Latex Allergy

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Background

Allergy to natural rubber latex is common and serious in children and adults. Latex is the milky fluid derived from the lactiferous cells of the rubber tree, Hevea brasiliensis. It is composed primarily of cis -1,4-polyisoprene, a benign organic polymer that confers most of the strength and elasticity of latex. It also contains a large variety of sugars, lipids, nucleic acids, and highly allergenic proteins.

More than 200 polypeptides have been isolated from latex. Latex proteins vary in their allergenic potential. Protein content varies with harvest location and manufacturing process. Basic knowledge of the manufacturing processes aids in understanding the medical problems related to latex exposure.[1]

Freshly harvested latex from Malaysia, Indonesia, Thailand, and South America is treated with ammonia and other preservatives to prevent deterioration during transport to factories. Latex is treated with antioxidants and accelerators to strengthen the product during the manufacturing process, including carbamates, mercaptobenzothiazoles, and thiurams, which have allergenic potential of their own.[2, 3] It is then shaped into the desired object and vulcanized to produce disulfide cross-linking of latex molecules.

After being dried and rinsed to reduce proteins and impurities, the product frequently is dry-lubricated with cornstarch or talc powder. Powder particles rapidly adsorb residual latex proteins; other proteins remain in soluble form on the surface of finished products.

Latex is ubiquitous in modern society and particularly in health care. William Halstead first used latex surgical gloves in 1890. Latex has been used in a myriad of medical devices for decades. In the late 1980s, however, latex glove use in healthcare skyrocketed, driven by efforts to reduce occupational exposure to blood-borne pathogens, particularly human immunodeficiency virus (HIV). Billions of pairs of medical gloves are imported to the United States annually, often as powdered, nonsterile examination gloves.

In the 1980s and 1990s, heightened demand for latex to manufacture gloves and other objects resulted in hundreds of new, poorly regulated latex factories in tropical countries. The incidence of minor and serious allergic reactions to latex began to rise rapidly among patients and health care workers (HCWs) around the world.[4, 5, 6, 7, 8] Latex sensitization can occur after skin or mucosal contact, after peritoneal contact during surgery, and after inhalation of aerosolized particles with adsorbed latex on their surfaces.

See All About Allergies: Be Ready for Spring, a Critical Images slideshow, to help identify a variety of allergens and symptoms.

For related information, see Medscape's Allergy & Immunology Resource Center.

Pathophysiology

Latex exposure is associated with 3 clinical syndromes.

Irritant dermatitis results from mechanical disruption of the skin due to the rubbing of gloves and accounts for the majority of latex-induced local skin rashes. It is not immune mediated, is not associated with allergic complications, and is not the subject of this article. It may be confused with Type IV hypersensitivity. Any chronic hand dermatitis in HCWs raises the risk of nosocomial infections, including blood-borne pathogens, and should be addressed to identify and remove irritants.

The second syndrome is a delayed (type IV) hypersensitivity reaction, resulting in a typical allergic contact dermatitis. Symptoms usually develop within 24-48 hours of cutaneous or mucous membrane exposure to latex in a sensitized person. The primary allergens are residual accelerators and antioxidants left from the original manufacturing process. Langerhans cells process the antigens and present them to cutaneous T cells. Multiple objects can cause sensitization, but the most common sources in this country are probably nonsterile examination gloves for adults and shoe soles for children. Type IV hypersensitivity is more common in atopic individuals. The dermatitis may predispose patients to further sensitizations or infections.

The third, most serious, and least common syndrome is immediate (type I) hypersensitivity. It is mediated by an immunoglobulin E (IgE) response specific for latex proteins. As noted, latex proteins are highly allergenic, and they are variable between lots from different plantations, factories, and manufacturers. Cross-linking of IgE molecules on mast cell and basophil cell membranes by latex protein allergens triggers the release of histamine and other mediators of the systemic allergic cascade in sensitized individuals.[9]

Exposure can occur following skin, mucous membrane, or visceral/peritoneal contact. Powdered latex examination gloves have been the most frequent source of sensitization in adults, causing cutaneous and inhalational exposures, most often affecting the HCWs wearing them. (Fortunately, their use is decreasing as many hospitals move toward powder-free, "low-allergen," or nonlatex glove products.)[10]

It also can follow inhalation of latex-laden particles or bloodstream exposure to soluble latex proteins following intravascular access procedures.[11] Anaphylaxis during anesthesia and in the perioperative period is increasingly recognized as a manifestation of type I allergy to latex.[12, 13, 14] It can be fatal without emergent treatment.[15]

Sensitization is more common in atopic individuals. Symptoms generally begin within minutes of exposure. The spectrum of clinical manifestations includes localized or generalized urticaria, rhinitis, conjunctivitis, bronchospasm, laryngospasm, hypotension, and full-blown anaphylaxis.

Epidemiology

Frequency

United States

Latex allergy is present in 1-5% of the general population, with an increased prevalence in atopic individuals. Latex allergy is increased in populations with chronic occupational exposure to latex.[16] It is found in 8-12% of HCWs[17] and in at least 10% of rubber industry workers. Symptoms of latex allergy have been described in 14% of a group of EMS providers and in 54% of a pediatric ED staff.[18, 19, 20] Atopy raises the risk of occupational sensitization.

The highest prevalence of latex allergy (20-68%) has been reported in patients with spina bifida or congenital urogenital abnormalities. Sensitization in these patients apparently follows multiple urinary tract, rectal, and thecal procedures, as well as multiple surgeries during early childhood. Children with spinal cord injuries also have increased incidence of latex allergy,[21]  although children with spinal dysraphism in one study had a low prevalence.[22] Patients with spina bifida may have a genetic predisposition for latex sensitization. Patients with spina bifida and human leukocyte antigen (HLA) alleles DRB and DQB1 were more likely to have a specific IgE response to a common latex antigen. Again, within this risk group, atopic children are at increased risk.

Other patients with a history of multiple surgeries or other latex-exposing procedures are also at increased risk relative to the general population. Patients with cerebral palsy, mental retardation, or paraplegia also appear to have increased risk of latex allergy, probably because of repeated medical exposures.

Finally, the prevalence of latex allergy is increased in persons with allergies to avocado, banana, chestnut, kiwi, papaya, peach, or nectarine. Cross-reacting antigens have been found between these tropical fruits and latex.

International

The occupational and nonoccupational risk patterns described above are similar in other developed countries, documented in an extensive international literature now focused more on interventions to reduce latex allergy in HCWs and other populations than on simply describing their increased risk.[2, 23, 24] Workers with occupational exposure during harvesting and/or processing latex in developing countries where H brasiliensis is grown have an increased risk relative to the general populations.[16, 25]

Mortality/Morbidity

Patients with type I hypersensitivity are at risk of developing anaphylaxis and/or respiratory obstruction, which can be fatal.

Deaths have been reported following the intraoperative or procedural use of latex devices. Latex anaphylaxis has occurred after childbirth, instrumentation, intravenous injection, balloon blowing, condom use, and hyperbaric treatment.[15, 12, 14, 13, 26]

Although most patients can be treated effectively for type IV and type I reactions without clinical sequelae, major allergy may prevent them from pursuing certain careers, using many household and workplace objects, and seeking timely medical care due to justified fear of latex exposure.

Sex

Incidence in males and females is equal.

Age

Latex allergy probably is more common in children and in younger working adults because of the increased medical and/or occupational exposure over the past decades.

History

Symptoms of delayed (type IV) hypersensitivity usually develop within 1-2 days of exposure. Immediate (type I) hypersensitivity causes symptoms within minutes of exposure. Immediate symptoms may include the following:

Physical

See the list below:

Causes

The source of latex exposure may be obvious or occult. The history of latex allergy may be known or unknown. Individuals may be exposed to latex through their skin, mucous membranes, or airway (ie, oral, nasal, or endotracheal tissue). Medical procedures may cause reactions in sensitized providers or patients. Inadvertent inhalational exposure is frequent in medical settings where aerosolized latex-laden glove powder may remain airborne for hours; this risk is reduced when powder-free products are used. Inhalational exposure also may occur outside hospitals from use of powder-lubricated latex products or even tire particles in heavy traffic areas. Common sources of latex exposure include, but are not limited to, the following:

Laboratory Studies

ED diagnosis and management depends on the history and the physical examination.[27] Results of laboratory tests sent from the ED are not generally available in a useful time frame. Several types of diagnostic studies are useful in nonemergent evaluations.

Total serum IgE may be elevated in patients with type I allergy, but it is neither sensitive nor specific.

Radioimmunoassay test (RAST) results for latex-specific IgE range from 50-100% sensitive and 63-100% specific. Predictive value depends on the exact test used, the patient population, and the source of allergen. RAST can be a useful and safe confirmatory test in patients with suggestive clinical histories. The sensitivity and specificity are improving with newer-generation testing methods.[28]

Enzyme-linked assays of latex-specific IgE (ELISA) may serve the same purpose.[29]

Genomic profiling may become a useful tool for predicting risk, guiding therapy, and understanding pathophysiology in latex allergy.[30]

Other Tests

See the list below:

Procedures

If type I latex allergy is suspected, all procedures should be performed with latex-free instruments, devices, and protective clothing.

Preprocedure screening by history should include risk factors such as occupational and nonoccupational risk groups, tropical fruit allergy, and atopy as well as documented latex allergy.

Prehospital Care

Prehospital providers should be aware of the risk of latex allergy in patients and providers.

Search for and read MedicAlert-type bracelets.

Note the patient's history of relevant allergies to medical devices or fruits.

To rule out latex allergy that could worsen with further medical exposure, review the patient's history of activities/exposures immediately preceding any systemic allergic reaction.

Use powder-free latex gloves or, ideally, high-quality nonlatex gloves to minimize risk to patients and providers in all circumstances. Latex-free resuscitation and intravenous (IV) access equipment should be available for high-risk patients. Do not give medication from rubber-topped multidose vials or through latex IV ports in latex-allergic patients.

Emergency Department Care

Patients with known or suspected latex allergy who seek care for unrelated medical conditions or injuries must be kept within a latex-safe environment to prevent serious complications. This includes all patients with spina bifida.

Patients presenting with frank symptoms of type I latex allergy are treated as any other patients with systemic allergic reactions, except they must be protected from further latex contact to avoid clinical deterioration. Many EDs, hospitals, and medical offices represent very high-risk environments for latex-sensitive patients, particularly if powdered latex gloves are still in use.

Consultations

Consultants must be aware of the need to scrupulously avoid exposing the patient to latex during exams and procedures.

Medication Summary

Latex allergies are best treated with patient education to avoid further exposure. Even HCWs may be poorly informed about latex allergy risk factors, clinical syndromes, and preventive approaches.[23] Type I reactions are treated as any other systemic allergic reaction. The cornerstones of treatment are epinephrine and H1 antihistamines. Systemic corticosteroids and H2 blockers may be useful. Please see articles on Anaphylaxis, Angioedema, and Asthma for details of therapy. No specific immunotherapy has been shown to be effective.

Type IV reactions (localized contact dermatitis) are unlikely to require ED treatment. They can be treated with topical steroids and patient education to avoid further exposures.

Further Outpatient Care

See the list below:

Further Inpatient Care

See the list below:

Inpatient & Outpatient Medications

See the list below:

Deterrence/Prevention

Hospitals should make policy and purchasing decisions to minimize latex exposure in the institution, with the goal being to protect sensitized patients and employees as well as to reduce the risk of primary sensitization. Several cost analyses have found that becoming latex-safe is cost-effective for health care facilities.[34, 35]

Minimally, this requires reducing or eliminating powdered latex examination gloves and substituting less allergenic latex gloves or, ideally, high-quality nonlatex gloves. This strategy has been shown to reduce natural rubber latex aeroallergen, sensitization of exposed HCWs, and incidence of asthma in HCWs.[36, 37] Follow-up studies of latex allergic HCWs have shown a reduction in latex-specific IgE antibodies after latex use is substantially reduced in the healthcare workplace.[38, 39, 40, 24]

It also requires clear guidelines for the safe treatment of sensitized patients and for the accommodation of sensitized employees.

Multidisciplinary hospital committees can be effective in accomplishing these goals.

Non-healthcare workplaces should address the risk of workplace anaphylaxis.[41]

Complications

See the list below:

Prognosis

See the list below:

Patient Education

See the list below:

Author

Amy J Behrman, MD, Associate Professor, Department of Emergency Medicine, Director, Division of Occupational Medicine, Perelman School of Medicine at the University of Pennsylvania

Disclosure: Nothing to disclose.

Specialty Editors

Francisco Talavera, PharmD, PhD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Received salary from Medscape for employment. for: Medscape.

Matthew M Rice, MD, JD, FACEP, Senior Vice President, Chief Medical Officer, Northwest Emergency Physicians of TeamHealth; Assistant Clinical Professor of Medicine, University of Washington School of Medicine Pending Approval

Disclosure: Nothing to disclose.

Chief Editor

Erik D Schraga, MD, Staff Physician, Department of Emergency Medicine, Mills-Peninsula Emergency Medical Associates

Disclosure: Nothing to disclose.

Additional Contributors

Mark Louden, MD, Assistant Professor of Clinical Medicine, Division of Emergency Medicine, Department of Medicine, University of Miami, Leonard M Miller School of Medicine

Disclosure: Nothing to disclose.

Acknowledgements

Marilyn Howarth, MD Center for Excellence in Environmental Toxicology, University of Pennsylvania

Marilyn Howarth, MD is a member of the following medical societies: American College of Occupational and Environmental Medicine

Disclosure: Nothing to disclose.

References

  1. Gawchik SM. Latex allergy. Mt Sinai J Med. 2011 Sep-Oct. 78(5):759-72. [View Abstract]
  2. Geier J, Lessmann H, Mahler V, Pohrt U, Uter W, Schnuch A. Occupational contact allergy caused by rubber gloves--nothing has changed. Contact Dermatitis. 2012 Sep. 67(3):149-56. [View Abstract]
  3. Pak VM, Watkins M, Green-McKenzie J. What is the role of thiurams in allergy to natural rubber latex products?. J Occup Environ Med. 2012 May. 54(5):649-50. [View Abstract]
  4. Agarwal S, Gawkrodger DJ. Latex allergy: a health care problem of epidemic proportions. Eur J Dermatol. 2002 Jul-Aug. 12(4):311-5. [View Abstract]
  5. Feng C, Wang H. Natural rubber latex allergy among health care workers. J Allergy Clin Immunol. 2007 Jun. 119(6):1561; author reply 1561. [View Abstract]
  6. Palosuo T, Antoniadou I, Gottrup F, Phillips P. Latex medical gloves: time for a reappraisal. Int Arch Allergy Immunol. 2011. 156(3):234-46. [View Abstract]
  7. Caballero ML, Quirce S. Identification and practical management of latex allergy in occupational settings. Expert Rev Clin Immunol. 2015 Sep. 11 (9):977-92. [View Abstract]
  8. Paul A, Chabaud M, Auber F, Peycelon M, Audry G. [Latex-free hospitals: Benefits and disadvantages]. Arch Pediatr. 2015 Sep 24. [View Abstract]
  9. Ahmed SM, Aw TC, Adisesh A. Toxicological and immunological aspects of occupational latex allergy. Toxicol Rev. 2004. 23(2):123-34. [View Abstract]
  10. Jackson EM, Arnette JA, Martin ML, Tahir WM, Frost-Arner L, Edlich RF. A global inventory of hospitals using powder-free gloves: a search for principled medical leadership. J Emerg Med. 2000 Feb. 18(2):241-6. [View Abstract]
  11. Sekiya K, Watai K, Taniguchi M, Mitsui C, Fukutomi Y, Tanimoto H. Latex anaphylaxis caused by a Swan-Ganz catheter. Intern Med. 2011. 50(4):355-7. [View Abstract]
  12. Bernardini R, Catania P, Caffarelli C, et al. Perioperative latex allergy. Int J Immunopathol Pharmacol. 2011 Jul-Sep. 24(3 Suppl):S55-60. [View Abstract]
  13. Caffarelli C, Stringari G, Miraglia Del Giudice M, Crisafulli G, Cardinale F, Peroni DG. Prevention of allergic reactions in anesthetized patients. Int J Immunopathol Pharmacol. 2011 Jul-Sep. 24(3 Suppl):S91-9. [View Abstract]
  14. Dong SW, Mertes PM, Petitpain N, Hasdenteufel F, Malinovsky JM,. Hypersensitivity reactions during anesthesia. Results from the ninth French survey (2005-2007). Minerva Anestesiol. 2012 Aug. 78(8):868-78. [View Abstract]
  15. Thong BY, Yeow-Chan. Anaphylaxis during surgical and interventional procedures. Ann Allergy Asthma Immunol. 2004 Jun. 92(6):619-28. [View Abstract]
  16. Ahmed DD, Sobczak SC, Yunginger JW. Occupational allergies caused by latex. Immunol Allergy Clin North Am. 2003 May. 23(2):205-19. [View Abstract]
  17. Occupational Safety and Health Administration. Latex Allergy. US Department of Labor. Available at http://www.osha.gov/SLTC/latexallergy/index.html. Accessed: June 28, 2013.
  18. Dorevitch S, Forst L. The occupational hazards of emergency physicians. Am J Emerg Med. 2000 May. 18(3):300-11. [View Abstract]
  19. Fein JA, Selbst SM, Pawlowski NA. Latex allergy in pediatric emergency department personnel. Pediatr Emerg Care. 1996 Feb. 12(1):6-9. [View Abstract]
  20. Galindo MJ, Quirce S, Garcia OL. Latex allergy in primary care providers. J Investig Allergol Clin Immunol. 2011. 21(6):459-65. [View Abstract]
  21. Schottler J, Vogel LC, Sturm P. Spinal cord injuries in young children: a review of children injured at 5 years of age and younger. Dev Med Child Neurol. 2012 Dec. 54(12):1138-43. [View Abstract]
  22. Goldberg H, Aharony S, Levy Y, Sivan B, Baniel J, Ben Meir D. Low prevalence of latex allergy in children with spinal dysraphism in non-latex-free environment. J Pediatr Urol. 2015 Sep 5. [View Abstract]
  23. Al-Niaimi F, Chiang YZ, Chiang YN, Williams J. Latex allergy: assessment of knowledge, appropriate use of gloves and prevention practice among hospital healthcare workers. Clin Exp Dermatol. 2013 Jan. 38(1):77-80. [View Abstract]
  24. Turner S, McNamee R, Agius R, Wilkinson SM, Carder M, Stocks SJ. Evaluating interventions aimed at reducing occupational exposure to latex and rubber glove allergens. Occup Environ Med. 2012 Dec. 69(12):925-31. [View Abstract]
  25. Liss GM, Sussman GL. Latex sensitization: occupational versus general population prevalence rates. Am J Ind Med. 1999 Feb. 35(2):196-200. [View Abstract]
  26. Marmo M, Sacerdoti C, Di Minno RM, Guarino I, Villani R, Di lorio C. Anaphylactic shock during hyperbaric oxygen therapy. Undersea Hyperb Med. 2012 Jan-Feb. 39(1):613-6. [View Abstract]
  27. Taylor JS, Erkek E. Latex allergy: diagnosis and management. Dermatol Ther. 2004. 17(4):289-301. [View Abstract]
  28. Hamilton RG, Peterson EL, Ownby DR. Clinical and laboratory-based methods in the diagnosis of natural rubber latex allergy. J Allergy Clin Immunol. 2002 Aug. 110(2 Suppl):S47-56. [View Abstract]
  29. Accetta Pedersen DJ, Klancnik M, Elms N, et al. Analysis of available diagnostic tests for latex sensitization in an at-risk population. Annals of Allergy, Asthma, & Immunology. February 2012. 108(2):94-7.
  30. Saulnier N, Nucera E, Altomonte G, Rizzi A, Pecora V, Aruanno A. Gene expression profiling of patients with latex and/or vegetable food allergy. Eur Rev Med Pharmacol Sci. 2012 Sep. 16(9):1197-210. [View Abstract]
  31. Blanco C, Carrillo T, Ortega N, Alvarez M, Dominguez C, Castillo R. Comparison of skin-prick test and specific serum IgE determination for the diagnosis of latex allergy. Clin Exp Allergy. 1998 Aug. 28(8):971-6. [View Abstract]
  32. Bernardini R, Mistrello G, Pucci N, et al. Diagnostic value of three different latex extracts. Int J Immunopathol Pharmacol. 2007 Apr-Jun. 20(2):393-400. [View Abstract]
  33. Food and Drug Administration. Natural rubber containing medical devices: user labeling.[Docket No. 96N-0119]. 21 CFR Part 801 Fed. Regist. 1997. 62:51021-51030.
  34. Korniewicz DM, Chookaew N, El-Masri M, Mudd K, Bollinger ME. Conversion to low-protein, powder-free surgical gloves: is it worth the cost?. AAOHN J. 2005 Sep. 53(9):388-93. [View Abstract]
  35. Phillips VL, Goodrich MA, Sullivan TJ. Health care worker disability due to latex allergy and asthma: a cost analysis. Am J Public Health. 1999 Jul. 89(7):1024-8. [View Abstract]
  36. Allmers H, Brehler R, Chen Z, Raulf-Heimsoth M, Fels H, Baur X. Reduction of latex aeroallergens and latex-specific IgE antibodies in sensitized workers after removal of powdered natural rubber latex gloves in a hospital. J Allergy Clin Immunol. 1998 Nov. 102(5):841-6. [View Abstract]
  37. LaMontagne AD, Radi S, Elder DS, Abramson MJ, Sim M. Primary prevention of latex related sensitisation and occupational asthma: a systematic review. Occup Environ Med. 2006 May. 63(5):359-64. [View Abstract]
  38. Filon FL, Radman G. Latex allergy: a follow up study of 1040 healthcare workers. Occup Environ Med. 2006 Feb. 63(2):121-5. [View Abstract]
  39. Yagami A, Suzuki K, Kano H, Matsunaga K. Follow-up study of latex-allergic health care workers in Japan. Allergol Int. 2006 Sep. 55(3):321-7. [View Abstract]
  40. Kelly KJ, Wang ML, Klancnik M, Petsonk EL. Prevention of IgE Sensitization to Latex in Health Care Workers After Reduction of Antigen Exposures. J Occup Environ Med. 2011 Aug. 53(8):934-40. [View Abstract]
  41. American College of Occupational and Environmental Medicine. Anaphylaxis awareness in the workplace. 2013. Available at http://www.acoem.org/anaphylaxis.aspx. Accessed: June 28, 2013.
  42. Biagini RE, MacKenzie BA, Sammons DL, et al. Latex specific IgE: performance characteristics of the IMMULITE 2000 3gAllergy assay compared with skin testing. Ann Allergy Asthma Immunol. 2006 Aug. 97(2):196-202. [View Abstract]