Toxic Shock Syndrome


Article Author:
Adam Ross


Article Editor:
Hugh Shoff


Editors In Chief:
Kranthi Sitammagari
Mayank Singhal


Managing Editors:
Orawan Chaigasame
Carrie Smith
Abdul Waheed
Frank Smeeks
Kristina Soman-Faulkner
Benjamin Eovaldi
Radia Jamil
Sobhan Daneshfar
Saad Nazir
William Gossman
Pritesh Sheth
Hassam Zulfiqar
Navid Mahabadi
Steve Bhimji
John Shell
Matthew Varacallo
Ahmad Malik
Mark Pellegrini
James Hughes
Beata Beatty
Hajira Basit
Phillip Hynes


Updated:
2/17/2019 9:19:51 AM

Introduction

Toxic shock syndrome (TSS) is an acute-onset illness characterized by fever, hypotension, sunburn-like rash, and end-organ damage. TSS was classically associated with high absorbency tampon use in menstruating women until eventually, these were taken off the market. Since that time, it has become important also to consider non-menstrual cases. The incidence of TSS is estimated to be around 0.8 to 3.4 per 100,000 in the United States.[1][2][3]

Etiology

TSS is most commonly caused by a toxigenic strain of Staphylococcus aureus or Group A Strep (Streptococcus pyogenes). Other strains of streptococci also produce superantigens, which can lead to TSS. The disease occurs most often in the setting of menstruation despite the discontinuation of high absorbency tampons. However, TSS can also present in non-menstrual settings such as in soft tissue infections, post-surgical infections, burns, retained foreign bodies such as nasal packing, and dialysis catheters. Staphylococcal TSS is typically the result of a localized infection such as an abscess, whereas streptococcal TSS may result from bacteremia, necrotizing fasciitis, or cellulitis.[4]

Epidemiology

The incidence of menstrual and non-menstrual TSS is estimated to be around 0.8 to 3.4 per 100,000 in the United States. The incidence tends to be higher in the winter and is more prevalent in developing countries. [5]

Pathophysiology

TSS is a toxin-mediated disease that is caused by toxin-producing streptococci or S. aureus. These toxins cause over-activation of cytokines and inflammatory cells resulting in the presenting signs and symptoms like fever, rash, hypotension, and end-organ failure due to capillary leak.

History and Physical

TSS typically presents with rapid onset of fever, rash, and hypotension. It may be preceded by a prodrome of fever and chills with nausea and vomiting as well as nonspecific symptoms such as myalgias, headache, or symptoms of pharyngitis (e.g., a sore throat, painful swallowing), which then progresses to sepsis and organ dysfunction. Risk factors include superabsorbent tampon use, nasal packing, post-operative wound infections, recent influenza infection, as well as immunocompromised states.

The Center for Disease Control and Prevention (CDC) clinical criteria for TSS includes fever, rash, hypotension, and multisystem organ involvement. Classically, the rash is a diffuse, blanching, macular erythroderma. The rash desquamates one to two weeks later followed by full-thickness peeling. There may be mucosal involvement with strawberry tongue and ulceration of the vaginal mucosa or conjunctival erythema. Patients may exhibit disorientation or altered mental status without focal deficits.

Evaluation

There is no specific lab test to identify TSS. A complete blood count (CBC) may show leukocytosis or leukopenia. Bandemia is common. Evaluation of multisystem organ involvement including CBC, CMP, CK, and coagulation studies should be drawn to evaluate for the clinical criteria of TSS. The CDC defines multisystem organ involvement as vomiting or diarrhea, myalgias, creatine phosphokinase (CPK) greater than two times the upper limit of normal, mucous membrane hyperemia (vaginal, oral, or conjunctival), BUN or creatinine two times the upper limit of normal, bilirubin or AST/ALT two times the upper limit of normal, Platelets less than 100,000, or altered level of consciousness without focal neurologic signs.[3]

Life-threatening hypocalcemia is prominent throughout the disease and should be repleted accordingly. Anemia, thrombocytopenia, and prolonged coagulation times are also common. Blood cultures and cultures from any suspected source should be obtained. Lumbar puncture should be performed in patients with fever and mental status change to evaluate for meningitis after obtaining coagulation studies.

Treatment / Management

Patients should receive aggressive intravenous (IV) fluid hydration with crystalloids. Soft tissue infections, especially necrotizing fasciitis should be sought out and managed. Any source of bacteria such as tampons or nasal packing should immediately be removed. Emergent surgical consultation should be obtained for any wound debridement or surgical cause. This is critical in the early management of toxic shock syndrome.[6][7]

Broad-spectrum antibiotics should be administered for those with an unidentified organism, if possible after blood cultures and cultures from the suspected source have been drawn. For most institutions, this will include vancomycin or linezolid given the high prevalence of methicillin-resistant Staphylococcus aureus (MRSA). Clindamycin should also be administered to suppress toxin production. Studies have shown improved outcomes when Clindamycin is added to antibiotic regimens. It should not be given alone as it is bacteriostatic, rather than bactericidal. Given that it is initially impossible to tell if the infection is polymicrobial, initial therapy should also cover gram-negative organisms.

Once the organism is identified, and sensitivities have been determined, antibiotics should be optimized and narrowed in the spectrum. Penicillin is the preferred antibiotic for group A strep. For MSSA, clindamycin is recommended, plus flucloxacillin or a beta-lactamase-resistant penicillin such as nafcillin. Current recommendations are to treat for seven to 14 days.

Vasopressors should be administered for patients with shock refractory to IV fluids. Most current guidelines recommend Norepinephrine as a first option. Intravenous immunoglobulin (IVIG) is thought to work by neutralizing the activity of the toxins produced and can be considered for shock refractory to fluids and vasopressors. While there are no randomized controlled trials supporting its use, observational trials have shown a reduction in mortality with IVIG compared to patients who only received antibiotics. The optimal dosing is not well established, but high dose at 2 g/kg is acceptable. All patients should be admitted to an intensive care unit. Although a small study from 1984 showed reduced illness severity with steroids, there was no improvement in mortality. Corticosteroids are currently not recommended as adjunctive therapy for TSS.

Differential Diagnosis

  • Scarlet fever
  • Kawasaki disease
  • Meningococcemia
  • Toxic epidermal necrolysis
  • Hemorrhagic shock
  • Gas gangrene
  • Drug eruption
  • Erythema multiforme

Pearls and Other Issues

All patients should be admitted to the intensive care until, with more severe cases going to a burn unit. The case fatality rate of Streptococcal TSS may exceed 50% whereas non-streptococcal TSS is less than 3%.  The CDC does not recommend routine screening and chemoprophylaxis of household contacts of patients with invasive Group A Strep (GAS) infections.

In two large prospective trials, only five cases of invasive GAS occurred amongst almost 2000 household contacts. However, based on risk factors for death from invasive GAS, the CDC states “health care providers may choose to offer chemoprophylaxis to household members aged 65 years or those at increased risk of sporadic invasive GAS infection”. While there are no large trials with evidence-based regimens, should you choose to treat household contacts, seven to ten days of oral cephalexin is a reasonable choice. For additional information see the CDC case definitions for Toxic Shock syndrome (other than Streptococcal) and Streptococcal Toxic Shock syndrome.

Enhancing Healthcare Team Outcomes

Toxic shock syndrome is a life-threatening disorder which carries a very high mortality. While the mortality rates have decreased over the past 2 decades, they still vary from 1.8-12%. For those patients who are misdiagnosed or the treatment is delayed, the mortality can exceed 50%. For this reason, healthcare workers should be aware of the disorder and even if they do not manage it, should be able to make a prompt referral. The key in the management of TSS is prevention. The patient needs to be educated on the early signs and symptoms of the disorder and when to seek medical care. In some cases, chemoprophylaxis of household contacts of the patient is recommended. The moment TSS is suspected, even during triage to the emergency department, an infectious disease consultant must be called right away. These patients need rapid resuscitation and admission to the ICU. Only with aggressive treatment can the high mortality rates be prevented.[8][9] (Level V)


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Toxic Shock Syndrome - Questions

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What is the most important immediate treatment for toxic shock syndrome?



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Which of the following organisms is most frequently implicated in the development of toxic shock syndrome?



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What causes toxic shock syndrome?



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A woman presents with high fever, lethargy, nausea, vomiting, and myalgias. Examination shows hypotension and a generalized erythematous rash with desquamation of the hands and feet. Laboratories show elevated WBC, BUN, and creatinine. Which of the following is the most likely diagnosis?



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Which of the following is least likely to be associated with the development of toxic shock syndrome?



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Which of the following statements about toxic shock syndrome (TSS) is NOT true?



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An organism that is a common cause of toxic shock syndrome is:



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A 17-year-old female presents with a 3-day history of an abscess on the back with cellulitis. The patient becomes hypotensive, vomits, and has diarrhea. There is a generalized macular erythematous rash, strawberry tongue, and injection of the oral mucosa and conjunctiva. Mental status deteriorates. Select the most likely etiology.



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Which organism is predominantly responsible for toxic shock syndrome?



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A previously healthy male presents with fever and rash after recently having nasal packing placed following surgery. He is tachycardic with an initial blood pressure of 80/50 mmHg and a temperature of 102 F. The rash is diffuse, red, and painful, and he has ulceration of the oral mucosa. Which of the following is the appropriate management and disposition?



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A 30 year old woman notes the sudden onset of a high fever, nausea, vomiting, diarrhea, and myalgias. Thereafter she develops diffuse erythroderma, hypotension, and confusion. The most likely diagnosis is:



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Toxic Shock Syndrome - References

References

Berg D,Gerlach H, Recent advances in understanding and managing sepsis. F1000Research. 2018     [PubMed]
Kim HI,Park S, Sepsis: Early Recognition and Optimized Treatment. Tuberculosis and respiratory diseases. 2018 Sep 28     [PubMed]
Vincent JL,Mongkolpun W, Current management of Gram-negative septic shock. Current opinion in infectious diseases. 2018 Oct 6     [PubMed]
Coopersmith CM,De Backer D,Deutschman CS,Ferrer R,Lat I,Machado FR,Martin GS,Martin-Loeches I,Nunnally ME,Antonelli M,Evans LE,Hellman J,Jog S,Kesecioglu J,Levy MM,Rhodes A, Surviving Sepsis Campaign: Research Priorities for Sepsis and Septic Shock. Critical care medicine. 2018 Aug     [PubMed]
Schmitz M,Roux X,Huttner B,Pugin J, Streptococcal toxic shock syndrome in the intensive care unit. Annals of intensive care. 2018 Sep 17     [PubMed]
Guirgis F,Black LP,DeVos EL, Updates and controversies in the early management of sepsis and septic shock. Emergency medicine practice. 2018 Oct     [PubMed]
Barrier KM, Summary of the 2016 International Surviving Sepsis Campaign: A Clinician's Guide. Critical care nursing clinics of North America. 2018 Sep     [PubMed]
Gaensbauer JT,Birkholz M,Smit MA,Garcia R,Todd JK, Epidemiology and Clinical Relevance of Toxic Shock Syndrome in US Children. The Pediatric infectious disease journal. 2018 Mar 27     [PubMed]
McCoy A,Das R, Reducing patient mortality, length of stay and readmissions through machine learning-based sepsis prediction in the emergency department, intensive care unit and hospital floor units. BMJ open quality. 2017     [PubMed]

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