| Home | E-Submission | Sitemap | Contact Us |  
Korean J Intern Med > Volume 30(6); 2015 > Article
Kang, Oh, Lee, and Lee: Survival benefits of warfarin in Korean patients with idiopathic pulmonary arterial hypertension



Idiopathic pulmonary arterial hypertension (IPAH) is an incurable disease with high mortality. Although most studies recommend anticoagulation treatment for IPAH, the benefits are uncertain, particularly in Korea, where it has not been studied. The purpose of this study was to evaluate survival outcomes of Korean patients with IPAH treated with warfarin.


We performed a retrospective cohort study of patients diagnosed previously with pulmonary arterial hypertension (PAH) at the Asan Medical Center in Korea, between January 1994 and February 2013. We excluded patients with associated PAH, patients who did not undergo right heart catheterization (RHC), and patients with a positive vasoreactivity test. Patients in the study cohort were classified into a “warfarin group” and a “non-warfarin group,” according to the treatment they received during the first year after diagnosis.


We identified 31 patients with IPAH and a negative vasoreactivity test on RHC. Median patient age was 36.0 years, and 23 patients (74.2%) were female. The median time from the onset of symptoms to diagnosis was 19.0 months, and the most common presenting symptom was dyspnea. Survival rates of the patients at 1, 3, 5, and 10 years were 90.2%, 79.5%, 62.7%, and 34.8%, respectively. The mean survival period was 12.0 years in the warfarin group and 6.1 years in the non-warfarin group. Warfarin treatment had significant survival benefits in patients with IPAH (p = 0.023).


Warfarin treatment substantially improved survival outcomes in Korean cases of IPAH.


Idiopathic pulmonary arterial hypertension (IPAH) is a rare and incurable disease that is not associated with an identifiable cause or family history and is categorized as group 1.1 in the Nice classification system [1]. As pulmonary vascular resistance (PVR) and right heart failure progresses in patients with IPAH, several symptoms may present, including dyspnea, chest pain, fatigue, peripheral edema, and syncope. Without appropriate treatment, the median survival period in IPAH cases is 2.8 years [2]. Many studies have been conducted to determine the best management approach for IPAH. An important pathophysiological finding of IPAH is thrombotic arteriopathy, which influences disease development if it progresses [3]. Biomarkers associated with hypercoagulability, such as fibrinogen, tissue plasminogen activator, plasminogen activator inhibitor-1, and von Willebrand factor, also increase in patients with IPAH [3,4]. In accordance with these findings, anticoagulation therapy with warfarin improves survival of patients with IPAH [5-9]. A recent large prospective cohort study also demonstrated a survival benefit from anticoagulation in patients with IPAH [10].
The full benefits and role of anticoagulation in the treatment of IPAH remain uncertain; however, some reports have suggested that warfarin has limited survival benefit in cases of IPAH [11,12] but no prospective randomized controlled studies of this treatment have been performed. In addition, these earlier studies mostly originated from Western countries [5,6,8-12], and there is no comparable warfarin treatment study on Korean patients with IPAH. The purpose of this study was to evaluate the survival benefits of warfarin in an IPAH cohort from a Korean tertiary hospital.


Study design and subjects

We performed a retrospective cohort study of patients > 20 years of age with a diagnosis of pulmonary arterial hypertension (PAH) made by one pulmonologist at a tertiary hospital in Korea between January 1994 and February 2013. To exclude patients with associated PAH, we reviewed the medical history (medications and previously diagnosed diseases) and test results (chest computed tomography [CT], ventilation/perfusion scan, echocardiography, liver ultrasonography, pulmonary function test [PFT], autoantibody test, liver function test, and human immunodeficiency virus test) for each patient. We then selected patients with IPAH who had undergone right heart catheterization (RHC) and excluded cases that did not meet the PAH diagnostic criteria, i.e., mean pulmonary artery pressure (PAP) > 25 mmHg, pulmonary capillary wedge pressure < 15 mmHg, and PVR > 3 Wood units at rest on RHC. We also excluded patients with IPAH who had positive vasoreactivity on RHC, which typically indicates a slower disease progression and a better prognosis than patients with a negative vasoreactivity test [6,13]. A positive vasoreactivity test is defined as a reduction in mean PAP ≥ 10 mmHg and an absolute final mean PAp < 40 mmHg without a decrease in cardiac output (CO). We divided the patients with IPAH confirmed to have negative vasoreactivity by RHC into a “warfarin group” or a “non-warfarin group” based on taking warfarin within 1 year of the diagnosis. This study was approved by the Institutional Review Board of Asan Medical Center. Because this was a retrospective study, the requirement for informed consent was waived. We used unique identifier numbers to maintain patient confidentiality.

Outcome measures

We evaluated the survival effects of warfarin on IPAH by comparing patient survival periods in the warfarin and non-warfarin groups. We judged survival status of the patients using the hospital electronic medical records or Korean National Health Insurance data. The survival period was calculated from the day of diagnosis to death or the last hospital follow-up day, and was compared between groups using the Kaplan-Meier method and the log-rank test.

Baseline data collection

We collected clinical and hemodynamic data on the patients with IPAH at the initial diagnosis, including sex, age, body mass index, smoking history, time from onset of symptoms to diagnosis, symptoms at admission, World Health Organization (WHO) dyspnea functional class, laboratory findings, PFT, echocardiography, RHC, chest CT, and medications. Another pulmonologist reviewed all patient medical records, hemodynamic variables, and vessel diameter on chest CT at least twice. To improve accuracy, all data were rechecked by two other specialists in the respiratory division.

Pulmonary function test

We measured diffusing capacity (DLCO) routinely and performed a 6-minute walk test according to the American Thoracic Society guidelines [14]. DLCO was measured using a single breath technique and the Vmax ENCORE 22 (CareFusion Corp., San Diego, CA, USA). The measurements were compared to predicted values using reference equations from Park and the European Community for Steel and Coal [15,16].


We evaluated ejection fraction (EF), left ventricular end-diastolic diameter (LVEDD), right ventricular end-diastolic diameter (RVEDD), and tricuspid regurgitation velocity by echocardiography. Echocardiography was usually performed using a Philips iE33 ultrasound system (Philips Healthcare, Andover, MA, USA). EF was measured by collating several methods and using the Quinones formula based on the parasternal views or using the quantitative two-dimensional biplane volumetric Simpson method from four- and two-chamber views [17,18]. LVEDD and RVEDD were measured using the two-dimensional linear or M-mode method from the parasternal long-axis view or the apical four-chamber view [18,19]. Systolic PAP was calculated using the trans-tricuspid gradient plus right atrial pressure (RAP), where the trans-tricuspid gradient is 4v2 (v = peak velocity of tricuspid regurgitation, m/second), and RAP was empirically estimated to be 10 mmHg [20]. Mean PAP was calculated from the equation: mean PAP = 0.61 × systolic PAP + 2 mmHg [21].

Right heart catheterization

We routinely performed RHC in our medical intensive care unit using a Swan-Ganz catheter (Swan-Ganz continuous CO/end diastolic volume thermodilution catheter models 777F8 or 777HF8, Edwards Lifesciences, Irvine, CA, USA) and a vigilance monitor (Edwards Lifesciences). We checked hemodynamic variables, such as systolic PAP, mean PAP, diastolic PAP, pulmonary capillary wedge pressure (PCWP), and CO, using the thermodilution method, as well as the response to the vasoreactivity test. PVR was estimated using RHC data and the formula: (mean PAP – PCWP) / CO. The cardiac index (CI) was calculated from the following formula: CI = CO / body surface area.

Chest computed tomography

We reviewed chest CT images using medical analysis software (PetaVision). We calculated the pulmonary artery to aorta ratio by measuring the diameter of the main pulmonary artery and the aorta at the level of the bifurcation of the left and right main pulmonary arteries. We repeated this process at least twice to increase accuracy.

Statistical analysis

Data are expressed as median (interquartile range) or as number (%). The clinical characteristics of the patients were analyzed using the Mann-Whitney U test and the chi-square test. Patient survival was analyzed by Cox-regression analysis and the Kaplan-Meier method. A p < 0.05 was significant. All analyses were performed with SPSS version 19 (IBM Co., Armonk, NY, USA).


A total of 85 patients with PAH were enrolled initially in our study. We isolated the patients with IPAH by excluding 16 patients with associated PAH (connective tissue disease [11], congenital heart disease [4], and portal hypertension [1]). Among the remaining 69 patients with IPAH, we further excluded 12 patients who did not undergo RHC, 20 who were not compatible with the PAH diagnostic criteria, and six with positive vasoreactivity on RHC. Of the final group of 31 patients with IPAH and a negative vasoreactivity test on RHC, 10 received warfarin (warfarin group) and 21 were treated without warfarin (non-warfarin group) within the first year after the diagnosis (Fig. 1).
The warfarin treatment international normalized ratio target was 1.5 to 2.5. The baseline characteristics of the study patients and both subgroups are presented in Table 1. Our study patients were young and predominantly female. The median time (interquartile range) from onset of symptoms to diagnosis was 19.0 months (interquartile range, 6.0 to 36.0). All PAH treatment drugs other than warfarin that were used within the first year from the IPAH diagnosis are listed in Table 2. Most of the patients received other treatments for IPAH, including conventional therapies (oxygen supplementation, digoxin, and diuretic therapy) and targeted therapies (prostanoids, endothelin receptor antagonists, and phosphodiesterase type 5 inhibitors) [22]. No differences were detected in the baseline characteristics or treatments between the warfarin and non-warfarin groups. The echocardiographic and RHC findings of the patients were compatible with PAH (Table 3). The hemodynamics findings, as measured by RHC, were similar with those of echocardiography. The diameter of the main pulmonary artery was larger than that of the aorta, as shown in Table 4 (median ratio of the pulmonary artery to the aorta, 1.2).
We analyzed survival in our patients using the Kaplan-Meier method (Fig. 2). The median follow-up period was 8.5 years, during which 14 patients died. The overall survival rates of the patients at 1, 3, 5, and 10 years were 90.2%, 79.5%, 62.7%, and 34.8%, respectively. The warfarin group had 2-fold higher mean survival (12.0 years in the warfarin group vs. 6.1 years in the non-warfarin group, p = 0.023). Survival rates at 1, 3, 5, and 10 years were 100.0%, 100.0%, 88.9%, and 74.1%, respectively, in the warfarin group, and 85.7%, 69.7%, 48.9%, and 16.3%, respectively, in the non-warfarin group. We also analyzed factors influencing survival using Cox regression analysis (Table 5). Both univariate and multivariate Cox regression analyses demonstrated that high mean PAP was negatively associated with survival, and use of warfarin was positively associated with survival.


This is the first Korean study to evaluate the efficacy of warfarin on long-term survival of patients with IPAH. We analyzed patients with IPAH > 20 years old with negative vasoreactivity confirmed by RHC between January 1994 and February 2013. Because a positive vasoreactivity test is associated with a good prognosis [6] and all IPAH patients with a positive vasoreactivity test were assigned to the non-warfarin group, we excluded such cases and analyzed the survival effect of warfarin in Korean patients with IPAH. As shown in Table 1, the baseline characteristics of the study patients were similar to those from the National Institutes of Health (NIH) and Chinese registries [23,24]. Our study patients were young and predominantly female, and dyspnea was the most common presenting symptom. The NIH registry, the Chinese registry, and our study patients were diagnosed approximately 2 years after symptom onset, showing that an early IPAH diagnosis remains difficult. In our current study, bosentan was not combined with the warfarin treatment (Table 2), as it can significantly reduce maximum prothrombin time (23% to 38%) [25].
We observed that survival in the warfarin group was greater than that in the non-warfarin group. The main pathophysiological findings in patients with IPAH are prothrombotic abnormalities and in situ thrombosis [10]. We believe that warfarin prevents this coagulation cascade from progressing and improves survival of patients with IPAH. No significant differences were observed between the two groups in baseline characteristics, drug treatment, hemodynamic variables measured by echocardiography and RHC, or vessel diameter on chest CT, consistent with previous studies [5-9]. We speculate that the lower WHO functional class, which has a tendency for more use of targeted agents, including sildenafil, iloprost, and ambrisentan in the warfarin group than those in the non-warfarin group, may have affected the survival outcomes of the groups.
As mentioned previously, the survival benefits of anticoagulation therapy in patients with IPAH was recently studied in a large prospective cohort [10]. Although the primary outcomes were similar between this previous study and our current analysis, the patients in that study had different baseline characteristics from those in our series (older, fewer females, higher WHO functional class, and shorter 6-minutes walking distance but lower mean PAP) and were also different from those recorded in most other PAH registries [23,24,26-28]. No prospective randomized controlled studies have been conducted on warfarin as a treatment for PAH; thus, this needs to be addressed in the future.
Here, we evaluated the survival benefits of warfarin in a group of carefully selected patients with IPAH confirmed by RHC with a negative vasoreactivity test, but our study had several limitations. First, our study population may have been subject to selection bias, as it originated from a single tertiary hospital in Korea. Therefore, our results may not be fully applicable to other community-based hospitals. Second, due to the retrospective nature of our analysis, some of the patient data including the RHC and/or chest CT findings were incomplete or difficult to decipher. Third, there may have been a lead-time bias between our two patient groups because of the long study period. Fourth, our study investigated a small sample size, i.e., only 10 warfarin patients and 21 non-warfarin patients. A larger sample size is required to make a more definitive conclusion about the efficacy of warfarin. Finally, our patients with IPAH were diagnosed by a single pulmonologist, which may have underestimated the prevalence of PAH in the initial cohort from which we selected our patients.
However, despite these limitations, this study is based on relatively long-term follow-up data and is the first to evaluate warfarin treatment in Korean patients with IPAH. Our findings suggest that warfarin has significant long-term survival benefits for patients with IPAH. The efficacy of anticoagulation therapy for treating IPAH is somewhat uncertain, but future prospective randomized studies are warranted to address this issue in Korean IPAH cases and patients with this condition in other countries.


1. Warfarin treatment may improve survival of Korean patients with idiopathic pulmonary arterial hypertension.

Conflict of interest

No potential conflict of interest relevant to this article was reported.

Figure 1.
Flow chart of the selection scheme used for patient enrollment.
Figure 2.
Survival analysis of the warfarin and non-warfarin groups using the Kaplan-Meier method.
Table 1.
Baseline characteristics of the patients with idiopathic pulmonary arterial hypertension in this study
Characteristic All patients (n = 31) Warfarin group (n = 10) Non-warfarin group (n = 21) p valuea
Sex > 0.999
 Male 8 (25.8) 2 (20.0) 6 (28.6)
 Female 23 (74.2) 8 (80.0) 15 (71.4)
Age at diagnosis, yr 36.0 (30.0–44.0) 32.5 (27.8–40.3) 36.0 (29.5–51.5) 0.186
Body mass index, kg/m2 22.1 (20.5–24.2) 22.3 (20.2–23.7) 21.8 (20.6–24.9) 0.746
Smoking > 0.999
 Non-smoker 22 (71.0) 7 (70.0) 15 (71.4)
 Smoker 9 (29.0) 3 (30.0) 6 (28.6)
Time from onset of symptoms to diagnosis, mon 19.0 (6.0–36.0) 16.5 (10.5–39.0) 21.0 (4.5–36.0) 0.755
Symptoms at admission
 Dyspnea on exertion 31/31 (100.0) 10/10 (100.0) 21/21 (100.0) > 0.999
 Chest pain 11/29 (37.9) 4/10 (40.0) 7/19 (36.8) > 0.999
 Syncope 5/18 (27.8) 3/8 (37.5) 2/10 (20.0) 0.608
 Hemoptysis 2/28 (7.1) 1/8 (12.5) 1/20 (5.0) 0.497
 Palpitation 8/25 (32.0) 4/9 (44.4) 4/16 (25.0) 0.394
 Pretibial pitting edema 8/22 (36.4) 2/8 (25.0) 6/14 (42.9) 0.649
WHO functional class 0.415
 Class I, II 17/27 (63.0) 4/8 (50.0) 13/19 (68.4)
 Class III, IV 10/27 (37.0) 4/8 (50.0) 6/19 (31.6)
Underlying disease
 Hypertension 5 (16.1) 0 5 (23.8) 0.147
 Hypothyroidism 2 (6.5) 1 (10.0) 1 (4.8) > 0.999
 Malignancy 2 (6.5) 0 1 (4.8) > 0.999
 Chronic kidney disease 1 (3.2) 0 1 (4.8) > 0.999
Pulmonary function test
 DLCO, pre-measure, % 74.5 (59.8–82.5) 70.5 (57.5–82.5) 74.5 (59.8–83.5) 0.650
(n = 30) (n = 10) (n = 20)
 6-minute walk distance, m 451.5 (363.3–487.0) 409.0 (260.0–487.0) 451.5 (384.5–486.8) 0.438
(n = 28) (n = 8) (n = 20)

Values are presented as number (%) or median (interquartile range).

WHO, World Health Organization; DLCO, diffusing capacity.

a Statistical comparisons of the data were performed using the chi-square test for categorical variables and the Mann-Whitney U test for continuous variables.

Table 2.
Treatments in the study cohort within the first year of diagnosis
Treatment All patients (n = 31) Warfarin group (n = 10) Non-warfarin group (n = 21) p valuea
Oxygen therapy 11 (35.5) 5 (50.0) 6 (28.6) 0.423
Digoxin therapy 8 (25.8) 1 (10.0) 7 (33.3) 0.222
Diuretic therapy 15 (48.4) 4 (40.0) 11 (52.4) 0.704
Beraprost 17 (54.8) 4 (40.0) 13 (61.9) 0.441
Bosentan 6 (19.4) 0 6 (28.6) 0.141
Sildenafil 7 (22.6) 4 (40.0) 3 (14.3) 0.172
Iloprost 4 (12.9) 2 (20.0) 2 (9.5) 0.577
Ambrisentan 1 (3.2) 1 (10.0) 0 0.323

Values are presented as number (%).

a Statistical comparisons of the data were performed using the chi-square test for categorical variables.

Table 3.
Hemodynamic variables of the warfarin and non-warfarin groups
Variable All patients (n = 31)
Warfarin group (n = 10)
Non-warfarin group (n = 21)
p valuea
No. Median (IQR) No. Median (IQR) No. Median (IQR)
Echocardiography findings
 EF, % 31 65.0 (60.0–69.0) 10 67.0 (58.8–75.3) 21 65.0 (60.0–68.0) 0.393
 LVEDD, mm 28 38.5 (35.0–43.8) 9 40.0 (34.5–43.0) 19 38.0 (35.0–44.0) 0.885
 RVEDD, mm 21 36.0 (32.5–40.0) 7 37.0 (36.0–39.0) 14 36.0 (30.5–41.0) 0.488
 Tricuspid regurgitation velocity, m/sec 31 4.5 (4.1–4.8) 10 4.5 (4.1–4.9) 21 4.6 (4.1–4.9) 0.819
 Systolic PAP, mmHgb 31 91.0 (77.2–102.2) 10 89.2 (76.4–104.1) 21 94.6 (75.6–104.1) 0.819
 Mean PAP, mmHgc 31 57.5 (49.1–64.3) 10 56.4 (48.6–65.5) 21 59.7 (48.1–65.5) 0.819
Right heart catheterization findings
 Systolic PAP, mmHg 30 89.0 (70.8–106.0) 9 89.0 (71.5–104.0) 21 89.0 (69.5–107.0) > 0.999
 Mean PAP, mmHg 31 59.0 (42.0–67.0) 10 59.5 (43.5–62.3) 21 57.0 (37.8–70.0) > 0.999
 Diastolic PAP, mmHg 30 39.0 (26.8–47.0) 9 33.0 (27.5–44.0) 21 39.0 (24.0–51.0) 0.625
 PVR, Woodd 31 11.9 (8.3–15.3) 10 11.1 (9.3–15.4) 21 12.5 (8.0–16.6) 0.852
 PCWP, mmHg 31 9.0 (8.0–10.0) 10 9.0 (7.5–10.0) 21 9.0 (7.5–12.5) 0.663
 CO, L/min 31 3.7 (3.4–4.6) 10 4.3 (3.6–4.5) 21 3.6 (3.2–4.6) 0.466
 CI, L/min/m2 31 2.4 (2.2–2.7) 10 2.6 (2.3–2.9) 21 2.4 (2.2–2.6) 0.250

IQR, interquartile range; EF, ejection fraction; LVEDD, left ventricular end diastolic diameter; RVEDD, right ventricular end diastolic diameter; PAP, pulmonary artery pressure; PVR, pulmonary vascular resistance; PCWP, pulmonary capillary wedge pressure; CO, cardiac output; CI, cardiac index.

a Statistical comparisons of the data were performed using the Mann-Whitney U test.

b Systolic PAP = 4v2 + 10 mmHg; v, tricuspid regurgitation velocity.

c Mean PAP = 0.61 × systolic PAP + 2 mmHg.

d PVR = (mean PAP − PCWP) / CO.

Table 4.
Aortic and pulmonary artery diameters of the warfarin and non-warfarin groups
Vessel diameter on chest CT All patients (n = 25) Warfarin group (n = 5) Non-warfarin group (n = 20) p valuea
Pulmonary artery diameter, mm 37.7 (35.0–42.7) 37.6 (33.1–39.6) 38.7 (34.7–43.1) 0.530
Aorta diameter, mm 29.7 (25.7–34.2) 29.7 (25.4–32.9) 28.8 (26.0–35.5) 0.717
Pulmonary artery:aorta ratio 1.2 (1.1–1.5) 1.3 (1.1–1.5) 1.2 (1.1–1.5) 0.869

Values are presented as median (interquartile range).

CT, computed tomography.

a Statistical comparisons of the data were performed using the Mann-Whitney U test.

Table 5.
Factors influencing survival in the patients with idiopathic pulmonary arterial hypertension by Cox regression analysis
Variable Univariate analysisa
Multivariate analysisa
p value OR (95% CI) p value OR (95% CI)
Sex 0.322 2.147 (0.474–9.726)
Age at diagnosis 0.514 0.983 (0.936–1.034)
WHO functional class (class I, II standards) 0.928 0.938 (0.233–3.770)
Hypertension 0.638 0.608 (0.077–4.825)
Hypothyroidism 0.060 14.248 (0.891–227.811)
Malignancy 0.676 0.046 (0.000–81,554.601)
Chronic kidney disease 0.648 0.046 (0.000–25,431.097)
DLCO, pre-measure % 0.625 0.990 (0.951–1.031)
6-minute walk distance, m 0.905 1.000 (0.995–1.005)
Mean PAP, measured by RHC 0.020b 1.035 (1.006–1.066) 0.031b 1.031 (1.003–1.059)
PVR, measured by RHC 0.066 1.067 (0.996–1.142)
Cardiac index, measured by RHC 0.486 0.712 (0.274–1.852)
Beraprost treatment 0.329 1.811 (0.550–5.961)
Bosentan treatment 0.241 2.262 (0.579–8.845)
Sildenafil treatment 0.178 0.244 (0.031–1.899)
Iloprost treatment 0.395 0.039 (0.000–70.010)
Warfarin treatment 0.039b 0.204 (0.045–0.926) 0.047b 0.210 (0.045–0.976)

OR, odds ratio; CI, confidence interval; WHO, World Health Organization; DLCO, diffusing capacity; PAP, pulmonary artery pressure; RHC, right heart catheterization; PVR, pulmonary vascular resistance.

a Statistical comparisons of the data were performed using Cox regression analysis.

b Statistically significant.


1. Simonneau G, Gatzoulis MA, Adatia I, et al. Updated clinical classification of pulmonary hypertension. J Am Coll Cardiol 2013;62(25 Suppl):D34–D41.
crossref pmid
2. D’Alonzo GE, Barst RJ, Ayres SM, et al. Survival in patients with primary pulmonary hypertension: results from a national prospective registry. Ann Intern Med 1991;115:343–349.
crossref pmid
3. Johnson SR, Granton JT, Mehta S. Thrombotic arteriopathy and anticoagulation in pulmonary hypertension. Chest 2006;130:545–552.
crossref pmid
4. Huber K, Beckmann R, Frank H, Kneussl M, Mlczoch J, Binder BR. Fibrinogen, t-PA, and PAI-1 plasma levels in patients with pulmonary hypertension. Am J Respir Crit Care Med 1994;150:929–933.
crossref pmid
5. Fuster V, Steele PM, Edwards WD, Gersh BJ, McGoon MD, Frye RL. Primary pulmonary hypertension: natural history and the importance of thrombosis. Circulation 1984;70:580–587.
crossref pmid
6. Rich S, Kaufmann E, Levy PS. The effect of high doses of calcium-channel blockers on survival in primary pulmonary hypertension. N Engl J Med 1992;327:76–81.
crossref pmid
7. Ogata M, Ohe M, Shirato K, Takishima T. Effects of a combination therapy of anticoagulant and vasodilator on the long-term prognosis of primary pulmonary hypertension. Jpn Circ J 1993;57:63–69.
crossref pmid
8. Roman A, Rodes-Cabau J, Lara B, et al. Clinico-hemodynamic study and treatment of 44 patients with primary pulmonary hypertension. Med Clin (Barc) 2002;118:761–766.
crossref pmid
9. Kawut SM, Horn EM, Berekashvili KK, et al. New predictors of outcome in idiopathic pulmonary arterial hypertension. Am J Cardiol 2005;95:199–203.
crossref pmid
10. Olsson KM, Delcroix M, Ghofrani HA, et al. Anticoagulation and survival in pulmonary arterial hypertension: results from the Comparative, Prospective Registry of Newly Initiated Therapies for Pulmonary Hypertension (COMPERA). Circulation 2014;129:57–65.
crossref pmid
11. Storstein O, Efskind L, Muller C, Rokseth R, Sander S. Primary pulmonary hypertension with emphasis on its etiology and treatment. Acta Med Scand 1966;179:197–212.
crossref pmid
12. Frank H, Mlczoch J, Huber K, Schuster E, Gurtner HP, Kneussl M. The effect of anticoagulant therapy in primary and anorectic drug-induced pulmonary hypertension. Chest 1997;112:714–721.
crossref pmid
13. Raffy O, Azarian R, Brenot F, et al. Clinical significance of the pulmonary vasodilator response during short-term infusion of prostacyclin in primary pulmonary hypertension. Circulation 1996;93:484–488.
crossref pmid
14. American Thoracic Society. Standardization of spirometry, 1994 update. Am J Respir Crit Care Med 1995;152:1107–1136.
15. Park JO, Choi IS, Park KO. Normal predicted values of single-breath diffusing capacity of the lung in healthy nonsmoking adults. Korean J Intern Med 1986;1:178–184.
crossref pmid pmc
16. Standardization of lung function testing in infants, children and adolescents. Paediatric Working Group, Cefalu, Palermo, October 4, 1982. Abstracts. Bull Eur Physiopathol Respir 1983;19:15P–24P.

17. Quinones MA, Waggoner AD, Reduto LA, et al. A new, simplified and accurate method for determining ejection fraction with two-dimensional echocardiography. Circulation 1981;64:744–753.
crossref pmid
18. Lang RM, Bierig M, Devereux RB, et al. Recommendations for chamber quantification: a report from the American Society of Echocardiography’s Guidelines and Standards Committee and the Chamber Quantification Writing Group, developed in conjunction with the European Association of Echocardiography, a branch of the European Society of Cardiology. J Am Soc Echocardiogr 2005;18:1440–1463.
crossref pmid
19. Shiran H, Zamanian RT, McConnell MV, et al. Relationship between echocardiographic and magnetic resonance derived measures of right ventricular size and function in patients with pulmonary hypertension. J Am Soc Echocardiogr 2014;27:405–412.
crossref pmid pmc
20. Currie PJ, Seward JB, Chan KL, et al. Continuous wave Doppler determination of right ventricular pressure: a simultaneous Doppler-catheterization study in 127 patients. J Am Coll Cardiol 1985;6:750–756.
crossref pmid
21. Chemla D, Castelain V, Humbert M, et al. New formula for predicting mean pulmonary artery pressure using systolic pulmonary artery pressure. Chest 2004;126:1313–1317.
crossref pmid
22. Ikeda D, Tsujino I, Sakaue S, et al. Pilot study of short-term effects of a novel long-acting oral beraprost in patients with pulmonary arterial hypertension. Circ J 2007;71:1829–1831.
crossref pmid
23. Rich S, Dantzker DR, Ayres SM, et al. Primary pulmonary hypertension: a national prospective study. Ann Intern Med 1987;107:216–223.
crossref pmid
24. Jing ZC, Xu XQ, Han ZY, et al. Registry and survival study in Chinese patients with idiopathic and familial pulmonary arterial hypertension. Chest 2007;132:373–379.
crossref pmid
25. Weber C, Banken L, Birnboeck H, Schulz R. Effect of the endothelin-receptor antagonist bosentan on the pharmacokinetics and pharmacodynamics of warfarin. J Clin Pharmacol 1999;39:847–854.
crossref pmid
26. Humbert M, Sitbon O, Chaouat A, et al. Pulmonary arterial hypertension in France: results from a national registry. Am J Respir Crit Care Med 2006;173:1023–1030.
crossref pmid
27. Tueller C, Stricker H, Soccal P, et al. Epidemiology of pulmonary hypertension: new data from the Swiss registry. Swiss Med Wkly 2008;138:379–384.
28. Badesch DB, Raskob GE, Elliott CG, et al. Pulmonary arterial hypertension: baseline characteristics from the REVEAL Registry. Chest 2010;137:376–387.
crossref pmid
Editorial Office
101-2501, Lotte Castle President, 109 Mapo-daero, Mapo-gu, Seoul 04146, Korea
Tel: +82-2-2271-6792   Fax: +82-2-790-0993    E-mail: kaim@kams.or.kr
Copyright © 2019 The Korean Association of Internal Medicine. All rights reserved.
About |  Browse Articles |  Current Issue |  For Authors and Reviewers
powerd by m2community