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Chapter 29 Sore Throat 361
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Auscultate the Lungs
Mycoplasma pneumoniae is frequently associated with sore throat in adolescents and young adults. If pneumo­nia is present, palpation, percussion, and auscultation of the lungs reveal an area of consolidation and adventi­tious breath sounds (see Chapter 13 for further discus­sion of the lung examination).
Palpate the Abdomen
Splenomegaly is found in about half the cases of mononucleosis, although hepatomegaly is rare. GERD may be associated with palpable upper epigastric tenderness.
LABORATORY AND DIAGNOSTIC STUDIES
The laboratory evaluation of sore throat is generally lim­ited to the identication of GABHS. Other infectious causes, such as gonorrhea or diphtheria, are rare, and testing is conducted only if the history indicates expo­sure. It is important to diagnose streptococcal pharyngitis so it can be treated promptly with antibiotics, avoiding serious sequelae, such as peritonsillar abscesses or rheu­matic fever.
Rapid Screening Tests
A throat swab is a rapid screen for streptococcal anti­gens and should be done if GABHS is suspected. If it is positive, the patient is treated without follow-up cultures. If the swab is negative, a throat culture is obtained. The test has a sensitivity of 75% to 85% and a specicity of 95% to 98%.
The Monospot is a rapid slide test that detects het­erophil antibody agglutination; it is not specic for EBV. It is most sensitive 1 to 2 weeks after symptoms appear and remains positive for up to 1 year. If chronic fatigue syndrome is being considered as a differential diagnosis, specic EBV antibody tests should be considered.
Antistreptolysin O Titer
GABHS produces enzymes that include streptolysin. An ASO titer is a serological test that detects the presence of a previous streptococcal infection. This titer does not increase until 1 to 6 months postinfec­tion, so it is of no diagnostic value. It is used to aid in the diagnosis of streptococci-associated in­fections, such as rheumatic fever, glomerulonephritis, and pericarditis. A caution, however, is that in as many as 50% of positive streptococcal cultures, an elevated ASO titer postinfection will not be found.
Potassium Hydroxide Smear for Wet Mount
Obtain a sample of pharyngeal discharge using a cotton-tipped applicator. Look under the microscope at the KOH slide for the presence of branching and budding hyphae that are characteristic of yeast infec­tion (see Chapter 34).
Complete Blood Count with Differential
Test results that show 50% lymphocytes and at least 10% atypical lymphocytes conrm the diagnosis of mononucleosis.
Computed Tomography Scan
Suspicion of an obstruction or swelling of the throat should be referred for further radiographic evaluation with a computed tomography scan.
Nasal Smear
Nasal cytology can be performed on nasal secretions obtained by having the patient blow the nose into a paper or by using a cotton-tipped swab to obtain secre­tions from the nose. The presence of eosinophils on a nasal smear stained with Wright’s stain viewed under a high-power microscope suggests an allergic, inam­matory process.
Culture
A throat culture to detect GABHS is the gold standard of diagnosis, with a 10% or lower false-negative rate. When obtaining a culture, rst remove crusts from lesions, taking care to touch only the throat or tonsils with the sterile swab. Avoid touching the tongue. Roll the throat swab over one tonsil, proceed across the posterior pharynx, and then swab the other tonsil. A culture for gonorrhea can conrm a diagnosis of gono­coccal pharyngitis.
DIFFERENTIAL DIAGNOSIS
Pharyngitis Without Ulcers
Epiglottitis
Epiglottitis is caused by infection with H. inuenzae type b that produces inammation and edema of the epiglottis and the surrounding areas, obstructing the ow of air. The edematous epiglottis may be pulled into the larynx during inspiration and can completely occlude the airway. Symptoms are respiratory distress, sore throat, difculty with secretions, drooling, pain
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on swallowing, and a toxic appearance. The infection occurs in both children and adults.
Peritonsillar/Retropharyngeal Abscess
A peritonsillar abscess, also called quinsy, is a collec­tion of pus between the tonsil and the capsule of the tonsillar pillar. This condition occurs in children but is more common in adults, especially in persons with a history of recurrent tonsillitis. The patient’s present­ing symptoms usually include a history of respiratory symptoms, difculty swallowing, otalgia, malaise, fever, and cervical lymphadenopathy. On examina­tion, there may be trismus; asymmetrical swelling of the uvula, tonsils, or posterior pharynx; or a visible abscess. Children’s presenting symptoms typically include fever, toxic appearance, refusal to swallow, drooling, and stridor. Children with retropharyngeal abscess are usually under the age of 4 and need immediate referral.
Viral Pharyngitis
Most sore throats are caused by viral infections. Patients usually have symptoms of malaise, fever, headache, cough, and fatigue. The pharynx is usually erythematous, or it may be pale, boggy, and swollen. There usually is no tonsillar or pharyngeal exudate or tonsillar enlargement present, although infection with an adenovirus may produce pharyngeal exudate. The presence of concomitant upper respiratory tract symp­toms such as cough and congestion makes the diagno­sis of viral pharyngitis more likely than that of strep­tococcal pharyngitis. Common cold viruses cause sore throats most frequently during the colder months of the year.
Streptococcal Pharyngitis
The major differential diagnoses for sore throat will be viral or bacterial infection. Fewer than 10% of adults and 30% of children who seek care for sore throat symptoms have streptococcal tonsillopharyngitis. However, reliance on clinical impression to arrive at a specic diagnosis is problematic. The symptoms most likely to occur with streptococcal pharyngitis include a fever with a temperature of 38.5° C (101.5° F) or higher, tonsillar exudate, anterior cervical adenopathy, and a history of recent exposure. The incidence of streptococcal pharyngitis increases from 10% in the summer and fall to 40% during the winter and early spring. GABHS cannot be reliably diagnosed on the
basis of signs and symptoms, and even when cultures are obtained, a causative agent may not be identied in 50% of patients. Table 29-2 shows the groups at risk for GABHS.
Mononucleosis
Mononucleosis causes about 5% of sore throats. It is most often a disease of young adults, and the causative agent is EBV in more than 90% of cases. History reveals a gradual onset, low-grade fever; mild sore throat; posterior cervical lymphadenopathy; and pro­nounced malaise and fatigue. Diagnosis can be con­rmed with a positive Monospot test and a complete
Table 29-2
Groups at Risk for Group A ß-Hemolytic Streptococcus (GABHS) Pharyngitis
RISK FACTORS DIAGNOSTIC TESTS
High Risk
Tonsillar exudate Temperature .38.5º C
(101.5º F)
Cervical
lymphadenopathy
Existing valvular rheu-
matic heart disease
Presumed Strep
Scarlet fever None; treat Strep epidemic Antibiotics already
started
Medium Risk
Exudate, nodes, or fever
present Prior rheumatic fever “Low risk” by PE but
,25 years old and no
URI Person with diabetes Recent “strep” exposure
Low Risk
No exudate, nodes,
or fever
PE, physical examination; URI, upper respiratory tract infection.
None; treat on basis of risk
factors
Rapid strep screen; if
positive, treat; if negative, do culture; treat if culture positive; do not treat if culture negative
Rapid strep screen; if posi-
tive, treat; if negative, do not culture; do not treat if culture negative
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blood count that shows greater than 50% lymphocyto­sis. Splenomegaly occurs in about 50% of cases, and palatine petechiae are a less common symptom. GABHS occurs concomitantly in 10% to 20% of cases.
Gonococcal Pharyngitis
This form of pharyngitis can occur in patients with a history of orogenital sexual activity. The patient may have no symptoms. Examination shows an exudative pharyngitis with bilateral cervical lymphadenopathy. Diagnosis is conrmed through Gram staining or culture.
Inflammation
Inammatory sore throat occurs in the presence of sinusitis or exposure to local irritants. The patient often reports a postnasal drip and allergic symptoms (itchy, watery eyes; runny nose) that may follow seasonal pat­terns. On examination, the patient may have sinus tenderness. The pharynx may be swollen or pale with posterior drainage present. The patient has no fever or lymphadenopathy.
Pharyngitis with Ulcers
Herpangina
Herpangina is an infection caused by the coxsackievi­rus. The patient reports a painful sore throat, fever, and malaise. Headache; anorexia; and neck, abdomen, and extremity pain may occur. Within 2 days of onset, small, grayish, papulovesicular lesions appear on the soft palate and pharynx. These progress to shallow ulcers, usually less than 5 mm in diameter. Outbreaks occur during the summer months. Coxsackievirus peaks in August, September, and October, although some cases occur during the winter months. It is more common in children and in immunosuppressed patients. Diagnosis is based on symptoms and charac­teristic oral lesions. An antibody titer can conrm diagnosis.
Vincent Angina
Vincent angina is caused by a fusospirochetal infec-
tion that results in necrotizing ulcerative gingivosto-
matitis. The patient’s symptoms include painful
ulcers, foul breath, and bleeding gums. Without sec-
ondary infection, there usually is no fever. On exami-
nation, gray, necrotic ulcers without vesicles are
apparent on the gingivae and interdental papillae.
Gram staining shows spirochetes and conrms the
diagnosis.
Aphthous Stomatitis
Aphthous stomatitis, or “canker sores,” appears as dis-
crete ulcers without preceding vesicles. The ulcers are
located on the inner lip, tongue, and buccal mucosa.
Lesions last about 1 to 2 weeks. The cause of the
lesions is unknown, but immunological mechanisms
play a major role.
Herpes Simplex Virus Type 1
An infection from herpes simplex virus type 1 (HSV-1)
is associated with fever, headache, sore throat, and
lymphadenitis. Characteristic clusters of yellow vesi-
cles appear on the palate, pharynx, and gingiva. Lesions
last 2 to 3 weeks. Recurrent lesions are characterized by
prodromal symptoms of burning, tingling, or itching.
Active lesions are usually painful. Recent studies indi-
cate that infections afict about 30% to 90% of the
U.S. population.
Candidiasis
Candidiasis is a yeast infection that produces white
plaques over the tongue and oral mucosa with ery-
thema; the plaques bleed when scraped. Candida
infection occurs commonly in otherwise normal
infants in the rst weeks of life; in immunocom-
promised persons, including those with diabetes;
and in persons taking antibiotics or using inhaled
steroids.
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DIFFERENTIAL DIAGNOSIS OF Common Causes of Sore Throat
CONDITION HISTORY PHYSICAL FINDINGS DIAGNOSTIC STUDIES
Pharyngitis Without Ulcers
Epiglottitis Sore throat, difficulty with
secretions, odynophagia (seen in pediatric patients ,2 years), unable to lie flat, unable to talk
Peritonsillar/
retropharyngeal abscess
Viral pharyngitis Scratchy, sore throat, malaise,
Group A
ß-hemolytic streptococcal pharyngitis
Mononucleosis
(Epstein-Barr virus)
Gonococcal
pharyngitis
Inflammation Exposure to irritants; postnasal
Pharyngitis with Ulcers
Herpangina
(coxsackievirus)
Fusospirochetal
infection (Vincent angina)
Aphthous stomatitis Oral trauma, ill-fitting dentures;
History of recurrent
tonsillitis; sore throat, difficulty swallowing, respiratory tract symptoms, fever, malaise
myalgias, headache, chills, cough, rhinitis
Most common in persons
5-15 years; known exposure; fall/winter season; sudden onset of fever, severe sore throat, and malaise; absence of cough and upper respiratory tract symptoms
Young adults; slow onset of
malaise, low-grade fever, mild sore throat
History of orogenital sexual
activity; may be asymptomatic
drip; allergic symptoms
More common in children;
immunosuppressed; painful throat; fever, malaise
Poor oral hygiene; painful
ulcers, foul breath, bleeding gums
painful ulcers vary in size; absence of other symptoms
Respiratory distress, drooling,
toxic appearance; DO NOT EXAMINE PHARYNX
Orthopnea, dyspnea, sym-
metrical swelling, abscess, trismus
Erythema, edema of throat,
tender posterior cervical nodes
Temperature .38.5º C
(101.5º F); exudate; anterior cervical lymphadenopathy
Presence/absence of
pharyngeal exudate, palatine petechiae, posterior cervical lymphadenopathy, splenomegaly
Pharyngeal exudate; bilateral
cervical lymphadenopathy
Sinus tenderness, pale or
swollen pharynx, postnasal drainage visible, no fever or lymphadenopathy
Lymphadenopathy; small
grayish papulovesicular lesions on soft palate and pharynx, progressing to shallow ulcers, usually ,5 mm in diameter
Gray necrotic ulcers without
vesicles on gingival margins and interdental papillae
Shallow ulcers, no vesicles;
indurated papules that progress to 1-cm ulcers; ulcer has yellow membrane and red halo; no fever or nodes
Refer immediately
Refer immediately: CT
scan; head and neck radiographs; laryngoscopy
None
Positive rapid strep
antibody screen; strep culture
Positive Monospot;
CBC with differential; .50% leukocytes
Gram stain; gonorrhea
culture
Eosinophils in nasal se-
cretions with allergies
Serology
Gram stain reveals
spirochetes
None
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DIFFERENTIAL DIAGNOSIS OF Common Causes of Sore Throat—cont’d
CONDITION HISTORY PHYSICAL FINDINGS DIAGNOSTIC STUDIES
Herpes simplex
infection
Candidiasis Immunosuppressed; persons
CBC, complete blood count; CT, computed tomography; KOH, potassium hydroxide.
History of trauma to mucosa;
pain, fever, headache
taking antibiotics or with diabetes; sore mouth/throat
Perioral lesions;
lymphadenitis; vesicles on palate, pharynx, gingiva
Curdlike white plaques that
bleed when scraped off
Viral culture
KOH smear shows
hyphae; culture
REFERENCES AND READINGS
Coby BA: Diagnosis and treatment of streptococcal pharyngitis,
Am Fam Physician 79:383, 2009.
Darrow DH, Siemens C: Indications for tonsillectomy and adenoid-
ectomy, Laryngoscope 112:8, 2002.
Ebell MH, Smith MA, Barry HC, Ives K, Carey M: The rational
clinical examination: does this patient have strep throat? JAMA 284:2912, 2000.
Gerber M: Diagnosis and treatment of pharyngitis in children, Pediatr
Clin North Am 52:729, 2005.
Linder JA: Evaluation and management of adult pharyngitis, Compr
Ther 34:196, 2008.
McPhee SJ, Papadakis MA: Current medical diagnosis and treatment,
ed 49, New York, 2010, McGraw-Hill.
Richardson MA: Sore throat, tonsillitis, and adenoiditis, Med Clin
North Am 83:75, 1999. Stevens D: A sore throat or something else? Pract Nurs 19:83, 2008. Vincent MT, Celstin N, Hussain AN: Pharyngitis, Am Fam Physician
69:1465, 2004.
C H A P T E R
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30
Syncope
yncope is the transient loss of consciousness and postural tone that results from a sudden decrease
S
in cerebral perfusion. It is distinct from a coma, seizures, shock, vertigo, and other states of altered con­sciousness. It is a symptom that about 10% of adults of any age will experience at least some time during their lives and the incidence exponentially increases in people over 70 years old. It is less common in children, except when there is a seizure disorder, primary cardiac arrhythmia, or a breath-holding incident.
The causes of syncope can be difcult to determine because patients generally are seen after the event has occurred. Syncope can be quite benign, such as a va­sovagal response, or it can indicate serious disease. However, even benign syncope can place the patient at risk for falls or injury. Cardiogenic syncope has high associated morbidity and mortality, and the emphasis in diagnosis is to rule out the most serious causes through a careful history and physical examination, with a few laboratory and diagnostic tests to establish a possible diagnosis. The Evidence-Based Practice box describes an evidence-based approach to the diag­nosis of syncope.
EVIDENCE-BASED PRACTICE
Diagnosing Syncope
DIAGNOSTIC REASONING: FOCUSED HISTORY
Is this really syncope?
Key Questions
n Did you lose consciousness? n Did you have any prodromal symptoms? n What were you doing when the event occurred? n If you lost consciousness, how long did it last? n Did your limbs jerk during the event? n Did anyone see you faint?
Loss of Consciousness
Distinguish syncope from other symptoms. Dizziness, vertigo, and presyncope do not cause loss of con­sciousness or postural tone.
Prodromal Symptoms
Sweating, vertigo, nausea, and/or yawning are prodromal symptoms that are associated with syncope; seizures may be associated with an aura or tongue biting. Aura also suggests migraine etiology.
Syncope is a common symptom with no diagnostic gold stan­dard and a range of prognoses. The authors of this guideline undertook an extensive review of the literature to help clini­cians maximize the diagnostic yield in the workup of syncope and here report the following key points that assist in the evaluation of syncope:
1. History, physical examination, and electrocardiography
(ECG) are the core of syncope workup (combined diag­nostic yield, 50%).
2. Neurological testing is rarely helpful unless additional neu-
rological signs or symptoms are present (diagnostic yield of EEG, CT, and Doppler ultrasound, 2% to 6%).
3. Patients in whom heart disease is known or suspected
and those with exertional syncope who are at higher risk
Data from Linzer M, Yang EH, Estes NA III, Wang P, Vorperian VR, Kapoor WN: Diagnosing syncope. Part 1: Value of history, physical examination, and electrocardiography. Clinical Efficacy Assessment Project of the American College of Physicians, Ann Intern Med 126:989-996, 1997.
366
for adverse outcomes should have cardiac testing, including echocardiography, stress testing, Holter moni­toring, or EPS, alone or in combination (diagnostic yield, 5% to 35%).
4. Syncope in the elderly often results from polypharmacy and abnormal physiological responses to daily events.
5. Long-term loop electrocardiography (diagnostic yield, 25% to 35%) and tilt-table testing (diagnostic yield, #60%) are most useful in patients with recurrent syncope in whom heart disease is not suspected.
6. Psychiatric evaluation can detect mental disorders associ­ated with syncope in up to 25% of cases.
7. Hospitalization may be indicated for patients at high risk for cardiac syncope or with acute neurological signs.
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Pre-event Characteristics
Characterize what precipitated the episodes. Loss of consciousness precipitated by pain, exercise, urination, defecation, or stressful events is probably not a seizure. Breath-holding spells are common in children, causing syncope. They are usually precipitated by pain, anger, a sudden startle, or frustration. Syncope occurs with rest or when supine during a seizure or arrhythmia. Syncope that occurs without warning is considered cardiovascular in origin.
Event and Postevent Characteristics
Rhythmic movements of extremities during the event usually indicate a seizure, although they can occur with syncope. Disorientation after the event, slow­ness in returning to consciousness, and unconscious­ness lasting longer than 5 minutes indicate seizure. Often children with breath-holding spells have asso­ciated cyanosis, clonic jerks, opisthotonos, and bradycardia.
Witness
The patient is unconscious when the syncopal event takes place and therefore is a poor historian. A careful history is needed from both the patient and a witness to help in the diagnosis. Adolescents who have hysterical syncope episodes generally have an audience when the event occurs and are able to describe details of the event that would not be known to an unconscious patient.
Does this require immediate referral?
Key Questions
n Do you have a history of heart disease? What is it? n Do you have a congenital heart problem? n Are you having chest pain and/or shortness of
breath?
n Did this occur after exercise?
History of Heart Disease/Congenital Heart Problem
The presence of structural heart disease increases the risk of sudden death. Patients with a history of coro­nary artery disease, congestive heart failure, or ven­tricular arrhythmia should be hospitalized. Cardiac syncope may be either arrhythmic or mechanical in origin. Cardiac outow obstruction from aortic or mitral stenosis or a prosthetic valve may cause
syncope. Complete heart block is a leading cause of syncope, the result of interruption of atrioventricular conduction. Children who have had cardiac surgery to correct severe congenital heart disease are at risk for arrhythmias.
Chest Pain or Shortness of Breath
Obstructive mechanical blockage may be caused by pulmonary embolism, cardiac ischemia, or myocardial infarction with pump failure.
After Exercise
Syncope that accompanies exercise should be consid­ered of cardiac origin unless proved otherwise. Syn­cope after exertion in a well-trained athlete who has no heart disease is likely vasovagal in origin.
What do associated symptoms tell me?
Key Questions
n What other symptoms did you have? n Do you have palpitations? n Do you have headaches? n Have you experienced vertigo, dizziness, or visual
changes?
Palpitations
Supraventricular or ventricular tachycardias are associ­ated with syncope and sudden death. Ventricular tachy­cardia with a heart rate of 200 beats per minute may be asymptomatic or cause syncope. Chaotic ventricular activity of ventricular brillation is always fatal unless it is reversed with electrical debrillation. (See Chapter 23 for more on palpitations.)
Headaches
The pain of migraine headaches and the effect of the migraine on the brainstem can cause syncope. Gener­ally the patient has associated symptoms, such as vomiting, photophobia, severe headache (often on one side), and a strong family history of migraines. The headache continues after consciousness is regained.
Vertigo, Dizziness, and Visual Symptoms
The presence of vertigo, dizziness, diplopia, or other visual changes may accompany migraine headache. Interruption in cerebral perfusion, such as with a tran­sient ischemic attack, also must be considered.
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Is this neurocardiogenic in origin?
Key Questions
n Did this occur in response to a specic situation
(e.g., stressful event, urination, defecation)?
n Were you sitting, standing, or lying at when you
fainted?
n Do you have a history of any heart problems?
medications, and recreational drugs (e.g., alcohol, co­caine) that produce orthostasis, bradycardia, or pro­longed QT interval. Adolescents may use drugs, such as amyl nitrite and butyl nitrite, as aphrodisiacs and euphoriants. These drugs lead to vasodilation, and syn­cope may occur.
Children may ingest medications that belong to family members, and a history of such activity must be investigated as a cause of the syncope.
Situational Fainting
Vasovagal syncope is the most common type seen in adults and healthy children. It is neurocardiogenic and tends to occur in families. It is often precipitated by emotional stress, fear, extreme fatigue, or injury. It can occur without any obvious antecedent cause. Warm temperature, anxiety, blood drawing, and crowded rooms may cause peripheral vasodilation. Lack of large muscle activity prevents the venous return that is needed for cardiac lling with consequent bradycardia and fainting. When supine, venous return to the heart occurs, awakening the patient. Rapid standing will cause recurrence of the episode. Mental alertness is present.
Situational syncope can occur in response to urina­tion, defecation, cough, or emotional stress. Posttussive syncope follows paroxysmal coughing caused by in­creased intrathoracic pressure, which is then transmitted to the intracranial circulation, increasing intracranial pressure and decreasing cerebral blood ow. Postmictu­rition syncope, occurring during or after urination, is caused by the release of intravascular pressure on urina­tion, which triggers vasodilation and vagally mediated bradycardia.
Is this orthostasis?
Other Health Problems or Conditions
Diabetes may induce hypoglycemia, causing a grad­ual syncope. Anemias and chronic gastrointestinal bleeding from an ulcer or another source may cause syncope.
Patients who are pregnant or dehydrated or who have been on prolonged bed rest are at risk for ortho­static hypotension and syncope.
Is this explained by other factors?
Key Questions
n Have you had this before? How often? n Did it occur with sudden head turning? n If a child: Has the child had Kawasaki disease? n Do you have Lyme disease?
Frequent Syncope with No Heart Disease
Psychogenic syncope is often associated with repeated episodes in which unpredictable motor reexes appear, with a lack of pathological reexes. Also, blood pres­sure and pulse rate measurements are normal, and skin and mucous membranes do not change color. Panic at­tacks, or hyperventilation, are often interpreted as feel­ing faint, but the patient does not usually appear pale, nor are the symptoms relieved when recumbent.
Key Questions
n What medications are you taking? n Have you recently started blood pressure medicine
or has the dose changed?
n What other health problems/conditions do you
have?
Medications
About 10% of syncopal episodes are caused by prescribed medications (e.g., antidepressants, anti­dysrhythmics, b-blockers, diuretics), over-the-counter
After Sudden Head Rotation
Carotid sinus hypersensitivity produces a cardioinhibi­tory response that results in a profound drop in heart rate or may induce an abrupt vasopressor response with a drop in blood pressure.
History of Kawasaki Disease
Syncope can occur in children who have had Kawasaki disease. These children are at risk for coronary heart disease, which may present as chest pain associated with exercise.
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Lyme Disease
Lyme disease can cause arrhythmia in the form of heart block, which can result in syncope.
What other things do I need to consider?
Key Questions
n Do you have a family history of sudden death? n Do you have a family history of fainting? n If a child: Did the mother have systemic lupus ery-
thematosus (SLE) while pregnant?
Family History of Sudden Death
A family history of idiopathic hypertrophic subaortic stenosis is a risk factor for sudden death, and referral is necessary to rule out this condition. A history of a fam­ily member who had a myocardial infarction before age 30 is a signicant risk factor for sudden death.
Family History of Fainting
Neurocardiogenic syncope is common in families.
Prenatal Systemic Lupus Erythematosus
SLE in a pregnant woman may cause autoimmune in­jury, resulting in congenital complete atrioventicular block.
DIAGNOSTIC REASONING: FOCUSED PHYSICAL EXAMINATION
Measure Blood Pressure and Pulse Rate
Obtain blood pressure readings in standing, sitting, and supine positions. Orthostatic hypotension is either a decrease in systolic blood pressure of at least 20 mm Hg or symptoms that prevent further standing, such as fainting, weakness, or lightheadedness.
Compare blood pressure readings in the two arms. Unequal measurements may indicate a cardiac cause of the syncope.
Bradycardia of 35 to 40 beats per minute usually does not compromise cerebral blood ow. Rates below this, however, will impair cerebral circulation and function. Tachycardia up to 180 beats per minute also does not usually compromise cerebral circulation.
Perform Heart and Lung Examination
Observe for jugular venous distention. Palpate the pre­cordium to assess the point of maximal impulse to es­timate the size of the left ventricle. Feel for lifts. Listen for heart rate and murmurs and for radiation of mur­murs. Listen for an abnormally loud S2 or the presence of an S3. Auscultate for carotid bruits and pericardial rub. Listen to the lungs to assess for rales associated with congestive heart failure.
Perform a Neurological Examination
Begin with a brief mental status examination. Assess cranial nerves, deep tendon reexes, and motor func­tion. Perform a Romberg test, as well as gait and pro­prioception evaluation. Assess pupillary asymmetry and look for nystagmus (see Chapter 12).
Perform an Abdominal Examination
Auscultate and observe for signs of aortic aneurysm.
Examine Extremities
Observe lower extremities for signs of thrombophlebi­tis, a source of pulmonary embolism.
LABORATORY AND DIAGNOSTIC STUDIES
Suspected or Known Cardiac Cause
Electrocardiogram
The usefulness of the electrocardiogram usually lies in identifying abnormalities that provide clues to underly­ing cardiac causes of syncope. These ndings include evidence of conduction disorder or signs of coronary artery disease or left ventricular hypertrophy. A 12-lead ECG is used for the basic evaluation. This should be rst evaluated for rhythm and rate. Hand-measured interval measurement should be made. A Q wave found in the anterolateral lead may indicate abnormal place­ment of the left coronary artery. A patient with a pro­longed QT interval or the presence of Q waves must be referred.
Complete heart block requires immediate referral
for pacemaker insertion.
Observe Hydration Status
Poor hydration status secondary to diuretic use, poor nutrition, or loss of uids from vomiting and diarrhea may be associated with syncope.
Carotid Sinus Massage
Carotid sinus massage (CSM) is done to evaluate pa­tients with suspected carotid sinus hypersensitivity. This can be performed at the bedside with the patient
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in a supine or upright position while under continuous ECG and blood pressure monitoring. Apply rm pres­sure and massage for 5 to 10 seconds one side at a time at the site of the strongest carotid pulsation. Carotid sinus hypersensitivity is diagnosed when CSM causes a $3 second pause, a $50 mm Hg fall in systolic blood pressure, or both, and associated syncope.
Event Monitoring or Continuous-Loop Monitoring
These measures are used in patients with suspected cardiac arrhythmias as the cause of the syncope. Holter (24 hours) or long-term (weeks, months) event monitoring is used to document electrocardiographic recordings. Holter monitoring is a continuous, 24-hour electrocardiographic recording to evaluate the type and amount of irregular heartbeats during regular activities, exercise, and sleep. The patient keeps a 24-hour diary to record daily activities and any symp­toms experienced.
Cardiac event monitoring is a continuous-loop, digi-
tal memory recorder worn for extended periods of time (up to 30 days or longer) that saves and records tran­sient events felt by the patient. Patients activate these monitors as symptoms occur. Loop monitors save infor­mation for a predetermined period prior to the patient trigger, and therefore can help identify the initiation sequence for arrhythmias. These stored events can be transmitted through a telephone for review.
Doppler Studies
Transcranial Doppler and carotid ultrasonography are used to detect hemodynamically signicant stenoses in the major intracranial or extracranial arteries.
Exercise Stress Test
Cardiac stress testing is used to evaluate exercise­associated arrhythmias and syncope. It can conrm the presence of coronary artery disease.
Echocardiography
This is used in patients with exercise-induced symptoms to exclude left ventricular outow tract obstruction.
Electrophysiological Studies
Electrophysiological studies (EPSs) are invasive tests that use electrical stimulation and monitoring to diagnose conduction disorders or the propensity for
the development of tachyarrhythmias. Electrodes are threaded through arm or leg veins and placed at stra­tegic positions in the ventricles, atria, or both. The electrodes record electrical signals and allow map­ping of electrical impulses. The electrodes also can electrically stimulate the heart at programmed rates to trigger latent ventricular tachycardias.
Suspected Neurological Cause
Baseline Blood Testing
Routine blood tests (electrolyte levels, renal function, blood glucose level, complete blood count) rarely yield useful diagnostic information. Most patients with abnor­malities in these areas have seizures rather than syncope.
Electroencephalography
Electroencephalography (EEG) may be useful in patients whose history suggests seizure.
Computed Tomography Scanning
Computed tomography (CT) may be useful if the patient has focal neurological ndings.
Unexplained Syncope
Toxicology Screen
Toxicology screening may be indicated on the basis of the history.
Tilt-Table Testing
Tilt-table testing is used to provoke vasovagal syn­cope in susceptible persons. Provocative agents such as isoproterenol or nitroglycerin may be used. Using the table, the patient is tilted upright while continuous minute-to-minute blood pressure, heart rate, and oxygen saturation measurements are re­corded. Patient symptoms are recorded in each po­sition. Patients with neurocardiogenic syncope de­velop a sudden drop in heart rate and/or blood pressure after their body has been tilted up for sev­eral minutes. If symptoms of lightheadedness or fainting occur during this test, the test is considered positive for neurocardiogenic syncope.
DIFFERENTIAL DIAGNOSIS
Cardiac Causes
Cardiac causes have a higher rate of mortality than do other causes of syncope. Cardiac causes include coro­nary artery disease, congenital and valvular disease,