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Coma blister

A coma blister, or coma bullae, is a skin lesion or blister that typically arises due to pressure in an individual with impaired consciousness. They vary in size, ranging from 4 to 5 centimeters in diameter, and may appear hemorrhagic or blood filled.[1] Coma blisters are usually found in the extremities and trunk.[2] These types of blisters have been associated with the overdose of central nervous system (CNS) depressants especially barbiturates, but also tricyclic antidepressants, hypnotics, benzodiazepines, opiates, antipsychotics, and alcohol.[3] However, studies have found that coma blisters are not caused by the toxicity of these drugs, but due to hypoxia and external pressure on the comatose individual's skin from being immobilized.[1] Coma blisters have been frequently found on individuals who have overdosed on drugs, but have also been found on individuals with chronic kidney failure, hypercalcemia, diabetic ketoacidosis, and a variety of neurologic conditions.[4] Coma blisters are more frequent in adults and less common among children as demonstrated by the few cases published in literature.[2]

Etiology

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The development of coma blisters derives from various causes in the setting of neurologic disease and other conditions, with crucial factors being inadequate amounts of oxygen at the tissue level and external pressure.[5] Examples of neurological disorders that are associated with coma blisters include cranioencephalic trauma, cerebrovascular disease, and meningoencephalitis.[6] Metabolic disorders such as diabetic ketoacidosis, hyperkalemia, and hypoglycemia are also associated with blister formation.[6] Drug overdose-induced comas are one of the most frequent predisposing factors of coma blister formation, where studies have reported the development of coma blisters in 4% of barbiturate overdose.[5][7] Recent studies also suggested that immune mechanisms play a role in the etiology of these blisters, specifically in the drug induced comas.[5] IgG, IgA, and C3 with fibrin are seen with direct immunoflourence staining.[8] Despite there being multiple causes of unconscious states, a common reoccurrence and feature of coma blisters include the death of body tissue or necrosis in the eccrine sweat glands.[9] However, it is still possible to see coma blisters in non-comatose individuals with granulomatosis with polyangiitis or long immobilization.[10][6]

Constant pressure forms blisters by causing tissue injury to the vessel walls, thereby interrupting blood and oxygen flow to the tissues.[5] This constant pressure is often caused by a reflex mechanism to counteract the low arterial blood pressure exacerbated by vasoactive drugs or shock.[11] A lack of oxygen to local tissue leads to the formation of necrotic bulla and the deterioration of the eccrine sweat glands, where metabolically active cells are present.[5] As a result of pressure, coma blisters most commonly develop on pressure points such as the ankles, heels, knees, elbows, fingers, and toes.[6]

Administration of antidepressants, antipsychotics, barbiturates, benzodiazepines, ethanol, or opioids are often connected to drug overdose-induced comas because of their vasoactive properties and possible toxicity on eccrine sweat glands.[7] Due to the over usage of vasoactive drugs, more pressure is applied to the arterial walls, thereby increasing the risk of tissue damage, loss of oxygen to local tissue, and blister formation.[12]

Blisters occur specifically at vasoactive pressure sites between 48 and 72 hours after the start of unconsciousness.[5] Although some lesions may heal on their own, the diagnosis of coma blisters are aided with specific histological characteristics.[5]

Diagnosis

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Coma blisters usually develop on pressure point sites within a few days on individuals who have been immobilized due to external events. Barbiturate overdose is the most frequent predisposing event, but coma or any other condition that renders an individual unconscious can lead to the formation of coma blisters. These blisters resolve on their own within one to two weeks and its diagnosis can be further characterized by histological evidence such as subepidermal bullae, focal necrosis of epidermis, dermis, subcutaneous tissue and all epidermal appendages. For non-drug induced coma blisters, the absence of inflammation along with the presence of thrombosis in dermal wall vessels are the two most significant differences from drug overdose-induced coma blisters. Necrosis on sweat glands and ducts usually occur in coma blisters, but its absence does not exclude the diagnosis.[5] In children, diagnosis may be dependent on careful clinicopathological correlation to omit other blistering diseases.[2]

Differential diagnosis

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Friction blisters

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Friction blisters are only found in areas that undergo repetitive friction. This type of blister is caused by frictional forces in which the epidermal cells are separated mechanically at the level of the stratum spinosum. Hydrostatic pressure causes the area of the separation to fill with fluid, a bullae that is characteristic for blisters.[13]

Edema blisters

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Edema Blisters form at the sites of swelling from acute volume overload, also as known as edema. Edema can occur for various reasons that may include renal or heart failure. Histopathology may show subepidermal edema, and a negative immunofluorescence staining may be performed to differentiate acute edema blisters from other bullous diseases.[14]

Bullous diabeticorum

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Bullous diabeticorum occurs in individuals with diabetes mellitus. Since the majority of diabetic individuals with bullous diabeticorum have nephropathy and neuropathy, it is suggested that the premature aging of local subbasement membrane zone connective-tissue may lead to these types of blisters.[15]

Epidermolysis bullosa

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Epidermolysis bullosa (EB) is a genetic disease that causes the skin to be extremely fragile and individuals with the disease are prone to blisters, even with minimal friction and trauma. There are thirty subtypes of epidermolysis bullosa which are arranged into four major categories: EB simplex (EBS), dystrophic EB (DEB), kindler EV, and junctional EB (JEB). There is currently no cure for epidermolysis bullosa and treatment is based on bandaging, wound management, and pain management.[16]

Bullous pemphigoid

Bullous pemphigoid is an autoimmune bullous disease that mainly affects older individuals. Individuals typically present with itchy rashes that transform into fluid filled bullous lesions on the skin. Although these blisters usually appear on the arms, legs, and trunk of the body, they can also be found in the mouth as sores. The most common treatment options for blisters caused by bullous pemphigoid are topical and systemic corticosteroids, which help to relive itching and heal the blistering skin.[17]

Treatment and management

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Coma blisters typically do not require treatment and will usually heal on their own within one to two weeks of formation.[5] Early identification and management of coma blisters is important and involves treating any underlying conditions that may have led to the formation of the blisters, and decreasing the risk of subsequent infections.[18]

Before starting any treatment, it is important to rule out other cases of potential bullous diseases, such as epidermolysis bullosa, bullous pemphigoid, bullous amyloidosis, and epidermolysis bullosa acquisita, since bullous lesions of the skin are characteristic in these conditions.[19] It is also important to differentiate coma blisters from other types of dermatologic lesions, such as friction blisters and edema blisters, as their characteristics may also be similar to coma blisters.[20] If treatment is needed, a possible option is topical antibiotics, which can be used to prevent infections of the blisters.[18]

Management and wound care can also be performed and involve sterile drainage of the blister, positioning the individual away from their wound to relieve any pressure on the site, and preventing the formation of pressure ulcerations. When draining the blisters, leaving the roof of the blister undamaged can allow the roof to act as an additional layer of dressing for the wound and the use of hydrocolloid dressings can also help to maintain moisture and promote healing.[21] Some individuals may experience visible scarring in the area after the blisters have healed, but this is non-concerning.[2]

Coma blisters are not seen as contraindications for other medications or therapies, therefore medications should be continued as needed to manage other co-morbidities even in the presence of coma blisters.[5]

See also

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References

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  1. ^ a b Agarwal A, Bansal M, Conner K (March 2012). "Coma blisters with hypoxemic respiratory failure". Dermatology Online Journal. 18 (3): 10. doi:10.5070/D35175b1pg. PMID 22483521.
  2. ^ a b c d Bosco L, Schena D, Colato C, Biban P, Girolomoni G (December 2013). "Coma blisters in children: case report and review of the literature". Journal of Child Neurology. 28 (12): 1677–1680. doi:10.1177/0883073812464684. PMID 23155203. S2CID 2299594.
  3. ^ "Coma blisters. A key to neurological diagnosis". Neurología (English Edition). Elsevier. Retrieved 2022-07-26.
  4. ^ Piede J, Wallace E (January 2011). "Coma bullae: associations beyond medications". Mayo Clinic Proceedings. 86 (1): e5. doi:10.4065/mcp.2010.0364. PMC 3012639. PMID 21193646.
  5. ^ a b c d e f g h i j Rocha J, Pereira T, Ventura F, Pardal F, Brito C (October 2009). "Coma Blisters". Case Reports in Dermatology. 1 (1): 66–70. doi:10.1159/000249150. PMC 2895214. PMID 20652118.
  6. ^ a b c d Vázquez-Osorio I, Gonzalvo-Rodríguez P, Rodríguez-Díaz E (2017). "Coma Blisters after an Overdose of Central Nervous System Depressants". Actas Dermo-Sifiliograficas. 108 (1): 81–83. doi:10.1016/j.adengl.2016.11.015. PMID 27737761.
  7. ^ a b Dinis-Oliveira RJ (2019). "Drug Overdose-Induced Coma Blisters: Pathophysiology and Clinical and Forensic Diagnosis". Current Drug Research Reviews. 11 (1): 21–25. doi:10.2174/1874473711666180730102343. PMID 30058500. S2CID 51863951.
  8. ^ Reilly GD, Harrington CI (December 1983). "Positive immunofluorescence in bullous lesions in drug-induced coma". The British Journal of Dermatology. 109 (6): 720. doi:10.1111/j.1365-2133.1983.tb00554.x. PMID 6360197. S2CID 32953723.
  9. ^ Asokan N, Binesh VG, Andrews AM, Jayalakshmi PS (November 2014). "Bullous lesions, sweat gland necrosis and rhabdomyolysis in alcoholic coma". Indian Journal of Dermatology. 59 (6): 632. doi:10.4103/0019-5154.143576. PMC 4248528. PMID 25484420.
  10. ^ Ferreli C, Sulica VI, Aste N, Atzori L, Pinna M, Biggio P (July 2003). "Drug-induced sweat gland necrosis in a non-comatose patient: a case presentation". Journal of the European Academy of Dermatology and Venereology. 17 (4): 443–445. doi:10.1046/j.1468-3083.2003.00695.x. PMID 12834457. S2CID 45514949.
  11. ^ Arndt KA, Mihm MC, Parrish JA (May 1973). "Bullae: a cutaneous sign of a variety of neurologic diseases". The Journal of Investigative Dermatology. 60 (5): 312–320. doi:10.1111/1523-1747.ep12723147. PMID 4758735.
  12. ^ Hollenberg SM (April 2011). "Vasoactive drugs in circulatory shock". American Journal of Respiratory and Critical Care Medicine. 183 (7): 847–855. doi:10.1164/rccm.201006-0972CI. PMID 21097695.
  13. ^ Knapik JJ, Reynolds KL, Duplantis KL, Jones BH (September 1995). "Friction blisters. Pathophysiology, prevention and treatment". Sports Medicine. 20 (3): 136–147. doi:10.2165/00007256-199520030-00002. PMID 8570998. S2CID 40287087.
  14. ^ Chen SX, Cohen PR (October 2017). "Edema Bullae Mimicking Disseminated Herpes Zoster". Cureus. 9 (10): e1780. doi:10.7759/cureus.1780. PMC 5732012. PMID 29255659.
  15. ^ Chouk C, Litaiem N (2022). "Bullosis Diabeticorum". StatPearls. Treasure Island (FL): StatPearls Publishing. PMID 30969694. Retrieved 2022-07-28.
  16. ^ Bardhan A, Bruckner-Tuderman L, Chapple IL, Fine JD, Harper N, Has C, et al. (September 2020). "Epidermolysis bullosa". Nature Reviews. Disease Primers. 6 (1): 78. doi:10.1038/s41572-020-0210-0. PMID 32973163. S2CID 221861310.
  17. ^ Miyamoto D, Santi CG, Aoki V, Maruta CW (2019-05-09). "Bullous pemphigoid". Anais Brasileiros de Dermatologia. 94 (2): 133–146. doi:10.1590/abd1806-4841.20199007. PMC 6486083. PMID 31090818.
  18. ^ a b Waring WS, Sandilands EA (2007). "Coma blisters". Clinical Toxicology. 45 (7): 808–809. doi:10.1080/15563650701709189. PMID 17952753. S2CID 5371293.
  19. ^ Northover JM, Pickard JD, Murray-Lyon IM, Presbury DG, Haskell R, Keith DA (June 1972). "Bullous lesions of the skin and mucous membranes in primary amyloidosis". Postgraduate Medical Journal. 48 (560): 351–353. doi:10.1136/pgmj.48.560.351. PMC 2495229. PMID 5049254.
  20. ^ Torres-Navarro I, Pujol-Marco C, Roca-Ginés J, Botella-Estrada R (September 2020). "Coma blisters. A key to neurological diagnosis". Neurologia. 35 (7): 512–513. doi:10.1016/j.nrleng.2018.11.007. PMID 30857784. S2CID 226194253.
  21. ^ Bluestein D, Javaheri A (November 2008). "Pressure ulcers: prevention, evaluation, and management". American Family Physician. 78 (10): 1186–1194. PMID 19035067.
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