Abstract
Background
Data regarding very severe acute hypertension, a serious problem in emergency departments (EDs), are scarce. We investigated the clinical characteristics, practice patterns, and long-term prognoses of patients presenting to the ED with very severe acute hypertension.
Methods
Cross-sectional study data were obtained from a single regional emergency medical center, including patients aged ≥ 18 years who were admitted to the ED between January 2016 and December 2019 for very severe acute hypertension, which was defined as systolic blood pressure of > 220 mmHg and/or diastolic blood pressure of > 120 mmHg. The patients were classified into two groups based on the presence or absence of hypertension-mediated organ damage (HMOD).
Results
Among 1,391 patients with very severe acute hypertension in the ED, half of the them (50.2%) had a previous medical history of hypertension, and 547 (39.3%) had acute HMOD. The overall 3-month, 1-year, and 3-year mortality rates were 5.2%, 11.9%, and 17.3%, respectively. In particular, patients with HMOD had a significantly higher mortality rate at each time point than those without HMOD. Among patients with HMOD, acute ischemic stroke was the most common (28.7%). Moreover, intravenous antihypertensive drugs were significantly more prescribed in patients with HMOD than in those without HMOD (79.0% vs. 22.2%, P < 0.001), but there were no differences in oral antihypertensive drugs between the two groups.
Conclusions
Patients with very severe acute hypertension had poor long-term clinical prognoses. Clinicians should be continuously monitoring and providing appropriate treatment and close follow-up for patients with very severe acute hypertension.
Supplementary Information
The online version contains supplementary material available at 10.1186/s40885-022-00208-3.
Keywords: Very severe acute hypertension, Emergency department, Hypertension-mediated organ damage, Mortality
Background
Hypertension is an important risk factor for cardiovascular and cerebrovascular events [1], and the number of patients with hypertension has steadily increased to more than 12 million in Korea [2]. Recently, although clinical trials and meta-analyses have strongly suggested intensive blood pressure (BP) lowering in patients with hypertension [3], approximately 1%–2% of patients eventually develop a severe acute increase in BP [4]. Hypertensive crisis or severe hypertension is defined as a BP elevation above 180 mmHg for systolic BP (SBP) and/or above 110–120 mmHg for diastolic blood pressure (DBP) according to the international practice guidelines for hypertension [5, 6]. Hypertensive emergency (HE) and hypertensive urgency, often referred to as hypertensive crisis, are distinguished by the presence or absence of new onset or worsening of acute organ damage [5–7]. According to our previous study, patients with severe acute hypertension accounted for 59 out of 1,000 emergency department (ED) visits at a single center in Korea, and their definition of severe acute hypertension was an SBP of ≥ 180 mmHg and/or a DBP of ≥ 100 mmHg [7]. However, a BP that is much higher than this threshold is often and is a life-threatening condition encountered in the EDs, which is highly associated with morbidity and mortality [8]. Immediate BP-lowering treatment is needed to prevent the progression of target organ damage in patients with severe acute BP elevation. Despite the clinical significance of severe acute BP elevation, epidemiologic studies and long-term outcomes in patients with very severe acute hypertension are scarce [6]. In this study, we investigated the clinical characteristics, practice patterns, and long-term prognosis of patients presenting to the ED with very severe acute hypertension.
Method
Study population and data collection
Cross-sectional study data were obtained from a single regional emergency medical center affiliated with an academic university hospital in Guri, Gyeonggi-do, Korea. The study design and primary results were published previously [7]. In brief, the medical records of 172,105 patients who visited the ED between January 2016 and December 2019 were reviewed; 2,087 patients who had an elevated initial SBP of > 220 mmHg and/or a DBP of > 120 mmHg were enrolled in this study (Fig. 1). Of these, patients who presented following acute trauma, for the certificates, or who visited the ED multiple times (revisits other than the first-visit) were excluded from this study. Finally, 1,391 patients with very severe acute hypertension were further classified based on the presence or absence of hypertension-mediated organ damage (HMOD). For this process, the National Emergency Department Information System (NEDIS) data were used to identify eligible patients who visited the ED. The system collects data, including initial vital signs and baseline clinical characteristics, and this information on all patients visiting the ED is automatically transmitted from each hospital to a central government server called the NEDIS.
Fig. 1.
Study population
The study was conducted in accordance with the Declaration of Helsinki and reviewed and approved by the Institutional Review Board of the researchers’ affiliated university hospital (GURI 2020–01-028), which waived the requirement for written informed consent.
Data collection
Data were collected using electronic medical records by experienced data collectors under principal investigator supervision. The following demographic and clinical characteristics were extracted: age, sex, initial BP in the ED, and traditional cardiovascular risk factors, including a history of hypertension, diabetes, dyslipidemia, ischemic stroke, hemorrhagic stroke, coronary artery disease, peripheral artery disease, heart failure, chronic kidney disease, and end-stage renal disease and smoking and alcohol consumption status.
The following laboratory data were extracted: serum creatinine, estimated glomerular filtration rate (eGFR) (mL/min/1.73 m2), troponin I, B-type natriuretic peptide (BNP), D-dimer, and proteinuria in a dipstick urinalysis. In addition, the diagnostic test findings to determine HMOD, types of antihypertensive drugs for controlling BP in the ED, and principal diagnosis at discharge were obtained.
The primary outcome was the development of all-cause mortality during the 3-year follow-up (until March 2021). The incidence of mortality and its timing were extracted from the National Health Insurance Service in South Korea. The secondary outcomes were all-cause mortality within 1 month, 3 months, and 1 year; hospital admission; discharge in the ED; discharge against medical advice; and mortality in the ED.
Definition
In this study, very severe acute hypertension was defined as an initial SBP of > 220 mmHg and/or DBP of > 120 mmHg when visiting the ED. HMOD was defined as hypertensive encephalopathy, cerebral infarction, intracerebral hemorrhage, retinopathy, acute heart failure, acute coronary syndrome, acute renal failure, and aortic dissection [9]. Hypertensive encephalopathy was defined as a severe increase in BP associated with other unexplained lethargy, seizures, cortical blindness, and coma [9]. Cerebral infarction and intracerebral hemorrhage were defined based on neurologic symptoms and brain imaging in the ED. Fundus examination confirmed retinopathy based on the presence of flame-like hemorrhages, cotton wool spots, or papilledema. Proteinuria was defined as a dipstick urinalysis result of 1 + or greater [10]. The BP was measured in the ED above the brachial artery using an automated BP machine, Spot Vital Signs LXi (Welch Allyn, Skaneateles Falls, NY, USA).
Statistical analysis
All categorical data are presented as frequencies and percentages, and data for continuous variables are expressed as means and standard deviations. Pearson’s chi-square test or Fisher’s exact test was used to compare categorical variables. Student’s t-test was used to compare continuous variables. The Kaplan–Meier survival analyses and log-rank tests were used to compare the cumulative mortality rates. Significance was defined as a P value of < 0.05. All analyses were performed using SPSS v26 (IBM Inc., Armonk, NY, USA).
Results
Clinical characteristics
Of the 172,105 patients who visited the ED during the study period, 1,391 (0.8%) had very severe acute hypertension, and 547 (39.3%) had HMOD. The patients’ baseline characteristics, including medical history, laboratory findings, and presenting symptoms, are presented in Table 1. The mean age of the total study population was 57.4 ± 17.2 years old, and 46.2% were women. Half of the patients (50.2%) had a previous medical history of hypertension. Of those who had hypertension previously, 358 (61.1%) were currently taking antihypertensive drugs. Blood tests (88.2%), chest radiography (84.5%), and electrocardiography (ECG) (79.7%) were performed in most patients with very severe acute hypertension, and brain imaging including brain computed tomography (CT) or magnetic resonance imaging (MRI) was performed in less than half (41.5%). Chest and abdominal CT, echocardiography, and fundoscopy were performed in a small number of patients. Patients with HMOD were significantly older and predominantly men compared with those without HMOD. In addition, patients with HMOD had significantly more traditional cardiovascular risk factors, including hypertension, diabetes, dyslipidemia, hemorrhagic stroke, coronary artery disease, heart failure, chronic kidney disease, end-stage renal disease, current smoking, and alcohol consumption than those without HMOD. Compared with patients without HMOD, those with HMOD presented with a significantly higher mean SBP (217.6 ± 29.0 vs. 198.2 ± 27.9 mmHg, P < 0.001). The DBP did not differ between the two groups. The mean eGFR was significantly lower in patients with HMOD than in those without HMOD, and proteinuria was more frequently observed in patients with HMOD. The mean BNP value was significantly higher in patients with HMOD, and cardiomegaly and congestion on chest radiography were significantly more observed in patients with HMOD than in those without HMOD. Abnormal findings on ECG, brain imaging, and fundoscopy were also more frequently observed in patients with HMOD.
Table 1.
Baseline characteristics
| All patients (n = 1,391) |
Patients with HMOD (n = 547) |
Patients without HMOD (n = 844) |
P value | |
|---|---|---|---|---|
| Mean age, years (SD) | 57.4 (17.2) | 62.1 (15.3) | 54.4 (17.7) | < 0.001 |
| Female sex, N (%) | 642 (46.2) | 225 (41.1) | 417 (49.4) | 0.003 |
| Medical history, N (%) | ||||
| Hypertension | 674 (50.2) | 326 (61.2) | 348 (43.0) | < 0.001 |
| Diabetes mellitus | 306 (23.1) | 149 (28.1) | 157 (19.8) | < 0.001 |
| Dyslipidemia | 89 (6.8) | 47 (8.9) | 42 (5.4) | 0.013 |
| Ischemic stroke | 80 (6.1) | 37 (7.0) | 43 (5.5) | 0.267 |
| Hemorrhagic stroke | 45 (3.4) | 25 (4.7) | 20 (2.6) | 0.035 |
| Coronary artery diseasea | 95 (7.2) | 60 (11.3) | 35 (4.5) | < 0.001 |
| Peripheral artery disease | 17 (1.3) | 6 (1.1) | 11 (1.4) | 0.666 |
| Heart failure | 61 (4.7) | 51 (9.6) | 10 (1.3) | < 0.001 |
| Chronic kidney disease | 108 (8.2) | 62 (11.7) | 46 (5.9) | < 0.001 |
| End-stage renal disease | 64 (4.9) | 33 (6.2) | 31 (4.0) | 0.062 |
| Social history, N (%) | ||||
| Cigarette smoking | 294 (32.5) | 162 (35.9) | 132 (29.0) | 0.042 |
| Alcohol consumption | 406 (43.7) | 216 (47.5) | 190 (40.0) | 0.022 |
| Triage vitals, mean (SD) | ||||
| SBP, mmHg | 205.4 (29.7) | 217.6 (29.0) | 198.2 (27.9) | < 0.001 |
| DBP, mmHg | 128.1 (15.6) | 128.3 (17.6) | 128.1 (14.1) | 0.814 |
| Laboratory tests done, N (%) | 1227 (88.2) | 539 (98.5) | 688 (81.5) | < 0.001 |
| Mean serum creatinine, mg/dL (SD) | 1.39 (1.9) | 1.62 (2.2) | 1.22 (1.7) | < 0.001 |
| Mean eGFR, mL/min/1.73 m2 (SD) | 79.5 (32.4) | 71.4 (32.3) | 85.7 (31.1) | < 0.001 |
| Troponin I, ng/mL (SD) | 0.249 (3.28) | 0.437 (4.67) | 0.080 (0.86) | 0.126 |
| BNP, pg/mL (SD) | 519.9 (971.2) | 677.1 (1051.1) | 305.8 (806.2) | < 0.001 |
| D-dimer, mg/L (SD) | 804.8 (2546.0) | 783.5 (2159.2) | 830.5 (2982.6) | 0.810 |
| Urinary analysis done, N (%) | 849 (61.0) | 406 (74.2) | 443 (52.5) | < 0.001 |
| Proteinuria, N (%)b | 329 (38.8) | 181 (44.6) | 148 (33.4) | < 0.001 |
| Chest X-ray done, N (%) | 1175 (84.5) | 530 (96.9) | 645 (76.4) | < 0.001 |
| Cardiomegaly, N (%) | 176 (14.7) | 96 (18.0) | 80 (12.0) | 0.003 |
| Congestion/fluid overload, N (%) | 97 (8.1) | 96 (18.0) | 1 (0.2) | < 0.001 |
| ECG done, N (%) | 1109 (79.7) | 525 (96.0) | 584 (69.2) | < 0.001 |
| LVH, N (%) | 190 (17.2) | 120 (22.9) | 70 (12.0) | < 0.001 |
| Myocardial ischemia, N (%) | 78 (7.1) | 58 (11.1) | 20 (3.4) | < 0.001 |
| Atrial fibrillation, N (%) | 79 (7.1) | 54 (10.3) | 25 (4.3) | < 0.001 |
| Brain CT or MR done, N (%) | 577 (41.5) | 328 (60.0) | 249 (29.5) | < 0.001 |
| Abnormal finding, N (%) | 281 (42.8) | 264 (75.9) | 17 (5.5) | < 0.001 |
| Chest and abdomen CT done, N (%) | 144 (10.4) | 55 (10.1) | 89 (10.5) | 0.769 |
| Echocardiography done, N (%) | 43 (3.1) | 39 (7.1) | 4 (0.5) | < 0.001 |
| Fundoscopy done, N (%) | 50 (3.6) | 22 (4.0) | 28 (3.3) | 0.491 |
| Abnormal finding, N (%) | 18 (13.8) | 13 (27.1) | 5 (6.1) | < 0.001 |
| Current antihypertensive drugs, N (%)c | 358 (61.1) | 186 (63.1) | 172 (59.1) | 0.327 |
| Presenting symptoms, n (%) | ||||
| Chest pain | 126 (9.1) | 82 (15.0) | 44 (5.2) | < 0.001 |
| Dyspnea | 201 (14.5) | 118 (21.6) | 83 (9.8) | < 0.001 |
| Headache | 110 (7.9) | 37 (6.8) | 73 (8.6) | 0.203 |
| Dizziness | 135 (9.7) | 32 (5.9) | 103 (12.2) | < 0.001 |
| Altered mental status | 180 (12.9) | 128 (23.4) | 52 (6.2) | < 0.001 |
| Focal neurologic deficit | 239 (17.2) | 187 (34.2) | 52 (6.2) | < 0.001 |
| Visual disturbance | 22 (1.6) | 12 (2.2) | 10 (1.2) | 0.141 |
| Epistaxis | 53 (3.8) | 0 (0) | 53 (6.3) | < 0.001 |
Data shown with percentages in parentheses represent numbers of participants, and other data represent mean values with standard deviation in parentheses; BNP B-type natriuretic peptide, CT computed tomography, DBP diastolic blood pressure, eGFR estimated glomerular filtration rate, ECG electrocardiogram, HMOD hypertension-mediated organ damage, LVH left ventricular hypertrophy, MR Magnetic resonance, N Number, SBP Systolic blood pressure, SD Standard deviation
aComposite of coronary artery disease, percutaneous coronary intervention, and coronary artery bypass graft
bProteinuria is defined as a dipstick urinalysis result of 1 + or more
cThe proportion of current antihypertensive drugs of those who had hypertension previously
Antihypertensive therapy and BP changes in the ED
Among 1,391 patients with very severe acute hypertension, 619 (44.5%) received intravenous antihypertensive drugs, and 268 (19.3%) received oral antihypertensive drugs in the ED (Table 2). Intravenous nicardipine was the most frequently prescribed (32.6%), and intravenous nitroglycerine was the second most common (15.2%). Among oral antihypertensive drugs, calcium antagonists were the most commonly prescribed drugs. Moreover, intravenous antihypertensive drugs were significantly more prescribed in patients with HMOD than in those without HMOD (79.0% vs. 22.2%, P < 0.001), but there was no difference in oral antihypertensive drugs between the two groups. Figure 2 shows the BP changes within 1 h and at discharge in both groups. The BP was measured within 1 h in only 39.0% of all patients (59.2% of patients with HMOD and 25.9% of those without HMOD), and the BP at discharge was assessed in 64.6% of all patients (80.1% of patients with HMOD and 54.6% of those without HMOD). Initially, the mean SBP and DBP were higher in patients with HMOD than in those without HMOD. The BPs within 1 h and at discharge were also higher in patients with HMOD.
Table 2.
Antihypertensive drugs used to control blood pressure for patient with very severe acute hypertension in ED
| All patients (n = 1,391) |
Patients with HMOD (n = 547) |
Patients without HMOD (n = 844) |
P value | |
|---|---|---|---|---|
| Oral antihypertensive drugs | 268 (19.3) | 106 (19.4) | 162 (19.2) | 0.932 |
| Calcium antagonistsa | 170 (12.2) | 38 (6.9) | 132 (15.6) | < 0.001 |
| Beta-blockerb | 62 (4.5) | 31 (5.7) | 31 (3.7) | 0.078 |
| Renin-angiotensin system inhibitorc | 22 (1.6) | 13 (2.4) | 9 (1.1) | 0.056 |
| Nitroglycerin | 73 (5.2) | 54 (9.9) | 19 (2.3) | < 0.001 |
| Intravenous antihypertensive drugs | 619 (44.5) | 432 (79.0) | 187 (22.2) | < 0.001 |
| Nicardipine | 453 (32.6) | 297 (54.3) | 156 (18.5) | < 0.001 |
| Labetalol | 35 (2.5) | 28 (5.1) | 7 (0.8) | < 0.001 |
| Esmolol | 14 (1.0) | 12 (2.2) | 2 (0.2) | < 0.001 |
| Nitroglycerin | 211 (15.2) | 173 (31.6) | 38 (4.5) | < 0.001 |
| Cessation due to iatrogenic hypotension | 71 (5.1) | 41 (7.5) | 30 (3.6) | 0.048 |
HMOD hypertension-mediated organ damage
aCalcium antagonists included amlodipine and nifedipine
bBeta-blocker included carvedilol, nebivolol, propranolol, atenolol, and bisoprolol
cRenin-angiotensin system inhibitor included perindopril, candesartan, losartan, and fimasartan
Fig. 2.
Blood pressure changes in the emergency department in patients with very severe acute hypertension according to hypertension-mediated organ damage
Patterns of HMOD and principal diagnosis at discharge
Among the 547 patients with HMOD, acute ischemic stroke was the most common (28.7%), followed by acute heart failure, intracerebral hemorrhage, acute coronary syndrome, acute kidney injury, subarachnoid hemorrhage, hypertensive encephalopathy, hypertensive retinopathy, and aortic dissection (Supplementary Table S1). Among the 1,391 patients, neurologic disorders, including ischemic stroke, hemorrhagic stroke, and seizures, were the most common primary diagnoses (29.3%) at discharge (Supplementary Table S2), followed by cardiovascular disorders (25.6%).
Clinical outcomes during the follow-up period
Overall, 755 (54.3%) patients were admitted, 487 (35.0%) were discharged, 146 (10.5%) were discharged against medical advice, and 3 (0.2%) died in the ED (Table 3). Most of the patients with HMOD (91.4%) were admitted to the general ward or intensive care units (ICU), and patients without HMOD were significantly more commonly discharged from the ED than those with HMOD (56.4% vs. 2.0%, P < 0.001).
Table 3.
Clinical outcome according to follow-up duration
| All patients (n = 1,391) |
Patients with HMOD (n = 547) |
Patients without HMOD (n = 844) |
P value | |
|---|---|---|---|---|
| Mortality rate within 1-month | 72 (5.2) | 50 (9.1) | 22 (2.6) | < 0.001 |
| Mortality rate within 3-months | 106 (7.6) | 71 (13.0) | 35 (4.1) | < 0.001 |
| Mortality rate within 1-year | 166 (11.9) | 99 (18.1) | 67 (7.9) | < 0.001 |
| Mortality rate within 3-years | 241 (17.3) | 136 (24.9) | 105 (12.4) | < 0.001 |
| Admission | 755 (54.3) | 500 (91.4) | 255 (30.2) | < 0.001 |
| Discharge at ED | 487 (35.0) | 11 (2.0) | 476 (56.4) | < 0.001 |
| Discharge against medical advice | 146 (10.5) | 35 (6.4) | 111 (13.2) | < 0.001 |
| Death in the emergency department | 3 (0.2) | 1 (0.2) | 2 (0.2) | 0.832 |
HMOD hypertension-mediated organ damage, ED emergent department
Among 1,391 patients, 214 (17.3%) died within 3 years, and the mortality rates increased over time from 1 month to 3 years. In particular, patients with HMOD had a significantly higher mortality rate at each time point than those without HMOD. Figure 3 shows the cumulative mortality rate in all patients according to the presence of HMOD using the Kaplan–Meier curves. Patients with HMOD had a significantly higher cumulative mortality rate than those without HMOD (log-rank P < 0.001).
Fig. 3.
Cumulative mortality rate in all patients and in those stratified according to the presence of hypertension-mediated organ damage
Of all patients, except 72 who died within a month, 1,009 (76.5%) of those discharged from the ED or after hospitalization attended their follow-up appointment (85.9% of patients with HMOD and 70.8% of those without HMOD). Among these patients, especially in patients with HMOD, the 1-year mortality rate was significantly higher in patients who were lost to follow-up than in those who were kept on follow-up appointments (20.0% vs. 8.2%, P = 0.002) (Supplementary Table S3).
Discussion
Based on the results of our study, the mortality rate within 3 years of patients who visited the ED for very severe acute hypertension was 17.3%, and especially, those with HMOD had worse prognosis. Although half of the patients (50.2%) were aware of their history of hypertension in this study, only 61.1% of them were taking antihypertensive drugs, suggesting that uncontrolled hypertension exists in patients receiving treatment as well as in untreated patients. Patients with very severe acute hypertension were most often diagnosed with neurologic disorders when discharged, and ischemic stroke was the most common among patients with HMOD.
Severe acute BP elevation is a prevalent and significant problem in patients visiting the ED. Although the BP criteria for severe hypertension follow the international practice guidelines for hypertension, there are no established criteria or definitions for BP that increases to a level that is significantly higher than that observed in severe hypertension [5, 6]. In addition, there are recommendations only for specific conditions in the treatment of patients presenting with very severe acute hypertension. In the European Society of Cardiology and European Society of Hypertension guidelines, for patients with a markedly elevated SBP or DBP (SBP of ≥ 220 mmHg, DBP of ≥ 120 mmHg), BP-lowering management is only mentioned in the presence of the acute phase of hemorrhagic and ischemic stroke [6]. Similarly, in the American College of Cardiology/American Heart Association guidelines, recommendations about BP-lowering management for patients with a markedly elevated BP of SBP higher than 220 mmHg are only described in the cerebrovascular disease part [5]. Acute intracerebral hemorrhage is common in patients with very severe acute hypertension (SBP of ≥ 220 mmHg and/or DBP of ≥ 120 mmHg), and these patients have an increased risk of death as well as a worse prognosis for neurologic recovery [11, 12]. However, few studies have evaluated patients visiting the ED for very severe acute hypertension regardless of the specific target organ damage, and there are few reports on the incidence rates, treatment status, and long-term prognosis. Our study showed that 0.8% (1,391 of 172,105) of patients who visited the ED during the study period had very severe acute hypertension and 60.7% (844 of 1,391) of patients with very severe acute hypertension had no HMOD. To the best of our knowledge, this study is the first to reveal antihypertensive drugs and clinical prognosis for very severe acute hypertension regardless of HMOD, which is rare but critical in the ED. In a previous study, Preston et al. [13] showed that 147 patients presenting to the ED at a single center with an SBP of ≥ 220 mmHg or DBP of ≥ 120 mmHg were evaluated for prognosis including repeat visits, target organ events, and hospitalizations for 2 years. They showed an increased risk of repeat visits (n = 389), new target organ events (n = 99), and hospitalizations (n = 76) in patients with very severe acute hypertension. While they did not reveal mortality data, we presented 1-month, 3-month, 1-year, and 3-year mortality data for a larger number of 1,391 patients and found that patients with very severe acute hypertension had a poor prognosis and high all-cause mortality rate within 3 years. Recently, we reported that the 1- and 3-year mortality rates for patients with severe acute hypertension were 8.8% and 13.9%, respectively [7]. In comparison, the 1- and 3-year mortality rates for patients with very severe acute hypertension in the present study were higher at 11.9% and 17.3%, respectively. We also showed the distribution of HMOD accompanied by very severe acute hypertension that acute ischemic stroke accounted for the most frequent HMOD, but acute heart failure, intracerebral hemorrhage, and acute coronary syndrome were also important accompanying organ damage. In addition, since neurologic and cardiovascular disorders account for most of the principal diagnoses at discharge, we suggest that the concept of a marked increase in the BP due to these causes should be considered when patients with very severe acute hypertension are encountered.
Since the guidelines recommend intravenous antihypertensive drugs for the treatment of BP-lowering in patients with HE [5, 6], intravenous antihypertensive drugs were prescribed significantly more for patients with very severe acute hypertension with HMOD in our study. Among the intravenous antihypertensive drugs recommended in the guidelines, nicardipine was administered the most, followed by nitroglycerine. Based on the results of our study, in addition to the worse clinical prognosis of very severe acute hypertension, the HMOD group had a significantly worse prognosis; therefore, more aggressive BP-lowering treatment would be needed than that in the non-HMOD group. Generally, it is recommended that patients with HMOD be treated in an ICU for close monitoring and reduction of the BP with parenteral antihypertensive drugs [5]. However, in our study, 8.4% of the patients with HMOD were discharged from the ED, and most of them were discharged against medical advice. Since the rate of follow-up loss among patients who were discharged from the ED was relatively high and the follow-up loss was associated with high mortality, the importance of hospitalization in patients with HMOD should be emphasized.
To our knowledge, we are the first to show the long-term natural course, including mortality, of patients who visit the ED due to acutely elevated blood pressure. Especially, a higher BP criterion (SBP of > 220 mmHg and/or a DBP of > 120 mmHg) could at least partially ameliorate the effect of typically transient BP elevations in acute ED settings. Very severe acute hypertension is associated with adverse outcomes and high utilization of medical services. In this context, understanding the natural processes, including all-cause mortality, in patients with very severe acute hypertension is pivotal in planning the basis for improving healthcare and prognosis.
Limitations
This study has some limitations. First, this was a retrospective study. There were missing data on variables highly related to very severe acute hypertension, such as alcohol consumption, smoking status, and drug history. We only examined the current status of antihypertensive drug usage but did not investigate its status following discharge. Second, this study was a single-center experience, which may not be representative of the entire population. However, the number of study patients was large, and meaningful results were derived from this. Third, the follow-up measurement of the BP in the ED was insufficient, especially for the patients in the non-HMOD group; the subsequent BP data were insufficient because the BP was not significantly measured after 1 h and at discharge. In particular, if there were data on the time when the target BP was reached, it would have been possible to quantitatively explain the outcomes. Further research regarding the clinical outcomes and presence of HMOD according to the time taken to control BP in patients with acute severe hypertension who visited the ED is needed. Finally, our study was unable to present cardiovascular mortality because there were no data available on the cause of death for the National Health Insurance Service. However, the data provided by the National Health Insurance Service on all-cause mortality and the date of death are accurate and reliable.
Conclusions
An SBP of > 220 mmHg and/or DBP of > 120 mmHg (very severe acute hypertension) is frequently accompanied by neurologic disorders, such as ischemic stroke, and patients with very severe acute hypertension have poor long-term clinical prognosis. In particular, both HMOD and non-HMOD groups had high all-cause mortality rate, although a significant difference in mortality rates was noted between the two groups. Clinicians should closely monitor and actively manage patients with very severe acute hypertension in the ED.
Supplementary Information
Additional file 1: Supplementary Table 1. Distribution of acute hypertension mediated-organ damage. Supplementary Table 2. Principaldiagnosis at discharge of all patients. Supplementary Table 3. Mortality rates at 3 monthsand 1 year according to follow-up visits.
Acknowledgements
None declared.
Abbreviations
- BNP
B-type natriuretic peptide
- BP
Blood pressure
- CT
Computed tomography
- DBP
Diastolic blood pressure
- ECG
Electrocardiography
- ED
Emergency department
- eGFR
Estimated glomerular filtration rate
- HE
Hypertensive emergency
- HMOD
Hypertension-mediated organ damage
- ICU
Intensive care units
- MRI
Magnetic resonance imaging
- SBP
Systolic blood pressure
Authors’ contributions
H-JK contributed to conceptualization, study design, data collection, data analysis, and data interpretation, drafted the article, was a major contributor in writing the manuscript. BSK was responsible for study design, data collection, data analysis, data interpretation, manuscript preparation, and also was an equally major contributor in writing the manuscript. J-HS was responsible for study design, data interpretation, and manuscript preparation. All authors read and approved the final manuscript.
Funding
This research was supported by grant KSH-R-2019–01 from the Korean Society of Hypertension.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Declarations
Ethics approval and consent to participate
This study was approved by the Institutional Review Board of the Hanyang University Guri Hospital and waived the requirement for written informed consent.
Consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
Footnotes
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Hyun-Jin Kim and Byung Sik Kim contributed equally to this work.
References
- 1.Fuchs FD, Whelton PK. High Blood Pressure and Cardiovascular Disease. Hypertens. 2020;75:285–292. doi: 10.1161/HYPERTENSIONAHA.119.14240. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Kim HC, Cho SMJ, Lee H, Lee HH, Baek J, Heo JE, et al. Korea hypertension fact sheet 2020: analysis of nationwide population-based data. Clin Hypertens. 2021;27:8. doi: 10.1186/s40885-021-00166-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Camafort M, Redon J, Pyun WB, Coca A. Intensive blood pressure lowering: a practical review. Clin Hypertens. 2020;26:21. doi: 10.1186/s40885-020-00153-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Chobanian AV, Bakris GL, Black HR, Cushman WC, Green LA, Izzo JL, Jr, et al. Seventh report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure. Hypertens. 2003;42:1206–1252. doi: 10.1161/01.HYP.0000107251.49515.c2. [DOI] [PubMed] [Google Scholar]
- 5.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: Executive Summary: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. Hypertens. 2018;71:1269–1324. doi: 10.1161/HYP.0000000000000066. [DOI] [PubMed] [Google Scholar]
- 6.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. Eur Heart J. 2018;39:3021–3104. doi: 10.1093/eurheartj/ehy339. [DOI] [PubMed] [Google Scholar]
- 7.Kim BS, Kim HJ, Lyu M, Kim WD, Lee Y, Kim M, Lee S, Park JK, Shin J, Shin H, Kim C, Shin JH. Clinical characteristics, practice patterns, and outcomes of patients with acute severe hypertension visiting the emergency department. J Hypertens. 2021;39(12):2506–2513. doi: 10.1097/HJH.0000000000002960. [DOI] [PubMed] [Google Scholar]
- 8.Saladini F, Mancusi C, Bertacchini F, Spannella F, Maloberti A, Giavarini A, et al. Diagnosis and treatment of hypertensive emergencies and urgencies among Italian emergency and intensive care departments. Results from an Italian survey: Progetto GEAR (Gestione dell’Emergenza e urgenza in ARea critica) Eur J Intern Med. 2020;71:50–6. doi: 10.1016/j.ejim.2019.10.004. [DOI] [PubMed] [Google Scholar]
- 9.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;5:37–46. doi: 10.1093/ehjcvp/pvy032. [DOI] [PubMed] [Google Scholar]
- 10.White SL, Yu R, Craig JC, Polkinghorne KR, Atkins RC, Chadban SJ. Diagnostic accuracy of urine dipsticks for detection of albuminuria in the general community. Am J Kidney Dis. 2011;58:19–28. doi: 10.1053/j.ajkd.2010.12.026. [DOI] [PubMed] [Google Scholar]
- 11.Rodriguez-Luna D, Pineiro S, Rubiera M, Ribo M, Coscojuela P, Pagola J, et al. Impact of blood pressure changes and course on hematoma growth in acute intracerebral hemorrhage. Eur J Neurol. 2013;20:1277–1283. doi: 10.1111/ene.12180. [DOI] [PubMed] [Google Scholar]
- 12.Sakamoto Y, Koga M, Yamagami H, Okuda S, Okada Y, Kimura K, et al. Systolic blood pressure after intravenous antihypertensive treatment and clinical outcomes in hyperacute intracerebral hemorrhage: the stroke acute management with urgent risk-factor assessment and improvement-intracerebral hemorrhage study. Stroke. 2013;44:1846–1851. doi: 10.1161/STROKEAHA.113.001212. [DOI] [PubMed] [Google Scholar]
- 13.Preston RA, Arciniegas R, DeGraff S, Materson BJ, Bernstein J, Afshartous D. Outcomes of minority patients with very severe hypertension (>220/>120 mmHg) J Hypertens. 2019;37:415–425. doi: 10.1097/HJH.0000000000001906. [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Additional file 1: Supplementary Table 1. Distribution of acute hypertension mediated-organ damage. Supplementary Table 2. Principaldiagnosis at discharge of all patients. Supplementary Table 3. Mortality rates at 3 monthsand 1 year according to follow-up visits.
Data Availability Statement
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.