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A BIOMETRIC STUDY OF SOME REPRODUCTIVE COMPONENTS OF THE MALE DOMESTIC LOCAL BREED CAT (Felis catus domestica) IN NORTHWEST NIGERIA.
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Indian Pet Journal www.indianpetjournal.com Vol 4 (1) Dec’13
5
Preliminary Clinical Observations Following Intravenous Blood
Transfusion In Local Domestic Mongrel Cat’s In Sokoto, Nigeria
M.A. Umarua, A. Bello*
b, S. Ladan
c, D. Musa
d, U.M. Mera
e
Usmanu Danfodiyo University, Sokoto, Nigeria aDepartment of Theriogenology and Animal production,
bDepartment of Veterinary Anatomy,
cMinistry of Animal Health and Fishery, Sokoto State,
dDepartment of Agriculture, Sokoto state Polytechnic, Sokoto Nigeria,
eDepartment of Veterinary Medicine, Usmanu Danfodiyo University, Sokoto, Nigeria.
*Corresponding author: [email protected]
Abstract
In this study a preliminary attempt was made to look into intravenous blood transfusion. In this part
of the country it is performed, neither in the few veterinary teaching hospitals, nor in our local
veterinary clinics. However, several clinical cases are regularly lost due to problems of anaemia, and
several other situations of blood insufficiencies. Eighteen (18) adult stray cats were used. Six as
donors, six as recipients, and six as control receiving normal saline. Blood was collected from the
jugular vein of cats under sedation, and transferred to sedated recipients. Vital parameters
(temperature, pulse, heart beat rate and respiratory rate.), packed cell volume (PCV) and clinical
reactions to the infusions were observed. The PCV of the recipients increased between 5-10% while
the temperature was seen to be increasing as the transfusion was taking place. There was an average
increase of 6-10c. In the body temperature .clinical signs observed during the initial blood
transfusion includes, salivation, urination, muscular tremors, vomiting, lacrimation, and bloat. While
the signs were more severe after the repeat transfusion two weeks afterwards, indicating serious
transfusion reactions such as severe salivation, urination, muscular tremors, vomiting, lacrimation,
mydriasis, lethargy, convulsions, facial oedema, opisthotonus and death. The control received
placebo and did not show any signs of adverse clinical reactions. A PCV of 26.83± 2.48%, before and
33.50±3.21%after the first transfusion, while the temperature of 37.72±0.64◦c before and 37.9±3.89oc
after the transfusion, a heart rate of 118±5.72beats/min before and 143.33±12.61 beats/min after the
first transfusion. The PCV for the repeat transfusion was 32.5 ± 2.66% before and 37.9±0.54oc before
and 39.4±0.29 after the second transfusion while heart rates of 119.33±7.06beat/minutes before and
151.33±7.65 beat /minutes after the second intravenous transfusions. These experiments showed that
blood transfusion in the local mongrel cats in northwest Nigeria can be performed to save the live of
a cat with problems of blood insufficiency. However, with some adverse reactions, a repeat blood
transfusion is not recommended because it can come with attendant severe transfusion reactions,
including death. The findings were discussed in the paper.
Key words: Clinical observation, Blood transfusion,Domestic mangrel cat, Intravenous,
Sokoto.
Introduction
Blood transfusion is the process of transferring blood or blood based products from one
individual into the circulatory system of another, blood transfusion can be like saving in
some situations, such as massive blood loss due to trauma, shock or can be used to replace
blood lost during surgery. Blood transfusion may also be used to treat severe anaemia or
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thrombocytopenia caused by blood disease in individuals suffering from haemophilia of
sickle cell disease which may require frequent transfusion. To obtain blood from cat’s,
sedation of anaesthesia is necessary to knock down the cat sufficiently to make safe blood
collection and donation. The blood is obtained directly, from large veins in the neck Jugular
vein using syringe profiled with anticoagulant and direct vain puncture or butterfly to catheter
fluids are often administered before and during blood collection. Up to 1/% of blood volume
can usually be taken without ill effect as a rough guide, one percent (1%) of the donor body
weight (30mL for a 30kg cat). The main blood groups system in cats can be grouped into type
A, type B and type AB. Like humans type A automatically react to type B blood and vice
versa. The rare AB blood group cats can receive blood from either type A or type B donors.
Transfusion reaction are usually separated into two categories immunological and Non-
immunological, the most common reaction of transfusions are vomiting and facial oedema.
Immunological transfusion reaction can be haemolytic or non-haemolytic in nature. Both
types can be separated into acute (Those occurring immediately after transfusion) and
delayed reactions, the worst type of reaction is the acute haemolytic reaction which can result
in death of the animal. An acute haemolytic reaction is due to a blood type incompatibility,
there is the non immunological transfusion reaction like circulatory overload, Haemolysis,
Bacterial contamination, etc.
Materials and Methods
Twelve adult of either six were used for this study. The goats were purchased from Sokoto
market with ages ranging from 10-12 months and body weight ranging between 25-30kg.
They were fed on bean haulm, wheat bran with fresh tap water. They were kept for 20 days.
Before the commencement of the experiment in order to stabilized and acclimatized with the
environment. During this period, a prophylaxis antibiotic along with deworming of the
animals was incorporated.
Blood samples were taken using EDTA bottles for PCV. The animals were divided into two
groups of 6 each i.e. 6 donor and 6 recipients. The donors were physically restrained and
jugular vein was prepared aseptically with Savlon and razor blade was used for shaving the
area. Commercial blood bags were prepared with 18g hypodermic needle was inserted via the
jugular vein. The quantity of blood depend on the weight of the animal i.e 10% of the blood
volume can usually be taken without any effect i.e rough guide of 1% of the donor body
weight i.e 100ml for 10kg as reported by Boden, (2001). Samples were stored in the
refrigerator for a period of two days before administration. Before administration the PCV
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were taken and were also warmed to body heat before administration according to Boden,
(2001). The recipients were prepared and mildly sedated; the site of choice for the transfusion
was the cephalic vein. Materials use include: Butterfly needle, Given set and adhesive tape
the animals were observed for any possible reaction with record taken at every stage. Clinical
observation during and after intravenous blood transfusion were conducted.
Results
The Packed Cell Volume (PCV) of each recipient increased between 5-10% while the
temperature was seen to be increasing as the transfusion is taken place, it has a marked
increase of about 6-100C this is expected as. A new substance has been introduced into the
circulation of the animal’s body consequently there is likely to be such increase in
temperature. Physiologically, as of the donors there is slight decrease in temperature after
blood collection. Other observations apart from increase in temperature after transfusion as
shown in table below includes salivation shivering, vomiting lacrimation and bloat before
recovery from anaesthesia.
The table 1 shows record of PCV levels and vital parameter of cats (Donors) before sample
were taken first transfusion. Table 4 shows the record of PCV levels and vital parameters of
the recipient before and after the first and second transfusion and in the first transfusion the
following signs were observed. They include salivation, urination, convulsion and vomition
which is as result of recovery from anaesthesia while bloat is a result of prolong as result of
recovery from anaesthesia while bloat is a result of prolong recumbency, the result obtained
from the transfusion indicate that there is no adverse reaction of hypersensitivity after first
transfusion and the cats were kept under close observation for one week. Therefore, its safe
and it was equally found that the first exposure can lead to a significantly marked increase in
parked cell volume, after the second transfusion, the following signs were observed in
addition to the first ones mentioned above, there was server hyperaemia on all the mucous
membranes and the extremities. There was server salivation and mydriasis and there was a
prolonged recovery from anaesthesia as compared with the first transfusion, two of the
recipient eventually died within 30 and 46mins respectively. There was marked increase in
PCV and temperature; three of the cats remain dull 2 days. This shows that there was
hypersensitivity reaction following the second transfusion and mydriasis observed in one of
the cats was indicative of aesthetic over dose.
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Table 1: Record of PCV levels and vital Parameter of cats (donors) before sample were taken
first transfusion
Donor animal PCV (%) Temperature before
collection (0
C)
Temperature before
collection (0
C)
D1 42 37.8 37.2
D2 51 39.0 38.7
D3 38 38.2 37.1
D4 44 37.7 37.0
D5 39 38.6 37.2
D6 40 37.9 37.1
Table 2: Record of PCV levels and vital parameters of the recipient before and after
transfusion.
Recipient
animal
PCV (%)
Vol. Before
transfusion
PCV(%)
Vol. after
transfusion
Temp.
Before
transfusion
Temp.
After
transfusion
Heart/rate b/m before &
after transfusion
Before After
R1 26 32 38.2 39.5 120 152
R2 29 36 37.0 30.0 126 163
R3 30 38 37.8 40.0 118 144
R4 27 34 37.0 39.2 110 128
R5 23 29 37.7 39.0 114 135
R6 26 32 38.6 39.7 122 138
Mean±SD 26.83±2.48 33.50±3.21 37.72±0.64 37.9±3.89 118.33±5.72 143.33±12.61
Table 3: Record of PCV levels and vital parameter of cats (donors) before sample were taken
Second blood transfusion.
Donor animal PCV (%) Temperature before
collection (0C)
Temperature before
collection (0C)
D1 44 37.7 37.0
D2 39 38.6 37.2
D3 36 37.9 37.3
D4 38 38.1 37.7
D5 39 38.2 37.5
D6 29 37.4 37.0
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Table 4: Record of PCV levels and vital parameters of the recipient before and after the
second Blood transfusion.
Recipient
animal
OCV (%)
Vol. Before
transfusion
PCV (%)
after
transfusion
Temp.
Before
transfusion
(0
C)
Temp.
After
transfusion
(0
C)
Heart/rate b/m before &
after transfusion
Before After
R1 31 39 37.5 39.2 110 138
R2 33 41 38.1 39.5 117 152
R3 35 44 37.2 39.6 113 155
R4 36 46 38.7 39.6 113 155
R5 31 38 38.2 39.7 127 161
R6 29 37 37.7 38.9 126 153
Mean±SD 32.5 ±2.66 40.83±3.54 37.9±0.54 39.4±0.29 119.33±7.06 151.33±7.65
Table 5. Physiological/clinical manifestations following intravenous blood transfusions in the
local mongrel cats.
Clinical
manifestations
Control(n=6)
Received placebo 1
st
transfusion(n=6) 2nd
transfusion(n=6)
Salivation
Urination
Muscular tremors
Lacrimation
Vomition
Mydriasis
Erythrema
facial oedema
Convulsion
Death
No salivation
No urination
No muscular
tremors
No lacrimation
No vomition
No mydriasis
No erythrema
No facial oedema
No convulsion
No death
Salivation
Urination
Muscular tremors
Lacrimation
Vomition
Mydriasis
Erythrema
Facial oedema
Convulsion
No death
Profuse salivation
urination
Severe muscular
tremors
Lacrimation
Vomition
Mydriasis
Erythrema
Severe facial oedema
severe convulsion
Death (33.3%)
Discussion and Conclusion
It’s important to perform blood transfusion particularly in Veterinary Clinic. This will boost
survival of the animal by treatment of chronic anaemia. Blood transfusion may also be life
saving where it is necessary to replace blood loss caused by accident, shocks surgeries as well
as post partum haemorrhages. The process of transfusion will therefore greatly contribute to
good reproductive health reducing loss of pets or highly price animals.
Other observations include drop in temperature of donors after collection an increase in
temperature, heart beat and respiratory rate of the recipients after transfusion. Other signs
observed after the second transfusion was indicative of typical signs of hypersensitivity
reaction. As of increase in body temperature is not surprising because physiologically the
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body react with any foreign agent that comes into it, some literature reported that such type of
increase in temperature are as a result of increases in blood flow into the vein (Boden, 2001).
Collapse which is a sudden failure of a system and Opisthotonos which is the position
assumed by the back bone during one of the convulsive seizure or epilepsy (Black Veterinary
Dictionary, 2001). Other signs observe include polycerthyamia, which is a redness of skin,
the skin surface blood vessels become gorged with blood and is seen in some bacterial
infection (Streptococcal infection) or in hypersensitivity reaction and the one observed here is
as a result of hypersensitivity reaction. As of the salivation and urination observed they could
be as a result of sedation of the animal resulting from the loss of voluntary activities by the
animals under general anaesthesia, specifically stage I and II. Prior to the transfusion in the
first attempt it is thus recommended that all recipients be cross matched prior to receive blood
cats requires cross matching and typing because most cats are born with isoantibodies against
the blood types. They are not example type B cat have strong naturally occurring antibodies
against type A blood. A small amount of 1 ml of type A blood given to type B cat can cause a
fatal transfusion reaction. Clinical observations during transfusion to recipient shows the
animals in distress, it is therefore difficult to perform in practice as it can be time consuming
and stressful to the animal. It was also observed that there was an increase in PCV after the
second transfusion (significantly of between 5 – 10% it’s therefore expected as appreciable
amount of blood (www.doctorslounge.com). In the course of this work the recipients were
sedated for ease of transfusion also according to other workers in the literature the recipient
should be mildly sedated (Cynthia et al., 2005, Boden, 2001).
Finally, there is great achievement and success in this project work because of the significant
increase observed in PCV and typical signs of hypersensitivity reaction observed in the
second transfusion. It also indicate that successful procedure is practicable and clinical
observation were mild especially in the first transfusion so also there was no abnormal
reaction of haemolytic or non haemolytic types in the first transfusion which was observed in
the second transfusion. It is therefore recommended that blood transfusion should be practice
where necessary due to its positive impact and contributions for the animal involved.
Acknowledgement
I wish to show my sincere gratitude to Mr. M. I Jimoh and Mr. O. Olushola of the
department of veterinary Anatomy, Faculty of veterinary medicine, Usmanu Danfodiyo
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university sokoto, for a job well-done in stabilising, handling and restraining the animals
during the research.
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