Definition
- Systolic BP ≥180 mmHg and/or diastolic BP ≥110 mmHg
- No symptoms or evidence of acute end-organ damage
- Urgent but not emergency situation
Causes
- Medication nonadherence
- Undiagnosed/undertreated hypertension
- Abrupt medication discontinuation (clonidine, beta blockers)
- Illicit drug use (cocaine, amphetamines)
- Medication effect (NSAIDs, steroids, SSRIs)
- Pain, anxiety
- Volume overload (renal failure, hyperaldosteronism)
Evaluation
- Repeat BP measurements to confirm
- Thorough history and physical exam
- Assess for symptoms of end-organ damage:
- CNS: headache, altered mental status, focal deficits
- Cardiac: chest pain, dyspnea, arrhythmia
- Renal: hematuria, oliguria
- Retina: vision changes, retinal hemorrhage
- Diagnostic tests:
- Basic metabolic panel
- Urinalysis
- ECG
- Cardiac enzymes if indicated
- Identify precipitating causes
Goals of Therapy
When it comes to managing blood pressure, it is important to do so gradually and systematically. Lowering blood pressure (BP) over a period of 24 to 48 hours is generally recommended for optimal results. The main goal during this process is to reduce the mean arterial pressure by approximately 25% within the first few hours.
It is crucial, however, to avoid excessive reductions in blood pressure, exceeding the recommended 25% mark. This is necessary to prevent the risk of inadequate blood supply (ischemia) to vital organs, which could lead to further complications. Therefore, finding the right balance is key.
To start, the target BP should be lowered to a level of 160/100 mmHg. Once this initial target is achieved, it is common practice to transition to an oral medication regimen for continued management of blood pressure in an outpatient setting. This gradual transition ensures a smoother adjustment, allowing for long-term maintenance of healthy blood pressure levels.
Management of previously treated hypertension
- If a patient was on a previous regimen, reinitiate that regimen
- Consider titrating to a higher dose.
Untreated Hypertension: Initiating Antihypertensive Therapy
- In patients not currently taking antihypertensive medications, the choice of initial agent(s) should take into account patient-specific factors, comorbidities, and compelling indications that favor certain drug classes.
- In patients without compelling indications, reasonable options for initial monotherapy include thiazide diuretics, ACE inhibitors, ARBs, and dihydropyridine calcium channel blockers. Based on evidence from head-to-head trials, ACE inhibitors, ARBs, and dihydropyridine CCBs may be preferred over thiazide diuretics.
Below is the table detailing the compelling indications for the use of specific antihypertensive agents:
Compelling Indication | Recommended Agents |
---|---|
Heart failure | Diuretics (e.g., thiazides, loop diuretics), ACE inhibitors, ARBs, beta blockers, aldosterone antagonists |
Post-myocardial infarction (MI) | Beta blockers, ACE inhibitors, ARBs |
Diabetic nephropathy | ACE inhibitors, ARBs |
Chronic kidney disease (CKD) | ACE inhibitors, ARBs |
Chronic kidney disease (CKD) with proteinuria | ACE inhibitors, ARBs |
Stroke prevention | Thiazide diuretics, ACE inhibitors, ARBs |
Atrial fibrillation with rapid ventricular response | Non-dihydropyridine calcium channel blockers (e.g., diltiazem, verapamil) |
Pregnancy or planning pregnancy soon | Methyldopa, labetalol, nifedipine extended-release, amlodipine |
- Medication choice should also account for comorbidities like CKD, orthostatic hypotension, and patient factors such as age, frailty, and pregnancy/childbearing potential. Frequent monitoring and up-titration is key during initiation.
- If blood pressure is ≥20/10 mmHg above goal, starting with two drugs is reasonable. Preferred combinations include a RAS inhibitor with a CCB or thiazide diuretic. Single pill combinations may improve adherence.
Oral Antihypertensive Agents
Captopril:
- ACE inhibitor
- Onset 15-30 minutes, peak 1-2 hours
- Duration 4-6 hours
- Dose: 25-50 mg PO
- Advantages: Rapid onset, well-tolerated
- Avoid in pregnancy, bilateral renal artery stenosis
Lisinopril
- Class of Agent: Lisinopril belongs to the class of drugs known as ACE inhibitors (Angiotensin-Converting Enzyme inhibitors).
- Onset: Lisinopril typically starts working within 1 to 2 hours after taking the medication.
- Duration: The effects of Lisinopril can last for 24 hours.
- Dosing: The typical starting dose of Lisinopril for hypertension is 10 mg once daily, with the dosage adjusted based on the individual’s response.
- Advantages: Lisinopril is effective in managing high blood pressure, reducing the risk of heart attack and stroke, and improving heart failure symptoms. It is generally well-tolerated and can be used in various patient populations.
Losartan
- Class of Agent: Losartan is an angiotensin II receptor blocker (ARB).
- Onset: The effects of Losartan can generally be seen within 6 hours
- Duration: The duration of action for Losartan is approximately 24 hours.
- Dosing: The usual starting dose of Losartan for hypertension is 50 mg once daily, with the dosage adjusted if necessary.
- Advantages: Losartan is effective in lowering blood pressure, reducing the risk of stroke, and managing certain heart conditions. It is well-tolerated and can be used in patients with diabetes or kidney problems.
Furosemide
- Class of Agent: Furosemide is a loop diuretic.
- Onset: Furosemide typically starts working within 30 minutes of oral administration or within 5 minutes if given intravenously.
- Duration: The effects of Furosemide can last for 4 to 6 hours.
- Dosing: The recommended starting dose for Furosemide varies depending on the condition being treated but is usually between 20-80 mg taken orally or intravenously.
- Advantages: Furosemide is effective in treating edema (fluid retention) associated with congestive heart failure, liver disease, or kidney disorders. It can help reduce symptoms such as swelling and shortness of breath.
Chlorthalidone
- Class of Agent: Chlorthalidone is a thiazide-like diuretic.
- Onset: Chlorthalidone typically starts working within 2 hours after oral administration.
- Duration: The duration of action for Chlorthalidone is approximately 24 to 72 hours.
- Dosing: The usual starting dose of Chlorthalidone is 25 mg to 50 mg once daily, with the dosage adjusted if necessary.
- Advantages: Chlorthalidone is effective in reducing blood pressure and managing edema. It is often used in the treatment of hypertension and can help improve overall cardiovascular health.
Hydrochlorothiazide
- Class of Agent: Hydrochlorothiazide is a thiazide diuretic.
- Onset: Hydrochlorothiazide generally starts working within 2 hours after oral administration.
- Duration: The effects of Hydrochlorothiazide can last for 6 to 12 hours.
- Dosing: The typical starting dose of Hydrochlorothiazide for hypertension is 12.5 mg to 25 mg once daily, with the dosage adjusted based on the individual’s response.
- Advantages: Hydrochlorothiazide is effective in lowering blood pressure, managing fluid retention, and can be used in various conditions, including hypertension, edema, and heart failure. It is often well-tolerated and is available in combination with other medications for enhanced effectiveness.
Clonidine:
- Central α2 agonist
- Onset 30-60 minutes, peak 2-4 hours
- Duration 6-12 hours
- Dose: 0.1-0.2 mg PO
- Advantages: Oral route, no dose adjustment in renal impairment
- Disadvantages: Rebound hypertension with abrupt discontinuation
Labetalol:
- Nonselective Beta-1 and Beta-2 receptor antagonist, minor alpha blocking activity
- Pros: PO/IV Push/Cont. Infusion, more-peripheral BB, quick onset
- Cons: Not for CHF or > 1st degree AV block, caution in bronchospastic disease
- Onset 30 minutes, peak 2-4 hours
- Duration 6-12 hours
- Dose: 200-400 mg PO
- Avoid in reactive airway disease, heart block
Metoprolol – Selective Beta-1 receptor antagonist
- Pros: Inexpensive, rapid onset, great for ACS or maintenance in CHF
- Cons: Hepatic metabolism, HR effect > BP effect
Amlodipine:
- Dihydropyridine calcium channel blocker
- Onset 2-4 hours, peak 6-12 hours
- Duration >24 hours
- Dose: 5-10 mg PO
- Advantages: Once daily dosing, few drug interactions
- Avoid in severe LV dysfunction
Hydralazine –
- Dosing: 10–50 mg orally, 2–4 times/day
- Pharmacokinetics: T1/2 = 3–7 hours, bioavailability ~26–50%
- Interferes with calcium transport, causing vasodilation
- Pros: PO/IV Push, rapid onset, short duration
- Cons: Multiple doses, lupus-like syndrome
Drug | Class | Onset | Duration | Dose | Advantages | Disadvantages |
---|---|---|---|---|---|---|
Captopril | ACE inhibitor | 15-30 min | 4-6 hours | 25-50 mg PO | Rapid onset, well-tolerated | Avoid in pregnancy, bilateral renal artery stenosis |
Lisinopril | ACE inhibitor | 1-2 hours | 24 hours | 10 mg once daily | Effective, well-tolerated | – |
Losartan | Angiotensin II receptor blocker (ARB) | 6 hours | 24 hours | 50 mg once daily | Effective in lowering BP, well-tolerated | – |
Furosemide | Loop diuretic | 30 min | 4-6 hours | 20-80 mg PO/IV | Effective in treating edema, reduces fluid retention | – |
Chlorthalidone | Thiazide-like diuretic | 2 hours | 24-72 hours | 25-50 mg once daily | Reduces BP, helps manage edema | – |
Hydrochlorothiazide | Thiazide diuretic | 2 hours | 6-12 hours | 12.5-25 mg once daily | Lowers BP, manages fluid retention | – |
Clonidine | Central α2 agonist | 30-60 min | 6-12 hours | 0.1-0.2 mg PO | Oral route, no dose adjustment in renal impairment | Rebound hypertension with abrupt discontinuation |
Labetalol | Nonselective Beta-1 and Beta-2 receptor antagonist, minor alpha blocking activity | 30 min | 6-12 hours | 200-400 mg PO | Multiple administration routes, quick onset | Not for CHF or > 1st degree AV block, caution in bronchospastic disease |
Metoprolol | Selective Beta-1 receptor antagonist | 1-2 hours | 6-12 hours | 25-50 mg PO | Rapid onset, great for ACS or maintenance in CHF | HR effect > BP effect |
Amlodipine | Dihydropyridine calcium channel blocker | 2-4 hours | >24 hours | 5-10 mg PO | Once daily dosing, few drug interactions | Avoid in severe LV dysfunction |
Hydralazine | Vasodilator | 0.5-1 hour | up to 12 hours | 10-50 mg orally, 2-4 times/day | Rapid onset, short duration, various administration routes | Multiple doses, lupus-like syndrome, |
Monitoring and Follow-up
- Frequent BP monitoring initially
- Assess for response to treatment and adverse effects
- Provide strong recommendations for outpatient follow-up
- Long-term lifestyle modifications – exercise, diet, sleep, stress management
- Ensure transition to an effective oral antihypertensive regimen
Summary
When it comes to managing high blood pressure, it’s important to consider a few key factors. First, it’s crucial to avoid the use of sublingual nifedipine due to the associated risks of a precipitous drop in blood pressure. This medication should be administered cautiously under medical supervision to prevent any potential complications.
Additionally, it’s essential not to lower blood pressure too rapidly, as this can increase the risk of ischemic events. Gradual reduction of blood pressure is recommended to ensure a smooth and safe transition.
For long-term management, transitioning to an oral antihypertensive regimen is typically the next step. This allows for outpatient management and brings the blood pressure under control effectively. Collaborating with a healthcare professional can help determine the most suitable medications and doses based on the individual’s health condition and response to treatment.
Lastly, close follow-up is crucial to monitor the progress and ensure that blood pressure remains adequately controlled. Regular check-ups and communication with a primary care provider will help make any necessary adjustments to the treatment plan to promote optimal health and well-being.
Remember, managing high blood pressure is a long-term commitment, and working closely with a healthcare professional is essential for personalized care and successful outcomes.