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https://doi.org/10.15836/ccar2023.225

Zbrinjavanje hitnih stanja vezanih uz arterijsku hipertenziju u izvanbolničkoj hitnoj medicinskoj službi

Điđi Delalić orcid id orcid.org/0000-0003-2102-2586 ; Sveučilište u Zagrebu, Medicinski fakultet, Zagreb, Hrvatska
Anđela Simić orcid id orcid.org/0000-0003-0428-1658 ; Zavod za hitnu medicinu Varaždinske županije, Varaždin, Hrvatska
Višnja Nesek Adam orcid id orcid.org/0000-0002-6521-4136 ; Klinička bolnica Sveti Duh, Zagreb, Hrvatska
Ingrid Prkačin orcid id orcid.org/0000-0002-5830-7131 ; Sveučilište u Zagrebu, Medicinski fakultet, Zagreb, Hrvatska


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Sažetak

SAŽETAK
Arterijska je hipertenzija najčešći uzrok kardiovaskularnih bolesti kao i smrtnosti. Znatno pridonosi učestalosti ostalih kroničnih bolesti, od kojih su najučestalije infarkt miokarda i moždani udar. Arterijska hipertenzija, bilo ona kronična neregulirana, a posebno u slučaju hipertenzivne hitnoće ili emergencije, kompleksno je stanje koje je potrebno odgovarajuće procijeniti i zbrinuti. Hipertenzivne emergencije nisu učestale u populaciji, ali su ozbiljna hitna stanja koja u kratkom vremenu, ako se odgovarajuće ne zbrinu, uzrokuju ireverzibilno oštećenje i gubitak funkcije ciljnih organa. Promptno i učinkovito postupanje u izvanbolničkoj hitnoj medicinskoj službi znatno doprinosi kvaliteti cjelokupnoga zdravstvenog sustava.

Ključne riječi

arterijska hipertenzija; izvanbolnička hitna medicinska služba

Hrčak ID:

304007

URI

https://hrcak.srce.hr/304007

Datum izdavanja:

13.6.2023.

Podaci na drugim jezicima: engleski

Posjeta: 562 *




Individual guidelines and consensuses differ with regard to grading arterial pressure values above the normal range and with regard to classification into pre-hypertension and “true” arterial hypertension (AH) (1-3). The definitions, diagnostic criteria, and grading for AH described in this review are based on the guidelines of the European Society of Cardiology (ESC) and the European Society of Hypertension (ESH) (1). According to the ESC/ESH guidelines, elevated blood pressure values in all patients above the age of 16 are graded as described inTable 1. These blood pressure (BP) values refer to standard in-office measurements performed in a doctor’s office.

TABLE 1 Grading of hypertension according to blood pressure values and the current Guidelines for the Management of Arterial Hypertension (1).
Grade of hypertensionSystolic blood pressure (mmHg)Diastolic blood pressure (mmHg)
Optimal blood pressure<120and<80
Normal blood pressure120-129and/or80-84
“Pre-hypertension/high normal” blood pressure130-139and/or85-89
Grade 1 hypertension140-159and/or90-99
Grade 2 hypertension160-179and/or100-109
Grade 3 hypertension≥180and/or≥110
Isolated systolic hypertension≥140and/or<90

Anamnesis and heteroanamnesis during a prehospital intervention

Emergency medical teams are often the first medical professionals coming into contact with patients who have elevated BP values. These values are usually measured by the patient using an at-home sphygmomanometer, in most cases an automatic one. BP values measured by such a device differ only minimally from those measured in-office, although scientific consensus among hypertension experts based on current studies indicates that measurements at home show BP values approximately 5 mmHg lower than those measured in a doctor’s office (4). Thus, hypertension guidelines have lowered the value for the classification of the first grade of AH (if it is diagnosed based on values measured at home) to ≥135/85 mmHg instead of ≥140/90 (1). When arriving to an intervention, if the patient is asymptomatic (but has elevated BP), it is necessary to ascertain whether the patient is taking the antihypertensive medication prescribed to them and at which doses and frequency, as well as whether their mode of intake matches the prescription in the medical documentation. It is recommended to assess the measurement values stored on the patient’s digital pressure measurement device (if the device supports this function) and to check whether the patient is leading an BP journal in order to assess the measured values and the time since the start of the hypertensive episode. The patient’s BP value should be measured. Although there are few studies comparing the validity of measuring BP values outside the hospital in comparison with in-hospital measurements, published studies found relatively small differences in BP measured by medical personnel outside the hospital in comparison with hospital conditions: the average variation in systolic BP is between -3.8 to -4.6 mmHg, and the average variation in diastolic BP ranges from +0.42 to -3.6 mmHg (5).

When measuring BP values, correct measurement techniques should be adhered to, while making sure of the following (6):

  • That the patient has not consumed caffeine or nicotine for at least 30 minutes before the measurement.

  • The patient should be seated in an upright position for at least 5 minutes before the measurement, without crossing their legs.

  • The cuff length should be 80% of the circumference of the upper arm, and the width should be 40% of the upper arm.

  • The patient should not speak during BP measurement.

  • The hand should be resting on a firm surface, approximately at the level of the heart.

  • Tight clothing should be removed from the patient’s upper arm before commencing the measurement.

It is important to perform anamnesis/heteroanamnesis and a clinical examination in order to establish suspicion of possible secondary causes of AH and differentiate newly-developed acute AH from undiagnosed chronic AH.

The following tables provide a brief overview of the most important recommendations.Table 2 shows the most important questions related to the patient’s medical history and the potential causes, i.e., the etiology, that they are used to assess.Table 3 describes the parts of the clinical examination that are important for assessing a patient with hypertension.Table 4 lists the most common causes of secondary hypertension and related items in the anamnesis and patient status.

TABLE 2 Personal medical history questions useful for establishing the differential diagnosis of hypertension etiology.
QuestionSuspected etiology
Has a physician ever told you/Do you know that you have high blood pressure?Open type question – a certain number of patients do not consider themselves as having arterial hypertension although they are taking or have been taking antihypertensive medications.
Do you have chest pain?Myocardial infarction. Aortic dissection.
Do you have shortness of breath/difficulty breathing?Myocardial infarction. Aortic dissection. Pulmonary edema. Heart failure.
Are you taking any medications or plant-based substances? Are you taking any supplements/drugs of abuse?Neuroleptic malignant syndrome. Serotonin syndrome. Cocaine abuse. Tetrahydrocannabinol abuse.
Have you recently stopped taking medications/plant-based substances/drugs of abuse/alcoholic beverages?Delirium tremens. Withdrawal syndromes. Rebound effect (with abrupt termination of beta blocker therapy).
Do you feel weakness in your arms or legs/confusion/dizziness/tingling/nausea? Are you having difficulties talking?Cerebrovascular incident. Transient ischemic attack. Intracranial hemorrhage.
Do you snore while sleeping? Do you wake up during the night? Do you feel tired during the day?Obstructive sleep apnea syndrome.
Have you ever had high blood pressure that did did not decrease with your usual blood pressure medications?Resistant renovascular hypertension. Hyperaldosteronism. Hyperthyroidism.
Has your physicians recently changed your blood pressure medications or their dose?Lowering of the dose of current antihypertensive medication or recent change of antihypertensive medication that could explain the sudden increase in blood pressure.
Which blood pressure medications do you take? How often?Survey of the patient’s medication-taking habits and whether they match with the prescribed therapeutic regime.
Do you urinate regularly? When was the last time you urinated? How much urine did you pass?Chronic kidney disease. Acute kidney injury.
TABLE 3 Clinical examination findings and their correlated etiologies.
Clinical examination findingCorrelated etiology
Precordial murmur.
Assymetrical extremity pulses.
Changes in the neurologic status.
Aortic dissection
Jugular vein distension.
Rhales on pulmonary auscultation.
Pretibial and perimalleolar edema.
Heart failure
Palpable, pulsating abdominal mass.
Auscultatory murmur over the abdomen
Abdominal aortic aneurysm
Extremity hyper/hypo-reflexia.
Palpable enlarged thyroid gland.
Hypo/hyperthyroidism
Hemorrhage,
papillary edema on fundoscopy.
Hypertensive retinopathy
TABLE 4 Secondary causes of hypertension and their correlated personal medical history and clinical examination findings, along with the indicated diagnostic workup.
Personal medical history/clinical examination findingEtiologyFurther diagnostic workup indicated in hospital unit
Murmur over the thoracic aorta (auscultated between the shoulder blades)
Barely palpable or nonpalpable femoral artery pulses
>20 mmHg difference in systolic BP between the upper and lower extremities
Coarctation of the aortaTransthoracic echocardiography
Multislice computed tomography of the aorta
Renal artery murmur (auscultated paraumbilically)
Increased serum creatinine concentration and/or proteinuria on urine dipstick test
Renal artery stenosisRenal artery Doppler ultrasonography
Multislice computed tomography of the renal arteries
Bradycardia/Tachycardia
Dysmenorrhea/Amenorrhea
Sudden weight loss or weight gain
Functional disorders of the thyroid glandLaboratory workup: measurement of serum thyroid stimulating hormone, free serum triiodothyronine, free serum thyroxine, anti-thyroid peroxidase antibodies
Hypokalemia
Hypernatremia
Primary hyperaldosteronismLaboratory workup: measurement of serum renin, aldosterone, aldosterone/renin ratio
Multislice computed tomography of the adrenal glands
Snoring during sleep
Apneic episodes and sudden waking from sleep
Fatigue during daytime
Obstructive sleep apnea syndromePolysomnography, drug induced sleep endoscopy
Pallor/Headache/Syncope
Tachycardia
Paroxysmal BP surges
PheochromocytomaLaboratory workup: measurement of metanephrine/normetanephrine and adrenaline/noradrenaline in a 24h urine sample
Abdominal obesity
“Buffalo hump”
“Moon facies”
Hyperglycemia
Red abdominal striations
Cushing’s disease/Insulin resistanceLaboratory workup: measurement of cortisol in a 24h urine sample
Dexamethasone suppression test
Measurement of serum insulin concentration and insulin resistance index

The role of the 12-lead electrocardiogram in emergencies

Electrocardiography (ECG) is an essential examination for AH. It is easily repeatable, non-invasive, and available in the patient’s home or the emergency services vehicle, and it is thus necessary to perform a 12-lead ECG during the first contact with the patient, repeating the examination when indicated. During the examination of a hypertensive patient, ECG has the most important role in discovering acute coronary syndrome, whether occlusion myocardial infarction (OMI) or non-occlusion myocardial infarction (NOMI). According to the 2022 recommendations of the American College of Cardiology for the treatment of acute chest pain in emergency services, physicians interpreting the ECG should pay special attention to findings that indicate OMI of one of the coronary arteries or their branches (7). Such ECG findings include ST-segment elevation in the relevant leads or equivalents such as posterior myocardial infarction with ST-elevation (STEMI), left branch block, or ventricular paced rhythm with positive or modified Sgarbossa criteria, de Winter sign, and hyperacute T-waves (7). More detailed descriptions of these findings are presented inTable 5.

TABLE 5 Electrocardiography findings correlated with myocardial ischemia (adapted from the 2022 American College of Cardiology guidelines on the evaluation of chest pain in the emergency department (7)).
FindingCriteria
ST-Elevation Myocardial Infarction equivalents
Posterior STEMIHorizontal ST-segment depression in V1-V3
Dominant R-wave (R/S ratio >1) in V2
Upright T waves in anterior leads
Prominent and broad R-wave (>30 ms)
Confirmation by ST-segment elevation of ≤0.5 mm in at least 1 of leads V7-V9
de Winter SignTall, prominent, symmetrical T waves arising from upsloping ST-segment depression >1 mm at the J-point in the precordial leads
0.5-1 mm ST-segment elevation may be seen in lead aVR
Hyperacute T-wavesBroad, asymmetric, peaked T waves may be seen early in ST-elevation myocardial infarction
Serial electrocardiograms over very short intervals are useful to assess for progression to ST-Elevation Myocardial Infarction
Left bundle branch block or ventricular paced rhythm
with Smith-modified Sgarbossa Criteria
Positive if any of the following are present:
Concordant ST-segment elevation of 1 mm in leads with a positive QRS complex
Concordant ST-segment depression of 1 mm in V1-V3
ST-segment elevation at the J-point, relative to the QRS onset, is at least 1 mm and has an amplitude of at least 25% of the preceding S-wave
Left bundle branch block or ventricular paced rhythm
with Sgarbossa Criteria
A total score ≥3 points is required:
Concordant ST-segment elevation ≥1 mm in leads with a positive QRS complex (5 points)
Concordant ST-segment depression ≥1 mm in leads V1-V3 (3 points)
Discordant ST-segment elevation ≥5 mm in leads with a negative QRS complex (2 points)
If there is discordant ST-segment elevation ≥5 mm, consider ST/S ratio <-0.25
Findings consistent with acute or subacute myocardial ischemia
Wellens syndromeBiphasic or deeply inverted and symmetric T waves in leads V2 and V3 (may extend to V6)
Recent angina
Absence of Q waves
ST-segment depressionHorizontal or downsloping ST-segment depression ≥0.5 mm at the J-point in 2 or more contiguous leads is suggestive of myocardial ischemia
Inverted T-wavesMay be seen in ischemia (subacute) or infarction (may be fixed and associated with Q waves) in continuous leads
ST-segment elevation in lead aVRST-segment elevation in aVR ≤1 mm
Multi-lead ST-segment depression in leads I, II, Val, and/or V4-V6
Absence of contiguous ST-segment elevation in other leads

In case of clinical suspicion, when the S1Q3T3 sign is present on the ECG, pulmonary embolism should be considered along with all the other diagnostic elements. Prospective studies that examined ECG findings showed that a quarter of patients with pulmonary embolism did not have the S1Q3T3 sign, i.e., no pathological ECG findings (8). Analysis of 212 ECG results showed that the S1Q3T3 sign was equally prevalent in patients with and without pulmonary embolism, and identified tachycardia (sensitivity 62.5%, specificity 77.5%) and newly-developed right branch block (sensitivity 93.3%, specificity 100.00%) as ECG findings that were statistically significantly associated with the diagnosis of pulmonary embolism (9).

Treatment approach

This review divides the treatment approaches to AH into approaches for hypertensive emergency or crisis, which is defined as elevated BP values leading to acute damage to target organs and requiring immediate reduction in order to preserve the function of affected organs and organ systems, and approaches for asymptomatic uncontrolled AH (2). The reason for this division is the fact that, although relatively rare, hypertensive emergency represents an emergency state which, if not treated in an adequate and timely manner, leads to permanent consequences in a very short period of time. Asymptomatic uncontrolled AH (previously known as “hypertensive urgency”) is the consequence of degenerative changes of the micro- and macro-vasculature that develop over several months or years that, although an independent risk factor for numerous diseases, does not represent a state of medical emergency that will lead to irreversible target organ damage within several hours (10). The choice of medication treatment and its goals differ significantly for these two pathophysiological entities and must therefore be addressed individually.

TREATMENT APPROACH FOR ASYMPTOMATIC UNCONTROLLED ARTERIAL HYPERTENSION

Approximately 6-8% of patients with elevated BP values measured at first contact with emergency services are diagnosed with AH at hospital discharge, with a prescription for antihypertensive medication (11,12). Although elevated BP values are not related to the reason for admission in approximately 75% of patients, some studies have shown that patients with significantly elevated values (grade 3 hypertension) in emergency departments had undiagnosed chronic AH, and that such findings cannot be ascribed solely to pain or anxiety (13,14).

When making a decision on commencing peroral antihypertensive treatment in a prehospital emergency setting for patients with asymptomatic uncontrolled AH, physicians must consider several important factors. Above all, they must consider the potential risk of the development of iatrogenic hypotension in patients above the age 80, fragile patients, and/or patients with comorbidities. They should also consider the benefits of short-term reduction of elevated BP values using peroral antihypertensive medication in the absence of other symptoms. Additionally, they should obtain information on the local availability of general practice physicians and the likelihood that further clinical treatment of AH will be performed. Studies that examined BP values from consecutive measurements in prehospital emergency interventions showed an average decrease of diastolic pressure of 11.6 mmHg in the second consecutive measurement that took place 20 minutes after the first. In patients with normal BP values at first measurement, the second measurement differed by only 3.5 mmHg (15). Thus, the decision to commence peroral treatment with antihypertensive medication depends on the physician’s assessment after considering factors tied to each individual patient, and the ESH guidelines recommend fixed antihypertensive therapy for AH grades 1 and 2 in order to simplify decisionmaking (1). Although they do not require emergency and immediate treatment, patients with asymptomatic and uncontrolled AH are still a vulnerable group that requires monitoring and treatment by primary healthcare physicians. A retrospective analysis conducted by Frei et al. found that 2.7% of patients presenting to emergency services due to elevated BP developed an adverse event within 7 days after being discharged from emergency services (75% of adverse events were heart failure, 25% were acute kidney damage) (16). It is crucial to emphasize the importance of consulting the patient’s family physician and recommending a treatment plan within 7 days, as well as providing instructions with regard to indications for contacting or presenting to emergency services.

If antihypertensive treatment should be commenced, the application of fixed oral antihypertensives is recommended in most patients. Combined peroral antihypertensive therapy is recommended in patients younger than 65 with newly-diagnosed AH grades 2 and 3, and the ESH/ESC Guidelines from 2018 recommend the application of a single-pill angiotensin-converting enzyme inhibitor (ACEI)/calcium antagonist ×1 perorally if the patient is edema-free, whereas a single-pill combination of an ACEI and diuretic is recommended for patients with edema. Other single-pill fixed combinations containing angiotensin receptor blockers, calcium channel blockers, or other thiazide diuretics or beta blockers (in case of tachycardia/atrial fibrillation/post-myocardial infarction) are prescribed depending on comorbid states and conditions. Starting with monotherapy is recommended in older/fragile patients (1). This usually consists of peroral application of a calcium antagonist (amlodipine 5 mg ×1) or ACEI (ramipril 5 mg). The application of anxiolytics has also been shown to be beneficial in out-of-hospital settings (17).

TREATMENT APPROACH IN HYPERTENSIVE EMERGENCY

Table 6 contains a list of the most common causes related to hypertensive emergency, which is a newly-developed acute hypertensive state that requires prompt and appropriate treatment for elevated BP. For the purpose of these recommendations, the definition of hypertensive emergency has been extended to states that present with a clinical picture of target organ damage, with BP values usually above 180/120 mmHg, given the limited capacity for laboratory and imaging examinations in prehospital emergency services.

TABLE 6 The most common etiologies leading to hypertensive emergencies.
Myocardial infarction
Pulmonary edema
Preeclampsia
Cerebrovascular incident
Hyperthyroidism
Aortic dissection
Sympathomimetic intoxication (i.e., cocaine)
Malignant hypertension with acute kidney injury

Treatment approach for hypertensive emergencies – treatment goals

In addition to defining hypertensive emergency, it is necessary to determine treatment goals before starting medication therapy. It is recommended to monitor mean arterial pressure (MAP) values when determining the baseline and target BP values in hypertensive emergencies (18). MAP is calculated using the formula: [2x(diastolic pressure) + systolic pressure]/3. Target MAP values are between 70-100 mmHg. If BP is measured using a semiautomated cuff-oscillometric device as found on most digital blood pressure devices and monitors, the displayed value is the MAP, while systolic and diastolic pressure are approximated using formulas and algorithms specific to individual manufacturers (19). MAP has a positive correlation with the level of target organ damage, the best indicator of the severity of hypertensive emergency (20). If possible, BP should be measured in both arms over several measurements in order to obtain the most precise possible baseline MAP value.

When forming the treatment plan, the patient’s medical history must be considered, i.e., whether they are a person with chronic, preexisting AH (in which case BP reduction should be performed at a slower pace and intensity) or a previously normotensive person with suddenly-developing AH (in which case BP reduction can be performed at a higher pace and intensity).

If medical history data are not available, a reasonable goal is to reduce MAP by approximately 20% within the first 2 hours, followed by reducing MAP to 125 mmHg over the course of 2-6 hours, depending on the etiology and patient comorbidities (3,21).

Before starting antihypertensive treatment, it is recommended to treat other potential causes of elevated BP in order to optimize AH control and prevent iatrogenic hypotension. Examples of such causes are presented inTable 7.

TABLE 7 The most common reversible secondary causes of an increase in blood pressure.
Cause of increased blood pressureTherapy
PainAnalgesic agents
Volume overloadDiuretic agents
Agitation/Acute psychosisAntipsychotic agents
Obstructive uropathy/Urinary retentionUrinary catheter placement

Choosing the best medication to treat individual patients and conditions is the decision of the treating physician, and we thus consider it inadvisable to provide specific algorithms for treatment in individual situations. Emergency patients with symptoms and signs that indicate hypertensive emergency often represent complex cases, and decisions on their treatment are multifactorial. The remainder of this text describes the pharmacokinetic and pharmacodynamic characteristics of medications that clinical practice and the literature have identified as most effective for acute reduction of elevated arterial pressure values. The availability of the medications described below varies between medical institutions.

INTRAVENOUS MEDICATIONS

1.

Intravenous medications can be divided into three groups based on the duration of their effect:

  1. Short-acting medications

    • Duration of action lower than 30 minutes – applied in continuous infusion

    • Short-acting effect allows titration

  2. Intermediate-acting medication

    • Duration of action between 30 minutes to 2 hours – applied in continuous infusion

    • Titration possible, but not as effective as in short-acting medications

  3. Long-acting medications

    • Duration of action longer than 2 hours – bolus application

    • Titration is more difficult due to long duration of action

Table 8 presents the intravenous medications most commonly applied in hypertensive emergencies. Literature data lists nicardipine, clevidipine, labetalol, nitroglycerine, esmolol, and urapidil (22-27). All of these are available in the Republic of Croatia, except for nicardipine and clevidipine

TABLE 8 Intravenous medications for blood pressure regulation in hypertensive emergency.
NameOnset of action/Duration of actionContraindicationsDoseComments
LabetalolOnset of action: 5-10 min
Duration of action: 3-6 h
Bradycardia, Atrioventricular block, Sick sinus syndrome, Cardiogenic pulmonary edema, Asthma exacerbation, Acute sympathomimetic intoxicationApplied in boluses. First bolus 20 mg, followed by a 40 mg bolus, then an 80 mg bolus up to 3 times maximum. Obligatory spacing between boluses: 15 minutes. Scheme: 20 mg - 40 mg - 80 mg-80 mg - 80mg
Maximum allowed cumulative dose: 300mg
Once the desired BP is achieved, apply 10-20 mg boluses according to MAP, not more often than every 10 minutes.
May cause bradycardia,
hyperkalemia
NitroglycerinOnset of action 2 min
Duration of action: 5-10 min
Use of phosphodiesterase 5 inhibitors within 48 hours (sildenafil, vardenafil, tadalafil). Suspected increased intracranial pressure.Applied as an infusion: 50-300 mcg/min, titrate according to MAPMedication of choice in acute cardiogenic pulmonary edema. Coronary venodilator, indicated in acute myocardial infarction (inferior/right sided myocardial infarction are relative contraindications)
EsmololOnset of action: 1-2 min Duration of action: 10-30 minBradycardia, Atrioventricular block, Sick sinus syndrome, Cardiogenic pulmonary edema, Asthma exacerbation, Acute sympathomimetic intoxicationLoading bolus 0.5 mg/kg, then a 50 mcg/kg/min infusion. If BP remains uncontrolled: repeat bolus 0.5 mg/kg, followed by a 50 mcg/kg/min infusion. Titrate infusion to MAP (max infusion rate 200 mcg/kg/min)May cause bradycardia,
hyperkalemia
UrapidilOnset of action 5 min Duration of action: 3 hAortic outflow tract stenosis. Arterio-venous shunt.Starting dose: 25mg bolus. If BP remains uncontrolled: repeat 25 mg bolus after 10 minutes. In case of persistently elevated BP: 50 mg bolus 10 minutes after the second bolus, followed by an infusion: 5-40 mg/hMost common medication for the management of hypertensive emergency in Croatia

2) SUBLINGUAL MEDICATIONS

Nitroglycerine can also be applied in a sublingual formulation, and it can also applied as a spray when indicated (28). One spray dose contains 400 mcg or 0.4 mg of nitroglycerine. Indications for the application of sublingual nitroglycerine in the context of hypertensive emergency are similar to those for intravenous application – acute cardiogenic pulmonary edema, acute myocardial infarction (suspected inferior wall or left ventricular myocardial infarction is a relative contraindication for their application). Absolute contraindications are the application of phosphodiesterase-5 inhibitors in a 48-hour period prior to the hypertensive episode and suspicion of elevated intracranial pressure. The most common side-effects are headache and facial erythema caused by vasodilatation. It is important to note that, given that sublingual application makes it more difficult to estimate the administrated dose, the patient should be placed in a sitting position after application of the medication due to the risk of rapid-onset hypotension. Although the sublingual formulation is not the standard for hypertensive emergency, examples from the literature show that its application is possible and effective. In a study by Prasanne et al., the authors administered one dose (0.4 mg) of sublingual nitroglycerine to patients with a hypertensive crisis and monitored the MAP values – after 10 minutes, an average MAP reduction of 16.3% was achieved (29). Hirschl et al. published studies that examined the application of sublingual nitroglycerine in doses of 0.8 mg every 10 minutes up to a cumulative dose of 3.2 mg in patients with hypertensive emergency and concluded that this form of treatment was equally effective as intravenous enalapril, but less effective than intravenous urapidil (30,31).

3) ORAL MEDICATIONS

Due to the long onset of action for most oral antihypertensive medications and the need for rapid and effective reduction of BP values in patients with hypertensive emergency, peroral antihypertensives have a limited role in prehospital emergency services. Switching to peroral therapy is generally not recommended until BP values have stabilized after intravenous application of medication. The slow onset and long duration of action in peroral application of medication should be considered, as it can lead to accumulation of the drug in the body and consequent iatrogenic hypotension, but studies have demonstrated that the peroral application of labetalol, losartan, and isosorbide dinitrate is safe and effective (32-34) (Table 9). The slow onset of action of peroral medications should also be considered in case of inclement weather or other conditions preventing the transport of patients to hospital care when treating patients on islands, in case of an insufficient venous approach (most common in oncological patients and patients with chronic kidney insufficiency), or limited capacity for osseous application of the medication (amputated limbs).

TABLE 9 Peroral medications for blood pressure regulation when transport if the patient to hospital care is not possible.
NameOnset of action/
Duration of action
ContraindicationsDoseComments
LabetalolOnset of action: 2 h
Duration of action: 10 h
Bradycardia, Atrioventricular block, Sick sinus syndrome, Cardiogenic pulmonary edema, Asthma exacerbation, Acute sympathomimetic intoxication1 200 mg oral tablet every 12 h. In case of suboptimal effect, another 200 mg oral tablet can be applied 2-4 h following the first. Maximum allowed dose: 1000 mg orally every 12 hMay cause bradycardia, hyperkalemia. In stable patients, following successful BP control with intravenous labetalol and stable BP values, treatment can be continued with peroral labetalol
LosartanOnset of action: 4-6 h
Duration of action: 24 h
Hyperkalemia, Acute kidney injury, Previously reported cough or angioedema with angiotensin converting enzyme inhibitors or angiotensin receptor blockersOne 50 mg oral tablet once daily. Maximum allowed dose: 100 mg dailyEfficacy differs between patients, depending on the renin/angiotensin/aldosterone system activity level of individual patients
Isosorbide dinitrateOnset of action: 1-2 h
Duration of action: 8 h
Increased intracranial pressure. Obstructive hypertrophic cardiomyopathyOne 20 mg oral tablet every 8 h. Maximum allowed dose: One 40 mg oral tablet every 8 hoursMay cause reflex tachycardia

The effectiveness of different antihypertensive medications

In the section below, we present a short overview of the two most commonly used intravenous antihypertensive medications listed inTable 8 and their effectiveness and safety in various clinical conditions.

Labetalol was assessed as a antihypertensive in numerous prospective studies and was shown to be an effective, fast-acting choice: the studies report the ratios of patients with BP successfully reduced to target values was 76% after 30 minutes and 96-100% after 60 minutes (35-37). In comparisons with other antihypertensives, labetalol was shown to be more effective than intravenous nitroglycerine (36), as effective as intravenous esmolol (38), and less effective than intravenous nicardipine (35) and peroral nifedipine (37).

Urapidil is an alpha-1 adrenergic receptor antagonist used for treating hypertensive emergencies. In prehospital conditions, it has been shown to be an effective antihypertensive medication that statistically significantly reduced BP values after as little as 5 minutes, without significant unwanted adverse effects (39). In hospital conditions, urapidil was also shown to be an effective, reliable, and fast-acting medication that was superior to oral captopril in achieving target BP values (40). A metanalysis comparing urapidil with nitroglycerine for the treatment of hypertensive acute heart failure showed that urapidil had a better safety profile and equal effectiveness as nitroglycerine in the treatment of hypertensive emergency and hypertensive crisis (41). Therefore, patients with hypertensive emergency should be treated the intravenous application of the medications described above, and, if MAP cannot be calculated, the goal is to achieve a 25% reduction in BP in comparison with baseline values within a one-hour standard. The treatment goal for patients with chronic uncontrolled hypertension (the previously employed term was “hypertensive urgency”) is the gradual reduction of BP to 20% in comparison with initial values, which is achieved through the application of peroral antihypertensive therapy (42).

Discussion

In prehospital emergency medical conditions, anamnesis and clinical examination of the patient have a significant role in the assessment and diagnosis of emergency states associated with hypertension (43). Raos et al. demonstrated a significant reduction in systolic pressure in prehospital conditions if benzodiazepine was prescribed alongside antihypertensive therapy. A reduction of BP of 19.5 ± 7.1% was achieved in the group of patients with chronic uncontrolled hypertension (previously called hypertensive urgency) who were prescribed benzodiazepine in comparison with the control group (BP reduced by 10.1 ± 7.0%) taking an antihypertensive medication without benzodiazepine (44). Its beneficial added anxiolytic effect should therefore be considered in prehospital treatment. The importance of clinical follow-up and further diagnostic examinations should be emphasized in patients with chronic uncontrolled arterial hypertension (which is also the most common reason for the arrival of an emergency medicine team) throughout primary and secondary healthcare, with a recommendation for further examination and treatment and exclusion of potentially curable secondary sources of AH, with special emphasis on the importance of recommending follow-up and control in hypertensiology clinics (42,44).

In case of hypertensive emergency, diastolic pressure should not be lower than 100 to 110 mmHg, in order to prevent further target organ damage due to hypoperfusion. Excessive BP reduction can indicate cerebral, coronary, or renal ischemia and must be avoided. Exceptions comprise patients with aortic dissection, pheochromocytoma crisis, and severe preeclampsia, as well as some patients with spontaneous intracerebral bleeding that require acute pressure reduction (42).

Proper management of hypertension, whether in prehospital or hospital emergency treatment, is crucial for the prevention of target organ damage as well as the prevention of cerebral, cardiac, renal, and vascular remodeling and untimely fibrosis of target organs such as the brain, heart, kidneys, and the vascular system.

Conclusion

Emergency service providers, as a form of a “safety net” for the healthcare systems, have an important role in informing patients on the importance of subsequent clinical treatment for chronic uncontrolled hypertension.

Knowledge of the etiology of emergency states related to hypertension and hypertensive emergency, as well as the pharmacokinetic and pharmacodynamic characteristics of medications available to physicians in emergency medical services, is crucial in order to provide patients with the best possible care in the context of available options, with the goal of achieving coordinated treatment and communication across prehospital and in-hospital emergency services.

LITERATURE

1 

Williams B, Mancia G, Spiering W, Agabiti Rosei E, Azizi M, Burnier M, et al. 2018 ESC/ESH Guidelines for the management of arterial hypertension: The Task Force for the management of arterial hypertension of the European Society of Cardiology and the European Society of Hypertension: The Task Force for the management of arterial hypertension of the European Society of Cardiology and the European Society of Hypertension. J Hypertens. 2018 October;36(10):1953–2041. https://doi.org/10.1097/HJH.0000000000001940 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/30234752

2 

nger T, Borghi C, Charchar F, Khan NA, Poulter NR, Prabhakaran D, et al. 2020 International Society of Hypertension global hypertension practice guidelines. J Hypertens. 2020 Jun;38(6):982-1004. https://doi.org/10.1097/HJH.0000000000002453 https://doi.org/10.1097/HJH.0000000000002453

3 

Whelton PK, Carey RM, Aronow WS, Casey DE Jr, Collins KJ, Dennison Himmelfarb C, et al. 2017 ACC/AHA/AAPA/ABC/ACPM/AGS/APhA/ASH/ASPC/NMA/PCNA Guideline for the Prevention, Detection, Evaluation, and Management of High Blood Pressure in Adults: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. J Am Coll Cardiol. 2018 May 15;71(19):e127–248. https://doi.org/10.1016/j.jacc.2017.11.006 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/29146535

4 

Bliziotis IA, Destounis A, Stergiou GS. Home versus ambulatory and office blood pressure in predicting target organ damage in hypertension: a systematic review and meta-analysis. J Hypertens. 2012 July;30(7):1289–99. https://doi.org/10.1097/HJH.0b013e3283531eaf PubMed: http://www.ncbi.nlm.nih.gov/pubmed/22499289

5 

Cienki JJ, DeLuca LA. Agreement between emergency medical services and expert blood pressure measurements. J Emerg Med. 2012 July;43(1):64–8. https://doi.org/10.1016/j.jemermed.2011.02.018 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/21982624

6 

Beevers G, Lip GY, O’Brien E. ABC of hypertension: Blood pressure measurement. Part II-conventional sphygmomanometry: technique of auscultatory blood pressure measurement. BMJ. 2001 April 28;322(7293):1043–7. https://doi.org/10.1136/bmj.322.7293.1043 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/11325773

7 

Kontos MC, de Lemos JA, Deitelzweig SB, Diercks DB, Gore MO, Hess EP, et al. 2022 ACC Expert Consensus Decision Pathway on the Evaluation and Disposition of Acute Chest Pain in the Emergency Department: A Report of the American College of Cardiology Solution Set Oversight Committee. J Am Coll Cardiol. 2022 November 15;80(20):1925–60. https://doi.org/10.1016/j.jacc.2022.08.750 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/36241466

8 

Chan TC, Vilke GM, Pollack M, Brady WJ. Electrocardiographic manifestations: pulmonary embolism. J Emerg Med. 2001 October;21(3):263–70. https://doi.org/10.1016/S0736-4679(01)00389-4 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/11604281

9 

Rodger M, Makropoulos D, Turek M, Quevillon J, Raymond F, Rasuli P, et al. Diagnostic value of the electrocardiogram in suspected pulmonary embolism. Am J Cardiol. 2000 Oct 1;86(7):807-9, A10. https://doi.org/10.1016/S0002-9149(00)01090-0 https://doi.org/10.1016/S0002-9149(00)01090-0

10 

Jacobs ZG. Hypertensive “Urgency” Is a Harmful Misnomer. J Gen Intern Med. 2021 September;36(9):2812–3. https://doi.org/10.1007/s11606-020-06495-6 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/33420559

11 

Tilman K, DeLashaw M, Lowe S, Springer S, Hundley S, Counselman FL. Recognizing asymptomatic elevated blood pressure in ED patients: how good (bad) are we? Am J Emerg Med. 2007 March;25(3):313–7. https://doi.org/10.1016/j.ajem.2006.09.007 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/17349906

12 

Bohan J, Fullerton L, Oakland B, Oldewage J. Hypertension in the ED: a multifaceted intervention to change provider practice. Am J Emerg Med. 2011 September;29(7):796–801. https://doi.org/10.1016/j.ajem.2010.05.003 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/20685061

13 

Baumann BM, Abate NL, Cowan RM, Chansky ME, Rosa K, Boudreaux ED. Characteristics and referral of emergency department patients with elevated blood pressure. Acad Emerg Med. 2007 September;14(9):779–84. https://doi.org/10.1197/j.aem.2007.05.008 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/17652640

14 

Tanabe P, Persell SD, Adams JG, McCormick JC, Martinovich Z, Baker DW. Increased blood pressure in the emergency department: pain, anxiety, or undiagnosed hypertension? Ann Emerg Med. 2008 March;51(3):221–9. https://doi.org/10.1016/j.annemergmed.2007.10.017 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/18207606

15 

Pitts SR, Adams RP. Emergency department hypertension and regression to the mean. Ann Emerg Med. 1998 February;31(2):214–8. https://doi.org/10.1016/S0196-0644(98)70309-9 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/9472183

16 

Frei SP, Burmeister DB, Coil JF. Frequency of serious outcomes in patients with hypertension as a chief complaint in the emergency department. J Am Osteopath Assoc. 2013 September;113(9):664–8. https://doi.org/10.7556/jaoa.2013.032 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/24005086

17 

Watson K, Broscious R, Devabhakthuni S, Noel ZR. Focused Update on Pharmacologic Management of Hypertensive Emergencies. Curr Hypertens Rep. 2018 June 8;20(7):56. https://doi.org/10.1007/s11906-018-0854-2 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/29884955

18 

Babbs CF. Oscillometric measurement of systolic and diastolic blood pressures validated in a physiologic mathematical model. Biomed Eng Online. 2012 August 22;11:56. https://doi.org/10.1186/1475-925X-11-56 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/22913792

19 

Liu J, Hahn JO, Mukkamala R. Error mechanisms of the oscillometric fixed-ratio blood pressure measurement method. Ann Biomed Eng. 2013 March;41(3):587–97. https://doi.org/10.1007/s10439-012-0700-7 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/23180030

20 

Papaioannou TG, Protogerou AD, Vrachatis D, Konstantonis G, Aissopou E, Argyris A, et al. Mean arterial pressure values calculated using seven different methods and their associations with target organ deterioration in a single-center study of 1878 individuals. Hypertens Res. 2016 September;39(9):640–7. https://doi.org/10.1038/hr.2016.41 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/27194570

21 

van den Born BH, Lip GYH, Brguljan-Hitij J, Cremer A, Segura J, Morales E, et al. ESC Council on hypertension position document on the management of hypertensive emergencies. Eur Heart J Cardiovasc Pharmacother. 2019 January 1;5(1):37–46. https://doi.org/10.1093/ehjcvp/pvy032 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/30165588

24 

Aronson S, Dyke CM, Stierer KA, Levy JH, Cheung AT, Lumb PD, et al. The ECLIPSE trials: comparative studies of clevidipine to nitroglycerin, sodium nitroprusside, and nicardipine for acute hypertension treatment in cardiac surgery patients. Anesth Analg. 2008 October;107(4):1110–21. https://doi.org/10.1213/ane.0b013e31818240db PubMed: http://www.ncbi.nlm.nih.gov/pubmed/18806012

29 

Prasanna N, Dissanayake HA, Constantine GR. Sublingual nitroglycerin for early blood pressure control in hypertensive emergencies: observations from an emergency department clinical audit in Sri Lanka. BMC Res Notes. 2018 June 5;11(1):355. https://doi.org/10.1186/s13104-018-3460-0 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/29871702

30 

Hirschl MM, Schreiber W, Woisetschläger C, Kaff A, Raab H. Sublinguales Nitroglyzerin oder intravenöses Enalaprilat in der präklinischen Behandlung von hypertensiven Patienten mit Lungenödem [Sublingual nitroglycerin or intravenous enalaprilat in preclinical treatment of hypertensive patients with pulmonary edema]. Z Kardiol. 1999 Mar;88(3):208-14. German. https://doi.org/10.1007/s003920050277 https://doi.org/10.1007/s003920050277

31 

Schreiber W, Woisetschläger C, Binder M, Kaff A, Raab H, Hirschl MM. The nitura study--effect of nitroglycerin or urapidil on hemodynamic, metabolic and respiratory parameters in hypertensive patients with pulmonary edema. Intensive Care Med. 1998 June;24(6):557–63. https://doi.org/10.1007/s001340050615 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/9681776

35 

Cannon CM, Levy P, Baumann BM, Borczuk P, Chandra A, Cline DM, et al. Intravenous nicardipine and labetalol use in hypertensive patients with signs or symptoms suggestive of end-organ damage in the emergency department: a subgroup analysis of the CLUE trial. BMJ Open. 2013 March 26;3(3):e002338. https://doi.org/10.1136/bmjopen-2012-002338 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/23535700

36 

Malik MA, Ahmad R, Beg M, Ahmad R. A comparative study of intravenous labetalol VS intravenous nitroglycerin in the treatment of hypertensive crises. Indian Heart J. 2022 July-August;74(4):332–4. https://doi.org/10.1016/j.ihj.2022.06.001 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/35667400

37 

Shekhar S, Sharma C, Thakur S, Verma S. Oral nifedipine or intravenous labetalol for hypertensive emergency in pregnancy: a randomized controlled trial. Obstet Gynecol. 2013 November;122(5):1057–63. https://doi.org/10.1097/AOG.0b013e3182a9ea68 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/24104790

38 

Muzzi DA, Black S, Losasso TJ, Cucchiara RF. Labetalol and esmolol in the control of hypertension after intracranial surgery. Anesth Analg. 1990 Jan;70(1):68-71. PubMed:https://pubmed.ncbi.nlm.nih.gov/1967515/

39 

Alijotas-Reig J, Bove-Farre I, de Cabo-Frances F, Angles-Coll R. Effectiveness and safety of prehospital urapidil for hypertensive emergencies. Am J Emerg Med. 2001 March;19(2):130–3. https://doi.org/10.1053/ajem.2001.20008 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/11239257

40 

Salkic S, Brkic S, Batic-Mujanovic O, Ljuca F, Karabasic A, Mustafic S. Emergency Room Treatment of Hypertensive Crises. Med Arch. 2015 October;69(5):302–6. https://doi.org/10.5455/medarh.2015.69.302-306 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/26622081

41 

Shi J, Li Y, Xing C, Peng P, Shi H, Ding H, et al. Urapidil, compared to nitroglycerin, has better clinical safety in the treatment of hypertensive patients with acute heart failure: a meta-analysis. Drug Des Devel Ther. 2018 December 27;13:161–72. https://doi.org/10.2147/DDDT.S185972 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/30643384

42 

Željković Vrkić T, Prkačin I, Jelaković B. Hipertenzivna kriza. Medix. 2018;24(130/131):218–26.

43 

Simić A, Nesek Adam V, Lukačević M. A Arterial hypertension in outpatient emergency practice – retrospective analysis of hypertensive patients at the Emergency Medicine Department of Varaždin County]. Cardiol Croat. 2017;12(3):64. Croatian. https://doi.org/10.15836/ccar2017.64

44 

Raos D, Paštrović F, Okštajner PK, Vodanović M, Prkačin I. Evaluation of hypertensive urgency management in out-of-hospital unit. Acta Med Croatica. 2020;74 Suppl 1:41–4.https://hrcak.srce.hr/236569


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