Jod-Basedow effect due to prolonged use of Lugol
Transcription
Jod-Basedow effect due to prolonged use of Lugol
Rev. Med. Chir. Soc. Med. Nat., Iaşi – 2014 – vol. 118, no. 4 INTERNAL MEDICINE - PEDIATRICS CASE REPORTS JOD-BASEDOW EFFECT DUE TO PROLONGED USE OF LUGOL SOLUTION-CASE REPORT Letiţia Leuştean¹, Cristina Preda¹, Maria-Christina Ungureanu¹*, R. Dănilă², Voichiţa Mogoş¹, Cipriana Ştefănescu³, Carmen Vulpoi¹ University of Medicine and Pharmacy ˮGrigore T. Popaˮ- Iaşi Faculty of Medicine 1. Department of Medical Specialties (II) 2. Department of Surgery 3. Department of Morpho-Functional Sciences *Corresponding author. E-mail: mariachristina11@yahoo.com JOD-BASEDOW EFFECT DUE TO PROLONGED USE OF LUGOL SOLUTION-CASE REPORT (Abstract): Graves' disease is the most common form of hyperthyroidism, accoun ting for 60-80% of all cases of thyrotoxicosis. If left untreated, it may lead to severe thyrotoxicosis with cardiovascular, ocular, psychiatric complication, and in extreme cases thyr otoxic crisis with a high mortality rate. We present the case of a 50-years-old woman diagnosed in another service with Graves' disease and treated for many years with antithyroid drugs (ATDs), admitted to our service for a relapse due to treatment discontinuation. The surgical treatment was planned and the preoperative preparation with Lugol solution was in itiated. Due to a misunderstanding, the administration of iodine solution was extended for a period of about 30 days, thus generating the so-called Jod-Basedow effect, with the exacerbation of the manifestations of thyrotoxicosis and risk of thyroid storm. The patient received treatment with high ATDs doses, glucocorticoids, and beta-blockers, resulting in the progressive improvement of symptoms. She was discharged from hospital and given the risk of thyrotoxic crisis the surgery was postponed. After a month, the patient underwent thyroide ctomy without preoperative preparation with iodine solution. The operative and postoperative courses were uneventful. Keywords: GRAVES' DISEASE, SURGICAL TREATMENT, LUGOL SOLUTION, THYROTOXIC CRISIS Graves' disease is the most common form of hyperthyroidism, accounting for 60-80% of all cases of thyrotoxicosis. Its prevalence is estimated to be about 0.6% of population, with a female-to-male ratio of 7:8/1. The disease mainly affects young women, aged 30-60 years (1, 2). It is an autoimmune disorder due to thyroid receptor autoantibodies (TRAb), also named thyroid-stimulated immunoglobulins (TSI), which stimulate growth of the thyroid gland and overproduction of thyroid hormones. The main clinical manifestations are hyperthyroidism, diffuse goiter, ocular signs, and more rarely dermopathy and acropachy (3). If left untreated it may lead to severe thyrotoxicosis with cardiovascular, ocular, psychiatric complication, and in extreme cases thyrotoxic crisis, with a high mortality rate of about 20% even in our days (4). 1013 Letiţia Leuştean et al. The optimal therapy for Graves' disease is still a subject of debate. The main treatment options are represented by antithyroid drugs (ATDs) and ablation therapy: radioactive iodine (RAI) or surgery (5). The used ATDs are methimazole, carbimazole, and propylthiouracil. They are acting by blocking thyroid hormone synthesis and may also control hyperthyroidism by immune suppression (6). A major disadvantage of ATDs treatment, which has traditionally been the first-line treatment in Europe, is the high risk of relapse after discontinuation (50-80% of patients) (5, 7). Surgery is an alternative therapeutic option for Graves' disease in many circumstances. Total thyroidectomy has negligible recurrence rates and high cure rates (8, 9, 10). Preoperative preparation with iodine is used by most surgeons in order to prevent thyrotoxic crisis and complications during thyroidectomy (11, 12). CASE REPORT We present the case of a 50-years-old woman, living in an urban area, nonsmoker, diagnosed in 2006 in another service with Graves' disease. She was treated with variable doses of methimazole. The patient was admitted to our service in January 2014 for agitation, sinus tachycardia, significant weight loss, and diarrhea. The patient discontinued the treatment with ADTs for 10 months without consulting her physician. Hormone profile revealed severe thyrotoxicosis: TSH < 0.004 µUI/ml, FT4 = 4.88 ng/dl, FT3 = 21.1 pg/ml, positive antithyroid antibodies (AAT) and TRAb. Thyroid ultrasound: increased thyroid volume (40 ml), intense hypoechoic appearance “hell-likeʺ vascularization. ECG: sinus tachycardia. Given the long course of Graves' disease, high thyroid volume and 1014 high TRAb levels, surgery was recommended. The preoperative preparation with Lugol solution 20 drops x 3/day for 9 days was initiated. Due to intercurrent respiratory infection surgery was delayed, but without discontinuing the administration of Lugol solution; the patient continued the administration of iodine solution at home for 30 more days. Readmitted for surgical treatment, the patient developed more severe symptoms of thyrotoxicosis (pulse = 140/min, intense sweating, agitation), the surgery being once again delayed, and the patient transferred to the Endocrinology Department. Clinical and laboratory assessments confirmed the diagnosis of Graves' disease; thyroid scan demonstrated the characteristic features of Jod-Basedow effect (large thyroid, highly increased thyroid uptake). Cardiac assessment: hyperkinetic heart, without signs of ventricular dysfunctions (fig. 1, 2). The patient received treatment with high methimazole doses (Thyrozol 60mg/day), glucocorticoids (Prednisone 30 mg/day) and beta-blockers (Propranolol 40 mg x 2/day). Due to leukopenia (white blood cell count to 2730/µl) with neutropenia (neutrophil count to 920/ µl) methimazole administration was temporary discontinued and continued the administration of corticosteroids with gradual return to normal of leukocyte formula that allowed resumption of high ATDs doses. The clinical signs had progressively improved and the patient was discharged after 14 days. The surgical treatment was once again postponed, given the risk of thyrotoxic crisis. The patient was ambulatory monitored every 2 weeks. In April 2014 thyroidectomy was performed without preoperative preparation with iodine solution. The operative and postoperative courses were Jod-Basedow effect due to prolonged use of Lugol solution-case report uneventful. The patient developed postoperative hypothyroidism, and currently she is under thyroid replacement therapy. Histopathology confirmed the Graves' disease. Fig. 1. Thyroid ultrasound showing an increased thyroid volume (63 ml), intense hypoechoic appearance, ʺhell-likeʺ vascularization Fig. 2. Thyroid scan: characteristic features of Jod-Basedow effect, large thyroid and highly increased thyroid uptake DISCUSSION In patients with Graves' disease treated for many years with ATDs, with an increased number of relapses, large goiter and high TRAb level, surgery may be a safe therapeutic option. Also, surgery provides rapid treatment and permanent cure of hyperthyroidism in most patients (8). Preoperative preparation of patients with hyperthyroidism to achieve euthyroid state is extremely important for avoiding perioperative complications due to severe thyrotoxicosis (13). This can be done using a combination of ATDs, beta-blockers and sometimes glucocorticoids (11). Thyroid storm is an exaggerated state of thyrotoxicosis that occurs in patients who have an inadequately treated thyrotoxicosis and a precipitating event such as thyroid surgery, with a mortality rate that has decreased over time from nearly 100% to approximately 20% in our days (4). Most surgeons administer iodine (as Lugol solution) to provide ≥ 30 mg of iodine/day for 10 days before surgery to decrease thyroid vascularity, the rate of blood flow, and intraoperative blood loss during thyroidectomy (12). These actions are explained by the Wolff-Chaikoff effect of excess iodine, an autoregulatory phenomenon that directly inhibits thyroid hormone synthesis and release. This effect lasts around 10 days, after which it is followed by an ”escape phenomenon”, with resumption of normal organification of iodine and normal thyroid function (14, 15). In our patient, the preoperative preparation with Lugol solution was extended for a period of about 30 days (due to a misunderstanding), thus providing excessive amounts of iodine to the thyroid gland for a long period of time, and generating the so-called Jod-Basedow effect, with the exacerbation of thyrotoxicosis and risk of thyroid storm. 1015 Letiţia Leuştean et al. This condition has a steep onset with fever, marked tachycardia, and arrhythmias, which may be accompanied by pulmonary edema, congestive heart failure, gastrointestinal dysfunction, and central nervous system involvement (16,17). Knowledge of these aspects and careful monitoring of the patient are extremely important because the diagnosis is mostly clinical, the point at which thyrotoxicosis becomes thyroid storm being subjective (17). Even though some authors have proposed a clinical score to confirm the diagnosis, in current practice patients presenting with significant symptoms of thyrotoxicosis should be considered as being at risk for thyroid storm and undergo aggressive treatment, rather than waiting for a specific score threshold (17, 18). In our case, the patient presented an impaired general condition with aggravation of the cardiovascular, digestive and mental manifestations of thyrotoxicosis, thus prompt treatment with high doses of ATDs, betablockers, glucocorticoids and sedatives was initiated in an attempt to block the synthesis and peripheral conversion of thyroid hormones, and to control the clinical symptoms. Besides minor adverse effects such as pruritus, skin rash, arthralgias, and slight elevations in liver enzymes levels, ATDs may rarely cause an aggravation of mild leukopenia that is common in Grave's disease, with risk of agranulocytosis (granulocyte count below 500/mm³). Agranulocytosis may occur even in patients who previously tolerated ATDs, and multiple exposures may represent a risk factor for developing hematological disturbances (19, 20). This situation was met in our patient, who presented under methimazole a worsening of initial leukopenia, with granulocytopenia and risk of agranulocytosis, which forced us to tem- 1016 porarily discontinue the administration of ATDs, and continue only with glucocorticoids, which gradually normalized the absolute neutrophil count. Normalization of white blood count allowed us to resume the treatment with high doses of methimazole, in order to obtain a more rapid improvement of symptoms, by blocking the synthesis of thyroid hormones. The clinical symptoms and hormone parameters gradually improved, and the patient was discharged after 14 days of hospital stay. It is important to know that in thyrotoxicosis ATDs are blocking the thyroid hormone synthesis, not the release of preformed thyroid hormones. Euthyroidism is obtained only when intrathyroidal hormone and iodine stores are depleted, and this process requires up to 6 weeks. Large goiters with abundant deposits of thyroid hormone, especially when iodine excess is present, often show a delayed response to thioanmides (19, 21). In these circumstances, knowing the history of massive thyroid iodine load, confirmed by the increased scintigraphic uptake and the ultrasonographic aspect of the thyroid gland with high volume and intense vascularization, the surgical intervention was postponed again, due to the high risk of thyrotoxic crisis. CONCLUSIONS Our case highlights that although preoperative preparation with iodine solution is preferred by most surgeons in order to prevent complications during thyroidectomy, this treatment must be performed in hospital under close supervision by medical personnel, in order to avoid such complications like Jod-Basedow phenomenon and thyroid storm. Thus, surgery remains a safe therapeutic option for Graves' disease in many circumstances. Jod-Basedow effect due to prolonged use of Lugol solution-case report REFERENCES 1. Tunbridge WMG, Evered DC, Hall R, et al. The spectrum of thyroid disease in the community: the Whickham survey. Clin Endocrinol (Oxf) 1977; 7: 481-493. 2. Vanderpump MPJ. The epidemiology of thyroid disease. Br Med Bull 2011; 99 (1): 39-51. 3. Ginsberg J. Diagnosis and management of Graves' disease. CMAJ 2003; 168(5): 575–585. 4. Karger S, Führer D. Thyroid storm-thyrotoxic crisis: an update. Dtsch Med Wochenschr 2008; 133(10): 479-484. 5. Wartofsky L, Glinoer D, Solomon B, et al. Differences and similarities in the diagnosis and treatment of Graves' disease in Europe, Japan, and the United States. Thyroid 1991; 1: 129–135. 6. Abraham P, Avenell A, Park CM , Watson WA, Bevan JS. A systematic review of drug therapy for Graves' hyperthyroidism. Eur J Endocrinol 2005; 154: 489-498. 7. Mohlin E, Filipsson Nyström H, Eliasson M. Long-term prognosis after medical treatment of Graves' disease in a northern Swedish population 2000–2010. Eur J Endocrinol 2014; 170: 419-427. 8. Genovese BM, Noureldine SI, Gleeson EM, Tufano RP, Kandil E. What is the best definitive treatment for Graves' disease? A systematic review of the existing literature. Ann Surg Oncol 2013; 20(2): 660-667. 9. Stålberg P, Svensson A, Hessman O, Akerström G, Hellman P. Surgical treatment of Graves' disease: evidence-based approach. World J Surg 2008; 32(7): 1269-1277. 10. Grigorovici A, Moruzi M, Malanca L, Costache M, Preda C, Dragomir C. Surgical treatment of Graves' disease. Rev Med Chir Soc Med Nat Iasi 2004; 108(3): 608-612. 11. Panzer C, Beazley R, Braverman L. Rapid preoperative preparation for severe hyperthyroid Graves' disease. J Clin Endocrinol Metab 2004; 89(5): 2142-2144. 12. Erbil Y, Ozluk Y, Giriş M, Salmaslioglu A, Issever H, Barbaros U. Effect of lugol solution on thyroid gland blood flow and microvessel density in the patients with Graves' disease. J Clin Endocrinol Metab 2007; 92(6): 2182-2189. 13. Kiyici S, Gul OO, Cander S, et al. Rapid preparation of patients with hyperthyroidism for thyroidectomy. Endocrine Abstracts 2009; 20: P67. 14. Panneels V, Juvenal G, Boeynaems JM, Durmont JE, Van Sande J. Iodide effects on the thyroid: biochemical, physiological, pharmacological, and clinical effects of iodide in the thyroid. In: Preedy VR, Burrow GN, Watson RR (editors). Comprehensive handbook of iodine: nutritional, biochemical, pathological and therapeutic aspects. Academic Press, USA, 2009, 303-314. 15. Eng P, Cardona G, Fang S, et al. Escape from the acute Wolff-Chaikoff effect is associated with a decrease in thyroid sodium/iodide symporter messenger ribonucleic acid and protein. Endocrinology 1999; 140(8): 3404-3410. 16. Nayak B, Burman K. Thyrotoxicosis and thyroid storm. Endocrinol Metab Clin North Am 2006; 4(35): 663-686. 17. Higgs M, Hull E, Lujan E. A case report of post-operative Jod-Basedow phenomennon following oral and i.v. iodine contrast administration. Case Rep Endocrinol 2014; doi: 10.1155/2014/980283. 18. Chen TS, Wen MJ, Hung YJ, Hsieh CH, Hsiao FC. A rare storm in a psychiatric ward: thyroid storm. Gen Hosp Psychiatry 2012; 2(34): 210 19. Marino M, Chiovato L, Pinchera A. Treatment of Graves' disease. In: Jameson JL, De Groot LJ (editors). Endocrinology: adult and pediatric. Philadelphia (PA), USA: Elsevier, 2010. 20. Dănciulescu Miulescu R, Carşote M, Trifănescu R, Ferechide D, Poiană C. Antithyroid drugs induced agranulocytosis and multiple myeloma: case report and general considerations. J Med Life 2013; 6(3): 327–331. 21. Diaconescu MR, Strat V, Chifan M, et al. The cardiac manifestations in hyperthyroidism. The surgical implications. Rev Med Chir Soc Med Nat Iasi 1993; 97(1): 405-410. 1017