Skip to main content Accessibility help
×
Hostname: page-component-78c5997874-4rdpn Total loading time: 0 Render date: 2024-11-06T11:44:14.112Z Has data issue: false hasContentIssue false

Chap. 24 - EMERGENCY MANAGEMENT OF CONNECTIVE TISSUE DISORDERS AND THEIR COMPLICATIONS

Published online by Cambridge University Press:  07 September 2011

Kristen Biggers
Affiliation:
West Virginia University School of Medicine
Noah Scheinfeld
Affiliation:
Columbia University College of Physicians and Surgeons
Ronni Wolf
Affiliation:
Kaplan Medical Center, Rehovot, Israel
Batya B. Davidovici
Affiliation:
Kaplan Medical Center, Rehovot, Israel
Jennifer L. Parish
Affiliation:
Jefferson Medical College of Thomas Jefferson University
Lawrence Charles Parish
Affiliation:
Jefferson Medical College of Thomas Jefferson University
Get access

Summary

COLLAGEN VASCULAR diseases are complex multiorgan states of pathologic dysfunction. The collagen vascular diseases that most commonly result in emergency situations include systemic lupus erythematosus (SLE), dermatomyositis (DM), and scleroderma. This chapter will review emergency management of connective tissue disorders and their complications. In particular, the clinical and laboratory aids required for diagnosis, therapy, and prognosis will be reviewed. Because we assume that the reader has a basic understanding of the diseases, the chapter does not review them.

SLE

SLE is a complex state of systemic dysregulation that can affect any organ system (see Figure 24.1). The noted writer Flannery O'Connor died at the age of 39, after surgery led to a reactivation and intensification of lupus that resulted in fatal kidney failure. As lupus can be a systemic disease, the most serious emergency management pertaining to it includes cardiovascular, pulmonary, hematologic, neurological, renal, and gastrointestinal (GI) dysfunctions. The prevalence of SLE for 15- to 44-year-old white women has been estimated to be between 18.3 and 40 cases per 100,000 and twice that for 15- to 44-year-old black women. The American College of Rheumatology has established a standard for the diagnosis of SLE, based on the patient having 4 of 11 criteria, including positive titers for various antibodies (Table 24.1).

Type
Chapter
Information
Emergency Dermatology , pp. 245 - 255
Publisher: Cambridge University Press
Print publication year: 2011

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Cervera, R, Khamashta, MA, Font, J, et al. Morbidity and mortality in systemic lupus erythematosus during a 5-year period. A multicenter prospective study of 1000 patients. Medicine. 1999; 78:167–75.CrossRefGoogle Scholar
Siegel, M, Lee, SL. The epidemiology of systemic lupus erythematosus. Semin Arthritis Rheum. 1973; 3:1–54.CrossRefGoogle ScholarPubMed
Brasington, RD, Kahl, , Ranganathan, P, et al. Immunologic rheumatic disorders. J Allergy Clin Immunol. 2003; 111:S593–S601.CrossRefGoogle ScholarPubMed
Boumpas, DT, Austin, HA, Fessler, BJ, et al. Systemic lupus erythematosus: emerging concepts: Part I. Renal, neuropsychiatric, cardiovascular, pulmonary and hematologic disease. Ann Intern Med. 1995; 122:940–50.CrossRefGoogle ScholarPubMed
Swaak, AJ, Brink, HG, Smeenk, RJ, et al. Systemic lupus erythematosus: clinical features in patients with a disease duration of over 10 years, first evaluation. Rheumatology (Oxford). 1999; 38:953–8.CrossRefGoogle ScholarPubMed
Jacobsen, S, Petersen, J, Ullman, S, et al. A multicentre study of 513 Danish patients with systemic lupus erythematosus: i. Disease manifestations and analyses of clinical subsets. Clin Rheumatol. 1998; 17:468–77.CrossRefGoogle ScholarPubMed
Wiedmann, HP, Matthay, RA. Pulmonary manifestations of systemic lupus erythematosus. J Thorac Imag. 1992; 7:1–18.CrossRefGoogle Scholar
Boulware, DW, Hedgpeth, MT. Lupus pneumonitis and anti-SSA(Ro) antibodies. J Rheumatol. 1989; 16:479–81.Google ScholarPubMed
Santos-Ocampo, AS, Mandell, BF, Fessler, BJ. Alveolar hemorrhage in systemic lupus erythematosus: presentation and management. Chest. 2000; 118:1083–90.CrossRefGoogle ScholarPubMed
Barile, , Jara, LJ, Medina-Rodriguez, F, et al. Pulmonary hemorrhage in systemic lupus erythematosus. Lupus. 1997; 6:445–8.CrossRefGoogle ScholarPubMed
Mulherin, D, Bresnihan, B. Systemic lupus erythematosus. Clin Rheumatol. 1994; 7:31–57.Google Scholar
Schwab, EP, Schumacher, HR., Freundlich, B, Callegari, PE. Pulmonary alveolar hemorrhage in systemic lupus erythematosus. Semin Arthritis Rheum. 1993; 23:8–15.CrossRefGoogle ScholarPubMed
Cervera, R, Khamashta, MA, Font, J, et al. Morbidity and mortality in systemic lupus erythematosus during a 10-year period: a comparison of early and late manifestations in a cohort of 1,000 patients. Medicine (Baltimore). 2003; 82:299–308.CrossRefGoogle Scholar
Noel, V, Lortholary, O, Casassus, P, et al. Risk factors and prognostic influence of infection in a single cohort of 87 adults with systemic lupus erythematosus. Ann Rheum Dis. 2001; 60:1141–4.CrossRefGoogle Scholar
Andonopoulos, AP, Constantopoulos, SH, Galanopoulou, V, et al. Pulmonary function of nonsmoking patients with systemic lupus erythematosis. Chest. 1988; 94:312–15.CrossRefGoogle Scholar
Traynor, AE, Corbridge, TC, Eagan, AE, et al. Prevalence and reversibility of pulmonary dysfunction in refractory systemic lupus: improvement correlates with disease remission following hematopoietic stem cell transplantation. Chest. 2005; 127:1680–9.CrossRefGoogle ScholarPubMed
Somers, E, Magder, LS, Petri, M. Antiphospholipid antibodies and incidence of venous thrombosis in a cohort of patients with systemic lupus erythematosus. J Rheumatol. 2002; 29:2531–6.Google Scholar
Ruiz-Irastorza, G, Egurbide, MV, Ugalde, J, et al. High impact of antiphospholipid syndrome on irreversible organ damage and survival of patients with systemic lupus erythematosus. Arch Intern Med. 2004; 164:77–82.CrossRefGoogle ScholarPubMed
Bankier, AA, Kiener, HP, Wiesmayr, MN, et al. Discrete lung involvement in systemic lupus erythematosus: CT assessment. Radiology. 1995; 196:835–40.Google ScholarPubMed
Fenlon, HM, Doran, M, Sant, SM, et al. High-resolution chest CT in systemic lupus erythematosus. AJR Am J Roentgenol. 1996; 166:301–7.CrossRefGoogle ScholarPubMed
Heffernan, MP, Do, JH, Mehta, J. Antinuclear antibodies in dermatology. Semin Cutan Med Surg. 2001; 20:2–13.CrossRefGoogle ScholarPubMed
Eiser, AR, Shanies, HM. Treatment of lupus interstitial lung disease with intravenous cyclophosphamide. Arthritis Rheum. 1994; 37:428–31.CrossRefGoogle ScholarPubMed
Bertolaccini, ML, Khamashta, MA. Laboratory diagnosis and management challenges in the antiphospholipid syndrome. Lupus. 2006; 15:172–8.CrossRefGoogle ScholarPubMed
McNeil, HP, Chesterman, CN, Krilis, SA. Anticardiolipin antibodies and lupus anticoagulants comprise separate antibody subgroups with different phospholipid binding characteristics. Br J Haematol. 1989; 73:506–13.CrossRefGoogle ScholarPubMed
Strand, V.New therapies for systemic lupus erythematosus. Rheum Dis Clin North Am. 2000; 26:389–406.CrossRefGoogle ScholarPubMed
Brey, RL, Escalante, A. Neurological manifestations of antiphospholipid antibody syndrome. Lupus. 1998; 7:S67.CrossRefGoogle ScholarPubMed
Takashi, Y.Livedo reticularis and central nervous system involvement in systemic lupus erythematosus. Arch Dermatol. 1986; 122:66–70.Google Scholar
Amigo, MC, Khamashta, MA. Antiphospholipid syndrome in systemic lupus erythematosus. Rheum Dis Clin North Am. 2000; 26:331–48.CrossRefGoogle ScholarPubMed
Kimberly, RP, Lockshin, MD, Sherman, RL, et al. High dose intravenous methylprednisolone pulse therapy in systemic lupus erythematosus. Am J Med. 1981; 70:817–24.CrossRefGoogle ScholarPubMed
Mackworth-Young, CG, David, J, Morgan, SH, Hughs, GR. A double blind placebo controlled trial of intravenous methylprednisolone in systemic lupus erythematosus. Ann Rheum Dis. 1988; 47:496–502.CrossRefGoogle ScholarPubMed
Fries, JF, Weyl, S, Hellman, HR. Estimating prognosis in disease activity. Am J Med. 1974; 57:561–6.CrossRefGoogle Scholar
Seleznick, MJ, Fries, JF. Variables associated with decreased survival in systemic lupus erythematosus. Semin Arthritis Rheum. 1991; 21:73–80.CrossRefGoogle ScholarPubMed
Alarcon, GS, McGwin, G, Bastian, HM, et al. Systemic lupus erythematosus in three ethnic groups VIII. Predictors of early mortality in the LUMINA cohort. Arthritis Care Res. 2001; 45:191–202.3.0.CO;2-2>CrossRefGoogle ScholarPubMed
Golbus, J, McCune, WJ. Lupus nephritis. Classification, prognosis, immunopathogenesis, and treatment. Rheum Dis Clin North Am. 1994; 20:213–42.Google ScholarPubMed
Ginzler, EM, Felson, DT, Anthony, JM, Anderson, JJ. Hypertension increases the risk of renal deterioration in systemic lupus erythematosus. J Rheumatol. 1993; 20:1694–700.Google ScholarPubMed
Briggs, WA, Choi, MJ, Scheel, PJ. Successful mofetil treatment of glomerular disease. Am J Kidney Dis. 1998; 31:213–17.CrossRefGoogle ScholarPubMed
Ho, A, Madger, L, Petri, M. The effect of azathioprine/mycophenolate on systemic lupus erythematosus activity. Arthritis Rheum. 1998; 41:S281.Google Scholar
Pashinian, N, Wallace, DJ, Klinenberg, JR. Mycophenolate mofetil for systemic lupus erythematosus. Arthritis Rheum. 1998; 41:S110.Google Scholar
Ortmann, RA, Klippel, JH. Update on cyclophosphamide for systemic lupus erythematosus. Rheum Dis Clin North Am. 2000; 26:363–75.CrossRefGoogle ScholarPubMed
Dourmishev, , Dourmishev, AL, Schwartz, RA. Dermatomyositis: cutaneous manifestations of its variants. Int J Dermatol. 2002; 41:625–30.CrossRefGoogle ScholarPubMed
Sunkureddi, P, et al. Signs of dermatomyositis. Hosp Physician. 2005; 41–4.Google Scholar
Katsambas, A, Stefanaki, C. Life-threatening dermatoses due to connective tissue disorders. Clin Dermatol. 2005; 23:238–48.CrossRefGoogle ScholarPubMed
Targoff, IN. Laboratory testing in the diagnosis and management of idiopathic inflammatory myopathies. Rheum Dis Clin North Am. 2002; 28:859–90.CrossRefGoogle ScholarPubMed
Callen, J. Dermatomyositis. Lancet. 2000; 355:53–7.CrossRefGoogle ScholarPubMed
Kovacs, SO, Kovacs, CS. Dermatomyositis. J Am Acad Dermatol. 1998; 39:899–920.CrossRefGoogle ScholarPubMed
Marie, I, Hachulla, E, Hantron, PY, et al. Polymyositis and dermatomyositis: short term and long term outcome, and predictive factors of prognosis. J Rheumatol. 2001; 28:2230–7.Google Scholar
Ramanan, AV, Feldman, BM. Clinical features and outcomes of juvenile dermatomyositis and other childhood onset myositis syndromes. Rheum Dis Clin North Am. 2002; 28:833–57.CrossRefGoogle ScholarPubMed
Yazici, Y, Kagen, LJ. Clinical presentation of the idiopathic inflammatory myopathies. Rheum Dis Clin North Am. 2002; 28:823–32.CrossRefGoogle ScholarPubMed
Callen, JP, Wortmann RL. Dermatomyositis. Clin Dermatol. 2006; 24:363–73.CrossRefGoogle ScholarPubMed
Dalakas, MC. Controlled studies with high-dose intravenous immunoglobulin in the treatment of dermatomyositis, inclusion body myositis and polymyositis. Neurology. 1998; 51:S37–S45.CrossRefGoogle ScholarPubMed
Rutter, A, Luger, TA. High dose intravenous immunoglobulins: an approach to treat severe immune mediated and autoimmune diseases of the skin. J Am Acad Dermatol. 2001; 44:1010–24.CrossRefGoogle Scholar
Marie, I, Hachulla, E, Levesque, H, et al. Intravenous immunoglobulins as treatment of life threatening esophageal involvement in polymyositis and dermatomyositis. J Rheumatol. 1999; 26:2706–9.Google ScholarPubMed
Oddis, CV. Idiopathic inflammatory myopathy: management and prognosis. Rheum Dis Clin North Am. 2002; 28:979–1001.CrossRefGoogle ScholarPubMed
Sontheimer, RD. Dermatomyositis: an overview of recent progress with emphasis on dermatologic aspects. Dermatol Clin. 2002; 20:387–408.CrossRefGoogle ScholarPubMed
Jansen, TL, Barrera, P, Engelen, BG, et al. Dermatomyositis with subclinical myositis and spontaneous pneumo-mediastinum with pneumothorax: case report and review of the literature. Clin Exp Rheumatol. 1998; 16:733–5.Google Scholar
Dourmishev, , Dourmishev, AL, Schwartz, RA. Dermatomyositis: cutaneous manifestations of its variants. Int J Dermatol. 2002; 41:625–30.CrossRefGoogle ScholarPubMed
Dawkins, MA, Jorizzo, JL, Walker, FO, et al. Dermatomyositis: a dermatology based case series. J Am Acad Dermatol. 1998; 38:397–404.CrossRefGoogle ScholarPubMed
Villalba, L, Adams, EM. Update on therapy for refractory dermatomyositis and polymyositis. Curr Opin Rheumatol. 1996; 8:544–51.CrossRefGoogle ScholarPubMed
Maeda, K, Kimura, R, Komuta, K, et al. Cyclosporine treatment for polymyositis/dermatomyositis: is it possible to rescue the deteriorating cases with interstitial pneumonitis?Scand J Rheumatol. 1997; 26:24–9.CrossRefGoogle ScholarPubMed
Nawata, Y, Kurasawa, K, Takabayashi, K, et al. Corticosteroid resistant interstitial pneumonitis in dermatomyositis/polymyositis: prediction and treatment with cyclosporine. J Rheumatol. 1999; 26:1527–33.Google ScholarPubMed
Sauty, A, Rochat, T, Schoch, OD, et al. Pulmonary fibrosis with predominant CD8 lymphocytic alveolitis and anti-Jo-1 antibodies. Eur Respir J. 1997; 10:2907–12.CrossRefGoogle ScholarPubMed
Caro, I. Dermatomyositis. Semin Cutan Med Surg. 2001; 20:38–45.CrossRefGoogle ScholarPubMed
Simenon, CP, Armadans, L, Fonollosa, V. Survival prognostic factors and markers of morbidity in Spanish patients with systemic sclerosis. Ann Rheum Dis. 1997; 56:723–8.CrossRefGoogle Scholar
Hesselstrand, R, Scheja, A, Akeson, A. Mortality and causes of death in a Swedish series of systemic sclerosis patients. Ann Rheum Dis. 1998; 57:682–6.CrossRefGoogle Scholar
Matucci-Cerinic, M, D'Angelo, S, Denton, CP, et al. Assessment of lung involvement. Clin Exp Rheumatol. 2003; 21:S19–S23.Google ScholarPubMed
Denton, CP, Black, CM. Pulmonary hypertension in systemic sclerosis. Rheum Dis Clin North Am. 2003; 29:335–49.CrossRefGoogle ScholarPubMed
Righi, A, Cerinic, MM. New treatments in scleroderma: the rheumatologic perspective. J Eur Acad Dermatol Venereol. 2002; 16:431–2.CrossRefGoogle ScholarPubMed
Wax, D, Garofano, R, Barst, RJ. Effects of long-term infusion of prostacyclin on exercise performance in patients with pulmonary hypertension. Chest. 1999; 116:914–20.CrossRefGoogle ScholarPubMed
Badesch, DB, Tapson, VF, McCoon, MD, et al. Continuous intravenous epoprostenol for pulmonary hypertension due to scleroderma spectrum of disease. A randomized controlled trial. Ann Intern Med. 2000; 132:425–34.CrossRefGoogle ScholarPubMed
Simonneau, G, Barst, RJ, Galie, N, et al. Continuous subcutaneous infusion of treprostinil, a prostacyclin analogue, in patients with pulmonary arterial hypertension: a double blind, randomized, placebo controlled trial. Am J Respir Crit Care Med. 2002; 165:800–4.CrossRefGoogle ScholarPubMed
Channick, RN, Simonnea, G, Sitbon, O, et al. Effects of the dual endothelin-receptor antagonist bosentan in patients with pulmonary hypertension: a randomized placebo controlled study. Lancet. 2001; 358:1119–23.CrossRefGoogle Scholar
Rubin, LF, Badesch, DB, Barst, RJ. Bosentan therapy for pulmonary hypertension. N Engl J Med. 2002; 346:896–903.CrossRefGoogle Scholar
Silver, EM, Warrick, JH, Kinsella, MB, et al. Cyclophosphamide and low dose prednisone therapy in patients with systemic sclerosis (scleroderma) with interstitial lung disease. J Rheumatol. 1993; 20:838–44.Google ScholarPubMed
White, B, Moore, W, Wingley, F, et al. Cyclophosphamide is associated with pulmonary function and survival benefit in patients with scleroderma and alveolitis. Ann Intern Med. 2000; 132:947–54.CrossRefGoogle ScholarPubMed
Pakas, I, Ioannides, JP, Malagari, K, et al. Cyclophosphamide with low or high dose prednisolone for systemic sclerosis lung disease. J Rheumatol. 2002; 29:298–304.Google ScholarPubMed
Steen, VD, Mayes, MD, Merkel, PA. Assessment of kidney involvement. Clin Exp Rheumatol. 2003; 21:S29–S31.Google ScholarPubMed
Steen, VD. Scleroderma renal crisis. Rheum Dis Clin North Am. 2003; 29:315–33.CrossRefGoogle ScholarPubMed
Steen, VD, Medsger, TA. Long term outcomes of scleroderma renal crisis. Ann Intern Med. 2000; 17; 600–3.CrossRefGoogle Scholar
Petri, M.Hopkins lupus cohort. 1999 Update. Rheum Dis Clin North Am. 2000; 26:199–213.CrossRefGoogle ScholarPubMed

Save book to Kindle

To save this book to your Kindle, first ensure [email protected] is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×