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Pharyngitis

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Venkata Sivakrishna Kumar Pulivarthi M.B.B.S [2]Delband Yekta Moazami, M.D.[3]

Synonyms and keywords: Sore throat; Bacterial pharyngitis; Group A streptococcal pharyngitis; Streptococcal pharyngitis; Viral pharyngitis

Overview

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Venkata Sivakrishna Kumar Pulivarthi M.B.B.S [2]Delband Yekta Moazami, M.D.[3]

Synonyms and keywords: Sore throat; Group A streptococcal pharyngitis; Bacterial pharyngitis; Viral pharyngitis; Acute pharyngitis; Chronic pharyngitis

Overview

A triad of sore throat, fever, and pharyngeal inflammation marked by erythema and edema are usually described as acute pharyngitis, although exudates, vesicles, or ulcerations may also be present. The inflammation of the pharynx, which presents as a sore throat, is pharyngitis. It is a painful inflammation of the pharynx and is colloquially referred to as a sore throat. Pharyngitis is a common medical problem in the outpatient medical setting, resulting in more than seven million pediatric visits each year. Most types of pharyngitis are caused by infectious etiologies. The most common cause of pharyngitis is a viral infection. However, some of the more serious types of pharyngitis are attributed to bacterial etiologies, such as group A-hemolytic Streptococcus pyogenes (GAS). Complications from GAS pharyngitis include rheumatic fever, deep space abscesses, and toxic shock. Although most episodes of pharyngitis are acute in nature, a small percentage becomes recurrent or chronic. With regards to chronic pharyngitis, non-infectious etiologies, such as Laryngopharyngeal reflux disease and periodic fever, aphthous ulcers, pharyngitis, and adenitis syndrome also need to be considered. Both medical and surgical therapies are effective in managing pharyngitis. Antibiotic treatment requires first-line medical therapy. Surgical management via adenotonsillectomy is recommended for certain indications. Adenotonsillectomy has been shown to be effective in reducing the burden of disease and improving the global quality of life and disease-specific. Several procedures, including traditional and intracapsular tonsillectomies, exist for adenotonsillectomy.

Historical Perspective

The sore throat was first described in the literature as ‘some variants of sore throat’ in the year 1879 by R. L. Bowles, M.D., in the British Medical Journal. Later, in 1885, David Newman, M.D., described pathology, symptoms, and treatment of pharyngitis.In 1910, the importance of bacteriological tests was shown in doubtful cases of pharyngitis. In 1931, three case reports were described and inferred that chronic non-tuberculous bronchial disease such as influenza, whooping cough, and measles is associated with chronic nasopharyngitis and also described the importance of conservative treatment in chronic nasopharyngitis.

Pathophysiology

The pathogenesis of the sore throat due to pharyngitis is poorly understood. The pharynx is often the first site of infection for many contagious diseases such as pharyngitis because pathogens such as viruses and bacteria often settle in the nasopharynx though inhalation or through droplets. Viral pharyngitis usually transmit from person to person through direct touch or through droplets transmission. The foreign invader reproduces rapidly after settling on the nasopharynx. Generally pharyngitis is a primary disease, but may be associated with systemic disorders such as the acute retroviral syndrome, or part of a more generalized upper respiratory tract infection.

Causes

Pharyngitis can be caused by infectious microorganisms or non-infectious agents. It is usually caused by viruses but may be caused by bacterial or fungal etiology. Gastroesophageal reflux disease (GERD) or particularly extra esophageal reflux (EER) can also cause an acid pharyngitis in adults and children.

Classification

Pharyngitis can be classified based on the duration as acute pharyngitis or chronic pharyngitis.

Differential Diagnosis

The major goal of the differentiating patients with sore throat or acute pharyngitis is to exclude potentially dangerous causes (e.g. Group A streptococcus), to identify any treatable causes, and to improve symptoms. Identifying the treatable causes is important because timely treatment with antibiotics helps prevent complications such as acute rheumatic fever, post streptococcal glomerulonephritis. Pharyngitis should be differentiated from other infectious causes which mimic sore throat that includes oral thrush, infectious mononucleosis, epiglottitis and peritonsillar abscess.

Epidemiology and Demographics

With more than 10 million outpatient visits per year, pharyngitis is one of the most common disorders in adults and children. Viruses are the single most common cause of pharyngitis and account for 25 percent to 45 percent of all cases. Group A streptococcus presents in up to 37% of all children presenting with a sore throat to an outpatient clinic or ED and 24% of those presenting at younger than 5 years. Group A streptococcus is by far the most common bacterial cause of acute pharyngitis, accounting for approximately 15 to 30 percent of cases in children and 5 to 10 percent of cases in adults. Peak seasons for sore throat include late winter and early spring.

Risk Factors

Pharyngitis is contagious, so anyone in close proximity to someone with the illness, is at risk. Social situations with prolonged close interpersonal contact are associated with a higher incidence of the disease, such as in schools, dormitories, or military barracks. Other common risk factors include a History of ill contact, Overcrowding, Frequent sinus infections, Smoking, attending daycare, immunocompromised patients, etc.

Natural History, Complications & Prognosis

Acute pharyngitis is typically described as the triad of sore throat, fever, and pharyngeal inflammation characterized by erythema and edema, although exudates, vesicles, or ulcerations may also be present. Although pharyngitis may be a primary disorder, sore throat and pharyngeal erythema may also be prominent in systemic disorders, such as the acute retroviral syndrome, or part of a more generalized upper respiratory tract infection. Most cases of acute pharyngitis are due to common viral infections and are benign, self-limited processes. The appropriate recognition of patients with more complicated infections that require diagnostic evaluations and treatment is one of the challenges of primary care medicine. An estimated 1-2% of acute pharyngitis progresses to recurrent or chronic disease.

Diagnosis

Key points in the evaluation of acute pharyngitis

  • Essential to diagnosis is the identification of treatable causes (e.g. Group A streptococcus) to prevent complications.
  • Testing for GAS pharyngitis should not be pursued in those with signs and symptoms indicative of a viral etiology.
  • Rapid antigen detection tests (RADTs) alone are sufficient for the diagnosis of GAS in adults, but negative results should be backed up by throat culture in children.
  • Specific techniques should be used to identify other causes where appropriate.
Guidelines Comparison for the Management of Acute Pharyngitis
Recommendation American College of Physicians (ACP) Infectious Diseases Society of America (IDSA)
Screening for acute pharyngitis Use Centor criteria Use clinical and epidemiologic findings to assess patient’s risk of GABHS (e.g., sudden onset of sore throat, fever, odynophagia, tonsillar erythema, exudates, cervical lymphadenitis, or history of streptococcal exposure)
Diagnostic testing RADT with Centor score of 2 or 3 only RADT or throat culture in all patients at risk
Back-up culture needed if RADT results negative? Adults: No

Children: Yes

Adults: No

Children: Yes

Who requires antibiotic treatment? Empiric antibiotics for Centor score of 3 or 4; treat patients with positive RADT result Positive RADT result or throat culture
Antibiotic of choice Oral penicillin V (Veetids; brand no longer available in the United States); intramuscular penicillin G benzathine (Bicillin L-A); oral amoxicillin with equal effectiveness and better palatability in children
Penicillin allergy Oral erythromycin; cephalosporin (first generation)

History and Symptoms

Pharyngitis is a very common inflammatory condition of the pharynx accompanied by a sore throat and occasionally difficulty in swallowing. Other symptoms depends on the etiology such as bacterial or viral.

Clinical features of acute pharyngitis
Group A streptococcal pharyngitis Viral pharyngitis

Physical Examination

Patients with pharyngitis typically have low-grade fever and pharyngeal erythema, suggestive of viral etiology or pharyngeal exudate or petechia, suggestive of GAS. Additional signs include enlarged edematous tonsils, enlarged and/or tender cervical adenopathy, the rash that may or may not be present. Scarlatiniform rash, which is marked by multiple small red papules that are widely and diffusely distributed but spare the palms and soles, is suggestive of GAS.

Centor criteria
The original Center score uses four signs and symptoms to estimate the probability of acute streptococcal pharyngitis in adults with a sore throat The score was later modified by adding age. It is important to evaluate for a definitive diagnosis to exclude GAS and to avoid unnecessary lab tests and antibiotic use. Centor criteria are a widely used and accepted clinical decision tool in identifying patients for whom neither microbiologic tests nor antimicrobial therapy is necessary. The Center score to use for children and adults with a sore throat to estimate the probability of Streptococcus pyogenes infection.

Modified Centor criteria Appropriate management according to the total score
Criteria Points Total score Chance of streptococcal infection in community

with usual levels of infection, %

Suggested management
Fever (temperature > 38°C) +1 0 2-3% No culture or antibiotic is required
Absence of cough +1 1 4-6%
Swollen and tender anterior cervical nodes +1 2 10-12% RADT or Culture and treat only if culture result is positive
Tonsillar swelling or exudates +1 3 27-28%
Age 3–14 yr +1 4 38–63% Culture all and treat emperically with penicillin on clinical grounds
Age 15–44 yr 0
Age ≥ 45 yr -1

Laboratory Findings

There is a broad overlap between the signs and symptoms of streptococcal and non-streptococcal (usually viral) pharyngitis, and the ability to identify streptococcal pharyngitis accurately on the basis of clinical grounds alone is generally poor. Therefore, except when obvious viral clinical and epidemiological features are present, a laboratory test should be performed to determine whether GAS is present in the pharynx. Even subjects with all clinical features in a particular scoring system can be confirmed to have streptococcal pharyngitis only about 35%–50% of the time and this is particularly the case in children. Swabbing the throat and testing for GAS pharyngitis with rapid antigen detection test (RADT)&/ culture should be performed because the clinical features alone do not reliably discriminate between GAS and viral pharyngitis except when overt viral features like rhinorrhea, cough, oral ulcers, and/or hoarseness are present.

  • The rapid streptococcal antigen tests are widely available and have been used and studied extensively as an adjunct to making the diagnosis of GAS pharyngitis. Specificity for the test has been reported to be as high as 95%, with a sensitivity of 80% to 90%. Throat cultures are much more sensitive, between 90% and 95%. However, they require up to 48 hours for results.
  • A test negative for GAS provides reassurance that the patient likely has a viral cause of pharyngitis. A negative test result also allows the clinician to safely avoid the use of antibiotics. Because of the general increase in rates of resistance to antibiotics, antimicrobial therapy should be prescribed only for proven episodes of GAS pharyngitis.

Special Considerations in the Diagnosis of Acute Pharyngitis in Adults

GAS causes only 5%–15% of cases of acute pharyngitis in adults. The risk of acute pharyngitis due to GAS among adults is higher for parents of school-age children and for those whose occupation brings them into close association with children. However, the risk of a first attack of ARF is extremely low in adults, even with an undiagnosed and untreated episode of streptococcal pharyngitis. Because of these epidemiological distinctions, the use of a clinical algorithm without microbiological confirmation has been suggested as an acceptable alternative basis for the diagnosis of infection in adults. However, use of this diagnostic strategy would result in treatment of an unacceptably large number of adults with non-streptococcal pharyngitis, which is an undesirable result in this age group, which has a low prevalence of GAS pharyngitis and a very low risk of rheumatic fever or rheumatic carditis. However, routine use of backup throat cultures for those with a negative RADT is not necessary for adults in usual circumstances, because of the low incidence of GAS pharyngitis in adults and because the risk of subsequent acute rheumatic fever is generally exceptionally low in adults with acute pharyngitis.

Special Considerations in the Diagnosis of Acute Pharyngitis in Children <3 Years

The prevalence of GAS pharyngitis is significantly lower for children <3 years of age, ranging from 10% to 14%, and if a corresponding rise in Antistreptococcal-O antibody (ASO) is required, the prevalence can be as low as 0%– 6%. Thus, diagnostic testing for GAS pharyngitis is not routinely indicated in children <3 years of age. However, if a child is <3 years of age and there is household contact with a school-aged sibling with documented streptococcal pharyngitis, then it is reasonable to consider testing the child if the child is symptomatic. Therefore, if a child is in daycare or another setting with a high rate of cases of GAS infections, then it is reasonable to test symptomatic children and treat them if they are found to be positive for GAS.

Algorithm for evaluation of acute pharyngitis

The major goal of the evaluation of patients with sore throat or acute pharyngitis is to exclude potentially dangerous causes (e.g. Group A streptococcus), to identify any treatable causes, and to improve symptoms. Identifying group A streptococcus (GAS) is important because timely treatment with antibiotics helps prevent post-streptococcal complications such as acute rheumatic fever. The evaluation includes a thorough history, focused physical examination, and diagnostic testing in selected patients.

Treatment

As is evident from potential etiologic agents of pharyngitis, group A streptococcus is the only commonly occurring form of acute pharyngitis for which antibiotic therapy is definitely indicated. Therefore, for a patient with acute pharyngitis, the clinical decision that usually needs to be made is whether or not the pharyngitis is attributable to GAS.

Medical Therapy

Patients with acute GAS pharyngitis should be treated with an appropriate antibiotic at an appropriate dose for a duration likely to eradicate the organism from the pharynx (usually 10 days). Based on their narrow spectrum of activity, the frequency of adverse reactions, and modest cost, penicillin or amoxicillin is the recommended drug of choice for those non-allergic to these agents. Treatment of GAS pharyngitis in penicillin-allergic individuals should include a first generation cephalosporin (for those not anaphylactically sensitive) for 10 days, clindamycin or clarithromycin for 10 days, or azithromycin for 5 days. Adjunctive therapy with nonsteroidal anti-inflammatory drugs (NSAIDs), acetaminophen, aspirin, or corticosteroids may be useful in the management of GAS pharyngitis.

Surgery

Tonsillectomy may be an option for patients with recurrent streptococcal infections.

Prevention

Accurate diagnosis of streptococcal pharyngitis followed by appropriate antimicrobial therapy is important for the prevention of acute rheumatic fever and for the prevention of suppurative complications such as peritonsillar abscess, cervical lymphadenitis, mastoiditis.

References

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Historical Perspective

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Venkata Sivakrishna Kumar Pulivarthi M.B.B.S [2]Delband Yekta Moazami, M.D.[3]

Overview

The sore throat was first described in the literature as ‘some variants of sore throat’ in the year 1879 by R. L. Bowles, M.D., in the British Medical Journal. Later, in 1885, David Newman, M.D., described pathology, symptoms, and treatment of pharyngitis.In 1910, the importance of bacteriological tests was shown in doubtful cases of pharyngitis. In 1931, three case reports were described and inferred that chronic non-tuberculous bronchial disease such as influenza, whooping cough, and measles is associated with chronic nasopharyngitis and also described the importance of conservative treatment in chronic nasopharyngitis.

Historical Perspective

  • Sore throat was first described in the literature as ‘some variants of sore throat’ in the year 1879 by R. L. Bowles, M.D., in the British Medical Journal.[1]
  • Later, in the Winter of 1885, David Newman, M.D., described pathology, symptoms, and treatment of pharyngitis in his lectures at the Glasgow Royal Infirmary.[2]
  • In 1910, Dr. Donelan illustrated the importance of bacteriological tests in doubtful cases of pharyngitis.[3]
  • In 1931, WM. W. PRIDDLE, B.A., M.D., described three case reports and inferred that chronic non-tuberculous bronchial disease such as influenza, whooping cough, and measles is associated with chronic nasopharyngitis and also described the importance of conservative treatment in chronic nasopharyngitis.[4]

References

  1. Bowles RL (1879) Some Varieties of Sore-Throat. Br Med J 1 (953):503-4. PMID: 20749164
  2. Newman D (1885) Two Lectures on Chronic Laryngitis and Chronic Pharyngitis: Their Pathology, Symptoms, and Treatment. Br Med J 2 (1279):5-7. PMID: 20751315
  3. Grant JD (1910) Secondary Specific Pharyngitis in a Young Woman. Proc R Soc Med 3 (Laryngol Sect):28. PMID: 19974411
  4. Priddle WW (1931) CHRONIC NASO-PHARYNGITIS AND CHRONIC BRONCHIAL INFECTION. Can Med Assoc J 25 (4):441-3. PMID: 20318472

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Classification

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Venkata Sivakrishna Kumar Pulivarthi M.B.B.S [2]

Overview

Pharyngitis can be classified based on the duration as acute pharyngitis or chronic pharyngitis. Additionally, pharyngitis may be classified broadly according to the causative agent as infectious or non-infectious.

Classification

Pharyngitis is a type of inflammation, most commonly caused by an upper respiratory tract infection. It may be classified as acute or chronic.

Pharyngitis can be classified according to the causative agent.[1][2]

Classification of pharyngitis
Infectious pharyngitis Non infectious pharyngitis

References

  1. Murray RC, Chennupati SK (2012) Chronic streptococcal and non-streptococcal pharyngitis. Infect Disord Drug Targets 12 (4):281-5. PMID: 22338589
  2. Chazan B, Shaabi M, Bishara E, Colodner R, Raz R (2003) Clinical predictors of streptococcal pharyngitis in adults. Isr Med Assoc J 5 (6):413-5. PMID: 12841012

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Pathophysiology

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Venkata Sivakrishna Kumar Pulivarthi M.B.B.S [2]Delband Yekta Moazami, M.D.[3]

Overview

The pathogenesis of the sore throat due to pharyngitis is poorly understood. The pharynx is often the first site of infection for many contagious diseases such as pharyngitis because pathogens such as viruses and bacteria often settle in the nasopharynx through inhalation or through droplets. Viral pharyngitis usually transmits from person to person through direct touch or through droplets transmission. The foreign invader reproduces rapidly after settling on the nasopharynx. Generally, pharyngitis is a primary disease, but may be associated with systemic disorders such as the acute retroviral syndrome, or part of a more generalized upper respiratory tract infection.

Pathophysiology

References

  1. Tsai HP, Kuo PH, Liu CC, Wang JR (2001). “Respiratory viral infections among pediatric inpatients and outpatients in Taiwan from 1997 to 1999”. J Clin Microbiol. 39 (1): 111–8. doi:10.1128/JCM.39.1.111-118.2001. PMC 87689. PMID 11136758.
  2. Ferri, Fred (2005). Md consult/first consult 14-month subscription : combo retail pack. Place of publication not identified: Elsevier Saunders. ISBN 9781416026075.
  3. Kline JA, Runge JW (1994) Streptococcal pharyngitis: a review of pathophysiology, diagnosis, and management. J Emerg Med 12 (5):665-80. PMID: 7989695
  4. Proud D, Naclerio RM, Gwaltney JM, Hendley JO (1990) Kinins are generated in nasal secretions during natural rhinovirus colds. J Infect Dis 161 (1):120-3. PMID: 2295843
  5. Bennett, John (2015). Mandell, Douglas, and Bennett’s principles and practice of infectious diseases. Philadelphia, PA: Elsevier/Saunders. ISBN 978-1455748013.
  6. Anjos LM, Marcondes MB, Lima MF, Mondelli AL, Okoshi MP (2014) Streptococcal acute pharyngitis. Rev Soc Bras Med Trop 47 (4):409-13. PMID: 25229278
  7. Murray RC, Chennupati SK (2012) Chronic streptococcal and non-streptococcal pharyngitis. Infect Disord Drug Targets 12 (4):281-5. PMID: 22338589
Causes

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ogheneochuko Ajari, MB.BS, MS [2]

Overview

Pharyngitis can be caused by infectious microorganisms or non-infectious agents. It is usually caused by viruses but may be caused by bacterial or fungal etiology. Gastroesophageal reflux disease (GERD) or particularly extraesophageal reflux (EER) can also cause acid pharyngitis in adults and children. 

Causes

Life Threatening Causes

Life-threatening causes include conditions that may result in death or permanent disability within 24 hours if left untreated.

Common Causes

Group A beta-hemolytic streptococcus (GABHS) is the most common bacterial cause of pharyngitis.[1]

Causes by Organ System

Cardiovascular Kawasaki disease
Chemical / poisoning Acetic acid, chemical exposure, hydrogen sulfide, platinosis
Dermatologic Behcets syndrome, lepidopterism, scarlet fever, scrumpox, Stevens-Johnson syndrome
Drug Side Effect Abacavir, abatacept, acetazolamide oral, acetohexamide , acyclovir, adalimumab, adefovir, alefacept, alfuzosin, allopurinol, altretamine, Amlodipine and Benazepril, amikacin sulfate, Amiloride and Hydrochlorothiazide, amobarbital, amphotericin B, ampicillin sodium, anagrelide, anakinra, anastrozole, anisindione, anticholinergic, antihemophilic factor (human), antihemophilic factor (recombinant), asparaginase, atorvastatin, auranofin, azelastine ophthalmic, aztreonam, benazepril, bevacizumab, bortezomib, bosentan, brinzolamide ophthalmic, budesonide inhalation powder, bumetanide, buspirone, busulfan, butabarbital, butorphanol, candesartan, capecitabine, captopril, carteolol, cefadroxil, cefamandole nafate, cefazolin sodium, cefepime, cefoperazone sodium, cefotaxime sodium, cefotetan disodium, cefoxitin sodium, cefpodoxime, ceftazidime, ceftizoxime sodium, ceftriaxone sodium, cefuroxime sodium, cephalexin, cephradine, cetuximab, chlorambucil, chlorothiazide, chlorpropamide, chlorthalidone, cilostazol, cladribine, clofarabine, clofibrate, co-trimoxazole, cromolyn sodium oral inhalation, cyanocobalamin nasal, cytarabine, dacarbazine, dactinomycin , dapsone, danazol, darbepoetin alfa, daunorubicin, desloratadine, desmopressin, dexmethylphenidate, diclofenac and misoprostol, diethylpropion, diphtheria, disopyramide, docetaxel, dornase alfa, doxorubicin, efalizumab, efavirenz, emtricitabine, enalapril, epinastine ophthalmic, epirubicin, epoetin alfa, eprosartan, erlotinib, erythromycin and sulfisoxazole, etanercept, ethacrynic acid, ethosuximide oral, etodolac, etoposide, ezetimibe, fentanyl skin patches, flavoxate, floxuridine, flunisolide nasal inhalation, fluorouracil, fluphenazine, fluticasone and salmeterol oral inhalation, formoterol, fosamprenavir, foscarnet sodium, fosinopril, fulvestrant, furosemide, gabapentin, ganciclovir, gatifloxacin, gemcitabine hydrochloride, glatiramer , glipizide, glyburide, grifulvin V, griseofulvin, hydrochlorothiazide, ibandronate, ifosfamide, imatinib, imipenem and cilastatin sodium, infliximab, insulin human (rDNA origin) inhalation, interferon beta-1a intramuscular, ipratropium and albuterol inhalation, irbesartan, ketotifen ophthalmic, lamotrigine, levetiracetam, levocetirizine, lisinopril, lomustine, loratadine, losartan, mechlorethamine, mefenamic acid, megestrol, melphalan, meprobamate, meropenem, mercaptopurine, mesalamine, methimazole, methotrexate, methsuximide oral, methyclothiazide, metolazone, metoprolol, minocycline, mitomycin, modafinil, moexipril, moxifloxacin ophthalmic, nafcillin sodium, natalizumab, nedocromil oral inhalation, nisoldipine, olopatadine ophthalmic, omeprazole, oxacillin sodium, oxaliplatin, oxcarbazepine, paclitaxel, palivizumab, pamidronate, peginterferon alfa-2a, penicillin G potassium or sodium, Penicillamine pentamidine isethionate, pentostatin, perindopril, phenobarbital, phenytoin oral, pindolol, pioglitazone, piperacillin sodium, plicamycin, pramlintide, prazosin and polythiazide, primaquine, primidone, procarbazine, promethazine, propafenone, propranolol oral, propylthiouracil, quetiapine, quinapril, rabeprazole, ramipril, ranitidine bismuth citrate, rifabutin, rimexolone, risedronate, risperidone, rifaximin, rituximab, ropinirole, rosiglitazone, rosuvastatin, salmeterol oral inhalation, sargramostim, scopolamine, secobarbital, sibutramine, silver sulfadiazine, sitagliptin, sodium dichloroisocyanurate, sodium oxybate, spironolactone, streptozocin, sulfadiazine, sulfasalazine, sulfinpyrazone, sulfisoxazole, tamsulosin, telmisartan, teniposide, terbinafine, teriparatide (rDNA origin), thioguanine, thiotepa, ticarcillin disodium, ticlopidine, tiotropium oral inhalation, tizanidine, tocainide, tolazamide, tolbutamide, topotecan hydrochloride, trandolapril, trastuzumab, trazodone, triamcinolone nasal inhalation, trimethadione, trimipramine, valproic acid, verapamil and trandolapril, vinblastine, vinorelbine tartrate, Von Willebrand factor, zalcitabine, zolmitriptan nasal, zonisamide
Ear Nose Throat Angina tonsillaris, Bezold’s abscess, dysphagia, ear pain, empty nose syndrome, epiglottitis, herpangina, laryngitis, Ludwig’s angina, oropharyngeal lesion, otalgia, post-nasal drip, retropharyngeal abscess, sinusitis, tonsillitis, tonsillolith, uvulitis, uvulopalatopharyngoplasty
Endocrine Thyroiditis
Environmental Environmental pollutants, lepidopterism
Gastroenterologic Dysphagia, esophagogastroduodenoscopy, GERD
Genetic Periodic fever, aphthous stomatitis, pharyngitis and adenitis
Hematologic Leukemia, Von Willebrand factor
Iatrogenic Endoscopy, invisalign, nasogastric intubation, uvulopalatopharyngoplasty
Infectious Disease Acute viral nasopharyngitis (common cold), adenovirus, allergic pharyngitis, angina tonsillaris, anthrax, arcanobacterium haemolyticum, arcanobacterium, Bezold’s abscess, blastomyces, candida albicans, cervical phlegmon, chickenpox, chlamydia pneumonia, chlamydophila pneumoniae, CMV pneumonitis, coccidioidomycosis, collinsonia canadensis, coronavirus, corynebacterium diphtheriae, coxsackie A virus, coxsackie B virus, cryptococcus, cytomegalovirus, deep neck infection, diphtheria, Duke’s disease, ebola, echovirus, encephalitis lethargica, epiglottitis, Epstein-Barr virus, francisella tularensis, fungal pharyngitis, fusobacterium necrophorum, fusobacterium, gonococcal pharyngitis, gonorrhea, Group A streptococcal infection, Group C streptococci, Group G streptococci, haemophilus influenzae, hand-foot-and-mouth disease, hantavirus pulmonary syndrome, herpangina, herpes simplex virus, herpesviridae, histoplasma, HIV, human parainfluenza viruses, influenza, Kikuchi-Fujimoto disease, klebsiella, laryngitis, lassa fever, Lemierre’s syndrome, lymphadenitis, metapneumovirus, moraxella catarrhalis, mumps, mycobacterium, mycoplasma pneumoniae, neisseria gonorrheae, non-specific urethritis, oral candidiasis, PANDAS, paracoccidioides, parainfluenza, pasteurella, pemphigus, periodic fever, aphthous stomatitis, pharyngitis and adenitis, peritonsillar abscess, pharyngoconjunctival fever, pneumococcus, poliovirus, Q fever, rabies, rat bite fever, respiratory syncitial virus, retropharyngeal abscess, rhinosporidium, rhinovirus, scarlet fever, scrumpox, severe acute respiratory syndrome, sinusitis, staphylococcus aureus, strep throat, streptococcal infections, streptococcus pneumoniae, streptococcus pyogenes, streptococcus suis, syphillis, the clap, tonsillitis, toxemia, tracheitis, tracheobronchitis, treponema pallidum, tularemia, upper respiratory tract infection
Musculoskeletal / Ortho No underlying causes
Neurologic Chronic fatigue syndrome, encephalitis lethargica
Nutritional / Metabolic Ariboflavinosis
Obstetric/Gynecologic Cervical phlegmon
Oncologic Laryngeal cancer, leukemia, lymphoma, lymphoproliferative disorders, nasopharyngeal carcinoma
Ophthalmologic No underlying causes
Overdose / Toxicity Cocaine, toxins
Psychiatric Chronic fatigue syndrome, PANDAS
Pulmonary Acute viral nasopharyngitis (common cold), CMV pneumonitis, epiglottitis, hantavirus pulmonary syndrome, hay fever, laryngitis, severe acute respiratory syndrome, tracheitis, tracheobronchitis, upper respiratory tract infection
Renal / Electrolyte No underlying causes
Rheum / Immune / Allergy Allergic pharyngitis, ankylosing spondylitis, arthralgia, Behcets syndrome, chronic fatigue syndrome, hay fever, immunocompromised host, lymphadenitis, lymphoproliferative disorders, periodic fever syndrome, platinosis, Still’s disease, TNF receptor associated periodic syndrome
Sexual No underlying causes
Trauma No underlying causes
Urologic No underlying causes
Miscellaneous Foreign body

[2][3]

Causes in Alphabetical Order

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References

  1. Pichichero ME (September 1998). “Group A beta-hemolytic streptococcal infections”. Pediatr Rev. 19 (9): 291–302. doi:10.1542/pir.19-9-291. PMID 9745311.
  2. Murray RC, Chennupati SK (2012) Chronic streptococcal and non-streptococcal pharyngitis. Infect Disord Drug Targets 12 (4):281-5. PMID: 22338589
  3. Kline JA, Runge JW (1994) Streptococcal pharyngitis: a review of pathophysiology, diagnosis, and management. J Emerg Med 12 (5):665-80. PMID: 7989695

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Differentiating Pharyngitis from other Diseases

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Venkata Sivakrishna Kumar Pulivarthi M.B.B.S [2]

Overview

Pharyngitis should be differentiated from other infectious causes which mimic sore throat that includes oral thrush, infectious mononucleosis, epiglottitis and retropharyngeal abscess.

Differentiating Pharyngitis from other Diseases

The major goal of the differentiating patients with sore throat or acute pharyngitis is to exclude potentially dangerous causes (e.g. Group A streptococcus), to identify any treatable causes, and to improve symptoms. Identifying the treatable causes is important because timely treatment with antibiotics helps prevent complications such as acute rheumatic fever, post-streptococcal glomerulonephritis.[1][2]

Disease/Variable Presentation Causes Physical exams findings Age commonly affected Imaging finding Treatment
Peritonsillar abscess Severe sore throat, otalgia fever, a “hot potato” or muffled voice, drooling, and trismus[3] Aerobic and anaerobic

bacteria most common is

Streptococcus

pyogenes.[4][5][6][7]

Contralateral deflection of the uvula,

the tonsil is displaced inferiorly and medially, tender submandibular and anterior cervical lymph nodes, tonsillar hypertrophy with likely peritonsillar edema.

The highest occurrence is in adults between 20 to 40 years of age.[3] On ultrasound peritonsillar abscess appears as focal irregularly marginated hypoechoic area.[8][9][10][11][8][9] Ampicillin-sulbactam, Clindamycin, Vancomycin or Linezolid
Croup Has cough and stridor but no drooling. Others are Hoarseness, Difficulty breathing, symptoms of the common cold, Runny nose, Fever Parainfluenza virus Suprasternal and intercostal indrawing,[12] Inspiratory stridor, expiratory wheezing, Sternal wall retractions[13] Mainly 6 months and 3 years old

rarely, adolescents and adults[14]

Steeple sign on neck X-ray Dexamethasone and nebulised epinephrine
Epiglottitis Stridor and drooling but no cough. Other symptoms include difficulty breathing, fever, chills, difficulty swallowing, hoarseness of voice H. influenza type b,

beta-hemolytic streptococci, Staphylococcus aureus,

fungi and viruses.

Cyanosis, Cervical lymphadenopathy, Inflamed epiglottis Used to be mostly found in

pediatric age group between 3 to 5 years,

however, recent trend favors adults

as most commonly affected individuals

with a mean age of 44.94 years

Thumbprint sign on neck x-ray Airway maintenance, parenteral Cefotaxime or Ceftriaxone in combination with Vancomycin. Adjuvant therapy includes corticosteroids and racemic Epinephrine.[15][16]
Pharyngitis Sore throat, pain on swallowing, fever, headache, abdominal pain, nausea and vomiting Group A beta-hemolytic

streptococcus.

Inflamed pharynx with or without exudate Mostly in children and young adults,

with 50% of cases identified

between the ages of 5 to 24 years

_ Antimicrobial therapy mainly penicillin-based and analgesics.
Tonsilitis Sore throat, pain on swallowing, fever, headache, and cough Most common cause is

viral including adenovirus,

rhinovirus, influenza,

coronavirus, and

respiratory syncytial virus.

Second most common

causes are bacterial;

Group A streptococcal

bacteria[17]

Fever, especially 100°F or higher. Erythema, edema and exudate of the tonsils,[18] cervical lymphadenopathy, and Dysphonia.Invalid parameter “ref” in <ref> tag. The supported parameters are: dir, follow, group, name.[19][20] Primarily affects children

between 5 and 15 years old.

Intraoral or transcutaneous USG may show an abscess making CT scan unnecessary.[21][19][20] Antimicrobial therapy mainly penicillin-based and analgesics with tonsilectomy in selected cases.
Retropharyngeal abscess Neck pain, stiff neck, torticollis, fever, malaise, stridor, and barking cough Polymicrobial infection.

Mostly; Streptococcus

pyogenes, Staphylococcus aureus and respiratory anaerobes (example; Fusobacteria, Prevotella,

and Veillonella species)[22][23][24][4][25][26]

Child may be unable to open the mouth widely. May have enlarged cervical lymph nodes and neck mass. Mostly between 2-4 years, but can occur in other age groups.[27][28] On CT scan, a mass impinging on the posterior pharyngeal wall with rim enhancement is seen[29][30] Immediate surgical drainage and antimicrobial therapy. emperic therapy involves; ampicillinsulbactam or clindamycin.

The table below summarizes the findings that differentiate pharyngitis from other conditions that cause fever, fatigue, abdominal pain and diarrhea:[31]

Disease Findings
Ebola Presents with fever, chills vomiting, diarrhea, generalized pain or malaise, and sometimes internal and external bleeding, that follow an incubation period of 2-21 days.
Typhoid fever Presents with fever, headache, rash, gastrointestinal symptoms, with lymphadenopathy, relative bradycardia, cough and leucopenia and sometimes sore throat. Blood and stool culture can confirm the presence of the causative bacteria.
Malaria Presents with acute fever, headache and sometimes diarrhea (children). A blood smears must be examined for malaria parasites. The presence of parasites does not exclude a concurrent viral infection. An antimalarial should be prescribed as an empiric therapy.
Lassa fever Disease onset is usually gradual, with fever, sore throat, cough, pharyngitis, and facial edema in the later stages. Inflammation and exudation of the pharynx and conjunctiva are common.
Yellow fever and other Flaviviridae Present with hemorrhagic complications. Epidemiological investigation may reveal a pattern of disease transmission by an insect vector. Virus isolation and serological investigation serves to distinguish these viruses. Confirmed history of previous yellow fever vaccination will rule out yellow fever.
Shigellosis & other bacterial enteric infections Presents with diarrhea, possibly bloody, accompanied by fever, nausea, and sometimes toxemia, vomiting, cramps, and tenesmus. Stools contain blood and mucous in a typical case. A search for possible sites of bacterial infection, together with cultures and blood smears, should be made. Presence of leucocytosis distinguishes bacterial infections from viral infections.
Leukemia Cancer of the blood or bone marrow and is characterized by an abnormal proliferation (production by multiplication) of blood cells, usually white blood cells (leukocytes). It is part of the broad group of diseases called hematological neoplasms.
Tonsillitis Tonsillitis is characterized by signs of red, swollen tonsils which may have a purulent exudative coating of white patches (i.e. pus). In addition, there may be enlarged and tender neck cervical lymph nodes.
Pharyngitis Typically characterized by sore throat, but commonly accompanied by fever, headache, joint pain and muscle aches, skin rashes, swollen lymph nodes in the neck, diphtheria and common cold.
Adenovirus infections Commonly presents by a cold syndrome, pneumonia, croup and bronchitis.
Influenza Symptoms of influenza can start quite suddenly one to two days after infection. Usually the first symptoms are chills or a chilly sensation but fever is also common early in the infection, with body temperatures as high as 39 °C (approximately 103 °F). Many people are so ill that they are confined to bed for several days, with aches and pains throughout their bodies, which are worst in their backs and legs. Common symptoms of the flu such as fever, headaches, and fatigue come from the huge amounts of proinflammatory cytokines and chemokines (such as interferon or tumor necrosis factor) produced from influenza-infected cells.[32] In contrast to the rhinovirus that causes the common cold, influenza does cause tissue damage, so symptoms are not entirely due to the inflammatory response.[33]
Others Leptospirosis, rheumatic fever, typhus, and mononucleosis can produce signs and symptoms that may be confused with Ebola in the early stages of infection.

The table below summarizes the findings that differentiate influenza from other conditions that cause fever, fatigue, abdominal pain and diarrhea:[34]

Disease Findings
Ebola Presents with fever, chills vomiting, diarrhea, generalized pain or malaise, and sometimes internal and external bleeding, that follow an incubation period of 2-21 days.
Typhoid fever Presents with fever, headache, rash, gastrointestinal symptoms, with lymphadenopathy, relative bradycardia, cough and leucopenia and sometimes sore throat. Blood and stool culture can confirm the presence of the causative bacteria.
Malaria Presents with acute fever, headache and sometimes diarrhea (children). A blood smears must be examined for malaria parasites. The presence of parasites does not exclude a concurrent viral infection. An antimalarial should be prescribed as an empiric therapy.
Lassa fever Disease onset is usually gradual, with fever, sore throat, cough, pharyngitis, and facial edema in the later stages. Inflammation and exudation of the pharynx and conjunctiva are common.
Yellow fever and other Flaviviridae Present with hemorrhagic complications. Epidemiological investigation may reveal a pattern of disease transmission by an insect vector. Virus isolation and serological investigation serves to distinguish these viruses. Confirmed history of previous yellow fever vaccination will rule out yellow fever.
Shigellosis & other bacterial enteric infections Presents with diarrhea, possibly bloody, accompanied by fever, nausea, and sometimes toxemia, vomiting, cramps, and tenesmus. Stools contain blood and mucous in a typical case. A search for possible sites of bacterial infection, together with cultures and blood smears, should be made. Presence of leucocytosis distinguishes bacterial infections from viral infections.
Leukemia Cancer of the blood or bone marrow and is characterized by an abnormal proliferation (production by multiplication) of blood cells, usually white blood cells (leukocytes). It is part of the broad group of diseases called hematological neoplasms.
Tonsillitis Tonsillitis is characterized by signs of red, swollen tonsils which may have a purulent exudative coating of white patches (i.e. pus). In addition, there may be enlarged and tender neck cervical lymph nodes.
Pharyngitis Typically characterized by sore throat, but commonly accompanied by fever, headache, joint pain and muscle aches, skin rashes, swollen lymph nodes in the neck, diphtheria and common cold.
Adenovirus infections Commonly presents by a cold syndrome, pneumonia, croup and bronchitis.
Influenza Symptoms of influenza can start quite suddenly one to two days after infection. Usually the first symptoms are chills or a chilly sensation but fever is also common early in the infection, with body temperatures as high as 39 °C (approximately 103 °F). Many people are so ill that they are confined to bed for several days, with aches and pains throughout their bodies, which are worst in their backs and legs. Common symptoms of the flu such as fever, headaches, and fatigue come from the huge amounts of proinflammatory cytokines and chemokines (such as interferon or tumor necrosis factor) produced from influenza-infected cells.[32] In contrast to the rhinovirus that causes the common cold, influenza does cause tissue damage, so symptoms are not entirely due to the inflammatory response.[35]
Others Leptospirosis, rheumatic fever, typhus, and mononucleosis can produce signs and symptoms that may be confused with Ebola in the early stages of infection.

Pharyngitis must be differentiated from other causes of dysphagia and fever

Variable Croup Epiglottitis Pharyngitis Bacterial tracheitis Tonsilitis Retropharyngeal abscess Subglottic stenosis
Presentation Cough Sore throat, pain on swallowing, fever, headache, abdominal pain, nausea and vomiting Barking cough, stridor,

fever, chest pain,

ear pain, difficulty breathing, headache, dizziness.

Sore throat, pain on swallowing, fever, headache, cough Neck pain, stiff neck, torticollis

fever, malaise, stridor, and barking cough

Depends on severity. May have respiratory distress at birth, exercise-induced dyspnea, intermittent wheezing. Inspiratory stridor. [36]
Stridor
Drooling
Others are Hoarseness, Difficulty breathing, symptoms of the common cold, Runny nose, Fever Other symptoms include difficulty breathing, fever, chills, difficulty swallowing, hoarseness of voice
Causes Parainfluenza virus H. influenza type b, beta-hemolytic streptococci, Staphylococcus aureus, fungi and viruses. Group A beta-hemolytic streptococcus. Staphylococcus aureus Most common cause is viral including adenovirus, rhinovirus, influenza, coronavirus, and respiratory syncytial virus. Second most common causes are bacterial; Group A streptococcal bacteria,[17]  Polymicrobial infection. Mostly; Streptococcus pyogenes, Staphylococcus aureus and respiratory anaerobes (example; Fusobacteria, Prevotella, and Veillonella species)[22][23][24][4][25][26] Congenital, trauma
Physical exams findings Suprasternal and intercostal indrawing,[12] Inspiratory stridor[37], expiratory wheezing,[37] Sternal wall retractions[38] Cyanosis, Cervical lymphadenopathy, Inflammed epiglottis Inflammed pharynx with or without exudate Subglottic narrowing with purulent secretions in the trachea[39][40] Fever, especially 100°F or higher.[41][42]Erythema, edema and Exudate of the tonsils.[18] cervical lymphadenopathy, Dysphonia.[43] Child may be unable to open the mouth widely. May have enlarged

cervical lymph nodes and neck mass.

Signs of respiratory distress, intermittent wheezing. Inspiratory stridor. [36]
Age commonly affected Mainly 6 months and 3 years old

rarely, adolescents and adults[14]

Used to be mostly found in

pediatric age group between 3 to 5 years,

however, recent trend favors adults

as most commonly affected individuals[44]

with a mean age of 44.94 years.

Mostly in children and young adults,

with 50% of cases identified

between the ages of 5 to 24 years.[45]

Mostly during the first six years of life Primarily affects children

between 5 and 15 years old.[46]

Mostly between 2-4 years, but can occur in other age groups.[27][28] May be congenital congenital or acquired. Mean age in acquired is 54.1 years[47]
Imaging finding Steeple sign on neck X-ray Thumbprint sign on neck x-ray Lateral neck xray shows intraluminal membranes and tracheal wall irregularity. Intraoral or transcutaneous USG may show an abscess making CT scan unnecessary.[21][19][20] On CT scan, a mass impinging on the posterior pharyngeal wall with rim enhancement is seen[29][30] Bronchoscopy reveals subglottic stenosis. Computed tomography may reveal a concentric stenotic tracheal segment.[48]
Treatment Dexamethasone and nebulised epinephrine Airway maintenance, parenteral Cefotaxime or Ceftriaxone in combination with Vancomycin. Adjuvant therapy includes corticosteroids and racemic Epinephrine.[15][16] Antimicrobial therapy mainly penicillin-based and analgesics. Airway maintenance and antibiotics Antimicrobial therapy mainly penicillin-based and analgesics with tonsilectomy in selected cases. Immediate surgical drainage and antimicrobial therapy. emperic therapy involves; ampicillin-sulbactam or clindamycin. Endoscopic balloon dilation for patients with low-grade subglottic stenosis,[49] glucocorticoid injections, and resection.[50]

References

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  2. Del Mar CB, Glasziou PP, Spinks AB (2006) Antibiotics for sore throat. Cochrane Database Syst Rev (4):CD000023. DOI:10.1002/14651858.CD000023.pub3 PMID: 17054126
  3. 3.0 3.1 Galioto NJ (2008). “Peritonsillar abscess”. Am Fam Physician. 77 (2): 199–202. PMID 18246890.
  4. 4.0 4.1 4.2 Brook I (2004). “Microbiology and management of peritonsillar, retropharyngeal, and parapharyngeal abscesses”. J Oral Maxillofac Surg. 62 (12): 1545–50. PMID 15573356.
  5. Megalamani SB, Suria G, Manickam U, Balasubramanian D, Jothimahalingam S (2008). “Changing trends in bacteriology of peritonsillar abscess”. J Laryngol Otol. 122 (9): 928–30. doi:10.1017/S0022215107001144. PMID 18039418.
  6. Snow DG, Campbell JB, Morgan DW (1991). “The microbiology of peritonsillar sepsis”. J Laryngol Otol. 105 (7): 553–5. PMID 1875138.
  7. Matsuda A, Tanaka H, Kanaya T, Kamata K, Hasegawa M (2002). “Peritonsillar abscess: a study of 724 cases in Japan”. Ear Nose Throat J. 81 (6): 384–9. PMID 12092281.
  8. 8.0 8.1 Lyon M, Blaivas M (2005). “Intraoral ultrasound in the diagnosis and treatment of suspected peritonsillar abscess in the emergency department”. Acad Emerg Med. 12 (1): 85–8. doi:10.1197/j.aem.2004.08.045. PMID 15635144.
  9. 9.0 9.1 Boesen T, Jensen F (1992). “Preoperative ultrasonographic verification of peritonsillar abscesses in patients with severe tonsillitis”. Eur Arch Otorhinolaryngol. 249 (3): 131–3. PMID 1642863.
  10. Bandarkar AN, Adeyiga AO, Fordham MT, Preciado D, Reilly BK (2016). “Tonsil ultrasound: technical approach and spectrum of pediatric peritonsillar infections”. Pediatr Radiol. 46 (7): 1059–67. doi:10.1007/s00247-015-3505-7. PMID 26637999.
  11. Scott PM, Loftus WK, Kew J, Ahuja A, Yue V, van Hasselt CA (1999). “Diagnosis of peritonsillar infections: a prospective study of ultrasound, computerized tomography and clinical diagnosis”. J Laryngol Otol. 113 (3): 229–32. PMID 10435129.
  12. 12.0 12.1 Johnson D (2009). “Croup”. BMJ Clin Evid. 2009. PMC 2907784. PMID 19445760.
  13. Giordano S, Adamo P, Monaci F, Pittao E, Tretiach M, Bargagli R (2009). “Bags with oven-dried moss for the active monitoring of airborne trace elements in urban areas”. Environ Pollut. 157 (10): 2798–805. doi:10.1016/j.envpol.2009.04.020. PMID 19457602.
  14. 14.0 14.1 Tong MC, Chu MC, Leighton SE, van Hasselt CA (1996). “Adult croup”. Chest. 109 (6): 1659–62. PMID 8769531.
  15. 15.0 15.1 Nickas BJ (2005). “A 60-year-old man with stridor, drooling, and “tripoding” following a nasal polypectomy”. J Emerg Nurs. 31 (3): 234–5, quiz 321. doi:10.1016/j.jen.2004.10.015. PMID 15983574.
  16. 16.0 16.1 Wick F, Ballmer PE, Haller A (2002). “Acute epiglottis in adults”. Swiss Med Wkly. 132 (37–38): 541–7. PMID 12557859.
  17. 17.0 17.1 Putto A (1987). “Febrile exudative tonsillitis: viral or streptococcal?”. Pediatrics. 80 (1): 6–12. PMID 3601520.
  18. 18.0 18.1 Stelter K (2014). “Tonsillitis and sore throat in children”. GMS Curr Top Otorhinolaryngol Head Neck Surg. 13: Doc07. doi:10.3205/cto000110. PMC 4273168. PMID 25587367.
  19. 19.0 19.1 19.2 Nogan S, Jandali D, Cipolla M, DeSilva B (2015). “The use of ultrasound imaging in evaluation of peritonsillar infections”. Laryngoscope. 125 (11): 2604–7. doi:10.1002/lary.25313. PMID 25946659.
  20. 20.0 20.1 20.2 Fordham MT, Rock AN, Bandarkar A, Preciado D, Levy M, Cohen J; et al. (2015). “Transcervical ultrasonography in the diagnosis of pediatric peritonsillar abscess”. Laryngoscope. 125 (12): 2799–804. doi:10.1002/lary.25354. PMID 25945805.
  21. 21.0 21.1 Kawabata M, Umakoshi M, Makise T, Miyashita K, Harada M, Nagano H; et al. (2016). “Clinical classification of peritonsillar abscess based on CT and indications for immediate abscess tonsillectomy”. Auris Nasus Larynx. 43 (2): 182–6. doi:10.1016/j.anl.2015.09.014. PMID 26527518.
  22. 22.0 22.1 Cheng J, Elden L (2013). “Children with deep space neck infections: our experience with 178 children”. Otolaryngol Head Neck Surg. 148 (6): 1037–42. doi:10.1177/0194599813482292. PMID 23520072.
  23. 23.0 23.1 Abdel-Haq N, Quezada M, Asmar BI (2012). “Retropharyngeal abscess in children: the rising incidence of methicillin-resistant Staphylococcus aureus”. Pediatr Infect Dis J. 31 (7): 696–9. doi:10.1097/INF.0b013e318256fff0. PMID 22481424.
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  25. 25.0 25.1 Wright CT, Stocks RM, Armstrong DL, Arnold SR, Gould HJ (2008). “Pediatric mediastinitis as a complication of methicillin-resistant Staphylococcus aureus retropharyngeal abscess”. Arch Otolaryngol Head Neck Surg. 134 (4): 408–13. doi:10.1001/archotol.134.4.408. PMID 18427007.
  26. 26.0 26.1 Asmar BI (1990). “Bacteriology of retropharyngeal abscess in children”. Pediatr Infect Dis J. 9 (8): 595–7. PMID 2235179.
  27. 27.0 27.1 Craig FW, Schunk JE (2003). “Retropharyngeal abscess in children: clinical presentation, utility of imaging, and current management”. Pediatrics. 111 (6 Pt 1): 1394–8. PMID 12777558.
  28. 28.0 28.1 Coulthard M, Isaacs D (1991). “Neonatal retropharyngeal abscess”. Pediatr Infect Dis J. 10 (7): 547–9. PMID 1876473.
  29. 29.0 29.1 Philpott CM, Selvadurai D, Banerjee AR (2004). “Paediatric retropharyngeal abscess”. J Laryngol Otol. 118 (12): 919–26. PMID 15667676.
  30. 30.0 30.1 Vural C, Gungor A, Comerci S (2003). “Accuracy of computerized tomography in deep neck infections in the pediatric population”. Am J Otolaryngol. 24 (3): 143–8. PMID 12761699.
  31. “WHO Infection Control for Viral Haemorrhagic Fevers in the African Health Care Setting” (PDF).
  32. 32.0 32.1 Schmitz N, Kurrer M, Bachmann MF, Kopf M (2005). “Interleukin-1 is responsible for acute lung immunopathology but increases survival of respiratory influenza virus infection”. J Virol. 79 (10): 6441–8. doi:10.1128/JVI.79.10.6441-6448.2005. PMC 1091664. PMID 15858027.
  33. Winther B, Gwaltney J, Mygind N, Hendley J. “Viral-induced rhinitis”. Am J Rhinol. 12 (1): 17–20. PMID 9513654.
  34. “WHO Infection Control for Viral Haemorrhagic Fevers in the African Health Care Setting” (PDF).
  35. Winther B, Gwaltney J, Mygind N, Hendley J. “Viral-induced rhinitis”. Am J Rhinol. 12 (1): 17–20. PMID 9513654.
  36. 36.0 36.1 Nussbaumer-Ochsner Y, Thurnheer R (2015). “IMAGES IN CLINICAL MEDICINE. Subglottic Stenosis”. N Engl J Med. 373 (1): 73. doi:10.1056/NEJMicm1404785. PMID 26132943.
  37. 37.0 37.1 Cherry, James D. (2008). “Croup”. New England Journal of Medicine. 358 (4): 384–391. doi:10.1056/NEJMcp072022. ISSN 0028-4793.
  38. Johnson D (2009). “Croup”. BMJ Clin Evid. 2009. PMC 2907784. PMID 19445760.
  39. Liston SL, Gehrz RC, Siegel LG, Tilelli J (1983). “Bacterial tracheitis”. Am J Dis Child. 137 (8): 764–7. PMID 6869336.
  40. Liston SL, Gehrz RC, Jarvis CW (1981). “Bacterial tracheitis”. Arch Otolaryngol. 107 (9): 561–4. PMID 7271556.
  41. Tonsillitis. Medline Plus. https://www.nlm.nih.gov/medlineplus/ency/article/001043.htm. Accessed May 2nd, 2016.
  42. “Tonsillitis – NHS Choices”.
  43. “Tonsillitis – Symptoms – NHS Choices”.
  44. Lichtor JL, Roche Rodriguez M, Aaronson NL, Spock T, Goodman TR, Baum ED (2016). “Epiglottitis: It Hasn’t Gone Away”. Anesthesiology. 124 (6): 1404–7. doi:10.1097/ALN.0000000000001125. PMID 27031010.
  45. Bennett, John (2015). Mandell, Douglas, and Bennett’s principles and practice of infectious diseases. Philadelphia, PA: Elsevier/Saunders. ISBN 978-1455748013.
  46. Sharav, Yair; Benoliel, Rafael (2008). Orofacial Pain and Headache. Elsevier. ISBN 0723434123.
  47. Nicolli EA, Carey RM, Farquhar D, Haft S, Alfonso KP, Mirza N (2017). “Risk factors for adult acquired subglottic stenosis”. J Laryngol Otol. 131 (3): 264–267. doi:10.1017/S0022215116009798. PMID 28007041.
  48. Nussbaumer-Ochsner Y, Thurnheer R (2015). “IMAGES IN CLINICAL MEDICINE. Subglottic Stenosis”. N Engl J Med. 373 (1): 73. doi:10.1056/NEJMicm1404785. PMID 26132943.
  49. Cui PC, Luo JS, Zhao DQ, Guo ZH, Ma RN (2016). “[Management of subglottic stenosis in children with endoscopic balloon dilation]”. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 51 (4): 286–8. doi:10.3760/cma.j.issn.1673-0860.2016.04.009. PMID 27095722.
  50. Nussbaumer-Ochsner Y, Thurnheer R (2015). “IMAGES IN CLINICAL MEDICINE. Subglottic Stenosis”. N Engl J Med. 373 (1): 73. doi:10.1056/NEJMicm1404785. PMID 26132943.
Epidemiology and Demographics

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Venkata Sivakrishna Kumar Pulivarthi M.B.B.S [2]

Overview

Pharyngitis is one of the most common disorders in adults and children, with more than 10 million ambulatories visits per year. Group A streptococcus is by far the most common bacterial cause of acute pharyngitis, accounting for approximately 15 to 30 percent of cases in children and 5 to 10 percent of cases in adults. Peak seasons for a sore throat include late winter and early spring. Transmission of typical viral and Group A streptococcus (GAS) pharyngitis occurs mostly by hand contact with nasal discharge, rather than by oral contact.

Epidemiology

Viruses are the most common causes of pharyngitis and account for 25% to 45% of all cases.[1][2] Group A streptococcus presents in up to 37% of all children presenting with a sore throat to an outpatient clinic or emergency room and 24% of those presenting at younger than 5 years.[3][4][5]

Demographics

Age

  • The highest burden of disease is found in children and young adults, with 50% of cases identified between the ages of 5 to 24 years.[6]
  • The GAS accounts for 5% to 10% of pharyngitis in adults and 15% to 30% in children.[7]
  • Infectious mononucleosis more common in the age group between 15 and 24 years of age.[8]

Gender

Men and women are affected equally by pharyngitis.

Race

The prevalence of pharyngitis does not vary by race.

References

  1. Alcaide ML, Bisno AL (2007) Pharyngitis and epiglottitis. Infect Dis Clin North Am 21 (2):449-69, vii. DOI:10.1016/j.idc.2007.03.001 PMID: 17561078
  2. Bisno AL, Kaplan EL (2006) Strep throat over and over: how frequent? How real? Mayo Clin Proc 81 (9):1153-4. DOI:10.4065/81.9.1153 PMID: 16970210
  3. Cirilli AR (2013) Emergency evaluation and management of the sore throat. Emerg Med Clin North Am 31 (2):501-15. DOI:10.1016/j.emc.2013.01.002 PMID: 23601485
  4. Bennett, John (2015). Mandell, Douglas, and Bennett’s principles and practice of infectious diseases. Philadelphia, PA: Elsevier/Saunders. ISBN 978-1455748013.
  5. Vincent MT, Celestin N, Hussain AN (2004) Pharyngitis. Am Fam Physician 69 (6):1465-70. PMID: 15053411
  6. Bennett, John (2015). Mandell, Douglas, and Bennett’s principles and practice of infectious diseases. Philadelphia, PA: Elsevier/Saunders. ISBN 978-1455748013.
  7. Bisno AL, Gerber MA, Gwaltney JM, Kaplan EL, Schwartz RH, Infectious Diseases Society of America (2002) Practice guidelines for the diagnosis and management of group A streptococcal pharyngitis. Infectious Diseases Society of America. Clin Infect Dis 35 (2):113-25. DOI:10.1086/340949 PMID: 12087516
  8. Bisno AL (2001) Acute pharyngitis. N Engl J Med 344 (3):205-11. DOI:10.1056/NEJM200101183440308 PMID: 11172144
Risk Factors

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Aysha Anwar, M.B.B.S[2], Venkata Sivakrishna Kumar Pulivarthi M.B.B.S [3]

Overview

Pharyngitis is contagious, so anyone in close proximity to someone with the illness, is at risk. Social situations with prolonged close interpersonal contact are associated with a higher incidence of the disease, such as in schools, dormitories, or military barracks. Droplet spread has been postulated as the method of transmission, and outbreaks have been associated with contaminated food and water, but fomites are not thought to play a role. The degree of contagion is probably related.

Risk Factors

Common risk factors for pharyngitis include:[1][2][3][4]

Less Common Risk Factors

References

  1. Kline JA, Runge JW (1994) Streptococcal pharyngitis: a review of pathophysiology, diagnosis, and management. J Emerg Med 12 (5):665-80. PMID: 7989695
  2. Koch A, Mølbak K, Homøe P, Sørensen P, Hjuler T, Olesen ME et al. (2003) Risk factors for acute respiratory tract infections in young Greenlandic children. Am J Epidemiol 158 (4):374-84. PMID: 12915503
  3. Carapetis JR, Steer AC, Mulholland EK, Weber M (2005) The global burden of group A streptococcal diseases. Lancet Infect Dis 5 (11):685-94. DOI:10.1016/S1473-3099(05)70267-X PMID: 16253886
  4. Dajani A, Taubert K, Ferrieri P, Peter G, Shulman S (1995) Treatment of acute streptococcal pharyngitis and prevention of rheumatic fever: a statement for health professionals. Committee on Rheumatic Fever, Endocarditis, and Kawasaki Disease of the Council on Cardiovascular Disease in the Young, the American Heart Association. Pediatrics 96 (4 Pt 1):758-64. PMID: 7567345
Screening

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Venkata Sivakrishna Kumar Pulivarthi M.B.B.S [2]

Overview

Routine screening for pharyngitis is not recommended. Testing for etiologic agents of pharyngitis should only be done in symptomatic patients.

Screening

Screening for etiologic agents of pharyngitis should only be done in symptomatic patients especially populations at risk. Anyone during the winter months is at risk of pharyngitis, especially those aged 5 to 15 years. Screening can be performed using rapid antigen detection test (RADT) or throat culture[1]

Screening of asymptomatic carriers can be considered in the following cases:

References


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Natural History, Complications,and Prognosis

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1];Associate Editor(s)-in-Chief: Aysha Anwar, M.B.B.S[2], Venkata Sivakrishna Kumar Pulivarthi M.B.B.S [3]

Overview

The sore throat, fever, and malaise associated with acute pharyngitis are distressing, but with few exceptions, these illnesses are both benign and self-limited. Many bacterial and viral organisms are capable of inducing pharyngitis, either as a single manifestation or as part of a more generalized illness. History and symptoms are essential to diagnosis to identify the treatable causes (e.g., GAS) to prevent complications.

Natural History

  • Acute pharyngitis is typically described as the triad of sore throat, fever, and pharyngeal inflammation characterized by erythema and edema, although exudates, vesicles, or ulcerations may also be present.
  • Although pharyngitis may be a primary disorder, sore throat and pharyngeal erythema may also be prominent in systemic disorders, such as acute retroviral syndrome, or part of a more generalized upper respiratory tract infection.
  • Most cases of acute pharyngitis are due to common viral infections and are benign,self-limited processes.[1]
  • The appropriate recognition of patients with more complicated infections that require diagnostic evaluations and treatment is one of the challenges of primary care medicine.[2] An estimated 1-2% of acute pharyngitis progresses to recurrent or chronic disease.[3]
  • Patients with recurrent episodes of pharyngitis and more than one episode of streptococcal pharyngitis at close intervals associated with laboratory evidence of GAS pharyngitis consider that they should also be alert to the possibility that the patient may actually be a chronic pharyngeal GAS carrier who is experiencing repeated viral infections.[4]

Group A Streptococcus

  • Strep pharyngitis occurs predominantly, though not exclusively, in school-age children.[1]
  • Symptoms develop after a short incubation period of 24 to 72 hours.[5]
  • Symptoms can vary widely, with some patients experiencing the full effects of the syndrome while others, such as those who have undergone tonsillectomy, may have milder symptoms.[1]
  • Untreated, group A beta-hemolytic streptococcus (GABHS) infection lasts 7-10 days. Patients with untreated streptococcal pharyngitis are infectious during the acute phase of the illness and for one additional week.
  • Effective antibiotic therapy shortens the infectious period to 24 hours, reduces the duration of symptoms by about one day, and prevents most complications.[5]

Corynebacterium diphtheriae

Complications

Identifying the cause of pharyngitis, especially GABHS, is important to prevent potential life-threatening complications.☃☃ Serious complications of pharyngitis may include peritonsillar abscess or retropharyngeal abscess.☃☃ Complications of pharyngitis based on the causing agent include the following: [6]

Common complications
Pathogen Complications
Group A Streptococcus

Suppurative complications

Non-suppurative complications

Influenza
Adenovirus
Cocksackie A virus
Epstein barr virus
Less common complications
Gonococcus
Diphtheria
Heamophilis influenza
Fusobacterium necrophorum
Parainfluenza virus

Group A Streptococcal Pharyngitis Complications

Rheumatic fever

Rheumatic fever is exceedingly rare in the United States and other developed countries (annual incidence of less than one case per 100,000). This illness should be suspected in any patient with joint swelling and pain, subcutaneous nodules, erythema marginatum or heart murmur, and a confirmed streptococcal infection during the preceding month. Patients will have an elevated antistreptolysin- O titer and erythrocyte sedimentation rate.[5]

Post-streptococcal glomerulonephritis

Post streptococcal glomerulonephritis is another rare complication of GABHS pharyngitis, although treatment with antibiotics does not prevent it. Patients present with hematuria and, frequently, edema in the setting of a recent streptococcal infection with an elevated antistreptolysin-O titer.[5]

Scarlet fever

Scarlet fever is another complication of GABHS pharyngitis and usually presents as a rash characterized by punctate, erythematous, branch able, sandpaper-like exanthematous rash. Rash distributes in the neck, groin, and axillae, and accentuate specifically in the body folds and creases. Other findings include pharynx and tonsils appear erythematous and covered with exudates and tongue appears as bright red with white coating, also known as strawberry tongue.

Prognosis

Most cases of pharyngitis go away on their own without complications.

References

  1. 1.0 1.1 1.2 1.3 1.4 Bisno AL (2001) Acute pharyngitis. N Engl J Med 344 (3):205-11. DOI:10.1056/NEJM200101183440308 PMID: 11172144
  2. Bennett, John (2015). Mandell, Douglas, and Bennett’s principles and practice of infectious diseases. Philadelphia, PA: Elsevier/Saunders. ISBN 978-1455748013.
  3. St Sauver JL, Weaver AL, Orvidas LJ, Jacobson RM, Jacobsen SJ (2006) Population-based prevalence of repeated group A beta-hemolytic streptococcal pharyngitis episodes. Mayo Clin Proc 81 (9):1172-6. PMID: 16970213
  4. Shulman ST, Bisno AL, Clegg HW, Gerber MA, Kaplan EL, Lee G et al. (2012) Clinical practice guideline for the diagnosis and management of group A streptococcal pharyngitis: 2012 update by the Infectious Diseases Society of America. Clin Infect Dis 55 (10):1279-82. DOI:10.1093/cid/cis847 PMID: 23091044
  5. 5.0 5.1 5.2 5.3 5.4 5.5 Vincent MT, Celestin N, Hussain AN (2004) Pharyngitis. Am Fam Physician 69 (6):1465-70. PMID: 15053411
  6. 6.0 6.1 6.2 6.3 Murray RC, Chennupati SK (2012). “Chronic streptococcal and non-streptococcal pharyngitis”. Infect Disord Drug Targets. 12 (4): 281–5. PMID 22338589.
Diagnosis

Diagnosis

Diagnostic Study of Choice | History and Symptoms | Physical Examination | Laboratory Findings | Electrocardiogram | Chest X Ray | CT | Ultrasound | Other Diagnostic Studies

Treatment

Treatment

Medical Therapy | Surgery | Primary Prevention | Secondary Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies

Case Studies

Case Studies

Case #1

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