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Addisonian Crisis

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ADRENAL CRISIS (ADDISONIAN CRISIS) โ€“ EMERGENCY PROTOCOL

CLINICAL MANAGEMENT GUIDELINE โ€“ INDIA


๐Ÿšจ MEDICAL EMERGENCY | IMMEDIATE TREATMENT REQUIRED
Mortality: 0.5-2% per crisis episode; Higher if delayed treatment
This is a CLINICAL diagnosis โ€“ TREAT FIRST, Confirm Later
Do NOT wait for lab results to initiate treatment

๐Ÿ”ฐ SYMBOL LEGEND

Symbol Meaning
๐Ÿšจ Emergency / Critical
โœ… Recommended / First-line
โš ๏ธ Caution / Important
โŒ Contraindicated / Avoid
๐Ÿ’Š Drug
๐Ÿ‡ฎ๐Ÿ‡ณ India-specific
โฑ๏ธ Time-critical

SECTION 1: RECOGNITION


1.1 DEFINITION

๐Ÿšจ Adrenal Crisis (Addisonian Crisis) = Life-threatening medical emergency due to acute cortisol deficiency, characterized by:
    • Severe hypotension / Shock (refractory to fluids and vasopressors)
    • Volume depletion
    • Often with precipitating event
๐Ÿ“Œ Can occur in KNOWN adrenal insufficiency (most common) OR as FIRST presentation

1.2 WHO IS AT RISK?

Patients with Known Adrenal Insufficiency
Condition
Primary adrenal insufficiency (Addisonโ€™s disease)
Secondary adrenal insufficiency (Pituitary disease)
Tertiary adrenal insufficiency (Chronic steroid use → HPA suppression)
Bilateral adrenalectomy
Congenital adrenal hyperplasia (CAH)
Patients Without Known Diagnosis (First Presentation)
Scenario
Undiagnosed Addisonโ€™s disease
Pituitary apoplexy
Bilateral adrenal hemorrhage (Waterhouse-Friderichsen)
Acute illness in patient with unrecognized adrenal insufficiency

1.3 PRECIPITANTS โ€“ THE TRIGGER

๐Ÿ“Œ Crisis is almost ALWAYS precipitated by a stressor in patients with adrenal insufficiency
๐Ÿšจ Common Precipitants
Infection (most common) โ€“ Gastroenteritis, Respiratory, UTI, Sepsis
Non-compliance / Discontinuation of glucocorticoid replacement
Inadequate stress dosing during illness/surgery
Vomiting / Diarrhea (cannot absorb oral steroids)
Surgery / Trauma without adequate steroid cover
Severe physical stress
Emotional stress (less common precipitant)
Other Precipitants
Adrenal hemorrhage (anticoagulants, sepsis, trauma)
Pituitary apoplexy
Drugs: Ketoconazole, Etomidate, Rifampicin (↑ cortisol metabolism), Phenytoin, Checkpoint inhibitors
Pregnancy / Labor
Burns
Myocardial infarction
Hyperthyroidism treatment (↑ cortisol clearance)

1.4 CAUSES OF ADRENAL INSUFFICIENCY LEADING TO CRISIS

Primary Adrenal Insufficiency
Cause Notes
Autoimmune adrenalitis
Most common in developed countries
Tuberculosis
Most common in India
Adrenal hemorrhage
Anticoagulants, Sepsis (Waterhouse-Friderichsen), Trauma
Bilateral adrenalectomy
Metastatic disease
Lung, Breast, Melanoma
Infections
Fungal (Histoplasma), HIV/CMV
Congenital adrenal hyperplasia
Adrenoleukodystrophy
Drugs
Ketoconazole, Etomidate
Secondary/Tertiary Adrenal Insufficiency
Cause Notes
Chronic glucocorticoid therapy
Most common cause overall
Pituitary tumors / Surgery / Radiation
Pituitary apoplexy
Acute
Sheehan syndrome
Postpartum pituitary necrosis
Hypophysitis
Autoimmune, Checkpoint inhibitor-induced
Hypothalamic disease
Traumatic brain injury

SECTION 2: CLINICAL FEATURES


2.1 CARDINAL FEATURES

๐Ÿšจ Feature Description
Hypotension / Shock
Often refractory to fluids and vasopressors
Volume depletion
Dehydration
Altered consciousness
Confusion, Lethargy, Obtundation, Coma
Abdominal symptoms
Pain, Nausea, Vomiting (may mimic acute abdomen)
Precipitating event
Usually identifiable

2.2 SYMPTOMS

Cardiovascular
Symptom
Dizziness / Lightheadedness
Syncope / Near-syncope
Palpitations (compensatory tachycardia)
Gastrointestinal
Symptom Notes
Nausea
Very common
Vomiting
May precipitate crisis (canโ€™t absorb oral meds)
Abdominal pain
Can be severe; May mimic acute abdomen
Diarrhea
Anorexia
Neurological
Symptom
Weakness (profound)
Fatigue (severe)
Confusion
Lethargy
Other
Symptom
Fever (if infection precipitant; Or due to crisis itself)
Leg cramps / Myalgia (electrolyte disturbances)

2.3 SIGNS

Vital Signs
Sign Finding
Blood pressure
↓↓ Hypotension; Often < 90/60 mmHg
Postural hypotension
Marked drop on standing
Heart rate
↑ Tachycardia (compensatory)
Temperature
↑ Fever (infection) OR ↓ Hypothermia
Respiratory rate
May be increased
General Examination
Sign Notes
Dehydration
Dry mucous membranes, Reduced skin turgor, Sunken eyes
Shock
Cold peripheries, Delayed capillary refill, Weak pulse
Altered consciousness
Confusion → Obtundation → Coma
Hyperpigmentation
PRIMARY AI only โ€“ Palmar creases, Buccal mucosa, Scars, Pressure points
Vitiligo
May be present (autoimmune association)
Abdominal tenderness
May mimic acute abdomen
Absent axillary/pubic hair
Women with chronic AI
Signs by Underlying Cause
Sign Suggests
Hyperpigmentation
PRIMARY adrenal insufficiency (high ACTH)
NO hyperpigmentation
SECONDARY/TERTIARY (low ACTH)
Visual field defect
Pituitary tumor
Bilateral adrenal mass/hemorrhage on imaging
Adrenal hemorrhage/metastases
Signs of underlying infection
Precipitant

2.4 CLASSIC PRESENTATION SCENARIOS

Scenario 1: Known Addisonโ€™s Disease + Illness
Features
Patient with known primary AI
Develops gastroenteritis (vomiting, diarrhea)
Unable to take/absorb oral hydrocortisone
Develops hypotension, Weakness, Confusion
Diagnosis: Adrenal crisis due to GI illness
Scenario 2: Patient on Chronic Steroids + Surgery
Features
Patient on long-term prednisolone for RA/Asthma
Undergoes surgery WITHOUT stress dose steroids
Post-operatively develops hypotension, Shock
Refractory to fluids and vasopressors
Diagnosis: Adrenal crisis due to inadequate steroid cover
Scenario 3: First Presentation
Features
Previously healthy (or chronic fatigue, Weight loss)
Develops severe infection
Presents with shock, Hyperpigmentation
Hypotension refractory to treatment
Hyponatremia, Hyperkalemia
Diagnosis: Adrenal crisis as first presentation of Addisonโ€™s
Scenario 4: Waterhouse-Friderichsen Syndrome
Features
Severe sepsis (especially Meningococcal)
Bilateral adrenal hemorrhage
Rapid deterioration, Purpura, DIC
Refractory shock
Diagnosis: Adrenal crisis due to adrenal hemorrhage

2.5 CLINICAL CLUES TO ADRENAL CRISIS

๐Ÿšฉ Red Flags โ€“ Think Adrenal Crisis If:
Shock refractory to fluids and vasopressors
Hypotension + Hyponatremia + Hyperkalemia
Hyperpigmentation
History of adrenal/pituitary disease
History of chronic steroid use
Recent steroid withdrawal
Hypoglycemia (especially with hypotension)
Unexplained fever + Hypotension
Abdominal pain + Hypotension + Confusion

SECTION 3: DIAGNOSIS


3.1 CLINICAL DIAGNOSIS

๐Ÿšจ CRITICAL PRINCIPLE
ADRENAL CRISIS IS A CLINICAL DIAGNOSIS
TREAT FIRST โ€“ Confirm Later
Do NOT wait for lab results
Delay in treatment = Increased mortality
Clinical Diagnostic Criteria
Criteria
Acute deterioration in health status
PLUS Hypotension (SBP < 100 mmHg) or Shock
PLUS Features that resolve with parenteral glucocorticoid
WITH Underlying adrenal insufficiency (known or suspected)

3.2 LABORATORY FINDINGS

Electrolytes
Finding Mechanism Notes
Hyponatremia
↓ Aldosterone (Na+ loss); ↓ Cortisol (↑ ADH) Common in PRIMARY
Hyperkalemia
↓ Aldosterone (K+ retention) Common in PRIMARY
Metabolic acidosis
↓ Aldosterone (H+ retention)
Normal electrolytes
May occur in SECONDARY (aldosterone intact)
Glucose
Finding Notes
Hypoglycemia
↓ Gluconeogenesis; More common in children and secondary AI
Renal Function
Finding Mechanism
Elevated urea
Dehydration; Prerenal
Elevated creatinine
Dehydration; Prerenal
Other
Test Finding
Calcium
May be elevated
CBC
Eosinophilia; Lymphocytosis; Anemia (chronic)
TSH
May be elevated (cortisol needed for TSH suppression)

3.3 HORMONAL CONFIRMATION (When Stable)

๐Ÿ“Œ Draw blood for cortisol BEFORE giving steroids if possible, but DO NOT DELAY TREATMENT
Cortisol
Test Interpretation
Random cortisol
Should be HIGH in acute illness/stress
< 3 μg/dL (83 nmol/L) = AI very likely
< 10 μg/dL (276 nmol/L) in critically ill = AI likely
< 15-18 μg/dL (414-500 nmol/L) in acute stress = Inappropriate
> 18-20 μg/dL (500-550 nmol/L) = AI unlikely
ACTH
Finding Interpretation
↑↑ High ACTH + ↓ Cortisol
PRIMARY adrenal insufficiency
↓ or Normal ACTH + ↓ Cortisol
SECONDARY/TERTIARY (Central)
Confirmatory Testing (Once Stable)
Test Protocol
Short Synacthen Test (ACTH Stimulation)
Give Synacthen 250 μg IV/IM; Measure cortisol at 0, 30, 60 min
Interpretation
Peak cortisol < 18-20 μg/dL (500 nmol/L) = AI confirmed

3.4 DISTINGUISHING PRIMARY VS SECONDARY AI

Feature Primary AI Secondary AI
ACTH
↑↑ ↓ or Normal
Aldosterone
Normal
Hyponatremia
โœ… Common May occur (dilutional)
Hyperkalemia
โœ… Common โŒ Absent (aldosterone intact)
Hyperpigmentation
โœ… Present โŒ Absent
Salt craving
โœ… Present โŒ Absent

3.5 ADDITIONAL INVESTIGATIONS

Investigation Purpose
ECG
Hyperkalemia changes; Arrhythmias
CXR
Infection; Small heart (chronic AI)
Blood cultures
Infection workup
Urine analysis/culture
UTI
Blood glucose
Hypoglycemia
CT Adrenals
Hemorrhage, Calcification (TB), Masses
CT/MRI Pituitary
If secondary AI suspected

SECTION 4: MANAGEMENT โ€“ OVERVIEW


4.1 Treatment Principles

๐Ÿšจ Adrenal Crisis Management

โฑ๏ธ Time-Critical: Treat Immediately
Do NOT wait for laboratory results before starting treatment.


Step 1: IV Hydrocortisone

๐Ÿ’Š 100 mg IV bolus immediately
Then 50โ€“100 mg IV every 6โ€“8 hours
OR 200 mg continuous IV infusion over 24 hours


Step 2: IV Fluids

Administer 0.9% Normal Saline for aggressive fluid resuscitation

  • 1 liter in the first hour

  • 4โ€“6 liters during the first 24 hours


Step 3: Treat Hypoglycemia

Check blood glucose levels.

If hypoglycemia is present, give IV Dextrose immediately.


Step 4: Identify and Treat Precipitating Cause

Identify the underlying trigger.

Most common cause: Infection

Start appropriate antibiotics if infection is suspected.


Step 5: Monitor and Taper

Closely monitor:

  • Vital signs

  • Electrolytes

  • Blood glucose

Once the patient is clinically stable, transition to oral maintenance steroid therapy.


4.2 KEY POINTS

๐Ÿšจ Critical Points
Hydrocortisone is life-saving โ€“ Give IMMEDIATELY
High-dose hydrocortisone has mineralocorticoid activity โ€“ No need for fludrocortisone acutely
Aggressive IV fluids โ€“ These patients are severely volume depleted
Treat the precipitant โ€“ Usually infection
Do NOT use dexamethasone if you need to do ACTH stim test later (dexamethasone doesnโ€™t cross-react with cortisol assay; hydrocortisone does โ€“ but treatment takes priority)

SECTION 5: STEP-BY-STEP MANAGEMENT


STEP 1: HYDROCORTISONE โ€“ IMMEDIATE

5.1 Initial Bolus
๐Ÿ’Š Drug Dose Route Timing
Hydrocortisone sodium succinate
100 mg
IV bolus
IMMEDIATELY
5.2 Maintenance
Regimen Dose
Intermittent bolus
50-100 mg IV q6-8h
OR Continuous infusion
200 mg IV over 24 hours (8.3 mg/hr)
5.3 Why Hydrocortisone?
Advantage
โœ… Has BOTH glucocorticoid AND mineralocorticoid activity
โœ… At high doses (≥ 50 mg), mineralocorticoid effect is sufficient
โœ… No need for separate fludrocortisone in acute phase
โœ… Rapid onset
โœ… Widely available
5.4 Alternative Glucocorticoids (If Hydrocortisone Unavailable)
๐Ÿ’Š Drug Dose Notes
Dexamethasone
4 mg IV
โš ๏ธ NO mineralocorticoid activity; May need fludrocortisone in primary AI
โœ… Use if ACTH stim test planned (doesnโ€™t interfere with cortisol assay)
Methylprednisolone
40 mg IV
Minimal mineralocorticoid activity
Prednisolone
25 mg IV/PO
Less preferred; Oral absorption may be impaired
5.5 Glucocorticoid Equivalence
Drug Equivalent Dose Mineralocorticoid Activity
Hydrocortisone 100 mg โ€“ โœ… Yes
Prednisolone 25 mg Minimal
Methylprednisolone 20 mg None
Dexamethasone 4 mg None

STEP 2: IV FLUID RESUSCITATION

5.6 Fluid Choice
๐Ÿ’ง Fluid Recommendation
0.9% Normal Saline
โœ… First-line
5% Dextrose in Normal Saline
โœ… If hypoglycemic
5.7 Fluid Volume
Time Volume
First hour
1000 mL (rapid bolus)
First 4-6 hours
2-3 L
First 24 hours
4-6 L (guided by response)
5.8 Why Aggressive Fluids?
Rationale
Patients are severely volume depleted
Aldosterone deficiency (PRIMARY AI) → Sodium and water loss
Vomiting/diarrhea worsen dehydration
Hypotension is primarily due to volume depletion
5.9 Fluid Monitoring
Monitor
Urine output โ€“ Target > 0.5 mL/kg/hr
Blood pressure โ€“ Target MAP > 65 mmHg
Heart rate โ€“ Should decrease with resuscitation
Clinical perfusion โ€“ Capillary refill, Skin temperature
โš ๏ธ Avoid overload in elderly/cardiac patients

STEP 3: CORRECT HYPOGLYCEMIA

5.10 Management
If Hypoglycemic
50 mL of 50% Dextrose IV bolus (25 g)
OR 100-200 mL of 25% Dextrose
OR 500 mL of 10% Dextrose
Switch to Dextrose-containing maintenance fluids (D5NS)
Monitor glucose q1-2 hours initially

STEP 4: IDENTIFY AND TREAT PRECIPITANT

5.11 Search for Precipitant
Investigation
History: Infection, Missed doses, Surgery, Trauma
Examination: Source of infection
Blood cultures
Urine analysis and culture
CXR
Other directed investigations
5.12 Treat Infection
If Infection Suspected
Empiric broad-spectrum antibiotics
Do NOT delay antibiotics
Adjust based on culture results
Common Regimens
Community-acquired: Ceftriaxone 2 g IV + Azithromycin (if respiratory)
Urinary source: Ceftriaxone or Fluoroquinolone
Sepsis/Unknown: Piperacillin-tazobactam or Meropenem

STEP 5: ADDITIONAL MEASURES

5.13 Vasopressors
When to Use
If hypotension persists despite adequate fluids and hydrocortisone
๐Ÿ’Š Noradrenaline โ€“ First-line vasopressor
Start at 0.05-0.1 μg/kg/min; Titrate to MAP > 65 mmHg
โš ๏ธ Important
Hypotension in adrenal crisis is often refractory to vasopressors UNTIL glucocorticoid given
Response to vasopressors improves after hydrocortisone
5.14 Correct Electrolyte Abnormalities
Abnormality Management
Hyponatremia
Usually corrects with IV NS + Hydrocortisone; Do NOT use hypertonic saline unless severe/symptomatic
Hyperkalemia
Usually corrects with IV NS + Hydrocortisone; Standard hyperkalemia treatment if severe (Calcium gluconate, Insulin-dextrose, Salbutamol)
5.15 Monitor for Complications
Complication Management
Arrhythmias (Hyperkalemia)
ECG monitoring; Treat hyperkalemia
Seizures (Hypoglycemia, Hyponatremia)
Correct glucose and sodium; Benzodiazepines
Shock (Refractory)
Vasopressors; Ensure adequate steroid dose

SECTION 6: MONITORING


6.1 ACUTE PHASE MONITORING

Parameter Frequency Target
Blood pressure
Continuous / q15 min initially SBP > 100; MAP > 65
Heart rate
Continuous Decreasing (compensation reducing)
Urine output
Hourly > 0.5 mL/kg/hr
Oxygen saturation
Continuous > 94%
Temperature
q2-4 hours Monitor for fever (infection)
Glucose
q1-2 hours initially > 70 mg/dL
Sodium
q6-12 hours Gradual normalization
Potassium
q6-12 hours < 5.5 mEq/L
Mental status
Frequent Improving

6.2 EXPECTED CLINICAL RESPONSE

Time Expected Response
1-2 hours
Blood pressure improving
4-6 hours
Significant hemodynamic improvement
12-24 hours
Clinical stabilization
24-72 hours
Resolution of acute crisis
Days
Electrolytes normalizing

6.3 SIGNS OF IMPROVEMENT

โœ… Improving
Blood pressure rising
Heart rate decreasing
Urine output increasing
Mental status clearing
Sodium rising
Potassium falling
Glucose stable

6.4 SIGNS OF NON-RESPONSE / DETERIORATION

๐Ÿšจ Worsening
Persistent hypotension despite treatment
Worsening mental status
Oliguria / Anuria
Worsening metabolic acidosis
Uncontrolled hyperkalemia
Action
Ensure adequate hydrocortisone dose
Ensure adequate fluid resuscitation
Consider alternative diagnosis
Escalate care (ICU if not already)
Look for uncontrolled precipitant

SECTION 7: TAPERING AND TRANSITION


7.1 WHEN TO TAPER

Criteria to Begin Taper
Hemodynamically stable
Eating and drinking
Precipitant controlled
Electrolytes improving
Usually after 24-72 hours

7.2 TAPERING PROTOCOL

Day Hydrocortisone Dose
Day 1 (Crisis)
100 mg IV bolus → 50-100 mg q6-8h
Day 2
50 mg IV/PO q6-8h (150-200 mg/day)
Day 3
25-50 mg PO q6-8h (75-150 mg/day)
Day 4
20 mg AM + 10 mg Noon + 10 mg PM (40 mg/day)
Day 5
20 mg AM + 10 mg PM (30 mg/day)
Day 6+
Return to maintenance (15-25 mg/day)

7.3 TRANSITION TO ORAL MAINTENANCE

Oral Hydrocortisone Regimen
๐Ÿ’Š Hydrocortisone Typical Maintenance
Dose
15-25 mg/day
Regimen
10 mg AM + 5 mg Noon + 5 mg Late afternoon
OR
15 mg AM + 5 mg Afternoon
Add Fludrocortisone (PRIMARY AI Only)
๐Ÿ’Š Fludrocortisone Dose
When to start
Once hydrocortisone < 50 mg/day
Dose
0.05-0.2 mg once daily (usually 0.1 mg)
Not needed in
Secondary/Tertiary AI (aldosterone intact)

7.4 DISCHARGE CRITERIA

โœ… Ready for Discharge
Hemodynamically stable on oral medication
Tolerating oral intake
Precipitant treated/controlled
Electrolytes stable
Patient/Family educated on sick day rules
Emergency injection kit provided
Medical alert identification arranged
Follow-up appointment scheduled

SECTION 8: PREVENTION OF FUTURE CRISES


8.1 SICK DAY RULES โ€“ PATIENT EDUCATION

Mild Illness (Cold, Minor Infection, Low-grade Fever)
Rule
DOUBLE the usual hydrocortisone dose
Continue fludrocortisone unchanged
Increase fluid and salt intake
Continue until recovered
Return to normal dose when well
Moderate Illness (Higher Fever, Vomiting, Diarrhea)
Rule
TRIPLE the usual hydrocortisone dose
If unable to keep oral meds down → Injectable hydrocortisone
Seek medical attention
Severe Illness / Emergency
๐Ÿšจ Rule
100 mg Hydrocortisone IM/IV immediately
Then 50-100 mg every 6-8 hours
Seek emergency medical care

8.2 STRESS DOSING FOR PROCEDURES

Procedure Recommendation
Minor (Dental work)
Double dose on morning of procedure
Moderate (Endoscopy)
50 mg IV/IM before procedure; Double oral × 24-48h
Major surgery
100 mg IV pre-op → 50-100 mg IV q8h → Taper over 3-5 days

8.3 EMERGENCY INJECTION KIT

Every Patient MUST Have
Hydrocortisone injection kit (100 mg)
Syringes and needles
Instructions for self-injection / Family injection
Train patient AND family on IM injection
Self-Injection Technique
Step Action
1 Reconstitute hydrocortisone (if powder)
2 Draw up 100 mg
3 Inject into outer thigh (IM)
4
Call for emergency help
5 Lie down; Do not drive

8.4 MEDICAL IDENTIFICATION

Every Patient MUST Have
Medical alert bracelet or necklace
Emergency card in wallet
Phone ICE contact with diagnosis
Card Should State
Information
โ€I have ADRENAL INSUFFICIENCYโ€œ
โ€In emergency, I need HYDROCORTISONE 100 mg IV/IM immediatelyโ€œ
โ€Do NOT wait for blood testsโ€œ
Emergency contact details
Doctorโ€™s contact

8.5 PATIENT EDUCATION CHECKLIST

โœ… Every Patient Must Know
Never stop steroids suddenly
Double dose if unwell
Triple dose if moderately ill
Use injection if vomiting / Canโ€™t take oral
Seek medical help if not improving
Always carry emergency injection
Wear medical alert identification
Inform all healthcare providers
Carry steroid card

SECTION 9: DRUG DOSES โ€“ QUICK REFERENCE


9.1 ACUTE CRISIS MANAGEMENT

Step Drug Dose
1
๐Ÿ’Š Hydrocortisone
100 mg IV bolus50-100 mg q6-8h OR 200 mg/24h infusion
2
๐Ÿ’ง 0.9% Normal Saline
1L in first hour4-6L in 24h
3
๐Ÿ’Š Dextrose
D50 50 mL IV if hypoglycemic
4
Antibiotics
Empiric if infection suspected
5
๐Ÿ’Š Noradrenaline
0.05-0.1 μg/kg/min if refractory hypotension

9.2 ALTERNATIVE GLUCOCORTICOIDS

Drug Dose Notes
Dexamethasone
4 mg IV q12h No mineralocorticoid effect
Methylprednisolone
40 mg IV q12h Minimal mineralocorticoid effect
Prednisolone
25 mg PO q6h If IV unavailable

9.3 MAINTENANCE THERAPY

Drug Dose
๐Ÿ’Š Hydrocortisone
15-25 mg/day in divided doses
๐Ÿ’Š Fludrocortisone (Primary AI only)
0.05-0.2 mg once daily

9.4 SICK DAY DOSING

Severity Hydrocortisone Dose
Mild illness
2× usual dose
Moderate illness
3× usual dose
Severe / Vomiting
100 mg IM/IV

9.5 SURGICAL STRESS DOSING

Surgery Pre-op Intra/Post-op
Minor
Double oral Double × 24h
Moderate
50 mg IV Double × 24-48h
Major
100 mg IV 50-100 mg IV q8h → Taper

SECTION 10: SPECIAL SITUATIONS


10.1 ADRENAL CRISIS IN PREGNANCY

Key Points
Consideration
Adrenal crisis can occur in pregnancy
Diagnosis can be challenging (Physiological changes mimic some features)
Hydrocortisone is SAFE in pregnancy
Fludrocortisone is SAFE in pregnancy
May need higher maintenance doses in 3rd trimester
Labor/Delivery: Stress dose hydrocortisone required
Labor and Delivery Protocol
Phase Dose
Early labor
Hydrocortisone 25-50 mg IV
Active labor
Hydrocortisone 100 mg IV
Delivery
Continue 50-100 mg IV q6-8h
Post-delivery
Taper over 24-72 hours

10.2 ADRENAL CRISIS IN CHILDREN

Key Points
Consideration
Hypoglycemia more common in children
Weight-based dosing required
CAH is common cause in infants
Family education critical
Pediatric Dosing
Drug Dose
Hydrocortisone
50-100 mg/m² IV bolus (or 2-4 mg/kg, max 100 mg)
Maintenance
50-100 mg/m²/day IV in divided doses
Fluids
20 mL/kg NS bolus → Maintenance
Dextrose
2-4 mL/kg of D25 if hypoglycemic

10.3 ADRENAL CRISIS IN PATIENTS ON ANTICOAGULANTS

Suspect Adrenal Hemorrhage
Clues
Patient on warfarin/heparin/DOACs
Sudden onset of: Abdominal/Flank pain, Hypotension, Fever
Falling hematocrit
CT: Bilateral adrenal hemorrhage
Management
Action
Treat crisis standard protocol (Hydrocortisone + Fluids)
Reverse anticoagulation if severe bleeding
CT Adrenals to confirm
Will likely need lifelong steroid replacement

10.4 BILATERAL ADRENALECTOMY

Key Points
Consideration
100% dependent on exogenous steroids
High risk of crisis
MUST have emergency injection kit
Education critical

10.5 SECONDARY ADRENAL INSUFFICIENCY

Key Differences
Feature Primary AI Secondary AI
Aldosterone
Normal
Hyperkalemia
Yes No
Hyperpigmentation
Yes No
Fludrocortisone needed
Yes
No
Management
Same as primary EXCEPT:
No fludrocortisone needed (aldosterone intact)
Usually less severe hyponatremia
Consider other pituitary hormone deficiencies

10.6 STEROID WITHDRAWAL CRISIS

Scenario
Features
Patient on chronic steroids (> 3 weeks)
Abruptly stops or rapidly tapers steroids
Develops fatigue, Hypotension, Nausea
Management
Action
Same treatment as adrenal crisis
Restart steroids
Slow, gradual taper when stable
May take months for HPA axis to recover

SECTION 11: ๐Ÿ‡ฎ๐Ÿ‡ณ INDIA-SPECIFIC CONSIDERATIONS


11.1 COMMON CAUSES IN INDIA

Cause Notes
Tuberculosis
Most common cause of primary AI in India
Autoimmune
Increasing, especially urban areas
Chronic steroid use
Common; Often over-the-counter; Hidden in Ayurvedic preparations
Post-TB
May have adrenal calcification

11.2 DRUG AVAILABILITY

Drug Availability Cost
Hydrocortisone injection 100 mg
โœ… Widely available โ‚น30-100
Hydrocortisone oral 10/20 mg
โœ… Available โ‚น50-150/month
Fludrocortisone 0.1 mg
โš ๏ธ Variable availability โ‚น200-400/month
Dexamethasone injection
โœ… Widely available โ‚น10-50
Normal Saline
โœ… Widely available โ‚น30-50/L

11.3 PRACTICAL CHALLENGES

Challenge Solution
Fludrocortisone availability
Patients should maintain adequate supply; Alternative suppliers
Non-compliance
Education; Family involvement; Regular follow-up
Hidden steroids in Ayurvedic preparations
Detailed medication history; Educate patients
Delayed presentation
Community awareness; Primary care education
Cost of long-term therapy
Generic options; Government schemes

Features
Findings
Most common cause in India
May have history of TB or TB contact
CT may show: Enlarged adrenals (acute) or Calcified adrenals (chronic)
May need ATT if active TB
Management
Action
Standard crisis management
Start ATT if active TB
โš ๏ธ Rifampicin increases cortisol metabolism โ€“ May need higher hydrocortisone doses during ATT (increase by 50-100%)
Adrenal function rarely recovers โ€“ Usually lifelong replacement needed

SECTION 12: SUMMARY TABLES


12.1 DIAGNOSTIC CLUES

Finding Suggests
Hypotension + Hyponatremia + Hyperkalemia PRIMARY AI
Hypotension + Hyponatremia (without hyperkalemia) SECONDARY AI
Hyperpigmentation PRIMARY AI
Hypoglycemia + Hypotension Adrenal crisis
Refractory shock Think adrenal crisis

12.2 IMMEDIATE MANAGEMENT CHECKLIST

โœ… Action Done
Hydrocortisone 100 mg IV bolus
โ˜
IV access × 2 large bore
โ˜
0.9% NS 1L rapid infusion
โ˜
Check glucose โ€“ Treat if low
โ˜
Blood samples: Cortisol, ACTH, U&E, Glucose, Cultures
โ˜
ECG (Hyperkalemia)
โ˜
Search for precipitant
โ˜
Continuous monitoring
โ˜

12.3 TREATMENT PROTOCOL SUMMARY

Step Intervention Dose/Details
1
Hydrocortisone IV 100 mg bolus → 50-100 mg q6-8h
2
IV Fluids NS 1L/hr × 1h → 4-6L/24h
3
Dextrose If hypoglycemic
4
Treat precipitant Antibiotics if infection
5
Monitor BP, HR, UO, Glucose, Electrolytes
6
Taper when stable → Oral maintenance over 3-5 days

12.4 SICK DAY RULES SUMMARY

Illness Severity Action
Mild
Double oral dose
Moderate
Triple oral dose
Severe / Vomiting
100 mg IM/IV + Seek help

12.5 PATIENT ESSENTIALS CHECKLIST

โœ… Every Patient Must Have
Emergency hydrocortisone kit
Training on self-injection
Medical alert ID
Steroid card
Written sick day rules
Emergency contact numbers
Regular follow-up

12.6 PRIMARY VS SECONDARY AI COMPARISON

Feature Primary AI Secondary AI
Site
Adrenal Pituitary/Hypothalamus
ACTH
↑↑ ↓/Normal
Aldosterone
Normal
Hyperkalemia
Yes No
Hyperpigmentation
Yes No
Fludrocortisone
Needed Not needed
Salt craving
Yes No

๐Ÿ“š ABBREVIATIONS

Abbreviation Full Form
ACTH Adrenocorticotropic Hormone
AI Adrenal Insufficiency
ATT Antitubercular Therapy
BP Blood Pressure
CAH Congenital Adrenal Hyperplasia
CMV Cytomegalovirus
CT Computed Tomography
D25/D50 25%/50% Dextrose
DIC Disseminated Intravascular Coagulation
DOAC Direct Oral Anticoagulant
ECG Electrocardiogram
GI Gastrointestinal
HIV Human Immunodeficiency Virus
HPA Hypothalamic-Pituitary-Adrenal
HR Heart Rate
ICE In Case of Emergency
ICU Intensive Care Unit
IM Intramuscular
IV Intravenous
MAP Mean Arterial Pressure
MRI Magnetic Resonance Imaging
NS Normal Saline
PO Per Oral
RA Rheumatoid Arthritis
SBP Systolic Blood Pressure
TB Tuberculosis
U&E Urea and Electrolytes
UO Urine Output
UTI Urinary Tract Infection

๐Ÿ“– KEY REFERENCES

Source
Bornstein SR et al. Diagnosis and Treatment of Primary Adrenal Insufficiency: An Endocrine Society Clinical Practice Guideline. JCEM 2016
Puar TH et al. Adrenal Crisis: Still a Deadly Event in the 21st Century. Am J Med 2016
Rushworth RL et al. Adrenal Crisis. NEJM 2019
Husebye ES et al. Adrenal Insufficiency. Lancet 2021
Bancos I et al. Diagnosis and Management of Adrenal Insufficiency. Lancet Diabetes Endocrinol 2015
Hahner S et al. High Incidence of Adrenal Crisis in Educated Patients with Chronic Adrenal Insufficiency. JCEM 2015
Harrisonโ€™s Principles of Internal Medicine, 21st Edition
Williams Textbook of Endocrinology, 14th Edition

Document Version: 1.0
Last Updated: December 2025
For: Healthcare Professionals Only
Related Guidelines: Addisonโ€™s Disease (Primary Adrenal Insufficiency); Cushingโ€™s Syndrome
Key Points:
    • ๐Ÿšจ TREAT FIRST โ€“ Do NOT wait for labs
    • ๐Ÿ’Š Hydrocortisone 100 mg IV immediately
    • ๐Ÿ’ง Aggressive IV Normal Saline
    • ๐Ÿ” Search for and treat precipitant
    • ๐Ÿ“‹ Patient education and emergency kit are ESSENTIAL for prevention

End of Guideline
๐Ÿ›ก๏ธ

Medical Advisory

Clinical guidelines are subject to change. Physicians should exercise their regular clinical judgment. This protocol does not replace individual institutional policies. Verified for Q1 2026.

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