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Dr. Manobla has been supportive, open minded and an
integral part of this project. When we first became that RD could be a problem,
he not only researched Renal Dysplasia himself, but he read the information I
had gathered. Dr. Manobla has made many phone calls, searching for help from
knowledgeable people. He learned how to do wedge biopsies, seeking guidance from
a veterinary surgeon. I could have never tackled RD without his help. I am
grateful and I would like to thank him.
Debby Rothman
conducted the following interview with Dr. David Manobla on March 28, 1997
during a wedge biopsy of a kidney.
DM – I’m in the abdomen. Now I’ll search for the kidney. I’m pulling up the
left kidney.
DR – Is the left kidney the one you always
biopsy?
DM – The left one is a little more accessible. I’ll isolate it. That’s a
normal looking kidney. There’s a layer of capsule over the kidney. The blood
vessels to the kidney are directly below the kidney. What I’m going to do now
is to take what’s called a wedge biopsy, which is a piece of kidney, going
through the capsule, the cortex and the medullar part of the kidney. That’s
what we’ll be sending in. The kidney has a fair amount of blood just because of
what it does in the body, so when I cut into it, it will be fairly bloody.
This is the piece of kidney we’re taking out. It will be sent off to two
different labs. I’ll put some gelfoam in, to slow down the bleeding. We’re
going to suture back up where we removed the piece of specimen.
DR – What kind of suture material are you using?
DM - #3-0 Maxon with a swedged on needle. It is absorbable. The kidney tissue
is extremely friable and not the best tissue to have to suture. On the other
hand, having so much vasculature, the kidney does heal rather quickly.
DR - Do you use a different type of suture
because it is so friable?
DM – No, not really. It’s just the normal type of suture I use for spays and
that type of stuff. It’s just that there’s a certain limit to how tight you can
tighten the suture because it will just tear out of the tissue.
DR – On the first biopsy
you used strip gelfoam, but now you use powdered gelfoam. Do you have a
preference?
DM – No, it just whatever we get, actually. If we get it from one distributor
it’s the strip; the other one will send us the powder gel. They both work the
same way.
So, I usually put three or four sutures in the kidney. After that we’ll apply
some pressure for a couple of minutes to make sure the bleeding has stopped.
Sometimes we have to hold it longer. This one’s actually not too bad. The dog
we did a couple of days ago seemed to bleed more than your other dogs, so we had
to apply pressure for five minutes.
DR – Do you usually do the standard preoperative
tests?
DM – Yes, we do a standard preop, check the BUN, ALT and protein level – total
protein. If any of those come out abnormal, we will add a creatinine test,
which is another test for kidney function. If any of the liver enzymes come out
abnormal, we would run several more liver tests. When we are doing a standard
preop it certainly wouldn’t be a bad idea to do a clotting test on these
animals, since we are involved with a fair amount of bleeding, to make sure that
they do have normal clotting factors. Then we just premedicate them normally.
So, this is it. It’s bleeding right now from where I placed a suture more than
anywhere else. Now we’ll time two minutes on the clock, putting some standard
pressure on incision. Hopefully that will be the end of the bleeding. We’ll
cut the kidney specimen into two pieces. We’ll send the larger half to Dr.
Bovee at the University of Pennsylvania. Dr. Bovee will do the normal pathology
report on it, looking for dysplastic cells in the kidney. The smaller piece
will go to VetGen, where a chemical DNA study is being done, to try to make a
noninvasive test for RD through either swab or blood test. The specimen to Dr.
Bovee will go in routine formalin. The specimen to VetGen for the DNA study
will go on dry ice, in a plastic bag.
Recovery has been routine. We’ve done at least 10+ of these. We haven’t had
any post op problems. Try to keep them fairly quiet. You may want to put an
older animal on IV fluids during surgery. That would certainly also be
recommended.
DR – How about antibiotics?
DM – I personally don’t routinely give antibiotics. Once again, if it’s an
older dog or if the animal seems to bleed more than normal, I’d certainly give
them an injection of antibiotic post surgically and send them home on
antibiotics.
DR – Do you think which lab the specimen is sent
to makes a difference?
DM – Yes, I think to determine the kidney cells you should send it to a
pathologist that’s familiar with this disease and who knows what they’re looking
for. The first one – when we necropsied Cisco - we sent one kidney to CSU and
one kidney to Dr. Bovee. CSU did not find any renal dysplastic cells. Dr. Bovee
did find dysplastic cells, so I do believe that we should probably send these to
one or two specialists in this field so that our results will correlate with
each other.
Okay, so we’ll release pressure on the kidney now. It’s been several minutes
and I’ll see what we have here. It’s bleeding a little bit. We’ll put some more
pressure on it. We’ll put some more gelfoam on it. It’s fairly quiet now.
We’ll put pressure on it for another minute and that should be the end of that.
Then just a routine closure of the abdominal incision. We’ll try to keep him
fairly quiet for the first 48 hours. Cage rest is really the best way to go.
For postop recovery we use a heated cage with some warm towels from the dryer.
If I feel like the dog has bled more than I would like, I would give the animal
IV fluids after the surgery or some subcutaneous fluids. So far, these animals
have recovered very uneventfully.
We have not done urinalysis on all of these dogs. We are finding that urine
results and blood results have been normal. We haven’t had any abnormal kidney
blood results, but we’ve probably had 50% of these dogs with kidney dysplasia.
All the blood work has been normal. And the urinalysis that we have run have
been normal. They’re concentrating urine correctly. Normal pH. No signs of
disease. Okay, I think we’re gonna pop that baby back in and sew him up.
DR – Why do you think it’s important to get a
percentage of fetal glomeruli reading?
DM – I think the percentage, at this point, is just giving us a handle on
prognosis for that particular animal. Dr. Bovee would certainly be able to
explain that better, but Dr. Bovee will tell us, from the percentages, life
expectancy of that particular animal. And what the chances are of that animal
coming down with clinical symptoms. Some people are using it as a gradient on
whether or not to breed that particular animal. Most of the ones we’ve done so
far have been mildly affected – anywhere from 2 – 5 %. Any dog that comes back
with 30% – 40% fetal glomeruli has a very short life expectancy of anywhere from
2 to 6 months, according to Dr. Bovee. And there’s the moderately affected that
come back at between 10% and 15%. I believe, at this point we’re thinking, at
some point some of those dogs will show clinical symptoms. The ones that come
back from 2 – 5 % are believed to not show any clinical symptoms throughout
their life, although they are considered carriers of the disease. I believe
most of ours so far have come back mildly affected. We’ve had one severely
affected with 40% fetal glomeruli.
DR – When we first started
exploring the options, when we became aware that this could be a problem, we
talked about doing an ultrasound guided needle biopsy. Can you comment on that
and why you decided wedge biopsy would be the best route to take?
DM – Well, once again, basically we’re following Dr. Bovee’s recommendations.
He, at this point, I believe is the best specialist in this field. He believes
that ultrasound guided biopsies do not give sufficient information. It
certainly would have been much easier for us to do that, but Dr. Bovee feels
that the information obtained from an ultrasound trucut biopsy does not give
enough information. The dysplastic cells are not throughout the entire kidney
and just doing a trucut biopsy – you’re really only getting specimen from one
area and you may miss catching any fetal cells at all. With a wedge biopsy,
it’s a fairly large piece of tissue and doing the biopsy with that method, we
are able to find the dysplastic tissue in the specimen. So, I would encourage
everyone else to continue do wedge biopsy as a means of diagnosing this
problem. The wedge biopsies have seemed to give us very good information.
I use a cutting needle. It has been recommended since the tissue is so friable
to use a tapered needle. I haven’t had any problems with a cutting needle. But
it has been suggested to use a tapered as another option.
DR – So have you found this to a somewhat
routine surgery?
DM – After the first five or so. (Laughter) I had never done one of these before
we started doing your dogs. The first several - I was a little nervous - but it
really is not a difficult procedure at all. The only thing you need to be aware
of is the hemorrhage that will be associated with cutting into the kidney. So
far we haven’t had any post op problems. I think the most important thing is to
apply good pressure during the surgery and to keep the dogs extremely quiet
after the surgery. Being that we’ve done so many dogs, we’ve tried to cut some
of the costs out of it by not using fluids on every animal and not doing a
barrage of blood testing. It would always be nice to do more lab work and put
every animal on intravenous fluids, but when you’re doing a whole breeding
population it can get cost prohibitive. But there really is not a whole lot to
it. It’s fairly quick and not that involved, once you’ve done a couple of
them. We’ve done ten or so now and haven’t had any problems at all with either
long-term hemorrhage or any other problems associated with surgery. We just do
a routing closure of the abdomen.
Are these the last two of your dogs to be biopsied?
DR – This is our second to
the last. I was just thinking about when we first became aware of RD. What I’d
like you to comment on is - you weren’t aware of this particular disease. I
believe many veterinarians are not aware of RD. Can you say anything about
that?
DM - I could. Basically, I think what’s happening is that as of late, with not
just this particular breed, but with a lot of breeds, we are beginning to
realize that there are a lot of diseases that are that have been around for
awhile and we have not realized it, both in the veterinary profession and in the
breeding world. There is a book out now. Basically, all that book covers is
genetic defects of every breed of dog. That book, I believe is about 300 pages
long. So we are becoming aware that a lot of these breeds have problems that we
should be aware of, especially being veterinarians, It’s very hard to know
everything about every breed. Obviously with something like this we need to
become more aware of these problems and try to solve the problem or talk to the
breeders and at least let them be aware of the possibilities of problems with
these particular breeds. I think right now there’s probably 15 or so breeds
that have some type of renal problem on a genetic basis. Ten years ago we may
have thought there may have been three or four breeds. We are becoming much
more aware of problems. I really think the only way to get to the bottom is to
do just what you’re doing. Find out who’s affected and take care of the
situation at that point. Certainly this breed is not the only breed where we’ll
find problems. The only way we will learn about this is to keep an open mind,
be aware of the problems and try to address them and not hide the facts. Hiding
the facts will basically slow down the progression of learning about the disease
and becoming aware of it. It’s not going to make the disease go away. I think
the responsibility, with both veterinarians and breeders is to learn about your
breed, learn about the breeds and what potential problems they have. To be
aware of those problems. To try to find out which animals in the population are
affected with it and to not use them as breeding stock.
DR – For me, the biggest eye opener was that
mildly affected animals will live an asymptomatic lifespan. Prior to finding
out about this problem, I thought my dogs were kidney disease free because they
live long lives. That is what has been the most startling thing that I’ve
found out through learning and through biopsies on these animals that I’ve
worked with for five generations.
DM – Right. Right. I think most people are not aware that just because they are
asymptomatic and are not showing any disease, that they can still have the
disease and transmit the disease. That’s certainly common with other problems
as well.
That’s the surgery. It took us twenty minutes or so.
DR – Is there any else you’d like to add?
DM – Just that it’s really a fairly easy procedure to do and I would recommend
that other breeders get in touch with their veterinarian or find a veterinarian
that's willing to do a wedge biopsy if their veterinarian would not like to do
it. Find another veterinarian in their area that would work with a breeder to
help to solve this question about which animals are affected.
Dr. David Manobla will be glad to talk further with your vet about this surgical
procedure. If anyone is interested in a copy of the videotape for their
veterinarian, I will send you one for the cost of a blank videotape, postage and
the mailing envelope. Dr. Manobla’s phone number is 303/670-0838.
Biopsy specimens should be preserved in formalin and sent to: University of
Pennsylvania, School of Veterinary Medicine, Laboratory of Pathology,
attention: Dr. Michael Goldschmidt, 3800 Spruce Street, Philadelphia, PA
19104-6051 Dr. Bovee's phone number is 215/898-8857. Phone calls must come from
your veterinarian.
Debby Rothman can
be reached on Mondays, Tuesdays and Wednesdays at 303/674-3297. Please leave a
message. If she can hear you she will pick up the phone, otherwise she will
return your phone call. Her email address is:
LhasaLhady@aol.com.
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