Name of the Corticosteroids Drugs
Systemic
- Hydrocortisone
- Prednisolone
Inhalational
- Beclomethasone dipropionate
- Budesonide
- Fluticasone propionate
- Flunisolide
- Ciclesonide
SYSTEMIC CORTICOSTEROID DRUGS
1.HYDROCORTISONE
| Hydrocortisone |
| Availability Cream, gel, lotion, ointment, solution: various strengths Injection: 25 mg/ml, 50 mg/ml; 100 mg/ vial, 250 mg/vial, 500 mg/vial, 1,000 mg/vial Intrarectal aerosol foam: 90 mg Oral suspension: 10 mg/5 ml Retention enema: 100 mg/60 ml Spray (topical): 1% Tablets: 5 mg, 10 mg, 20 mg |
| Administration and handling Adults and children: 20 to 240 mg/day P.O. ● Adults and children: 5 to 75 mg by intra-articular injection q 2 to 3 weeks (intrarectal foam) ● Adults and children: r b.i.d. for 2 to 3 weeks; every other day ● Adults and children: 15 to 240 mg/day I.M., or I.V. ● Adults and children: 100 to 500 mg I.M. or I.V.; may repeat at 2-, 4-, or 6-hour intervals |
| Mechanism of action Suppresses inflammatory and immune responses, mainly by inhibiting migration of leukocytes and phagocytes and decreasing inflammatory mediators |
| Indications Replacement therapy in adrenocortical insufficiency; hypercalcemia due to cancer; arthritis; collagen diseases; dermatologic diseases; autoimmune and hematologic disorders; trichinosis; ulcerative colitis; multiple sclerosis; proctitis; nephrotic syndrome; aspiration pneumonia hydrocortisone, hydrocortisone cypionate |
| Contraindications Hypersensitivity to hydrocortisone or its components, idiopathic thrombocytopenic purpura (I.M.), intestinal conditions prohibiting intrarectal steroids (P.R.), recent live-virus vaccination, systemic fungal infection |
| Precautions ● hypertension, osteoporosis, glaucoma, renal or GI disease, hypothyroidism, cirrhosis, thromboembolic disorders, myasthenia gravis, heart failure ● pregnant or breastfeeding patients ● children ages 6 and younger (safety not established). |
Patient monitoring
In high-dose therapy (which should not exceed 48 hours), watch closely for signs and symptoms of depression or psychotic episodes.
- Monitor blood pressure, weight, and electrolyte levels regularly.
- Assess blood glucose levels in diabetic patients. Expect to increase insulin or oral hypoglycaemic dosage. 2Monitor patient’s response during weaning from drug. Watch for adrenal crisis, which may occur if drug is discontinued too quickly.
Patient teaching
- Instruct patient to take daily P.O. dose with food by 8 A.M. 2Urge patient to immediately report unusual weight gain, face or leg swelling, epigastric burning, vomiting of blood, black tarry stools, irregular menstrual cycles, fever, prolonged sore throat, cold or other infection, or worsening of symptoms.
- Tell patient using topical form not to apply occlusive dressing unless instructed by prescriber.
- Advise patient to discontinue topical drug and notify prescriber if local irritation occurs.
- Instruct patient to eat small, frequent meals and to take antacids as needed to minimize GI upset.
- Tell patient that response to drug will be monitored regularly.
- Caution patient not to stop taking drug abruptly.
- In long-term use, instruct patient to have regular eye exams.
- Instruct patient to wear medical identification stating that he’s taking this drug.
2.PREDNISOLONE
| Prednisolone |
| Availability: Oral solution: 5 mg/ml Suspension for injection (acetate): 25 mg/ml, 40 mg/ml, 50 mg/ml Suspension (ophthalmic): 0.12%, 0.125%, 1% Syrup: 5 mg/5 ml, 15 mg/5 ml Tablets: 5 mg Tablets (orally disintegrating, sodium phosphate): 10 mg, 15 mg, 30 mg |
| Administration and handling: Adults: 200 mg P.O. daily for 1 week, followed by 80 mg every other day for 1-month Children:1 to 2 mg/kg/day as a single dose or in divided doses; may continue for 3 to 10 days Children: 60 mg/m2 P.O. daily in three divided doses for 4 weeks, |
| Mechanism of action: Binds to intracellular glucocorticoid receptors and suppresses inflammatory and immune responses by: • inhibiting neutrophil and monocyte accumulation at inflammation site and suppressing their phagocytic and bactericidal activity • stabilizing lysosomal membranes • suppressing antigen response of macrophages and helper T cells • inhibiting synthesis of inflammatory response mediators, such as cytokines, interleukins, and prostaglandins. |
| Indications |
| Contraindications: Hypersensitivity to prednisolone or its components, idiopathic thrombocytopenic purpura (I.M. form), systemic fungal infection |
| Precautions ● diabetes mellitus, glaucoma, renal or hepatic disease, hypothyroidism, cirrhosis, diverticulitis, nonspecific ulcerative colitis, recent intestinal anastomoses, inflammatory bowel disease, thromboembolic disorders, seizures, myasthenia gravis, heart failure, hypertension, osteoporosis, ocular herpes simplex, immunosuppression, emotional instability ● pregnant or breastfeeding patients ● children younger than age 6 (younger than age 2 when treated for nephrotic syndrome; younger than age 1 month when treated for aggressive lymphomas and leukaemia’s with ODT form) |
INHALATION CORTICOSTEROID DRUGS
1.BECLOMETHASONE DIPROPIONATE
| Beclomethasone dipropionate |
| Availability: Inhalation aerosol: 40-mcg metered inhalation in 7.3-g canister; 80-mcg metered inhalation in 7.3-g canister Inhalation capsules: 100 mcg, 200 mcg Nasal spray: 0.042% (25-g bottle containing 180 metered inhalations) |
| Administration and handling: Adults and children ages 12 and older: 40 to 80 mcg by oral inhalation b.i.d.; maximum of 320 mcg bid Children ages 5 to 11: 40 mcg by oral inhalation b.i.d.; maximum of 80 mcg b.i.d. Administration: ● Use spacer device to ensure proper delivery of dose and to help prevent candidiasis and hoarseness. ● After inhalation, tell patient to hold his breath for a few seconds before exhaling. ● For greater efficacy, wait 1 minute between inhalations. ● If patient is also receiving a bronchodilator, administer it at least 15 minutes before beclomethasone. ● Discontinue drug after 3 weeks if symptoms don’t improve markedly. |
| Mechanism of action: May decrease number and activity of cells involved in the inflammatory response of asthma, allergies, and rhinitis, such as mast cells, eosinophils, basophils, lymphocytes, macrophages, and neutrophils. Also, may inhibit production or secretion of chemical mediators, such as histamine, eicosanoids, leukotrienes, and cytokines. May produce direct smooth-muscle cell relaxation and decrease airway hyperresponsiveness |
| Indications: Maintenance treatment of asthma as prophylaxis; asthma patients who require systemic steroids for whom adding an inhaled steroid may reduce or eliminate the need for systemic steroids |
| Contraindications: Hypersensitivity to beclomethasone’s ingredients, infrequent oral corticosteroid treatment, primary treatment of status asthmaticus or other acute asthma attack, relief of acute bronchospasm or of asthma controlled by bronchodilators or other nonsteroidal drugs, treatment of Non asthmatic bronchitis |
| Precautions: ● active untreated infections, diabetes mellitus, glaucoma, underlying immunosuppression ● patients receiving concurrent systemic corticosteroids ● pregnant or breastfeeding patients ● children younger than age |
Nursing Considerations
- Instruct patient to hold inhaled drug in airway for several seconds before exhaling and to wait 1 minute between inhalations.
- Advise patient to rinse mouth after using inhaler and to wash and dry inhaler thoroughly to help prevent fungal infections and sore throat.
- Encourage patient to document use of drug and his response in a diary.
- If patient is also using a bronchodilator, teach him to use it at least 15 minutes before beclomethasone.
- As appropriate, review all other significant and life-threatening adverse reactions.
PATIENT TEACHING
- Advise patient not to abruptly stop taking beclomethasone because adrenal insufficiency may occur. Urge her to notify prescriber if she develops signs of adrenal insufficiency, such as nausea, fatigue, anorexia, dyspnoea, hypotension, fever, malaise, dizziness, and fainting.
- Before patient uses nasal spray for first time, instruct her to prime pump by placing her thumb on its base and her index and middle fingers on its shoulder area and then pressing her thumb firmly and quickly against the bottle several times or until fine mist appears. Before patient uses nasal inhalation canister for first time, instruct her to shake it and check that it’s working properly by spraying it once in the air while looking for fine mist.
- Teach patient to inhale deeply after each nasal spray or inhalation, exhaling through mouth and tilting head back to let drug spread over the nasopharynx.
- Teach patient how to properly use oral inhalation aerosol, shaking canister well before using. If patient has trouble using device and coordinating inhalation with it, suggest using a spacer device.
- If two inhalations are prescribed, advise patient to wait a minute between them.
- If patient uses an inhaled bronchodilator with beclomethasone oral inhalation, tell her to use bronchodilator first, wait 5 minutes, and then use beclomethasone.
2.BEDESONIDE
| Budesonide |
| Availability: Capsules (extended-release): 3 mg Inhalation powder: 90 mcg (Pulmicort Flex haler), 180 mcg (Pulmicort Flex haler) Inhalation suspension (Repulse): 0.25 mg/2 ml, 0.5 mg/2 ml, 1 mg/ml Nasal spray: 32 mcg/metered spray (7-g canister) |
| Administration and handling: Adults: 360 mcg (powder for oral inhalation) inhaled b.i.d. Children aged 6 to 17: 180 mcg (powder for oral inhalation) inhaled bid Administration ● If patient also uses a bronchodilator, give that drug at least 15 minutes before budesonide. ● Know that using a spacer reduces risk of candidiasis and hoarseness. ● Make sure patient swallows’ capsules whole without crushing or chewing them. |
| Mechanism of action: Inhibits inflammatory cells and mediators, possibly by decreasing influx into nasal passages or bronchial walls. As a result, nasal or airway inflammation decreases. Oral inhalation form also inhibits mucus secretion in airways, decreasing the amount and viscosity of sputum. |
| Indications: Maintenance treatment of asthma as prophylactic therapy Seasonal or perennial allergic rhinitis Mild to moderate active Crohn’s disease involving ileum, ascending colon, or both |
| Contraindications: Hypersensitivity to budesonide or its components, recent septal ulcers or nasal surgery or trauma (nasal spray); status asthmaticus or other acute asthma episodes (oral inhalation) |
| Precautions: renal disease, hepatic disease, heart failure, active untreated infections, systemic infections, hypertension, osteoporosis, diabetes mellitus, glaucoma, underlying immunosuppression, hypothyroidism, diverticulitis, nonspecific ulcerative colitis, recent intestinal anastomoses, thromboembolic disorders, seizures, myasthenia gravis, ocular herpes simplex infection ● patients receiving concurrent systemic corticosteroids ● pregnant or breastfeeding patients ● children younger than age |
Nursing Considerations
- Use budesonide cautiously if patient has tubercular infection; untreated fungal, bacterial, or systemic viral infection; or ocular herpes simplex.
- Closely monitor a child’s growth pattern; budesonide may stunt growth. WARNING Assess patient who switches from a systemic corticosteroid to inhaled budesonide for adrenal insufficiency (fatigue, hypotension, lassitude, nausea, vomiting, weakness), which may be life-threatening. Hypothalamic-pituitary-adrenal axis function may take several months to recover after stopping systemic corticosteroids. Stopping budesonide abruptly may cause adrenal insufficiency.
- Administer Repulse by jet nebulizer connected to an air compressor.
- Patient exposed to chickenpox may receive varicella zoster immune globulin or pooled I.V. immunoglobulin. If chickenpox develops, give antiviral as ordered. A patient exposed to measles may need pooled I.M. immunoglobulin.
- Assess patient for effectiveness of budesonide therapy, especially if being weaned from a systemic corticosteroid. If patient has increased asthma or an immunologic condition previously suppressed by systemic corticosteroid—such as rhinitis, conjunctivitis, an eosinophilic condition, eczema, or arthritis—notify prescriber.
- Pulmicort Flexhaler contains small amounts of lactose, which may trigger coughing, wheezing, or bronchospasm in a patient with a severe milk-protein allergy.
- Monitor patient for evidence of hypersensitivity, such as contact dermatitis, rash, urticaria, angioedema, bronchospasm, or anaphylaxis. If present, notify prescriber immediately. Expect to stop budesonide and provide emergency supportive care.
Patient teaching
- Teach patient proper use of inhaler.
- Tell patient to swallow capsules whole without crushing or chewing them. 2Instruct patient to contact prescriber immediately if he develops itching, rash, fever, swelling of face and neck, or difficulty breathing.
- Encourage patient to document medication use and his response in diary.
- Advise patient to report signs and symptoms of fungal infections of mouth.
- Tell female patient to inform prescriber if she is pregnant or plans to become pregnant.
- Caution patient to avoid exposure to chickenpox and measles, if possible.
- Emphasize importance of rinsing mouth after each inhaler treatment and washing and drying inhaler thoroughly after each use.
- Instruct patient to avoid high-fat meals, grapefruit, and grapefruit juice.
- As appropriate, review all other significant and life-threatening adverse reactions and interactions, especially those related to the drugs and foods mentioned above.
3.FLUTICASONE PROPIONATE
| Fluticasone propionate |
| Availability: Inhalation aerosol, metered (Flovent HFA): 44 mcg, 110 mcg, 220 mcg Inhalation powder, metered (Flovent Discus): 50 mcg, 100 mcg, 250 mcg Nasal spray (Floneses): 50 mcg Topical cream (Cultivate): 0.005% Topical ointment (Cultivate): 0.005% fluticasone furoate Nasal spray (Veramyst): 27.5 mcg fluticasone furoate in each 50-microliter spray in 10-g bottle containing 120 sprays |
| Administration and handling: Adults and adolescents aged 12 and older: 110 mcg (2 sprays per nostril) once daily Children ages 2 to 11: 55 mcg (1 spray per nostril) once daily Administration: ● Know that Floneses may cause immediate hypersensitivity reaction (contact dermatitis). ● Be aware that topical ointment should be used in adults only. ● Prime Veramyst nasal spray before first use, when not used for more than 30 days, or if cap has been left off bottle for 5 days or more. ● Administer inhalation powder by oral inhalation only. |
| Mechanism of action: Unknown. Has potent vasoconstrictive and anti-inflammatory properties |
| Indications: Prophylaxis of asthma and treatment of asthma for patients requiring oral corticosteroid therapy |
| Contraindications: Hypersensitivity to drug or its components ● Primary treatment of status asthmaticus or other acute asthma episodes necessitating intensive measures (Flovent FHA, Flovent Discus) ● Severe allergy to milk proteins (Flovent Discus) |
| Precautions: ● recurrent epistaxis, recent nasal septal ulcer, nasal surgery, or trauma ● severe hepatic disease (Veramyst) ● glaucoma and cataracts ● tuberculosis; respiratory tract infection; fungal, bacterial, viral, or parasitic infections; ocular herpes simplex ● hypercriticism and adrenal suppression (when used at higher than recommended dosages or in susceptible persons) ● concurrent use of other CYP3A inhibitors (such as ketoconazole; use not recommended with ritonavir) ● Candida albicans infection (Flovent, Veramyst) ● elderly patients (Floneses, Veramyst) |
Patient monitoring
- Monitor patient for withdrawal symptoms after Flovent is discontinued.
- Stay alert for systemic corticosteroid effects when administering Flovent, Floneses, or Veramyst.
- Observe for reduced growth rate in child or adolescent using Flovent, Floneses, or Veramyst.
- When giving Flovent, watch for eosinophilic conditions, such as Churg Strauss syndrome.
- When giving Floneses, assess for epistaxis, wheezing, nasal septum perforation, cataracts, glaucoma, and increased intraocular pressure (rare reaction).
- When giving Veramyst, assess for epistaxis, nasal septum perforation, cataracts, glaucoma, and increased intraocular pressure (rare reaction).
Patient teaching
- Tell patient to take drug exactly as prescribed.
- Teach patient proper use of prescribed form. 2Advise patient to immediately report signs of allergic reaction.
- Caution patient to avoid exposure to people with chickenpox or measles.
- Advise female patient taking Floneses, Flovent, or Veramyst to inform prescriber if she is pregnant or breastfeeding.
- As appropriate, review all other significant and life-threatening adverse reactions and interactions, especially those related to the drugs and tests mentioned above.
4.FLUNISOLIDE
| Flunisolide |
| Availability: Spray solution: 25 ml (each actuation delivers approximately 25 mcg) |
| Administration and handling: Adults and adolescents aged 15 and over. 500 mcg (2 inhalations) bid Children ages 6 to 15. 500 mcg (2 inhalations) b.i.d. Maximum: 1,000 mcg daily |
| Mechanism of action: Inhibits cells involved in inflammatory response, such as mast cells, eosinophils, basophils, lymphocytes, macrophages, and neutrophils. Also inhibits production of chemical mediators, such as histamine, eicosanoids, leukotrienes, and cytokines |
| Indications: To provide maintenance treatment of asthma, alone or with oral corticosteroids to relieve symptoms of seasonal or perennial rhinitis |
| Contraindications: ● Hypersensitivity to drug or its components ● Untreated local infections of nasal mucosa |
| Precautions: ● localized Candida albicans infection; tuberculosis; untreated fungal, bacterial, or systemic viral infections; ocular herpes simplex ● patients receiving immunosuppressive therapy |
Nursing Considerations
- Use flunisolide cautiously in patients with ocular herpes simplex, pulmonary tuberculosis, or untreated systemic bacterial, fungal, parasitic, or viral infection.
- If patient receives an oral corticosteroid, expect to taper it slowly 1 week after changing to flunisolide. For patient who receives prednisone, expect to reduce it by no more than 2.5 mg daily at weekly intervals, beginning at least 1 week after flunisolide therapy starts
- Monitor growth in children; corticosteroids may increase risk of growth suppression.
Patient teaching
Teach patient to recognize and immediately report serious adverse reactions.
- Teach patient proper use of drug. Caution him not to use more than prescribed amount; doing so may cause serious side effects.
- Tell patient maximum drug effects may not occur for several weeks.
- Tell patient to avoid people with measles, chickenpox, and other transmissible infections.
- Caution patient to withhold dose and contact prescriber if infection occurs.
- Instruct female patient to tell prescriber if she becomes pregnant.
- Tell female patient not to breastfeed without consulting prescriber.
- As appropriate, review all other significant and life-threatening adverse reactions and interactions, especially those related to the tests mentioned above.
5.CICLESONIDE
| Ciclesonide |
| Availability: INHALATION AEROSOL 1. 80mcg/inhalation 2. 160mcg/inhalation |
| Administration and handling: INHALATION AEROSOL Adults and children aged 12 and overusing bronchodilator therapy. Initial: 80 mcg b.i.d. Maximum: 160 mcg b.i.d. Adults and children aged 12 and over Initial: 80 mcg b.i.d., adjusted to lowest effective dose when stabilized. Maximum: 320 mg b.i.d Adults and children age 12 and older maximum: 320 mcg b.i.d., |
| Mechanism of action: Inhibits cells involved in the asthma inflammatory response, such as mast cells, eosinophils, basophils, lymphocytes, macrophages, and neutrophils. Ciclesonide also inhibits production or secretion of chemical mediators, such as histamine, eicosanoids, leukotrienes, and cytokines. |
| Indications: To prevent asthma attacks as part of maintenance therapy to treat nasal congestion in seasonal or allergic rhinitis |
| Contraindications: Hypersensitivity to ciclesonide or its components, primary treatment of status asthmaticus or other acute asthma episodes that require intensive measures |
| •Precautions: •Avoid being near people who are sick or have infections. Call your doctor for preventive treatment if you are exposed to chicken pox or measles. These conditions can be serious or even fatal in people who are using steroid medication. •You should not stop using ciclesonide inhalation suddenly. |
Nursing Considerations
- Use cautiously in patients with tuberculosis; fungal, bacterial, viral, or parasitic infection; ocular herpes simplex; or measles or chickenpox because these conditions may worsen with ciclesonide therapy.
- Also use cautiously in patients with a history of increased intraocular pressure, glaucoma, or cataracts because ciclesonide may increase intraocular pressure or cause cataract formation and in patients with major risk factors for decreased bone mineral content, such as prolonged immobilization, family history of osteoporosis, or long-term use of drugs that can reduce bone mass, such as anticonvulsants and oral corticosteroids.
- Inspect patient’s oral cavity regularly for abnormalities. Have patient rinse mouth following inhalation of ciclesonide to reduce risk of oral candidiasis. If oral candidiasis occurs, expect to continue ciclesonide therapy, unless severe.
- If patient takes a systemic corticosteroid, expect to taper dosage by no more than 2.5 mg/day at weekly intervals, starting 1 week after ciclesonide therapy begins
PATIENT TEACHING
- Urge patient to use ciclesonide regularly, as prescribed, but not for acute bronchospasm. Also tell her never to increase or decrease the dosage without consulting prescriber.
- Tell patient to use ciclesonide only with the actuator supplied with the product. Explain that when the dose indicator shows a red zone in the window, about 20 inhalations are left, indicating a need for a refill. When the indicator shows zero, she should discard the inhaler. Advise against relying solely on the dose indicator, especially if inhaler has been dropped, but to keep track of number of inhalations used.
- Instruct patient to use inhaler according to package instructions. Stress needs to make sure canister is firmly seated in the plastic mouthpiece adapter before each use and to press inhaler slowly but firmly until it can go no further in the adapter for each spray. Inform patient that she doesn’t need to shake inhaler before use.
- Tell patient to always replace cap after use, to keep mouthpiece clean, and to clean mouthpiece once a week with a clean, dry tissue or cloth.
- Explain that the full effect of drug may not occur for 4 weeks or more
REFERENCES
- Robert Kizior, Keith Hodgson, Saunders Nursing Drug handbook,1st edition 2024, Elsevier Publications. ISBN-9780443116070
- McGraw Hill- Drug Handbook, Seventh Edition, 2013, McGraw Hill Education Publications,9780071799430.
- April Hazard, Cynthia Sanoski, Davi’s Drug Guide for Nurses -Sixteenth Edition 2019, FA Davis Company Publications,9780803669451.
- Jones and Bartlet, Pharmacology for Nurses, Second Edition, 2020, Jones and Bartlet Learning Publications, ISBN 9781284141986.
- Nursebro.com, Search – Nursebro
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