Difference between revisions of "Feline Infectious Anaemia"

Latest revision as of 10:15, 8 March 2022

Summary
Cause:	Mycoplasma haemofelis
Signalment:	Male cats with outdoor access
Associated conditions:	Feline retroviruses
Differential diagnoses:	Other causes of anaemia
Diagnosis:	PCR, blood smear examination
Treatment:	Doxycycline

Also known as: FIA — Haemoplasmosis — Hemoplasmosis; previously known as: Haemobartonellosis

Caused by: Mycoplasma haemofelis (Mhf) (previously known as Haemobartonella felis), Candidatus M. haemominutum (Mhm) — Candidatus M. turicensis (Mtc)

Introduction

Feline Infectious Anaemia is a regenerative anaemia of cats caused by Mycoplasma haemofelis (Mhf). The disease occurs worldwide and should be considered as a differential diagnosis for any cat presenting with anaemia.

Aetiology

Mhf is one of a group of organisms known as haemotropic mycoplasmas which infect many mammalian species. The causative organism was previously called Haemobartonella felis and thus the disease was known as haemobartonellosis. Polymerase chain reaction (PCR) assays allowing DNA analysis resulted in the reclassification of the organism as a mycoplasma in 2001^[1]. Two other haemotropic mycoplasmas (Candidatus M. haemominutum (Mhm) and Candidatus M. turicensis (Mtc)) have also been identified in cats but appear to be less pathogenic^[2].

Mhf can vary in shape from cocci to rods and is sometimes present as chains of organisms on the surface of erythrocytes.

Mycoplasma haemofelis on the surface of an erythrocyte

Transmission

The mode of transmission of Mhf is poorly understood. Several possibilities have been proposed but none have been able to be reliably demonstrated. These include:

Biting and fighting activities. Infection by this route has not been able to be demonstrated experimentally.
Fleas. The fact that Mhf infection can be prevalent in areas where fleas are uncommon makes this less likely.^[3]
Arthropods. Geographic variation in rates of Mhf infection does exist and could be due to transmission by an arthropod. ^[4]

As transmission has been shown to occur through blood transfusion due to the ability of the organism to survive in stored blood products for up to 7 days ^[5], it is recommended that blood donors be screened.^[6]

Signalment

The major group at risk for Mhf infection are young male cats who spend time outdoors. In many areas of the world an association has been shown between Mhf and retroviral infections^[2]. It has been demonstrated that cats infected with Mhf and feline leukaemia virus (FeLV) are likely to develop more severe anaemia that cats infected only with Mhf ^[6].

Pathogenesis

The pathogenesis of Mhf is not fully understood. It is thought that the presence of the parasite on the surface of the erythrocytes may induce antibody production^[7], resulting in haemolysis which is primarily extravascular. The haemolysis may be due to direct damage of erythrocytes by the organism or as a result of the antibodies produced by the infected animal ^[6].

Cats can produce an immune response which results in the disappearance of organisms from the blood. Production of uninfected erythrocytes can then result in an increase in haematocrit.

It is thought that recovered cats can become subclinical carriers, with the potential for the disease to recrudesce if the animal is in a stressed state eg pregnancy, illness.^[8]

Mycoplasma haemofelis on the surface of blood cells

Clinical signs

Infected cats most commonly present for lethargy and decreased appetite. Physical examination findings are non-specific and can include signs of anaemia, such as mucous membrane pallor, tachypnoea and tachycardia, pyrexia, and occasionally splenomegaly and jaundice. Pyrexia is frequently intermittent and spikes when parasite numbers are highest ^[6]. The anaemia can be severe and rapidly fatal in some cases.

Differential diagnosis

There are multiple causes of both regenerative and non-regenerative anaemia in cats which must be considered as differential diagnoses.

For cats showing signs of regeneration, causes of blood loss or haemolysis must be considered:

primary immune-mediated haemolytic anaemia
Heinz body haemolytic anaemia (onions, garlic, propofol)
other infectious causes such as Babesia felis and Cytauxzoon felis
neoplasia

Major differential diagnoses for cats with non-regenerative anaemia include:

neoplasia
chronic inflammatory conditions
underlying conditions such as diabetes mellitus and renal disease
Feline Immunodeficiency Virus(FIV) and FeLV infections
bone marrow diseases

Diagnosis

The most commmon findings from complete blood counts from cats with Mhf infections are a macrocytic, hypochromic regenerative anaemia. Reticulocytes and Howell-Jolly bodies may be identified on cytologic examination.

Mhf infection can be definitively diagnosed by identification of organisms on a blood smear, appearing as cocci or rods and sometimes forming short chains of organisms. However, examination of a single blood smear is less than 50% sensitive ^[7] as the animal's immune response causes organisms to disappear from the blood stream for several days, often to reappear a few days later. One study found that smears should be examined every four days over a minimum of three four day cycles^[9], making it possible to have eight days between presentation and diagnosis. It also has the potential for misidentification of organisms.

The gold standard for diagnosis of Mhf infection is polymerase chain reaction (PCR), which detects the 16S RNA gene. The test is widely available through veterinary diagnostic laboratories. There are two types of PCR tests; conventional PCR which uses the presence or absence of bands on a gel to assess infection, and real-time PCR assays which uses fluoresence to mark a segment of DNA unique to the organism, making it highly sensitive and species-specific and thus the test of choice ^[2]. Treatment with antimicrobials may result in false negatives on PCR so collecting before beginning therapy is preferable.

Treatment

The treatment of choice for Mhf infection is doxycycline for at least two weeks. Only cats who are anaemic and have clinical signs and laboratory results consistent with haemoplasmosis should be treated as the drug does not reliably eliminate the organism^[2]. For this reason a PCR-positive cat may not become negative despite treatment and therapy cannot be used to ensure blood donor cats are free from infection.

Enrofloxacin is also an effective treatment ^[10] but is a second choice due to the risk of acute retinal damage in cats.

A blood transfusion may also be required in cases of severe anaemia.

Antimicrobial therapy and blood transfusions should be initiated before PCR results are known, as this may take several days. In cats testing negative for Mhf and failing to respond to therapy, alternative diagnoses should be considered.

The use of glucocorticoids to suppress immune-mediated damage to erythrocytes has been suggested. However, as this treatment may cause reactivation of a latent infection it is recommended that they only be used in cats not responding to doxycycline and/or for whom there is no definitive diagnosis.

Prognosis

Prognosis for infected cats is related to the severity of the anaemia at presentation. If an animal survives the initial anaemia prognosis for clinical recovery is good. However, antibiotics do not clear the infection so many cats become carriers of the organism. Affected animals may also have intercurrent disease, such as retroviral infections, which will also affect the prognosis.

Feline Infectious Anaemia Learning Resources
Vetstream To reach the Vetstream content, please select	Canis, Felis, Lapis or Equis
Flashcards Test your knowledge using flashcard type questions	Small Animal Emergency and Critical Care Medicine Q&A 12
Literature Search Search for recent publications via CAB Abstract (CABI log in required)	Mycoplasma haemofelis publications Feline Infectious Anaemia publications
Full Text Articles Full text articles available from CAB Abstract (CABI log in required)	Diagnosis and management of Hemoplasma infections. Lappin, M. R.; The North American Veterinary Conference, Gainesville, USA, Small animal and exotics. Proceedings of the North American Veterinary Conference, Orlando, Florida, USA, 17-21 January, 2009, 2009, pp 655-656, 23 ref. Bartonellosis and hemoplasmosis in dogs and cats: emerging issues. Lappin, M. R.; The North American Veterinary Conference, Gainesville, USA, Small animal and exotics. Proceedings of the North American Veterinary Conference, Volume 21, Orlando, Florida, USA, 2007, 2007, pp 629-631

References

↑ Niemark H, Johansson KE, Rikihisa Y, et al (2001) Proposal to transfer some members of the genera Haemobartonella and Eperythrozoon to the genus Mycoplasma with descriptions of Candidatus Mycoplasma haemofelis, Candidatus Mycoplasma haemomuris, Candidatus Mycoplasma haemosuis and Candidatus Mycoplasma wenyonii Int J Sys Evol Microbiol 51(3) pp891-9
↑ ^2.0 ^2.1 ^2.2 ^2.3 Sykes, JE (2010) Feline Hemotropic Mycoplasmas Vet Clinics of North America: Small Animal Practice pp. 1157-1170
↑ Jensen WA, Lappin MR, Kamkar S et al (2001) Use of a polymerase chain reaction assay to detect and differentiate two strains of Haemobartonella felis in naturally infected cats. Am J Vet Res 62(4):604-8
↑ Willi B, Boretti FS, Baumgartner C et al (2006) Prevalence, risk factor analysis and follow-up of infections caused by three feline haemoplasma species in Switzerland. J Clin Microbiol 44(3):961-9
↑ Gary AT, Richmond HL, Tasker S etal (2006) Survival of Mycoplsma haemofelis and Candidatus Mycolplasma haemominitum in blood of cats used for transfusions J Feline Med Surg 8(5):321-6
↑ ^6.0 ^6.1 ^6.2 ^6.3 Wardrop J, Reine N, Birkenheuer A et al (2005) Canine and feline blood donor screening for infectious disease J Vet Intern Med 19(1) pp.135-42.
↑ ^7.0 ^7.1 Hagiwara, MK (2009) Anemia in Cats: Is It Mycoplasma? Proceedings of the 34th World Small Animal Veterinary Congress
↑ Harvey JW and Gaskin JM (1978)Feline haemobartonellosis;attempts to induce relapses of clinical disease in chronically infected cats.J Am Anim Hosp Assoc14:453
↑ Ettinger, S.J, Feldman, E.C. (2005) Textbook of Veterinary Internal Medicine (6th edition, volume 2) W.B. Saunders Company
↑ Tasker, S, Helps CR, Day MJ et al.(2004) Use of a Taqman PCR to determine the response to Mycoplasma haemofelis infection to antibiotic treatment. JMicrobiol Methods 56(1):63-71

Extra references

Merck & Co (2008) The Merck Veterinary Manual (Eighth Edition) Merial

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[Niemark-1] Niemark H, Johansson KE, Rikihisa Y, et al (2001) Proposal to transfer some members of the genera Haemobartonella and Eperythrozoon to the genus Mycoplasma with descriptions of Candidatus Mycoplasma haemofelis, Candidatus Mycoplasma haemomuris, Candidatus Mycoplasma haemosuis and Candidatus Mycoplasma wenyonii Int J Sys Evol Microbiol 51(3) pp891-9

[Sykes-2] 2.0 ^2.1 ^2.2 ^2.3 Sykes, JE (2010) Feline Hemotropic Mycoplasmas Vet Clinics of North America: Small Animal Practice pp. 1157-1170

[Jensen-3] Jensen WA, Lappin MR, Kamkar S et al (2001) Use of a polymerase chain reaction assay to detect and differentiate two strains of Haemobartonella felis in naturally infected cats. Am J Vet Res 62(4):604-8

[Willi-4] Willi B, Boretti FS, Baumgartner C et al (2006) Prevalence, risk factor analysis and follow-up of infections caused by three feline haemoplasma species in Switzerland. J Clin Microbiol 44(3):961-9

[Gary-5] Gary AT, Richmond HL, Tasker S etal (2006) Survival of Mycoplsma haemofelis and Candidatus Mycolplasma haemominitum in blood of cats used for transfusions J Feline Med Surg 8(5):321-6

[Wardrop-6] 6.0 ^6.1 ^6.2 ^6.3 Wardrop J, Reine N, Birkenheuer A et al (2005) Canine and feline blood donor screening for infectious disease J Vet Intern Med 19(1) pp.135-42.

[Hagiwara-7] 7.0 ^7.1 Hagiwara, MK (2009) Anemia in Cats: Is It Mycoplasma? Proceedings of the 34th World Small Animal Veterinary Congress

[Harvey-8] Harvey JW and Gaskin JM (1978)Feline haemobartonellosis;attempts to induce relapses of clinical disease in chronically infected cats.J Am Anim Hosp Assoc14:453

[Ettinger-9] Ettinger, S.J, Feldman, E.C. (2005) Textbook of Veterinary Internal Medicine (6th edition, volume 2) W.B. Saunders Company

[Tasker-10] Tasker, S, Helps CR, Day MJ et al.(2004) Use of a Taqman PCR to determine the response to Mycoplasma haemofelis infection to antibiotic treatment. JMicrobiol Methods 56(1):63-71

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-{{unfinished}}
+{{OpenPagesTop}}
+{{Summary
+|cause = ''Mycoplasma haemofelis''
+|signalment = Male cats with outdoor access
+|associated = Feline retroviruses
+|differentials = Other causes of anaemia
+|diagnosis = PCR, blood smear examination
+|treatment = Doxycycline
+}}
+Also known as: '''''FIA — Haemoplasmosis — Hemoplasmosis'''''; previously known as: ''Haemobartonellosis''
-==Desciption==
+Caused by: '''''Mycoplasma haemofelis (Mhf)''''' (previously known as ''Haemobartonella felis''), '''''Candidatus M. haemominutum (Mhm) — Candidatus M. turicensis (Mtc)'''''
-An infectious disease of the cat caused by ''[[Mycoplasma haemofelis]]'' which until recently was known as ''Haemobartonella felis''.
-The organism is found on the surface of [[Erythrocytes|erythrocytes]] and is considered an opportunistic infection that causes illness following predisposing factors. It is possible to be transmitted via bite wounds, biting arthropods, via blood transfusions and from a queen to her kittens. The organism causes a cyclic parasitaemia in affected cats and infected animals despite mounting an immune response will become carriers of the organism.
+==Introduction==
+Feline Infectious Anaemia is a [[Regenerative_and_Non-Regenerative_Anaemias|regenerative anaemia]] of cats caused by '''''Mycoplasma haemofelis''''' (Mhf). The disease occurs worldwide and should be considered as a differential diagnosis for any cat presenting with anaemia.
+==Aetiology==
+Mhf is one of a group of organisms known as haemotropic [[Mycoplasmas|mycoplasmas]] which infect many mammalian species. The causative organism was previously called ''Haemobartonella felis'' and thus the disease was known as haemobartonellosis. [[Polymerase_Chain_Reaction|Polymerase chain reaction]] (PCR) assays allowing DNA analysis resulted in the reclassification of the organism as a mycoplasma in 2001<ref name="Niemark">Niemark H, Johansson KE, Rikihisa Y, et al (2001) Proposal to transfer some members of the genera ''Haemobartonella'' and ''Eperythrozoon'' to the genus ''Mycoplasma'' with descriptions of Candidatus ''Mycoplasma haemofelis'', Candidatus ''Mycoplasma haemomuris'', Candidatus ''Mycoplasma haemosuis'' and Candidatus ''Mycoplasma wenyonii'' '''Int J Sys Evol Microbiol 51(3) pp891-9</ref>. Two other haemotropic mycoplasmas (''Candidatus M. haemominutum'' (Mhm) and ''Candidatus M. turicensis'' (Mtc)) have also been identified in cats but appear to be less pathogenic<ref name="Sykes">Sykes, JE (2010) Feline Hemotropic Mycoplasmas '''Vet Clinics of North America: Small Animal Practice''' pp. 1157-1170</ref>.
+Mhf can vary in shape from cocci to rods and is sometimes present as chains of organisms on the surface of [[Erythrocyte|erythrocytes]].
+[[File:M haemofelis2.jpg|thumb|''Mycoplasma haemofelis'' on the surface of an erythrocyte]]
+==Transmission==
+The mode of transmission of Mhf is poorly understood. Several possibilities have been proposed but none have been able to be reliably demonstrated. These include:
+* Biting and fighting activities. Infection by this route has not been able to be demonstrated experimentally.
+*[[Fleas|Fleas]]. The fact that Mhf infection can be prevalent in areas where fleas are uncommon makes this less likely.<ref name="Jensen"> Jensen WA, Lappin MR, Kamkar S et al (2001) Use of a polymerase chain reaction assay to detect and differentiate two strains of ''Haemobartonella felis'' in naturally infected cats. '''Am J Vet Res''' 62(4):604-8 </ref>
+*[[Arthropods|Arthropods]]. Geographic variation in rates of Mhf infection does exist and could be due to transmission by an arthropod. <ref name="Willi">Willi B, Boretti FS, Baumgartner C et al (2006) Prevalence, risk factor analysis and follow-up of infections caused by three feline haemoplasma species in Switzerland. '''J Clin Microbiol''' 44(3):961-9</ref>
+As transmission has been shown to occur through blood transfusion due to the ability of the organism to survive in stored blood products for up to 7 days <ref name="Gary">Gary AT, Richmond HL, Tasker S etal (2006) Survival of ''Mycoplsma haemofelis'' and ''Candidatus'' Mycolplasma haemominitum in blood of cats used for transfusions '''J Feline Med Surg''' 8(5):321-6</ref>, it is recommended that blood donors be screened.<ref name="Wardrop">Wardrop J, Reine N, Birkenheuer A et al (2005) Canine and feline blood donor screening for infectious disease '''J Vet Intern Med''' 19(1) pp.135-42.</ref>
 ==Signalment==
-Almost half of the cats infected have concurrent [[Feline Leukaemia Virus|Feline Leukaemia Virus]] (FeLV).
+The major group at risk for Mhf infection are young male cats who spend time outdoors. In many areas of the world an association has been shown between Mhf and [[Retroviridae|retroviral infections]]<ref name="Sykes" />. It has been demonstrated that cats infected with Mhf and [[Feline_Leukaemia_Virus|feline leukaemia virus (FeLV)]] are likely to develop more severe anaemia that cats infected only with Mhf <ref name="Wardrop"></ref>.
-The disease is common in roaming Tom cats 1-3 years old.
+==Pathogenesis==
+The pathogenesis of Mhf is not fully understood. It is thought that the presence of the parasite on the surface of the erythrocytes may induce [[Immunoglobulins_-_Overview|antibody production]]<ref name="Hagiwara"></ref>, resulting in [[Regenerative_and_Non-Regenerative_Anaemias#Haemolysis|haemolysis]] which is primarily extravascular. The haemolysis may be due to direct damage of erythrocytes by the organism or as a result of the antibodies produced by the infected animal <ref name="Wardrop"></ref>.
+Cats can produce an immune response which results in the disappearance of organisms from the blood. Production of uninfected erythrocytes can then result in an increase in [[haematocrit]].
+It is thought that recovered cats can become subclinical carriers, with the potential for the disease to recrudesce if the animal is in a stressed state eg pregnancy, illness.<ref name = "Harvey">Harvey JW and Gaskin JM (1978)Feline haemobartonellosis;attempts to induce relapses of clinical disease in chronically infected cats.'''J Am Anim Hosp Assoc'''14:453</ref>
+[[File:M haemofelis.jpg|thumb|''Mycoplasma haemofelis'' on the surface of blood cells]]
+==Clinical signs==
+Infected cats most commonly present for lethargy and decreased appetite. Physical examination findings are non-specific and can include signs of anaemia, such as mucous membrane pallor, tachypnoea and tachycardia, pyrexia, and occasionally splenomegaly and [[Icterus|jaundice]]. Pyrexia is frequently intermittent and spikes when parasite numbers are highest <ref name="Wardrop"></ref>.  The anaemia can be severe and rapidly fatal in some cases.
+==Differential diagnosis==
+There are multiple causes of both [[Regenerative and Non-Regenerative Anaemias|regenerative and non-regenerative anaemia]] in cats which must be considered as differential diagnoses.
+For cats showing signs of regeneration, causes of blood loss or haemolysis must be considered:
+*[[Immune_Mediated_Haemolytic_Anaemia|primary immune-mediated haemolytic anaemia]]
+*Heinz body haemolytic anaemia (onions, garlic, [[propofol]])
+*other infectious causes such as [[Babesia|''Babesia felis'']] and [[Cytauxzoon#Cytauxzoon_felis|''Cytauxzoon felis'']]
+*[[Neoplasia_-_Pathology|neoplasia]]
+Major differential diagnoses for cats with non-regenerative anaemia include:
+*neoplasia
+*chronic inflammatory conditions
+*underlying conditions such as [[Diabetes_Mellitus|diabetes mellitus]] and [[Chronic_Renal_Failure|renal disease]]
+*[[FIV|Feline Immunodeficiency Virus(FIV)]] and [[FeLV]] infections
+*[[Regenerative_and_Non-Regenerative_Anaemias#Failure_of_the_bone_marrow_stem_cells_to_produce_erythroid_cells|bone marrow diseases]]
 ==Diagnosis==
-The organism can be intermittently seen microscopically on the surface of red blood cells on Giemsa-stained blood smears. The organism stains blue and look like rings or rods.
-Erythrophagocytosis may be evident and parasitised erythrocytes will become spherical.
+The most commmon findings from complete blood counts from cats with Mhf infections are a '''macrocytic, hypochromic regenerative anaemia'''. [[Reticulocyte|Reticulocytes]] and [[Howell-Jolly Bodies|Howell-Jolly bodies]] may be identified on cytologic examination.
+Mhf infection can be definitively diagnosed by identification of organisms on a blood smear, appearing as cocci or rods and sometimes forming short chains of organisms. However, examination of a single blood smear is less than 50% sensitive <ref name="Hagiwara"> Hagiwara, MK (2009) Anemia in Cats: Is It Mycoplasma? '''Proceedings of the 34th World Small Animal Veterinary Congress'''</ref> as the animal's immune response causes organisms to disappear from the blood stream for several days, often to reappear a few days later. One study found that smears should be examined every four days over a minimum of three four day cycles<ref name="Ettinger>Ettinger, S.J, Feldman, E.C. (2005) Textbook of Veterinary Internal Medicine (6th edition, volume 2) W.B. Saunders Company</ref>, making it possible to have eight days between presentation and diagnosis. It also has the potential for misidentification of organisms.
-The organism must be differentiated from Howell-Jolly bodies and other parasites. Due to the cyclic parasitaemia the organism causes, negative blood smears will not rule out the disease.
-Additionally Immunofluorescence of blood smears can demonstrate the organism.
+The gold standard for diagnosis of Mhf infection is polymerase chain reaction (PCR), which detects the 16S RNA gene. The test is widely available through veterinary diagnostic laboratories. There are two types of PCR tests; conventional PCR which uses the presence or absence of bands on a gel to assess infection, and real-time PCR assays which uses fluoresence to mark a segment of DNA unique to the organism, making it highly sensitive and species-specific and thus the test of choice <ref name="Sykes"></ref>. Treatment with antimicrobials may result in false negatives on PCR so collecting before beginning therapy is preferable.
-Haematology will show a decreased packed cell volume and a low Red blood cell count.
+==Treatment==
+The treatment of choice for Mhf infection is [[Tetracyclines|doxycycline]] for at least two weeks. Only cats who are anaemic and have clinical signs and laboratory results consistent with haemoplasmosis should be treated as the drug does not reliably eliminate the organism<ref name="Sykes"></ref>. For this reason a PCR-positive cat may not become negative despite treatment and therapy cannot be used to ensure blood donor cats are free from infection.
-===Clinical signs===
+[[Fluoroquinolones|Enrofloxacin]] is also an effective treatment <ref name="Tasker">Tasker, S, Helps CR, Day MJ et al.(2004) Use of a Taqman PCR to determine the response to ''Mycoplasma haemofelis'' infection to antibiotic treatment. '''JMicrobiol Methods''' 56(1):63-71</ref> but is a second choice due to the risk of acute retinal damage in cats.
-The peracute disease is associated with severe anaemia and immunosuppression, and can be rapidly fatal.
-Fever, anaemia, depression, weakness and jaundice occur in the acute form. In the chronic form animals present with anaemia, lethargy and weight loss.
+A [[:Category:Transfusion Medicine|blood transfusion]] may also be required in cases of severe anaemia.
-Cyclic fever may also occur during the transient period of parasitaemia.
+Antimicrobial therapy and blood transfusions should be initiated before PCR results are known, as this may take several days. In cats testing negative for Mhf and failing to respond to therapy, alternative diagnoses should be considered.
-Recovery can occur with a regenerative bone marrow response however severe anaemia may occur in the presence of [[Feline Leukaemia Virus|feline leukaemia virus]] (FeLV).
+The use of [[Steroids|glucocorticoids]] to suppress immune-mediated damage to erythrocytes has been suggested. However, as this treatment may cause reactivation of a latent infection it is recommended that they only be used in cats not responding to doxycycline and/or for whom there is no definitive diagnosis.
-===Treatment===
+==Prognosis==
-Infected cats should be treated with [[Tetracyclines|doxycycline]] for 3 weeks twice daily. [[Fluoroquinolones|Enrofloxacin]] is also a good treatment choice especially in refractory cases when combined with doxycycline.
+Prognosis for infected cats is related to the severity of the anaemia at presentation. If an animal survives the initial anaemia prognosis for clinical recovery is good. However, antibiotics do not clear the infection so many cats become carriers of the organism. Affected animals may also have intercurrent disease, such as retroviral infections, which will also affect the prognosis.
-A blood transfusion may als be required in cases of severe anaemia.
-As blood sucking endoparasites such as [[:Category:Fleas|Fleas]] are thought to spread disease the animal should also recieve flea treatment.
+{{Learning
+|flashcards = [[Small Animal Emergency and Critical Care Medicine Q&A 12]]
+|literature search = [http://www.cabdirect.org/search.html?rowId=1&options1=AND&q1=%22Mycoplasma+haemofelis%22&occuring1=title&rowId=2&options2=OR&q2=%22Haemobartonella+felis%22&occuring2=title&rowId=3&options3=AND&q3=&occuring3=freetext&x=48&y=12&publishedstart=yyyy&publishedend=yyyy&calendarInput=yyyy-mm-dd&la=any&it=any&show=all ''Mycoplasma haemofelis'' publications]
-Prednislone is also advised to treat the immune mediated mechanisms and to prevent further erythrophagocytosis.
+[http://www.cabdirect.org/search.html?q=%28title%3A%28%22Infectious+Anaemia%22%29+OR+title%3A%28Haemobartonellosis%29+OR+title%3A%28%22Mycoplasma+haemofelis%22%29+OR+title%3A%28%22Haemobartonella+felis%22%29%29+AND+od%3A%28cats%29 Feline Infectious Anaemia publications]
+|full text = [http://www.cabi.org/cabdirect/FullTextPDF/2009/20093115252.pdf ''' Diagnosis and management of Hemoplasma infections.''' Lappin, M. R.; The North American Veterinary Conference, Gainesville, USA, Small animal and exotics. Proceedings of the North American Veterinary Conference, Orlando, Florida, USA, 17-21 January, 2009, 2009, pp 655-656, 23 ref.]
-==Prognosis==
+[http://www.cabi.org/cabdirect/FullTextPDF/2007/20073119573.pdf ''' Bartonellosis and hemoplasmosis in dogs and cats: emerging issues.''' Lappin, M. R.; The North American Veterinary Conference, Gainesville, USA, Small animal and exotics. Proceedings of the North American Veterinary Conference, Volume 21, Orlando, Florida, USA, 2007, 2007, pp 629-631]
-Varied depending on the severity of the anaemia at presentation. If not treated 1/3 of affected animals will die. Antibiotics do not clear the infection so many cats become carriers of the organism however relapses are uncommon.
+|Vetstream = [https://www.vetstream.com/felis/Content/Disease/dis60170 Feline infectious anemia]
+}}
 ==References==
-Ettinger, S.J, Feldman, E.C. (2005) '''Textbook of Veterinary Internal Medicine''' (6th edition, volume 2)''W.B. Saunders Company''
+<references/>
+==Extra references==
 Merck & Co (2008) '''The Merck Veterinary Manual''' (Eighth Edition) ''Merial''
-[[Category:Anaemia]]
-[[Category:Cat]][[Category:To Do - Caz]]
+{{Rebekah Brown
+|date = July 3, 2012 }}
+{{OpenPages}}
+[[Category:Anaemia|5]]
+[[Category:Lymphoreticular and Haematopoietic Diseases - Cat]][[Category:Cat Bacteria]]
+[[Category:Expert_Review - Small Animal]]