degenerative mitral valve disease. J Vet Cardiol 2012;14:127-48.

Fox P. Pathology of myxomatous mitral valve disease in the dog. J Vet Cardiol 2012;14:103-26.

 

randyhermandvm

Peters recent comment

Peters recent comment (although not proven) is that Pimo reduces L atrial pressures better than Enalapril. I have taken that to “heart” and I have started Pimo sooner than I used to. I see no downside other than cost. I guess that agrees with EL use in B2 cases.

 

Anonymous

Thanks EL and Randy. I also
Thanks EL and Randy. I also feel I would start pimobendan at this stage just because I feel dogs stabilize faster… I’m not sure if you find the same. I guess I wanted to check whether there is any particular finding in the echo related to contractility which would be the sign for starting it or it just depends on whether there are symptoms or not ( that is B2 or C1). Thanks.
I hope I get to scan this patient right after treatment as you suggest, but owners find it difficult to understand the necessity of re-scanning once the dog is better on treatment…

EL

I agree from B2 on they just

I agree from B2 on they just do better. Pimo gets the patient into trouble when there isnt volume overload and can cause or be part of sudden death. This issue historicaly is one of the reasons it took pimo so long to get to the US from europe in 2002 on. It was being used by some vets in europe in cases that were not cardiogenic but were thought to be and were treated erroneously because there was a murmur but no real volume overload and sudden death was occurring and I believe was taklen off the market for a while but not sure. Regardless the big pharma campaign was thought ot be implicated as well and we all know how that can happen. This is a summary from a lecture form Lombard (I think) a number of years ago at acvim I believe….. one of those lectures that stick out in my history where the concept is lived daily:) I started using Pimo in NJ in 2002 when my clients had to do all the fda paperwork t be able to use it in the US. One of the benefits of attending ecvim and acvim nearly every year for the last 12 years is gettign the forest and not the trees on the treatment potentials… I suggest the dualing medicine conferences to anyone that wants to globalize their medicine and get both sides of the medicine story. ECVIM was in Lisbon this year and we had an abstract on mapping of pancreatitis and clinical signs and got second place award for best oral abstract:) Fun stuff… sorry for the tangent I have run-on-itis today:)

Im sure Peter knows this story more precisely on pimo.

So B2 on for sure and there is a big study going on right now to support pimo in B2 and I hear the results are +.

Anonymous

Thanks, that’s really
Thanks, that’s really interesting stuff. I actually had heard of that previously from when I worked in UK. In any case, all this comments are being very helpful and clarifying and reassuring so that I can communicate better with my colleagues with appropriate base. Thanks again.

Peter

Hi!
I would use Pimo in this

Hi!

I would use Pimo in this case by all means. There is clear evidence of advanced disease with marked volume overload and systolic impairment.

The story about cardiac death is – as far as I know – the human story (reason why they dont use it in humans). 

Pimo is a very safe drug and one of the most effective we have in veterinary cardiology. Initially, there was concern that Pimo could worsen the progression of DMVD or cause arrhythmias. The latter has been sufficiently refuted and many cardiologists use it even before the onset of CHF if there is evidence of systolic dysfunction (off level, though).

Of course, it should never be used in a stage B1 case!

Peter

 

 

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