Professional Documents
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D i s t res s : E t i o l o g y,
D i a g n o s i s , a n d Tre a t m e n t
Susan E. Orosz, PhD, DVM, DABVP (Avian), DECZM (Avian)a,*,
Marla Lichtenberger, DVM, DACVECCb
KEYWORDS
Respiratory distress Avian Anatomy and physiology
Infraobital sinus Upper respiratory infection
Paleopulmonic respiratory system
Neopulmonic respiratory system
budgerigars, the cere is usually blue (Fig. 1); in adult females it is usually brownish
pink. Changes in the normal color pattern of the cere are suggestive of gonadal tumors
in this species. Each species has a characteristic size and shape and any variation
should be noted on the physical examination.
The nares or nostrils are located dorsally within the area of the cere in psittacine
birds. The openings may be shaped abnormally as a result of chronic upper respira-
tory infection and should be noted on the physical examination (Fig. 2). Air moves
through the nares into the nasal cavity. In Amazon parrots and Galliformes, a rounded,
keratinized structure called the operculum is found in the rostral-most extent of the
nasal cavity. It acts as a baffle to deflect and prevent inhalation of foreign bodies.
In most species, the nasal cavity is divided by a nasal septum. Within the lateral
walls of the cavity are highly vascularized nasal conchae (Fig. 3). Most birds have 3
conchae: the rostral, middle, and caudal nasal conchae. The middle nasal concha is
the largest. A clinically important anatomic feature is the relationship of this concha
to the openings of the infraorbital sinus, the only true paranasal sinus of birds. This
sinus opens dorsally into both the middle and caudal nasal conchae. The caudal nasal
concha drains only into the nasal cavity by its dorsal opening into the infraorbital sinus.
As a result, the only passageway for drainage of mucopurulent material in the infraor-
bital sinus is the caudal nasal concha up through the dorsal opening, or over the
middle nasal concha into the nasal cavity. Pus collects in the sinus and can distend
it around the eye.
The infraorbital sinus is located ventromedial to the orbit and has numerous diver-
ticuli. A rostral diverticulum extends into the maxillary rostrum or bill, a preorbital diver-
ticulum lies rostral to the orbit, a postorbital diverticulum may be subdivided to
surround the opening of the ear, and a mandibular diverticulum extends into the man-
dibulary rostrum. In addition to its communication with the nasal conchae, the infraor-
bital sinus also communicates with the cervicocephalic air sac at its caudal-most
extent. Knowledge of the relationship of this sinus and air sac with the bones of the
skull is important during examination of the upper respiratory system and during irri-
gation and surgical drainage procedures.
History
The owner will often describe nasal discharge, redness or swelling of a portion of the
infraorbital sinus and particularly around the eye (Fig. 4), feather loss on the head and
ocular discharge, and some birds will rub their beak on the perch or scratch the sides
of their head.
Fig. 1. Blue cere in a male budgerigar (Melopsittacus undulatus). Males typically have a blue
cere at the base of the beak, whereas females have a brownish pink one.
Avian Respiratory Distress 243
Fig. 2. Severe upper respiratory tract infection, double yellow-headed Amazon parrot (Am-
azona oratrix). The feathers are missing from head rubbing in an attempt to reduce pressure
within the infraorbital sinus. Excoriated areas just distal to cere indicate where the rostral
portion of the infraorbital sinus is now exposed.
Etiology
The differential diagnoses for a URI are a secondary response to hypovitaminosis A;
other nutritional deficiencies; squamous metaplasia; altered immunocompetence;
infections from predominantly gram-negative bacteria, mycobacteria, mycoplasma,
Fig. 3. Cross-sectional anatomy of the nasal conchae and infraorbital sinus in fowl, from (A)
(rostral) to (D) (caudal). The anatomic plan is similar among species. Note the only connec-
tion between the nasal cavity and infraorbital sinus is dorsal over the middle nasal conchae.
(Reprinted from King AS, McLelland J. Birds: their structure and function. 2nd edition. Bath
(United Kingdom): Bailliere Tindall; 1984. p. 111; with permission.)
244 Orosz & Lichtenberger
Fig. 4. Gouldian finch (Erythrura gouldiae) with an infraorbital sinusitis. Pus collects in the
infraorbital sinus and distends it laterally, making the periorbital area swollen.
and fungal elements (such as Aspergillus sp or yeast); viral infections, including avipox
virus,6 and Chlamydophila; and parasitic infections, such as trichomonads, Capillaria,
nematode cysts, and Knemidokoptes. The clinician should examine the choanal slit in
the roof of the oropharynx (Fig. 5). Blunting of the papillae is associated with disease
processes or hypovitaminosis A in those species with papillae.
Although passerines with conjunctivitis and other symptoms of upper respiratory
tract infections are associated with mycoplasma, psittacines can also be affected.
Diagnosis is often based on polymerase chain reaction (PCR) samples taken from
swabs of the conjunctiva or fluid from flushes of the nasal cavity. Isolation and culture
is often difficult.7 Common serotypes of paramyxovirus (PMV) of passerines include
PMV-1, 2, and 3 and these can produce respiratory signs in passerines and other
avian species. Often the birds show respiratory signs along with gastrointestinal (GI)
and neurologic signs, but can die acutely.
Noninfectious causes may include airborne toxins, cigarette smoke, polytetrafluoro-
ethylene, allergies, foreign-body inhalation, and subcutaneous swellings of unknown
etiology.
Diagnostic tests
A nasal flush (Fig. 6) or infraorbital sinus aspiration should be performed. The fluid
obtained can be gram stained, a cytology performed, or culture and sensitivity
done. Endoscopy of the choanal area and biopsy of any lesions could be considered
as the next diagnostic procedure for those that are nonresponsive to initial treatment.
Radiographs of the head and computed tomographic scans of sinuses may be useful.
Various PCR tests may be used based on the differential diagnoses.
Avian Respiratory Distress 245
Fig. 5. Choanal slit from a robin (Turdus migratorius). The clinician should examine the roof
of the oropharynx. Many species have caudally directed papillae normally. Blunting is asso-
ciated with hypovitaminosis A and a variety of diseases.
Treatment
Many times a nasal flush will help remove mucous and discharge so that the bird can
breathe easier. Initial cytology and gram stains of the fluid can help the clinician decide
on treatment (antibiotics, antifungals) pending cultures and sensitivity results.
Fig. 6. Nasal flush of an orange-winged Amazon (Amazona amazonica). Holding the bird in
this position allows the flush to move from the nostril through the rostral portion of the
nasal cavity and out the choanal slit without aspirating the bird. Use pH-balanced saline.
246 Orosz & Lichtenberger
why it is easier to intubate birds than mammals. This increased diameter directly
reflects one physiologic adaptation of birds: the use of their beaks for the manipulation
of objects. The increased length of the trachea is part of an adaptation in birds
whereby the increased length of their necks allows use of their beak to manipulate
objects. However, the increase in length causes an increased air resistance. A wider
rima glottis, as well as a wider trachea, is necessary to reduce this resistance. To
compensate for the wider and longer trachea and its corresponding increase in
dead space, the respiratory rate of birds is less than that of mammals, with a larger
tidal volume. These anatomic and physiologic differences are important when select-
ing endotracheal tubes for anesthetic procedures. In addition, the tracheal rings of
birds are complete. They are shaped like a signet ring and overlap to form a more rigid
trachea than that of a comparably sized mammal. These two facts are important to
reduce the possibility of tracheal kinking when moving the neck. Overinflation of a cuf-
fed endotracheal tube is potentially easier in a bird because of the less expansive
nature of the trachea. Overinflation can lead to mucosal edema and difficulty
breathing. Whenever possible, uncuffed endotracheal tubes should be used.
The trachea often bifurcates immediately after entering the thoracic inlet. At this
bifurcation is the syrinx (Fig. 7), which represents the voice box of birds. The syrinx
is highly variable among species but represents several cartilages, which may be ossi-
fied, and syringeal muscles and membranes. Most syringeal muscles are external to
the tracheal bifurcation. Depending on the species, birds may also have internal syrin-
geal muscles within the space of the trachea or bronchi. This narrowed internal diam-
eter of the syrinx is a common site for tracheal granulomas and foreign bodies.
History
The bird may have demonstrated inspiratory stridor that has increased in intensity or
the respiratory distress could be acute because of complete obstruction.
Etiology
Causes of large airway disease include obstruction by a foreign body (ie, seed in
cockatiels), mass, Aspergillus granuloma (Fig. 8A) or oropharyngeal granulomas,
Mycobacterium genavense infection causing a granuloma,8 and tracheal fibrinous
seal.9
Diagnostic tests
Radiographs (see Fig. 8B), complete blood count (CBC) and a biochemical profile,
transtracheal wash, and endoscopy can help to diagnose the cause of airway obstruc-
tion. Material removed by endoscopy can be submitted for PCR, culture, and
cytology.
Treatment
Large airway obstruction requires rapid anesthetic induction with sevoflurane/isoflur-
ane anesthesia, rapid intubation and ventilation with 100% oxygen. If there is a total
upper airway obstruction, emergency air sac tube placement is performed. The bird
will relax and breathe easier under inhalant anesthesia. Endoscopy can be used to
remove an obstruction as a granuloma or seed caught at the syrinx.
Avian Respiratory Distress 247
Fig. 7. Ventral view of the tracheal bifurcation and syrinx from a tufted duck. Ducks often
have a syringeal bulla that is a diverticulum to enhance sound production. Psittacine birds
do not have one; however, sound is produced at the tracheal bifurcation in birds, not at
the tracheal opening (larynx) as in mammals. (Reprinted from King AS, McLelland J. Birds:
their structure and function. 2nd edition. Bath (United Kingdom): Bailliere Tindall; 1984.
p. 119; with permission.)
Small Airway
Anatomy and physiology
The mainstem or primary bronchi (Fig. 9) represent the continuation of the syrinx. Each
perforates the septal surface of the lung and continues into the lung parenchyma as the
intrapulmonary primary bronchus. The portion of the bronchus is long as it continues to
the caudal extremity of the lung. Its diameter is variable among species but is widest at
its entrance into the lung tissue and then tapers progressively. The epithelium of the
primary bronchus is pseudostratified with goblet cells and there are areas with ridges
carrying cilia. There are 4 groups of secondary bronchi that arise from the primary bron-
chus. Their anatomy is described with the description of the lung parenchyma.
History
A blue and gold macaw will present with the history of periodic respiratory distress and
is commonly raised with a cockatoo or African gray. The offending toxin, such as
smoke, aerosol, or cigarettes, will be identified on history. Bird may appear open
mouthed with increased abdominal effort on expiration.
Fig. 9. The septal surface of the right lung of the domestic fowl, which shows the anatomic
arrangement of the medioventral (MV-arising dorsally) and the lateroventral (LV-arising
ventrally) secondary bronchi as they arise from the primary bronchus. Also shown are the medi-
odorsal (MD) secondary bronchi. The direction of origin of the secondary bronchi and the termi-
nation of the primary bronchus into the abdominal air sac explains opacities that can be observed
radiographically. (Reprinted from King AS, McLelland J. Birds: their structure and function. 2nd
edition. Bath (United Kingdom): Bailliere Tindall; 1984. p. 122; with permission.)
Avian Respiratory Distress 249
Etiology
Small airway disease includes inhalant respiratory irritants, such as smoke, polytetrafluoro-
ethylene toxicity, aerosols, cigarette smoke, candles, heated polytetrafluoroethylene,10
and overheated microwave.11 Granulomas in the small airways may also cause this expi-
ratory distress.
Diagnostic tests
Stabilize the bird for 12 to 24 hours with bronchodilators and oxygen. Radiographs,
CBC, and chemistry profile should be performed to rule out an infectious disease.
Birds with aspergillosis often have high white counts with total protein levels of
approximately 7.
Treatment
The most effective bronchodilators are pharmaceutical agents that stimulate b-adren-
ergic receptors in bronchial smooth muscle and promote smooth muscle relaxation.
For this reason they have become the authors’ first line of treatment for bronchocon-
striction causing acute respiratory distress. These b-receptor agonists are most effec-
tive and least toxic when they are given as an aerosol that is inhaled. b-agonists, such
as terbutaline, can be given IM in birds (0.01 mg/kg every 6–8 hours) initially and then
continued by nebulization.
Nebulizers are designed to convert liquids to appropriately sized aerosol particles
for inhalation. The nebulizer consists of a disposable or reusable nebulizer and a pres-
surized gas (air or oxygen) source. A small volume of medication and a larger volume
of diluent are placed into the nebulizer chamber.
Ultrasonic nebulizers generate an aerosol through ultrahigh-frequency vibration of
a piezoelectric crystal at the bottom of a liquid. The advantages of using an ultrasonic
nebulizer include faster nebulization time, longer product life, smaller particle size, and
quieter operation compared with a jet nebulizer. The veterinarian nebulizer used most
commonly is an ultrasonic nebulizer (DVM pharmaceuticals, Inc, IVAX Corp, Miami,
FL, USA), which costs about $150, delivers particle size of 2 to 7 mm, and can be
used by an owner in the home. It is not known if the particle size will reach the atria
of the lung, but use of this nebulizer will deliver particles to the bronchi for treatment
of bronchoconstriction.
History
The bird will likely have a history of lethargy, decreased appetite, and not doing well
before the respiratory distress.
Etiology
Causes of coelom space disease include fluid accumulation heart disease, hypoalbu-
minemia, liver disease, egg-related peritonitis,12 organomegaly (hepatic lipidosis), and
mass (neoplasia, abscess, egg).
using a lateral view. The mainstem bronchi divide into secondary bronchi. These
bronchi subsequently divide into parabronchi. All parabronchi anastomose freely
with other parabronchi and have expansions within their walls, called atria, which
allows for gas exchange. Parabronchi (Fig. 10) maintain a constant mean diameter
within a species.
The mediodorsal and medioventral secondary bronchi connect to form a functional
unit. These bronchi terminate at the cranial pulmonary air sacs and form the basis of
the paleopulmonic respiratory system (Fig. 11). The parabronchi of the lateroventral
secondary bronchi connect with the laterodorsal secondary bronchi. The cranial
pulmonary air sacs are expandable sacs that are connected to the lungs by these
bronchial arrangements and include the cervical, clavicular, and cranial thoracic air
sacs. The lateroventral bronchi are connected with the caudal pulmonary air sacs of
the lungs. These caudal air sacs are the caudal thoracic and abdominal air sac. This
latter arrangement represents the neopulmonic respiratory system. Air sacs, in
general, are histologically similar to a peritoneum, with squamous to columnar epithe-
lium, a basement membrane, and an underlying connective tissue support. Only in the
area immediately surrounding an opening of a parabronchus does the tissue change
to ciliated columnar epithelium. The paleopulmonic and neopulmonic systems are
best defined physiologically rather than anatomically.
Birds do not have a diaphragm and therefore rely on changes in pressure between
their air sacs relative to the atmospheric pressure to move air through a nonexpand-
able lung. The pressure changes within the air sacs are the result of volume changes in
the thoracoabdominal cavity. On inspiration, the ribs move cranioventrally, thereby
increasing the thoracoabdominal space. This action results in a lowering of the pres-
sure in the air sacs. On expiration, the ribs move caudodorsally, thereby reducing the
space in the chest and increasing the pressure in the air sacs. Expiration is also an
active process requiring skeletal muscle contraction. For this reason, it is extremely
Fig. 10. The cross section of the parabronchi of the domestic fowl. In the paleopulmonic
portion of the lungs, the parabronchi form a series of parallel tubes with the lung parenchyma
between. (Reprinted from King AS, McLelland J. Birds: their structure and function. 2nd
edition. Bath (United Kingdom): Bailliere Tindall; 1984. p. 125; with permission.)
252 Orosz & Lichtenberger
Fig. 11. Diagram of the lower respiratory tract after Fedde. The paleopulmonic system has
the parallel parabronchi that connect with the cervical, clavicular, and cranial thoracic air
sacs. This system, through aerodynamic valving, moves air in one direction. The neopul-
monic system moves air in and out of the same parabronchial tubes bilaterally. The neopul-
monic system includes the caudal thoracic and abdominal air sacs.
important when holding a bird that the sternum can move freely or the bird will
suffocate.
Gas exchange occurs in the walls of the parabronchi, the atria, and more impor-
tantly in the air capillaries, which are the avian equivalent of alveoli (Fig. 12). The
blood-gas barrier of birds is similar to that of mammals in that it consists of an endo-
thelial capillary cell, a common basal lamina, and an air capillary epithelium of squa-
mous cells. The difference is that the blood-gas barrier is much thinner in birds than
in mammals. The diameter of the air capillaries of birds is much smaller than that of
a mammalian alveolus, allowing for a much larger number of air capillaries in a given
space when compared with mammals. For this reason, fluid can accumulate in the air
capillary faster than an alveolus. Clinically then, birds crash faster than mammals
because of their unique anatomy and physiology of the parenchyma of the lungs.
Because of the unidirectional continuous flow of air of the paleopulmonic system,
birds are more efficient than mammals in capturing oxygen and removing carbon
dioxide. The nonoxygenated blood enters at an approximately 90 angle from the par-
abronchus. This crosscurrent gas exchange enhances the ability to oxygenate blood.
The epithelial cells of the lung act as fixed macrophages and transfer engulfed mate-
rial to interstitial macrophages. Air that enters the caudal air sacs is filtered less than
that of the cranial air sacs, making the caudal air sacs more susceptible to disease.
History
There is usually a history of not doing well, lethargy, and anorexia.
Fig. 12. The anatomy of the exchange surface of the lungs. The blood air barrier is much
thinner in birds compared with mammals. It consists of the endothelial blood capillary
cell, a common basal lamina, and the squamous epithelial cell of the air capillary. (Reprinted
from King AS, McLelland J. Birds: their structure and function. 2nd edition. Bath (United
Kingdom): Bailliere Tindall; 1984. p. 128; with permission.)
Etiology
Differential diagnoses for lower respiratory tract signs include infectious causes and
noninfectious causes. Companion avian patients may have infections that result
from a variety of agents and these include bacteria (often gram-negative rods), fungi
(Aspergillus), viruses pox, Amazon tracheitis virus, Pacheco disease, polyomavirus,
reovirus, exotic Newcastle disease, other PMVs, Chlamydophila, and parasites
(air sac mites, species of Syngamus, Toxoplasma/Atoxoplasma, Encephalitozoan,
Sarcocystis).
Aspiration is often secondary to crop disorders and may result in bacterial, yeast, or
mycelial phase fungal infections. Birds may also aspirate because of foreign bodies in
their upper GI tract; a goiter (parakeets) blocking the outflow of the crop, and overfilling
of the crop when hand feeding or gavage feeding. Other conditions that cause inflam-
matory problems for the lower respiratory tree include toxicity (polytetrafluoroethy-
lene, heavily scented products, and cigarette smoke), neoplasia, and a ruptured air
sac. Metabolic causes may produce respiratory signs. Allergens are becoming more
of a problem and they are suspected in pneumonitis observed in blue and gold
macaws. Extrarespiratory causes reduce the available air sac space and do not allow
254 Orosz & Lichtenberger
adequate exchange across the blood air barrier. Common reasons for this to happen
are ascites and an enlarged abdominal organ.
Parenchymal disease
Parenchymal disease may benefit from use of parental or nebulization of bronchodila-
tors and antibiotics. An air sac tube may partially improve respiration in birds with
primary lung and air sac disease.
Careful auscultation is indicated for a heart murmur or gallop or persistent
arrhythmia suggestive of cardiogenic edema. If heart failure is suspected, administer
furosemide (2–4 mg/kg intravenously) and nitroglycerine ointment on the back and
allow the bird to stabilize before further diagnostics.
Birds with a history of regurgitation or vomiting may benefit from broad-spectrum
antibiotics (eg, enrofloxacin, trimethoprim sulfadiazine, amoxicillin/clavulanic acid)
and bronchodilators when aspiration pneumonia is suspected. Birds administered
antibiotics particularly long-term should also be administered an antifungal drug to
reduce the incidence of secondary infections.
Birds suspected of aspergillosis (leukocytosis with a monocytosis, increased
total protein and pulmonary nodules) should be treated with appropriate antifungal
drugs.
Birds suspected of psittacosis (leukocytosis, clinical signs varying from chronic
unthriftiness to acute anorexia, diarrhea, respiratory distress, and lime green feces)
should be treated with drugs inhibiting the growth of Chlamydophila species. Doxycy-
cline is the drug of choice. Most commonly, a real-time PCR test for psittacosis that
includes a swab of the conjunctiva, oropharynx, and choanal and cloaca with some
whole blood is recommended from a clinical perspective. For further details, see the
Compendium of Measures to Control Chlamydophila psittaci Infection Among
Humans (Psittacosis) and Pet Birds (Avian Chlamydiosis), 2010, issued by the
National Association of State Public Health Veterinarians (www.nasphv.org/
documentsCompendiaPsittacosis).
REFERENCES
7. Sandmeir P, Coutteel P. In: Harrison GJ, Lightfoot TL, editors, Clinical avian medi-
cine. Management of canaries, finches, and mynahs, vol. II. Palm Beach (FL):
Spix Publishing; 2006. p. 879–913.
8. Kiehn TE, Hoefer H, Bottger EC, et al. Mycobacterium genavense infections in pet
animals. J Clin Microbiol 1996;34(7):1840–2.
9. Good DA, Heatley TN, Tully Jr, et al. Anesthesia case of the month. Partial
obstruction of the trachea was a differential diagnosis for the bird’s respiratory
problems. J Am Vet Med Assoc 2001;219(11):1529–31.
10. Wells RE, Slocombe RF, Trapp AL. Acute toxicosis of budgerigars (Melopsittacus
undulates) caused by pyrolysis products from heated polytetrafluoroethylene:
clinical study. Am J Vet Res 1982;43(7):1238–42.
11. Zanen AL, Rietveld AP. Inhalation trauma due to overheating in a microwave
oven. Thorax 1993;48(3):300–2.
12. Gorham SL, Akins M, Carter B. Ectopic egg yolk in the abdominal cavity of a cock-
atiel. Avian Dis 1992;36(3):816–7.