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Leatha Heaton

Leatha Heaton, 19

Algeria

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    https://eliteline.us/employer/growth-hormone-boosters-showdown-sermorelin-vs-ipamorelin-explained/

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What Are The Risks Of Steroid Use? For Teens

The High‑Dose, Long‑Term Use of Steroids: A Detailed Look at the Risks



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1. Why Clinicians Turn to Corticosteroids




Potent anti‑inflammatory and immunosuppressive properties that can control disease activity rapidly.


Widely used for a spectrum of conditions:


Autoimmune disorders (e.g., rheumatoid arthritis, systemic lupus erythematosus)

Allergic reactions and asthma exacerbations

Severe dermatologic lesions (psoriasis, eczema)

Certain neurologic diseases (multiple sclerosis relapses)





Offer a \"bridge\" to other disease‑modifying therapies while patients wait for slower‑acting drugs.




Clinical Dilemma


Despite their benefits, corticosteroids can lead to serious side effects. Clinicians must weigh the risk/benefit ratio on an individual basis and consider tapering strategies or steroid‑sparing agents.



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1️⃣ Side Effects of Long‑Term Corticosteroid Use



System Common Adverse Effect Typical Onset Key Clinical Signs


Metabolic Weight gain, central obesity, dyslipidemia, hyperglycemia Weeks–Months Fatty pads around abdomen; increased BMI; elevated fasting glucose/ HbA1c


Endocrine Adrenal suppression, Cushingoid features Months Moon facies, buffalo hump, purple striae


Musculoskeletal Osteoporosis, muscle wasting, myopathy 3–6 months Bone pain; easy fractures; proximal muscle weakness


Dermatologic Skin thinning, bruising, easy cuts Weeks–Months Thin translucent skin; wide ecchymoses


Cardiovascular Hypertension, arrhythmias Weeks–Months Elevated BP readings; palpitations


Neuropsychiatric Mood swings, anxiety, insomnia Weeks–Months Sleep disturbance; irritability


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4. Evidence‑Based Prevention and Management Strategies



A. Prevention in Patients with Normal BMI (≥18.5 kg/m²)



Strategy Evidence Level Key Points


Baseline cardiovascular risk assessment (including blood pressure, lipids, fasting glucose) Strong (guidelines: ACC/AHA 2021) Detects pre‑existing risk; informs treatment intensity.


Lifestyle counseling – diet rich in fruits/vegetables, lean protein, whole grains; limit sodium and saturated fats Moderate (RCTs such as DASH, Mediterranean diets) Reduces blood pressure and improves lipid profile.


Physical activity ≥150 min/week moderate intensity Strong (WHO 2020 physical activity guidelines) Lowers hypertension, improves insulin sensitivity.


Avoid smoking; limit alcohol to ≤1 drink/day for women, ≤2 for men Strong (USPSTF) Reduces cardiovascular risk significantly.


Routine monitoring of BP and lipids at each visit Moderate (guideline recommendation: AHA/ACC 2017) Enables timely adjustment of therapy.


Consider pharmacologic agents early if BP >140/90 or lipid abnormalities persist after lifestyle Strong (ACC/AHA 2018 hypertension guideline; ACC/AHA 2013 cholesterol guideline) Evidence shows early treatment reduces events.



Rationale






Lifestyle: Proven to lower blood pressure and LDL, reduce inflammation, improve insulin sensitivity.


Monitoring: Allows detection of subclinical disease progression or inadequate response.


Early pharmacologic intervention: Multiple trials (e.g., SPRINT for hypertension; ACCORD for diabetes) show early treatment reduces cardiovascular events.







3. Evidence‑Based Lifestyle Interventions



Intervention Key Study/Guideline Effect Size / Outcome


Weight loss ≥5 % (dietary caloric restriction, Mediterranean diet, low‑carb) Look AHEAD trial; DASH & Mediterranean diet studies ↓ SBP 5–10 mmHg; ↓ LDL 15–20 mg/dL; ↑ HDL 3–4 mg/dL


Physical activity ≥150 min/week moderate (aerobic + resistance) ACC/AHA physical activity guideline ↑ insulin sensitivity, ↓ visceral fat, ↓ BP


Reduce alcohol to ≤2 drinks/day AHA alcohol recommendations ↓ SBP 3–5 mmHg; ↓ triglycerides


Quit smoking CDC smoking cessation guidelines ↓ CVD risk 40% over 10 years


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6. Monitoring & Adjustment




Blood pressure – home BP monitoring daily (morning & evening) for first month, then weekly.


Weight & waist circumference – every 4 weeks.


HbA1c – at baseline and after 12 weeks; repeat at 24 weeks if needed.


Serum lipids – baseline, 12 weeks, and 24 weeks (or sooner if symptoms/side‑effects).


Medication adherence & side‑effects – review at each visit.



Adjustments:


Situation Next Step


BP >140/90 after 2 weeks on diet alone Add low‑dose thiazide diuretic (e.g., chlorthalidone 12.5 mg)


BP still uncontrolled after adding thiazide Consider ACE inhibitor (lisinopril 10 mg) or ARB (losartan 50 mg)


Elevated serum creatinine (>1.4 mg/dL) on ACEi/ARB Re‑evaluate; consider reducing dose or switching to diuretic


Serum potassium >5.0 mmol/L with ACEi/ARB Add K‑spend (spironolactone 25 mg) and monitor closely


Weight gain (>2 kg), edema after ACEi/ARB Consider adding furosemide 20–40 mg/d; adjust diuretic dose


Persistent edema >6 weeks despite diuretics Increase diuretic dose or add thiazide‑like (chlorthalidone) if needed


Monitoring Plan




Parameter Frequency Target / Note


Weight Daily at home ≥0.5 kg ↑ → review diuretics


BP Every 3–4 h in hospital, then twice daily at home 150/90 may need adjustment


Serum electrolytes (Na⁺, K⁺, Cl⁻) Daily during hospitalization; repeat 48‑hr after diuretic changes K⁺ 3.5–5 mEq/L; Na⁺ 135–145 mEq/L


Creatinine/CrCl Daily If CrCl ↓ 2 kg weight gain over baseline is significant


Symptom review (dyspnea, orthopnea) Daily Worsening symptoms may indicate fluid overload


When to seek medical attention:





Rapid weight gain (>5 lb/2.3 kg in 24 h).


New or worsening dyspnea, orthopnea, edema.


Persistent headache, confusion, seizures (possible hypertensive crisis).


Severe abdominal pain, nausea, vomiting (signs of GI toxicity).







4. Managing Adverse Reactions



Symptom Immediate Action Follow‑up


Nausea/vomiting Encourage small, frequent sips of water; administer oral antiemetic (e.g., ondansetron) if needed. If vomiting >3 times/day or unable to keep down medication → notify provider; consider dose reduction or alternate day dosing.


Abdominal pain / bloating Take a break from the drug for 1–2 days; monitor pain intensity. Persistent or severe pain (> 48 h) → seek medical attention.


Headache, dizziness, faintness Rest in a safe environment; keep hydrated. If headache >moderate severity or associated with visual changes → consult healthcare professional.


Gastrointestinal bleeding signs (dark stools, blood) Stop medication immediately and contact your provider urgently.


Weight loss >5 % of body weight Reevaluate dosage and frequency.


> Tip: Keep a symptom diary to track any new or worsening side‑effects.



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4. Managing Weight Loss



How Much Weight Do You Expect?




On average, people lose about 0.5–1 kg (1–2 lbs) per week while on the program.


The rate can vary based on diet, exercise, and starting weight.




Why We Monitor Your Weight




Too Rapid Loss: Can lead to loss of muscle mass or nutritional deficiencies.


Very Slow Loss (2 kg/month → Reduce daily caloric deficit by ~200 kcal.


Weight gain >1 kg/month (without strength gains) → Increase caloric intake or decrease training volume slightly.


Strength plateau for 3+ weeks → Add a progressive overload stimulus (e.g., increase weight, add sets).







Quick Reference Table



Parameter Target


Resting HR 40 ms


Sleep 7–9 h/night


Macro Ratio 30% protein, 30% fat, 40% carbs


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4. Data‑Driven Analysis & Recommendations



4.1 Data Summary (Hypothetical)



Parameter Baseline Current Goal


VO₂max 35 ml/kg/min 42 ml/kg/min 50+


Resting HR 72 bpm 68 bpm 40


Sleep Duration 6.5 h 7 h 8 h


Body Fat % 28% 26%

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