Introduction
Corticosteroids have been in use for longer than 40 years. Over time, they have become indispensable in controlling a variety of disease states. Currently, glucocorticoids (GC) are available in numerous formulations: oral, topical, ophthalmic solutions and ointments, oral inhalers, nasal formulations, parenteral and rectal preparations. GC, especially when they are used throughout the course in geriatrics is not devoid of side effects and complications due, in part, to physiological changes of agin. The aim of our study was to evaluate the frequency and type of side effects and complications of long-term corticosteroid therapy in the elderly.
Materials and methods
A retrospective study was performed in 23 patients aged 65 years older and collected in internal medicine department of the Habib Thameur hospital from January 2000 to December 2004. The adverse effects of corticosteroids were recorded throughout the monitoring period. We selected the following as inclusion criteria: an age greater than or equal to 65 years, at least one hospitalization during the included period, and the indication of a general glucocorticoid treatment on long-term excluding inhaled and topical corticosteroids. We noted the following for each patient: age, sex, medical history, reasons for hospitalization, clinical features, paraclinical explorations conducted, diagnosis retained. We systematically analyzed the prescription of treatment and the treatment protocol described by specifying: the type of drugs used, the type of use (oral or IV bolus), the period of the different phases (in particular the treatment time of attack), levels of degression and maintenance therapy, the dose used during each phase in mg/kg/day, the terms of degression, the occurrence of relapses and the evolutionary times and recurrence. We evaluated our patients, for side effects and complications that occurred during the evolution recalling the therapeutic adjuvant used. Data were entered using Excel software and analyzed using SPSS version 11.5.
Results
The complete retrospective study of the 23 patients can be seen in Table 1.
Table 1. The retrospective study of the 23 patients including the adverse effects of corticosteroids.
Case
|
Age
|
Sex
|
Antecedents
|
Hospitalized for
|
Diagnosis
|
Glucocorticoid
|
Complications
|
---|
1 | 85 | F | Cataract operated Diabetes | Temporal headache Paresthesia of scalp fever | Temporal arteritis | 0.7 mg/Kg/d during 4 weeks then digression until 5 mg/j during 18 months | Herpes zoster Iatrogenic diabetes |
2 | 79 | F | Hypertension Diabetes | Temporo-frontal headache Paresthesia of scalp Arthralgia Biological inflammatory syndrome | Temporal arteritis | 0.7 mg/Kg/d during 4 weeks then digression until 5 mg/j during 18 months | Infectious Pulmonary disease Iatrogenic diabetes Arterial hypertension |
3 | 72 | F | - | Temporal headache Prolonged fever Weight loss Biological inflammatory syndrome | Temporal arteritis | 0.7 mg/Kg/d during 4 weeks then digression until 5 mg/j during 18 months | Urinary infection Iatrogenic diabetes |
4 | 75 | F | Hypertension Cardiac failure cataract | Temporal headache Intermittent claudication of jaw Weight loss Biological inflammatory syndrome | Temporal arteritis | 0.7 mg/Kg/d during 4 weeks then digression until 5 mg/j during 18 months | Intestinal infection Arterial hypertension |
5 | 82 | F | Diabetes | Weight loss Biological inflammatory syndrome | Temporal arteritis | 0.7 mg/Kg/d during 4 weeks then digression until 5 mg/j during 18 months | Dental abscess Iatrogenic diabetes Cataract |
6 | 72 | H | Smoking | Atrocious headache Paresthesia of scalp Intermittent claudication of jaw | Temporal arteritis | 0.7 mg/Kg/d during 4 weeks then digression until 5 mg/j during 18 months | Urinary Infection Iatrogenic diabetes |
7 | 72 | H | Smoking | Temporo-frontal headache Intermittent claudication of jaw Weight loss Biological inflammatory syndrome | Temporal arteritis | 0.7 mg/Kg/d during 4 weeks then digression until 5 mg/j during 18 months | Onyxis Dental abscess Arterial hypertension |
8 | 87 | F | Hypertension Diabetes Cataract | Temporal headache Paresthesia of scalp Intermittent claudication of jaw Weight loss | Temporal arteritis | 0.7 mg/Kg/d during 4 weeks then digression until 5 mg/j during 18 months | Infectious Pulmonary disease Iatrogenic diabetes |
9 | 71 | F | Hysterectomy | Polyarthritis Weight loss Biological inflammatory syndrome | Rheumatoid arthritis | 10 mg/j for life | Urinary infection Iatrogenic diabetes |
10 | 66 | F | Hypertension Diabetes Obesity | Polyarthritis | Rheumatoid arthritis | 10 mg/j for life | Eczema marginatum Iatrogenic diabetes |
11 | 66 | F | Pulmonary tuberculosis Cataract | Polyarthritis Weight loss Biological inflammatory syndrome | Rheumatoid arthritis | 10 mg/j for life | Reactivation of tuberculosis Arterial hypertension |
12 | 66 | F | - | Polyarthritis Biological inflammatory syndrome | Rheumatoid arthritis | 10 mg/j for life | Erysipelas Iatrogenic diabetes |
13 | 78 | F | Cataract | Anemia | Rheumatoid arthritis | 10 mg/j for life | Intertrigo Arterial hypertension |
14 | 69 | F | Hypertension Smoking | Arthritis of knee | Rheumatoid arthritis | 10 mg/j for life | Otitis |
15 | 68 | F | Obesity Smoking | Diabetes | Rheumatoid arthritis | 10 mg/j for life | Onyxis Iatrogenic diabetes |
16 | 77 | F | - | lower back pain Weight loss Monoclonal gammaglobulinemia | Multiple myeloma | Dexamethasone treatment monthly as part of an established protocol | Urinary infection Arterial hypertension |
17 | 71 | F | Hypertension fracture of neck of femur | Bone pain Weight loss Biological inflammatory syndrome Renal failure | Multiple myeloma | Dexamethasone treatment monthly as part of an established protocol | Erysipelas Arterial hypertension |
18 | 70 | F | - | Weight loss | Multiple myeloma | Dexamethasone treatment monthly as part of an established protocol | Sinusitis Arterial hypertension |
19 | 68 | F | Hypertension | Sclerodactyly Cutaneous sclerosis Arthritis Weight loss | Scleroderma | 10 mg/d | Intertrigo Osteoporosis Depression |
20 | 72 | F | Hypertension | Arthralgia Myalgia Biological inflammatory syndrome | Scleroderma | 0.5 mg/Kg/d | Sinusitis Intertrigo Arterial hypertension |
21 | 71 | F | Hypertension Diabetes Vertebral compaction | Photo sensitive rash Edema of lower limbs Proteinuria Haematuria | Systemic lupus erythematosus | 1 mg/Kg/d during 6 weeks then digression until 10 mg/j | Herpes zoster Iatrogenic diabetes Osteoporosis |
22 | 67 | H | Hypertension Thrombosis of left lower limb | Renal failure | Retroperitoneal fibrosis | 0.5 mg/Kg/d during 3 months then digression until 5 mg/Kg/d | Septic osteoarthritis Depression |
23 | 73 | F | Hypertension Psoriasis of elbows and knees Hysterectomy | Weight loss Fever Cough | Psoriatic arthritis | 30 mg/d during 4 weeks then digression until 10 mg/Kg/d | Erysipelas |
There were 20 women and 3 men aged 66 to 87 years with a mean age of 75.7 years. The diagnoses were 8 cases of temporal arteritis, 7 cases of rheumatoid arthritis, 3 cases of multiple myeloma, 2 scleroderma, 1 case of systemic lupus erythematosus, 1 case of retroperitoneal fibrosis and 1 case of psoriatic arthritis. We selected 66 complications (Table 2). Infectious complications were found in 26 cases (39.3%): 2 viral infections, 7 fungal infections and 17 bacterial infections including 4 urinary infections, 3 bronchopulmonary infections, 3 skin infections, 2 Otorhinolaryngologic infections, 2 stomatological infections, 1 osteoarticular infection, 1 gastrointestinal infection and 1 case of reactivation of latent tuberculosis (Table 3).
Table 2. Complications of long-term corticosteroid treatment identified in the 23 patients of the study.
Complications
|
Number
|
%
|
---|
Infections | 26 | 39.3 |
Iatrogenic diabetes | 11 | 16.7 |
Arterial hypertension | 9 | 13 |
Osteoporosis | 2 | 3 |
Depression | 2 | 3 |
Cataracts | 1 | 1.5 |
Table 3. Type of infection complications in the 23 patients of the study.
Etiology
|
Localization
|
Type
|
Number (26)
|
---|
Viral | – | Herpes zoster | 2 |
Bacterial | Pulmonary
Urinary Cutaneous Osteoarticular Otorhinolaryngologic Gastroenterologic Stomatologic | Disease of the lungs Reactivation of tuberculosis Urinary infection Erysipelas Septic osteoarthritis Sinusitis Intestinal infection Dental abscess | 3 1 4 3 1 2 1 2
|
Mycotic | – | Eczema marginatum Intertrigo Onyxis Otitis | 1 3 2 1 |
Among the metabolic complications we identified 11 cases (16.7%) of iatrogenic diabetes that was aggravated by corticosteroids in 6 cases or discovered during treatment in 5 cases. High blood pressure (hypertension) aggravated or induced by corticosteroid treatment has been notified in 9 patients (13%). Osteoporosis is reported in 2 cases (3%), depression in 2 cases (3%), cataracts in 1 case.
Discussion
As in the literature, infectious complications were most common in our study followed by metabolic complications. Infectious complications were particularly found with systemic diseases such as vasculitis or giant cell arteritis, or connective tissue disorders such as rheumatoid arthritis or lupus erythematosus, infection being the leading cause of death in the latter disorder1. Thus, in a study on complications due to steroid therapy in 164 patients aged 75 and older and suffering from temporal arteritis, a total of 111 complications were reported, including infectious complications in 31 cases and 20 cases of pulmonary infection2. In contrast, a second study reviewing the complications of corticosteroid therapy in giant cell arteritis and polymyalgia rheumatica, including a total of 500 patients from 5 different studies, found a low number of infectious complications: in total, 9 patients including 7 cases of herpes zoster3. In rheumatoid arthritis, many infections are reported, even with steroids at a dose below 10 mg/day4. In the current literature, there are many observations describing severe infections that have been found (e.g. shingles, fungus ...)5. In a series5 about the adverse effects of corticosteroid therapy in rheumatoid arthritis, there were three more severe infections in the group treated with long-term corticosteroids compared with the group not receiving cortisone. In total in this series5, 8 patients with herpes zoster were identified, 5 of pneumonia, 4 of septic arthritis and 2 cases of urinary tract infections among a total of 22 severe infections. On the other hand, we must insist on the morbidity associated to long-term corticosteroids during systemic lupus erythematosus6,7. Although our sample is small, our results are comparable to those of Chevalet2, as we found that infections accounted for 39.3% of total complications of long-term corticosteroid treatment in our investigations.
Among the metabolic complications, we identified 11 cases (16.7%) of iatrogenic diabetes, and this was aggravated by corticosteroids in 6 cases or discovered during treatment in 5 cases. According to Agard8, diabetes affects 10% of patients with giant cell arteritis. Treatment based on a diabetic diet and insulin therapy should be preferred to oral antidiabetic drugs8. Corticosteroids, (even at low doses), can reveal diabetes, justifying minimum carbohydrate restriction, or can exacerbate pre-existing diabetes, temporarily insulin use9. High blood pressure (hypertension) aggravated or induced by corticosteroid treatment has been noted in 9 patients, at a rate of 13%. For 5 of the patients, hypertension was aggravated to a degree significant enough to warrant remission to previous antihypertensive treatment. For the other 4 patients, hypertension appeared, but was managed with the initiation of a low-sodium diet or mild antihypertensive therapy. Hypertension is more frequent during steroid treatment, but its relationship with dose and duration of treatment is unclear. Pre-existing hypertension appears to be a risk factor which is why thiazide diuretics are recommended in the first place10. Hypertension is the most important parameter to monitor. According to Agard8, it is often pre-existing in giant cell arteritis and is aggravated in 15 to 30% of cases which requires increasing the antihypertensive treatment. Among our 23 patients, we observed a case of femoral neck fracture in the 7th month of corticosteroid therapy in a woman of 72 years treated for temporal arteritis at a dose of 10 mg/day, and treated by nail plate with secondary loosening. This incident suggests an iatrogenic cause. A second patient had clinical features suggestive of vertebral fracture associated with radiographic images confirming the diagnosis. This complication is associated with taking long-term steroids, as in the patient's history; there was no case of previous vertebral collapse. According to some authors, the side-effects of corticosteroid therapy in giant cell arteritis are more common in patients aged 75 years or over receiving at least 40 mg/day prednisone treatment5. Furthermore, in a meta-analysis combining 11 studies collecting data from more than 1,000 patients, steroids was noted to cause side effects in 29% of patients, and cause a complication in 10% of rheumatology cases8. Glucocorticoid-induced osteoporosis is the most common complication of temporal arteritis for at least 10% of patients and 15% at 1 year of treatment of those aged over 75 years. Rheumatological complications related to corticosteroids are the most prevalent complication in those over 75 years. Within a group of 229 people treated with prolonged corticosteroid therapy, a prevalence of 46% of vertebral fractures was observed in the age group 70–79 years vs. 32% in that age group not using steroids, and respectively 60% versus 40% after 80 years. The subjects of 70–79 years have a vertebral slice fracture risk 5 times higher than those less than 60 years11. In two of our patients (8.6%), we observed the appearance of a depression with mood, character and behavior. According to some authors, psychiatric disorders do not appear to be increased with low doses of cortisone2. In a series involving subjects aged 75 years, psychiatric complications were reported in 13 cases including 7 cases of depressive disorders and, 6 cases of agitation with confusion or mania2. In 126 subjects with giant cell arteritis, 20 patients (16%) had psychiatric complications with corticosteroids. The onset of these disorders occur most often in the first month of treatment, taking on various forms such as: mood with irritability, sleep disorder, depression, manic states syndrome and anxiety disorders in vascular dementia12. The systematic implementation of a Mini Mental State or Geriatric Depression Scale in all patients receiving prolonged oral corticosteroids especially before the onset of rapid cognitive decline or psychiatric symptoms especially in patients treated for giant cell arteritis, should help target surveillance of subjects at risk12. We found one case of steroid-induced cataracts diagnosed in the 42nd month of corticosteroid therapy in a patient treated for rheumatoid arthritis. Eye problems, mainly represented by a posterior subcapsular cataract, and did not tend to regress to the withdrawal of corticosteroid therapy, even at low doses5. Cataract is deemed to be a complication of high-dose corticosteroids or related to the total dose and duration of treatment. This complication has also been reported with low dose corticosteroids, but it is uncommon. Its relative risk is 1.8 to 2.5 times higher with prolonged steroid treatment13. A mucocutaneous disorder was reported in one case, and these are linked to metabolic disturbances and obesity through fat overload or facial-nerve block. These treatment-related disorders are more difficult to prevent since they are often also linked to the condition being treated long-term14.
Conclusion
Glucocorticoids are among the most commonly prescribed agents in clinical practice. Their varied physiological effects make them ideal agents for treating several disease states. Infectious and metabolic complications were the most common in our study. Physician education on risk factors might improve prescribing glucocorticoids in elderly patients. The knowledge of drug-use patterns is extremely important, particularly when treating a member of the aged-population who is a high-risk subject.
Comments on this article Comments (1)