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ORIGINAL ARTICLE
Year : 2014  |  Volume : 9  |  Issue : 4  |  Page : 209-215
Pulmonary arterial hypertension in Saudi Arabia: Patients' clinical and physiological characteristics and hemodynamic parameters. A single center experience


1 Division of Pulmonary Medicine, Department of Medicine, PSMMC, Riyadh, Saudi Arabia
2 Department of Pediatric Cardiology, Section of Congenital Heart Disease, PSCC, Riyadh, Saudi Arabia
3 High Institute of Public Health, Alexandria University, Alexandria, Egypt
4 Department of Cardiac Sciences, Section of Adult Cardiology, King Khalid University Hospital, Riyadh, Saudi Arabia
5 Saudi Association for Pulmonary Hypertension, Riyadh, Saudi Arabia

Date of Submission14-Apr-2014
Date of Acceptance26-Jun-2014
Date of Web Publication4-Sep-2014

Correspondence Address:
M M Idrees
Division of Pulmonary Medicine, Prince Sultan Medical Military City, PO Box 7897 (C-110), Riyadh - 11159
Saudi Arabia
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DOI: 10.4103/1817-1737.140127

PMID: 25276239

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   Abstract 

Aims: The main objective of this study is to describe patients' clinical characteristics and physiological and hemodynamic parameters at the time of diagnosis in a pulmonary hypertension center in Saudi Arabia.
Materials and Methods: This study reports the results from a single pulmonary hypertension specialized center in Riyadh, Saudi Arabia, namely Prince Sultan Medical Military City/Cardiac Center (PSMMC & CC). Both newly diagnosed (incidence) and referred (prevalence) cases of pulmonary arterial hypertension are included. All characteristics, including clinical, physiological, and hemodynamic parameters at the time of diagnosis are described.
Results: A total of 107 patients were identified as having pulmonary arterial hypertension as diagnosed by right heart catheterization. The mean age at diagnosis was 36 (± 9) years, and there was a female preponderance of 62.6%. The mean duration between symptom onset and diagnosis was 27.8 (± 9.0) months. At the time of enrollment, 56.1% of patients were in functional class III and 16.8% were in functional class IV. Fifty five patients (51.4%) were diagnosed as idiopathic pulmonary arterial hypertension, 29 patients (27.1%) as congenital heart disease associated with pulmonary arterial hypertension, 16 patients (15.0%) as connective tissue diseases associated with pulmonary arterial hypertension, 4 patients (3.7%) as heritable pulmonary arterial hypertension, and 3 patients (2.8%) as portopulmonary hypertension.
Conclusion: This data highlights the current situation of pulmonary arterial hypertension in Saudi Arabia. Our patients are much younger than patients described in other international registries but still detected as late in the course of the disease. A majority of patients displays severe functional and hemodynamic compromise.


Keywords: Hemodynamics, pulmonary arterial hypertension, registry, Saudi Arabia, Saudi association for pulmonary hypertension, six minute walk test


How to cite this article:
Idrees M M, Al-Najashi K, Khan A, Al-Dammas S, Al-Awwad H, Batubara E, Al Otai A, Abdulhameed J, Fayed A, Kashour T, SAPH Registry Taskforce. Pulmonary arterial hypertension in Saudi Arabia: Patients' clinical and physiological characteristics and hemodynamic parameters. A single center experience. Ann Thorac Med 2014;9:209-15

How to cite this URL:
Idrees M M, Al-Najashi K, Khan A, Al-Dammas S, Al-Awwad H, Batubara E, Al Otai A, Abdulhameed J, Fayed A, Kashour T, SAPH Registry Taskforce. Pulmonary arterial hypertension in Saudi Arabia: Patients' clinical and physiological characteristics and hemodynamic parameters. A single center experience. Ann Thorac Med [serial online] 2014 [cited 2020 Oct 26];9:209-15. Available from: https://www.thoracicmedicine.org/text.asp?2014/9/4/209/140127



   Introduction Top


Pulmonary arterial hypertension (PAH) is characterized by progressive increase in pulmonary vascular resistance (PVR) and pulmonary artery pressure (PAP) that can lead to right heart failure and death. [1] The understanding of PAH pathobiology and the management of the disease have undergone significant advances during the last decade. Despite such improvement, PAH remains progressive and often fatal.

The National Institutes of Health (NIH) conducted the first registry of primary pulmonary hypertension (now known as idiopathic PAH [IPAH]) in the early 1980s. [2] Subsequently, a number of registries have been published to describe the natural history of PAH in different countries. [3],[4],[5],[6],[7] These registries have significantly improved our understanding on many aspects of PAH. The French registry of 674 adults with PAH has described the prevalence and incidence of the disease as well as the clinical and hemodynamic characteristics of IPAH patients. [3] Other surveys from America have focused mainly on the association between the environmental factors, particularly appetite suppressive drugs, and PAH. [8],[9] A large prospective study (REVEAL Registry) in USA has described the characteristics of the demographics, clinical course, hemodynamic features, and disease management of PAH patients. [4]

The prognostic markers in PAH include a composite of measures that includes clinical characteristics and physiological and hemodynamic parameters. The modified New York Heart Association (NYHA) functional class has been recognized as an important prognostic measure. Furthermore, exercise tolerance and biochemical and hemodynamic markers are also essential tools for categorizing PAH patients from both prognostic and therapeutic aspects.

The true burden of PAH in the Middle East and Saudi Arabia remains unknown, and the disease characteristics are yet to be determined. In the present study, we described the characteristics of PAH patients at the time of diagnosis in one center in Saudi Arabia.


   Materials and Methods Top


The present study describes the results of prospectively collected and longitudinally followed cohort of patients diagnosed with PAH (both incidence and prevalence cases) in one tertiary specialized pulmonary hypertension (PH) center, Prince Sultan Medical Military City and Cardiac Center (PSMMC&CC), in Saudi Arabia over 3-year period.

Between December 2009 and November 2012, all patients referred to the pulmonary hypertension unit with suspected or confirmed diagnosis of WHO group I disease (PAH) were screened by using echocardiograph.

The diagnostic right heart catheterization (RHC) was necessary to meet the study inclusion criteria. RHC was performed in resting position using the Saudi Association for Pulmonary Hypertension (SAPH) RHC protocol. If appropriate wedging was not possible, left ventricular end-diastolic pressure (LVEDP) was directly measured.

The study protocol was reviewed and approved by the Registry and Research taskforces of the Saudi Association of Pulmonary Hypertension and by the Research and Ethics Committee of Prince Sultan Medical Military City.

Participants

Patients with newly diagnosed (incidence case) or previously diagnosed (prevalence case) PAH were eligible for enrollment if they fulfilled the definition of pulmonary hypertension (PH) group I PAH, as per the Nice 5 th PH World Congress. [10] This includes patients with PAH that is idiopathic, heritable, or associated with congenital systemic-to-pulmonary shunts, connective tissue diseases, portal hypertension, drugs or toxins, HIV infection, or schistosomiasis.

The inclusion criteria were:

  1. Age ≥ 14
  2. PAH group 1 diseases (as described above)
  3. Mean pulmonary arterial pressure (mPAP) ≥ 25 mmHg at rest and pulmonary artery wedge pressure (PAWP) or LVEDP ≤ 15 mmHg, as measured by RHC.


Patients with splenectomy or hemoglobinopathies were excluded as this group has been moved from PAH group I diseases to PH group V diseases as per the Nice 5 th PH World recommendation.

Data was collected using the SAPH-modified diagnostic and treatment protocol. The baseline assessment includes medical and drugs history, onset of symptoms, time of diagnosis, modified NYHA functional class at time of diagnosis, tests used to diagnose PAH that include pulmonary function test (PFT) including diffusion capacity, high resolution chest computerized tomography scan (HRCT), CT pulmonary angiography, V/Q scan, abdominal ultrasound, hepatic virology screen and liver function tests, immune screening, Schistosoma titer, and HIV serology. PHA group I disease category was also identified at this stage.

Physiological assessment at the time of diagnosis includes six-minute walk test (6MWT), NT pro BNP level, and echocardiographic evaluation for pericardial effusion and right ventricular function (TAPSE score).

RHC for hemodynamic parameters was performed in all patients (except 2) and included mPAP, right atrial pressure (RAP), cardiac index (CI), PAWP or LVEDP, and PVR. Only idiopathic and congenital heart diseases patients underwent vasoreactive testing using intravenous or inhaled Iloprost as per the protocol. The positive vasoreactive response is defined as a drop in mPAP by more than 10 mmHg to reach an absolute value of less than 40 mmHg in response to administration of acute vasodilator agent.

Statistical analysis

Descriptive statistics in terms of mean, standard deviations and percentages were used to describe characteristics of the studied patients. Comparison of categorical variables was conducted by Chi-Square test or Fisher's exact test accordingly. After assessment of normality distribution of variables, Student t-test and ANOVA test were used if data had normal distribution whilst Mann-Whitney and Kruskal-Wallis test were used in skewed data. A P-value less than 0.05 was considered a significant test. SPSS version 17 was used for all statistical analysis.


   Results Top


A total of 128 patients with clinically suspected WHO group I PAH were evaluated. Of these, 107 patients (83.6%) met the study entry criteria and are described in this study [95 (89%) incidence cases and 12 (11%) prevalence cases]. Of those excluded, 2 patients had a normal RHC despite abnormal echocardiography (one patient had systemic sclerosis, SSc) and the other had pulmonary fibrosis with suspected "out of proportion" PAH); 4 patients had a high PAWP with normal transpulmonary gradient compatible with left-ventricular diastolic dysfunction; nine patients had WHO group IV chronic thromboembolic pulmonary hypertension (CTEPH); 3 patients had veno-occlusive disease (group I'), and 3 patients had WHO group III diseases. [Figure 1] illustrates the distribution of the study population.
Figure 1: The distribution of the study cohort RHC = Right heart catheterization, PAH = Pulmonary arterial hypertension, Pts., patients, WHO = World Health Organization, IPAH = Idiopathic pulmonary arterial hypertension, PAH-ACHD = Congenital heart disease-associated pulmonary arterial hypertension, PAH-ACTD = Connective tissue disease-associated pulmonary arterial hypertension, HPAH = Heritable pulmonary arterial hypertension, Po-APAH = Portal hypertension-associated pulmonary arterial hypertension (portopulmonary hypertension)

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Demographics

The mean age at diagnosis was 36 (± 9) years. Out of the 107 patients, 67 (62.6%) were female. Three patients (2.8%) were non-Saudi in origin (1 Sudanese, 1 Jordanian, and 1 Yemeni). Eighty-four patients (78.5%) were geographically from the central province. [Table 1] illustrates the demography of the patients enrolled in the study.
Table 1: Demography, clinical, and physiological characteristics of all patients

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Baseline clinical characteristics

At the time of diagnosis, 29 patients (27.1%) were in modified NYHA functional class II, 60 patients (56.1%) were in functional class III, and 18 patients (16.8%) were in functional class IV. In the whole cohort of patients, the mean (± SE) time from symptoms onset to diagnosis was 27.8 (± 9.0) months. Fifty-five patients (51.4%) were diagnosed as IPAH, 29 patients (27.1%) as PAH associated with congenital heart disease (PAH-ACHD), 16 patients (14.9%) as PAH associated with connective tissue disease (PAH-ACTD) [systemic sclerosis (n = 11), mixed connective tissue disease (n = 4), systemic lupus erythematosus (n = 1)], 4 patients (3.7%) as heritable pulmonary arterial hypertension (HPAH) [based on strong family history but genetic testing was not performed], and 3 patients (2.9%) as portopulmonary hypertension (PoPH) [all with hepatitis B virus and portal hypertension]. The HPAH subgroup patients were younger than the other subgroups (mean age 19 (± 2) years), while the PAH-ACTD patients subgroup were the eldest (mean age 49 (± 5) years) and had more severe symptoms at diagnosis. [Table 1] illustrates the baseline characteristics of the patients enrolled in the study.

Physiological and hemodynamics characteristics

The results of the physiological characteristics are shown in [Table 1]. Exercise capacity had been evaluated at the time of diagnosis in 104 patients (97.1%) by 6MWT. Cardiopulmonary exercise test was not performed in any patient. Echocardiograph results were available for all patients (100%) at the time of diagnosis. Systolic pulmonary arterial pressure estimation, TAPSE scoring, presence of pericardial effusion, and evaluation of diastolic and systolic function of the left ventricle were included in echocardiographic evaluation. Blood NT-pro BNP level was available in 80 patients (74.8%) at the time of diagnosis.

Diagnostic RHC was available in 105 patients (98.1%) at the time of diagnosis. Two patients were diagnosed as a very complex PAH-ACHD (complex single ventricle physiology with Eisenmenger), and both had previous cardiac cath done by their congenital heart disease specialist. The treating physician considered repeat RHC unnecessary and probably risky, and so the evaluation was made by echocardiography only.

The results of hemodynamics measurement are shown in [Table 2].
Table 2: Hemodynamic measurements of all patients

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Acute vasodilator challenge was performed in all 55 IPAH patients (100%) and in 17 patients (58.6%) of those diagnosed with PAH-ACHD. As per SAPH protocol, PAH-ACTD, HPAH, and PoPH patients were not tested for vasodilator challenge. Intravenous prostacyclin was used as the testing agent in 48 patients (66.5%), while inhaled Iloprost was used in 14 patients (19.4%) and IV adenosine in 10 patients (14.1%). The rate of positive acute vasodilator response was overall low and reported in 5 patients (6.9%) only.

Incidence versus prevalence cases

Incident cases were those newly diagnosed patients for whom diagnosis was first made during the recruitment phase of the study, while prevalent cases were those patients with a known diagnosis of PAH and referred to our center for further management.

Ninety-five (89%) incidence cases were diagnosed during the recruitment period, while 12 (11%) cases were referred to our center with an established diagnosis of PAH (prevalent cases). All prevalence cases had a repeat RHC at enrollment for complete hemodynamic study and confirmation of the diagnosis. Clinical and hemodynamic data for incident versus prevalent cases are shown in [Table 3].
Table 3: Clinical and hemodynamic data for incidence versus prevalence cases

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Finally, the correlation between the modified NYHA functional class and both physiological and hemodynamic parameters at the time of diagnosis is illustrated in [Table 4].
Table 4: Physiological & hemodynamic parameters according to NYHA FC at the time of diagnosis

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   Discussion Top


PAH is a disease characterized by progressive increase in PVR and PAP secondary to progressive narrowing of the pulmonary arteries lumen. [1] Such abnormality is caused in part by smooth muscle contraction secondary to the imbalance between the vasoconstrictive and vasodilator mediators produced by the injured endothelial cells. More importantly, vascular remodeling caused by abnormal proliferation of all layers of the pulmonary arteries combined with a state of apoptosis resistance have been recently recognized as the main cause behind the abnormal rise in PVR in PAH. [10],[11],[12],[13]

The first recognizable work on pulmonary hypertension was in year 1981, when NIH created a national registry of 187 patients with "primary" pulmonary hypertension". [2],[14] Such early effort has led to major advances in the understanding of this disease. More recently, it has been recognized that several diseases or conditions could be associated with PAH. These diseases share similar clinical and pathobiological features with IPAH. [15] During the last PH World congress 2013 in Nice, the classification of PH group was updated and PAH continues to be categorized as Group I diseases. This group includes IPAH, HPAH, drug- and toxin-induced PAH, and PAH associated with CHD, CTD, HIV, portopulmonary, and schistosomiasis. [16]

The present study describes the characteristics of PAH in the largest population of patients in Saudi Arabia to date. The clinical characteristics used in this study was limited to the modified NYHA functional class since this clinical parameter was found to have prognostic significance both at baseline [17] and follow up. [18] The physiological characteristics included 6 MWT, NT-pro BNP biomarker level, and TAPSE scoring as measured by echocardiography. 6MWT is a straightforward, safe, and reproducible test, which measures the distance walked in 6 minutes. It has been found to have a prognostic measure in PAH patients. [18],[19] Similarly, both NT-pro BNP and TAPSE scoring have also been found to carry prognostic values. [20],[21] Finally, hemodynamic characteristics included both diagnostic (mPAP and PAWP) and prognostic (RAP, CI, PVR, and vasoreactivity) parameters. [22],[23]

In the current study, 107 adult PAH patients (95 incident cases and 12 prevalent cases; [Table 1]) were included. The mean age of the whole cohort at the time of diagnosis was significantly lower than the mean age reported by other registries. [3],[4],[6],[7] This can probably be explained by the young age of the Saudi Arabian population, as more than 50% of the whole Saudi population is younger than 20 years of age.

The mean duration between symptom onset and diagnosis was unacceptably long (27.8 ± 9.0 months). As a result, 72.8% of the patients were in functional class III or IV at presentation. This delayed diagnosis is consistent with similar findings reported in many studies. [3],[4],[6] Because baseline modified NYHA functional class is a well-recognized predictor of outcome in PAH patients, the long duration of symptoms before establishing the diagnosis indicates insufficient awareness about the disease in Saudi Arabia. Alhamad et al., have recently published a single-center experience in managing PH in Saudi Arabia. [24] In his cohort of 112 PH patients, only 12 (10.7%) belonged to group I PAH, and almost all of them were related to IPAH and PAH-ACTD. Of interest, the reported symptoms duration before establishing the diagnosis was significantly shorter (7.3 ± 5.7 months) in that cohort.

IPAH was the most common subtype of PAH in our study. This observation has been recognized by other international registries. [3],[5],[25] Our IPAH patients were predominantly female and significantly older than the HPAH and PAH-ACHD patients but younger than PAH-ACTD (P < 0.001 between the groups). Similar to other registries, the majority of patients were at functional class III or IV at the time of diagnosis [Table 1].

PAH-ACHD patients were the second most common PAH subgroup and had the best physiological parameters compared to other groups. The high prevalence of PAH-ACHD in this cohort probably reflects the current practice of late detection of CHD patients in Saudi Arabia and delayed surgical corrections. Despite a relatively long duration of symptoms, those patients were more likely to be in modified NYHA functional class II compared to other group, although this did not reach the statistically significant level (P = 0.08 between the groups). Nevertheless, PAH-ACHD patients showed a significantly better physiological profile when compared to other PAH groups.

SSc was the leading cause of PAH-ACTD in our cohort. In SSc, the occurrence of PAH has been reported in more than 10% of patients and is known to have a major negative impact on outcome and survival. [26],[27] Currently, international guidelines recommend to screen all asymptomatic SSc patients on an annual basis. [28] Our PAH-ACTD patients were significantly older than the other groups (P < 0.001 between groups) and had the longest duration of symptoms before confirming the diagnosis (P < 0.001 between groups). This is presumably related to the presence of other comorbidities that might be associated with CTD and can also lead to pulmonary symptoms, such as interstitial lung disease, heart failure, or myopathy. Furthermore, PAH-ACTD patients had significantly more physiological limitation when compared to other PAH groups (P < 0.001).

HPAH patients were the youngest among the groups. Both HPAH and PoPH patients had the shortest symptoms duration before establishing the diagnosis compared to other groups (P < 0.001). This is presumably related to the lower threshold for making the diagnosis because of involvement of other family members, and because of the severity of the symptoms.

Finally, although schistosomiasis is prevalent in certain regions of Saudi Arabia, we could not identify a single PAH case related to this infectious process. This could be attributed to detection or referral bias.

Hemodynamically, the HPAH group showed the most severe profile (P < 0.001 for RAP and PVR; P = 0.001 for CI; [Table 2]). The aggressive nature and poor outcome of HPAH has been well-recognized. [29] Conversely, and despite the worse physiological presentation, the PAH-ACTD patients expressed the most relatively benign profile. This discrepancy between the physiological and hemodynamic profiles in PAH-ACTD has been reported by others. [23],[30],[31] Patients with IPAH expressed a middle range of severity in our cohort. The relatively good CI observed in PAH-ACHD and PoPH was relatively due to the milder nature of the disease in the former and to known high cardiac output status in chronic liver disease in the latter condition [Table 2]. In addition, our data represent that acute responders to vasodilator challenge occur only in a small minority of patients (5 patients, 6.9%; [Table 2]). Because calcium channel blocker therapy is only indicated in positive acute vasodilator patients, we confirm that this therapy should never be used as an empirical trial. [32],[33] Furthermore, the vasoreactive patients tended to have more benign physiological and hemodynamic profiles when compared to non-vasoreactive patients (NYHA FC II/III/IV 80%/20%/0% vs. 25%:57%:18%; 6MWT 388 m vs. 293 m; TAPSE 19 mm vs. 17 mm; NT-proBNP 668 pmol/l vs. 1429 pmol/l; mPAP 47 mmHg vs. 51 mmHg; CI 2.9 L/m/m 2 vs. 2.3 L/m/m 2 ; and PVR 12 WU vs. 16 WU, respectively; P < 0.01).

Finally, there were no distinctive features between the incidence and the prevalence cases in regard to clinical, physiological, or hemodynamic parameters [Table 3]. This could in part be related to the small number of prevalence cases in this study but may also be related to the recent time of diagnosis in some prevalent cases, which put them in a similar category as the incident cases. Traditionally, it is believed that the incidence cases have a worse prognosis when compared with prevalence cases. [34] Prevalence and incidence of PAH in Saudi Arabia cannot be calculated based on this early study and will be determined once the data from other centers involved in Pulmonary Arterial Hypertension in Saudi Arabia (PATENTS) registry conducted by the Saudi Association of Pulmonary Hypertension (SAPH) becomes available.

In conclusion, this descriptive study confirmed many characteristics similarities between Saudi PAH patients and the international data. Our patients still present very late in the course of the disease, and the majority of them display severe physiological and hemodynamic compromise. Of note, our patients are much younger when compared to the international registries.

 
   References Top

1.Tuder RM, Marecki JC, Richer A, Fijalkowska I, Flores S. Pathology of pulmonary hypertension. Clin Chest Med 2007;28:23-42.  Back to cited text no. 1
    
2.D′Alonzo GE, Barst RJ, Ayres SM, Bergofsky EH, Brundage BH, Detre KM, et al. Survival in patients with primary pulmonary hypertension. Ann Intern Med 1991;115:343-9.  Back to cited text no. 2
    
3.Humbert M, Sitbon O, Chaouat A, Bertocchi M, Habib G, Gressin V, et al. Pulmonary arterial hypertension in France: Results from a national registry. Am J Respir Crit Care Med 2006;173:1023-30.  Back to cited text no. 3
    
4.Badesch DB, Raskob GE, Elliott CG, Krichman AM, Farber HW, Frost AE, et al. Pulmonary arterial hypertension: Baseline characteristics from the REVEAL Registry. Chest 2010;137:376-87.  Back to cited text no. 4
    
5.Escribano-Subias P, Blanco I, Lopez-Meseguer M, Lopez-Guarch CJ, Roman A, Morales P, et al. Survival in pulmonary hypertension in Spain: Insights from the Spanish registry. Eur Respir J 2012;40:596-603.  Back to cited text no. 5
    
6.Jing ZC, Xu XQ, Han ZY, Wu Y, Deng KW, Wang H, et al. Registry and survival study in chinese patients with idiopathic and familial pulmonary arterial hypertension. Chest 2007;132:373-9.  Back to cited text no. 6
    
7.Peacock AJ, Murphy NF, McMurray JJ, Caballero L, Stewart S. An epidemiological study of pulmonary arterial hypertension. Eur Respir J 2007;30:104-9.  Back to cited text no. 7
    
8.Rich S, Rubin L, Walker AM, Schneeweiss S, Abenhaim L. Anorexigens and pulmonary hypertension in the United States: Results from the surveillance of North American pulmonary hypertension. Chest 2000;1173:870-74.  Back to cited text no. 8
    
9.Walker AM, Langleben D, Korelitz JJ, Rich S, Rubin LJ, Strom BL, et al. Temporal trends and drug exposures in pulmonary hypertension: An American experience. Am Heart J 2006;1523:521-6.  Back to cited text no. 9
    
10.Tuder RM, Abman SH, Braun T, Capron F, Stevens T, Thistlethwaite PA, et al. Development and pathology of pulmonary hypertension. J Am Coll Cardiol. 2009;54:S3-9.  Back to cited text no. 10
    
11.Morrell NW, Adnot S, Archer SL, Dupuis J, Jones PL, MacLean MR, et al. Cellular and molecular basis of pulmonary arterial hypertension. J Am Coll Cardiol 2009;54:S20-31.  Back to cited text no. 11
    
12.Tuder RM, Archer SL, Dorfmüller P, Erzurum SC, Guignabert C, Michelakis E, et al. Relevant issues in the pathology and pathobiology of pulmonary hypertension. J Am Coll Cardiol 2013;62(25 Suppl):D4-12.  Back to cited text no. 12
    
13.Idrees MM. Pulmonary hypertension: Another light in the dark tunnel. Learning the lesson from cancer. Ann Thorac Med 2013;8:69-70.  Back to cited text no. 13
[PUBMED]  Medknow Journal  
14.Rich S, Danzker DR, Ayres SM, Bergofsky EH, Brundage BH, Detre KM, et al. Primary pulmonary hypertension: A national prospective study. Ann Intern Med. 1987;107:216-23.  Back to cited text no. 14
    
15.Galie` N, Hoeper MM, Humbert M, orbicki A, Vachiery JL, Barbera JA, et al; ESC Committee for Practice Guidelines (CPG). Guidelines for the diagnosis and treatment of pulmonary hypertension: The Task Force for the Diagnosis and Treatment of Pulmonary Hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS), endorsed by the International Society of Heart and Lung Transplantation (ISHLT). Eur Heart J Eur Heart J 2009;30:2493-37.  Back to cited text no. 15
    
16.Simonneau G, Gatzoulis MA, Adatia I, Celermajer D, Denton C, Ghofrani A, et al. Updated clinical classification of pulmonary hypertension. J Am Coll Cardiol 2013;62(25 Suppl):D34-41.  Back to cited text no. 16
    
17.McLaughlin VV, Shillington A, Rich S. Survival in primary pulmonary hypertension: The impact of epoprostenol therapy. Circulation 2002;106:1477-82.  Back to cited text no. 17
    
18.Sitbon O, Humbert M, Nunes H, Parent F, Garcia G, Hervé P, et al. Long-term intravenous epoprostenol infusion in primary pulmonary hypertension: Prognostic factors and survival. J Am Coll Cardiol 2002;40:780-8.   Back to cited text no. 18
    
19.Miyamoto S, Nagaya N, Satoh T, Kyotani S, Sakamaki F, Fujita M, et al. Clinical correlates and prognostic significance of six-minute walk test in patients with primary pulmonary hypertension: Comparison with cardiopulmonary exercise testing. Am J Respir Crit Care Med 2000;161:487-92.  Back to cited text no. 19
    
20.Nagaya N, Nishikimi T, Uematsu M, Satoh T, Kyotani S, Sakamaki F, et al. Plasma brain natriuretic peptide as a prognostic indicator in patients with primary pulmonary hypertension. Circulation 2000;102:865-70.  Back to cited text no. 20
    
21.Forfia PR, Fisher MR, Mathai SC, Housten-Harris T, Hemnes AR, Borlaug BA, et al. Tricuspid annular displacement predicts survival in pulmonary hypertension. Am J Respir Crit Care Med 2006;174:1034-41.  Back to cited text no. 21
    
22.Nickel N, Golpon H, Greer M, Knudsen L, Olsson K, Westerkamp V, et al. The prognostic impact of follow-up assessments in patients with idiopathic pulmonary arterial hypertension. Eur Respir J 2012;39:589-96.  Back to cited text no. 22
    
23.Weir EK, Rubin LJ, Ayres SM, Bergofsky EH, Brundage BH, Detre KM, et al. The acute administration of vasodilators in primary pulmonary hypertension. Experience from the National Institutes of Health Registry on Primary Pulmonary Hypertension. Am Rev Respir Dis 1989;140:1623-30.  Back to cited text no. 23
    
24.Alhamad EH, Cal JG, Alfaleh HF, Alshamiri MQ, Alboukai AA, Alhomida SA. Pulmonary hypertension in Saudi Arabia: A single center experience. Ann Thorac Med 2013;8:78-85.  Back to cited text no. 24
[PUBMED]  Medknow Journal  
25.McGoon MD, Miller DP. REVEAL: A contemporary US pulmonary arterial hypertension registry. Eur Respir Rev 2012;21:8-18.   Back to cited text no. 25
    
26.Koh ET, Lee P, Gladman DD, Abu-Shakra M. Pulmonary hypertension in systemic sclerosis: An analysis of 17 patients. Br J Rheumatol 1996;35:989-93.  Back to cited text no. 26
    
27.MacGregor AJ, Canavan R, Knight C, Denton CP, Davar J, Coghlan J, et al. Pulmonary hypertension in systemic sclerosis: Risk factors for progression and consequences for survival. Rheumatol (Oxford) 2001;40:453-9.  Back to cited text no. 27
    
28.Hachulla E, Gressin V, Guillevin L, Carpentier P, Diot E, Sibilia J, et al. Early detection of pulmonary arterial hypertension in systemic sclerosis: A French nationwide prospective multicenter study. Arthritis Rheum 2005;52:3792-800.  Back to cited text no. 28
    
29.Sitbon O, Jais X, Savale L, Dauphin C, Natali D, O′Callaghan D, et al. Upfront triple combination therapy of IV epoprostenol with oral Bosentan and sildenafil in idiopathic and heritable pulmonary arterial hypertension. Am J Respir Crit Care Med 2011;183:A5910.  Back to cited text no. 29
    
30.Fisher MR, Mathai SC, Champion HC, Girgis RE, Housten-Harris T, Hummers L, et al. Clinical differences between idiopathic and scleroderma-related pulmonary hypertension. Arthritis Rheum 2006;54:3043-50.  Back to cited text no. 30
    
31.Girgis RE, Mathai SC, Krishnan JA, Wigley FM, Hassoun PM. Long-term outcome of bosentan treatment in idiopathic pulmonary arterial hypertension and pulmonary arterial hypertension associated with the scleroderma spectrum of diseases. J Heart Lung Transplant 2005;24:1626-31.  Back to cited text no. 31
    
32.Humbert M, Sitbon O, Simonneau G. Treatment of pulmonary arterial hypertension. N Engl J Med 2004;351:1425-36.  Back to cited text no. 32
    
33.Sitbon O, Humbert M, Jais X, Ioos V, Hamid AM, Provencher S, et al. Long-term response to calcium channel blockers in idiopathic pulmonary arterial hypertension. Circulation 2005;111:3105-11.  Back to cited text no. 33
    
34.Humbert M, Sitbon O, Yaïci A, Montani D, O′Callaghan DS, Jaïs X, et al. French Pulmonary Arterial Hypertension Network. Survival in incident and prevalent cohorts of patients with pulmonary arterial hypertension. Eur Respir J 2010;36:549-55.  Back to cited text no. 34
    


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    Tables

  [Table 1], [Table 2], [Table 3], [Table 4]

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