Skip to main content

Assessing the spectrum of pulmonary hypertension identified at an Egyptian expert referral center

Abstract

Background and objective

Pulmonary hypertension is an assorted state that encompasses a spectrum of diseases and is categorized into five groups. The registries are necessary for the identification of risk factors, progression of the disease, outcomes, and effect of treatment strategies on the progression of the disease. The aim of this work was to identify different groups of PH identified at an Egyptian referral center and to compare the demographic and clinical characteristics of each group.

Patients and methods

This study included 132 patients who were diagnosed with a right heart catheter in the Chest Department, Kasr El-Aini Hospital, Faculty of Medicine, Cairo University, in the period from January 2017 to January 2019. Patients were classified into different groups, then received medical treatment accordingly. Demographic and clinical data were documented. Arterial blood gases, spirometry, and 6-minute walk test (6MWT) were performed.

Results

The mean age of cases was (43.9±13.69) years; the majority of them were females (72.7%). More than half of the patients (57.5%) had pulmonary artery hypertension (PAH), while 22.7% and 18.3% had pulmonary hypertension due to chronic thrombo-embolic cause and lung cause respectively. The 1-year survival rate was 81.8%.

Conclusions

The results of the study showed female predominance, the PAH type was the commonest, and the overall 1-year survival rate was 81.8%.

Background

The definition of pulmonary hypertension (PH) is elevated mean pulmonary artery pressure (mPAP) more than 25mmHg at right heart catheterization (RHC). It is classified into five different groups: group 1, pulmonary arterial hypertension (PAH); group 2, PH due to left heart disease (LHD); group 3, PH due to lung disease; group 4, chronic thromboembolic PH (CTEPH); and group 5, PH with unclear multifactorial mechanisms [1].

It is a severe, progressive disease associated with significant morbidity and mortality [2]. However, it is a rare disease; the registries are necessary for the identification of risk factors, progression of the disease, outcomes, and effect of treatment strategies on the progression of the disease.

For more than two decades, the National Institutes of Health (NIH) registry has collected data on the epidemiology of the idiopathic, familial, and anorexigen-associated forms of PAH, providing important information on survival and prognostic markers among these patients [3].

In recent years, some registries put into practice the description of the natural history of PH, raising the awareness of that silent disease and promoting more and more options for its discovery and treatment. From that point of view; the current study brings to light the Egyptian experience of a single pulmonary hypertension center, identifying the demographic and clinical characteristics of different PH groups.

Subjects and methods

Study design and population

A descriptive retrospective study was conducted in the Chest Department, Kasr El-Aini Hospital, Faculty of Medicine, Cairo University, in the period from January 2017 to January 2019. It involved 132 cases with pulmonary hypertension. Informed written consent was obtained from all participants. The ethical committee of the Faculty of Medicine, Cairo University, approved the study.

Inclusion criteria

  • All patients who were diagnosed by right heart catheter (RHC) to have mean pulmonary artery pressure (mPAP) ≥25mmHg.

Exclusion criteria

  • Patients refusing the procedure of RHC.

Preparation and laboratory evaluation

All patients were subjected to complete history tacking and clinical evaluation, the dyspnea scale according to NYHA association, complete blood picture, arterial blood gases, spirometry, and 6-minute walk test (6MWT).

Radiological evaluation

All patients underwent chest high-resolution computerized tomography (HRCT) or CT pulmonary angiography (CTPA), abdominal ultrasound, and echocardiography and ventilation/perfusion (VQ) scan.

Right heart catheter

Swan-Ganz catheter (TriOxTM PA Catheter, 8F, 110cm, J-tip, Heparin coated) was used. In addition to the balloon at the tip for flotation, it consists of an endhole port, a side-hole port 30 cm from the catheter tip. The pressure transducer was set to zero level at the mid-thoracic line with the patient in a supine position, halfway between the anterior sternum and bed surface, which represents the level of the left atrium [4].

Under visualization by ultrasound, Swan-Ganz catheter was introduced through the internal jugular vein to obtain pressure measurements in the right atrium, right ventricle, pulmonary artery, pulmonary artery wedge position. To obtain measurements of pulmonary artery wedge pressure (PAWP), the balloon was inflated in the right atrium, from where the catheter was advanced until it reaches the PAWP position [5].

Repeated inflations and deflations in the wedge position were avoided to avoid pulmonary artery rupture. Mixed venous oxygen saturation (SvO2) was measured while the tip of the catheter was in the pulmonary artery, whereas systemic oxygen saturation was acquired noninvasively by oximetry [6]. Cardiac output was calculated by the Fick method:

$$\mathrm{Cardiac}\ \mathrm{output}\ \left(\mathrm{l}/\min \right)=\mathrm{oxygen}\ \mathrm{consumption}\ \left(\mathrm{ml}/\min \right)/\left(\Delta \mathrm{A}-\mathrm{V}\ {\mathrm{O}}_2\times 1.36\times \mathrm{Hemoglobin}\ \left(\mathrm{mg}/\mathrm{dL}\right)\times 10\right)$$

where ΔA-V O2 is the arterial-venous oxygen saturation difference and the constant 1.36 is the oxygen-carrying capacity of hemoglobin (expressed in mL O2/g Hgb). In addition to the evaluation of cardiac output, the cardiac index was calculated as the ratio of cardiac output to body surface area. Pulmonary vascular resistance (PVR) was calculated as: PVR = mPAP–mean PAWP)/cardiac output [7]. Pulmonary vascular resistance index (PVRI) was calculated as the ratio of PVR to body surface area.

Statistical analysis

All statistical calculations were done using computer programs Microsoft Excel 2003 (Microsoft Corporation, NY, USA) and SPSS version 17 statistical program (Statistical Package for the Social Science; SPSS Inc., Chicago, IL, USA). A probability value (p value) less than 0.05 was considered statistically significant.

All comparisons between two groups were performed using Student’s t test. P value <0.05 was considered statistically significant.

Results

Patient’s characteristics

This study included 132 patients diagnosed by RHC as having pulmonary hypertension, most of them were females (72.7%). The mean age was 43.9±13.69 years (Table 1). The youngest patients were present in groups 2 and 3 PHT, hence the mean age in these two groups was 28 and 33 years respectively.

Table 1 Patients’ characteristics (n=132)

Clinical and laboratory evaluation in different groups

In the current study; the most common group was PAH (57.5%, n=76), followed by CTEPH (22.7%, n=30), group 3 (18.3%, n=24), then group 2 PH due to left ventricular dysfunction (1.5%, n=2) (Table 1). The mean distance in performing 6MWT was 209±120m. The majority of cases presented by grade III of dyspnea (60.6%, n=80), and the rest of them were grades II and IV (28.7%, n=38 and 10.7%, n=14, respectively) (Table 2).

Table 2 Patients’ clinical evaluation (n=132)

General and hemodynamic characteristics in PAH and CTEPH groups and its correlation with survival

The hemodynamic parameters of the two biggest groups are summarized in (Table 3).

Table 3 Hemodynamic parameters of PAH and CTEPH groups

Mean 6MWT distance was 209m±120m. After 1 year, the mean distance was 244m±127m.

After 1 year follow-up, the overall survival rate in all cases was 81.8%. All patients (n=2) in group 2 were still alive, while survival in groups 1, 3, and 4 was 89.4%, 66.6%, and 73.3%, respectively (Table 4). The present study found the mean age of survivors to be 42.4±14.3 years in PAH and 40.2±9.8 years in CTEPH, while in the non-survivors, it was 40.7±12.5 years in PAH (p>0.05) and 47±20.7 years in CTEPH (p>0.05). Moreover, in PAH, the mean 6MWT distance in survivors was 232.9±113.6m while it was 131.2±123m in non-survivors (p>0.05). On the other hand, the mean 6MWT distance in survivors with CTEPH was 238.5±100.5m while it was 141±128.4m in non-survivors (p>0.05). Hence, there was an insignificant role of age and 6MWT in predicting the survival in each group.

Table 4 Survival rate in 1-year follow-up

Moreover, considering the relation between survival and patients’ hemodynamic parameters, we found no statistically significant differences (p>0.05) between survivors and non-survivors (Table 5).

Table 5 Comparison between survivors and non-survivors of PAH and CTEPH groups

Discussion

Pulmonary hypertension is defined as an increase in mean pulmonary arterial pressure (mPAP) ≥25 mmHg at rest as assessed by right heart catheterization (RHC) [8]. Although 5 PH groups are recognized, the majority of studies in PH have focused on PAH and CTEPH. The aim of this study was to identify different groups of PH and assess the survival among its different groups.

As mentioned before, the most common group was PAH (57.5%, n=76), followed by CTEPH (22.7%, n=30), then group 3 (18.3%, n=24). The least cases were those of group 2 PH due to left ventricular dysfunction (1.5%, n=2) because those patients are usually diagnosed and managed by cardiologists and are not referred to our center. Group 1 (PAH) had a lower share than in COMPERA (Comparative, Prospective Registry of Newly Initiated Therapies for Pulmonary Hypertension), a prospective European registry in 28 centers in 6 countries, in which 71% of all patients had PAH and 29% had non-PAH-PH [8]. On the other hand, in ASPIRE registry that enrolled 1344 patients, the commonest group was PAH (49.62%), followed by CTEPH (20%), group 3 (14.7%), group 2 (12.98%), and the least common was group 5 (2.6%) [9].

Furthermore, the Giessen Pulmonary Hypertension Registry enrolled 2067 patients; 33.1% had PAH, 14.9% had PH due to left heart disease, 26.4% had PH due to lung disease, 22.2% had CTEPH, and 3.4% had group 5 PH [10]. The percentage of PAH in this study was higher than those of ASPIRE registry and Giessen registry, but lower than that of COMPERA, which may be due to different sample sizes in each study.

Female predominance was reported in the current work; 72.7% of the cases were females while 27.3% were males. That came in accordance with ASPIRE registry, in which female predominance of 62% was also reported [9]. Moreover, in the Giessen Pulmonary Hypertension Registry, the female percentage was 58.94% with a female-to-male ratio of 1.24:1 [10].

In the same line, the National Registry evaluating the characterization of Primary Pulmonary Hypertension (US-NIH) which enrolled 187 PAH patients from 32 centers, women were more frequently affected, with a female predominance of 63% [3]. Another French registry enrolled 674 PAH cases; females were 65% [11]. In addition, REVEAL registry showed marked female predominance (80% of PAH) [12]. There was a female predominance in all registries of PAH, and this can be explained by the role for hormonal influences (particularly estrogen) in the pathogenesis of PAH, as estrogen may promote cellular proliferation [13].

Considering the age of patients with PH, the mean age of all patients in this study was 43±13.69 years which was lower than that of ASPIRE registry and Giessen registry, in which the mean age at diagnosis was 59±17 years and 59.6 years respectively [9, 10]. In the same line, French and REVEAL registries reported higher age of patients, with a mean age of 50±15 years and 53±14 years, respectively [11, 12].

On the other hand; the mean age of PAH was lower than the current study, as it was 36±15 and 36±9 years in US-NIH and Saudi registry respectively [3, 14]. This could be explained by different demographics and awareness.

In the present work, 28.7% of cases presented with grade II dyspnea, 60.6% with grade III dyspnea, and 10.7% with grade IV dyspnea. That came in harmony with ASPIRE and Giessen registry: dyspnea grade III counted for 65% of cases in both registries, while grade IV was 16% and 22%, respectively [9, 10]. Moreover, in the REVEAL registry, dyspnea grade III was 50% and grade IV was 5.6% [12]. These differences may be due to a lack of awareness and the vague symptoms of PH, which may delay seeking medical advice.

In the present work, 1-year survival rate in all cases was 81.8%. However, the ratio was different among the different groups; 89.4% in group 1, 100% in group 2, 66.6% in group 3 and 73.3% in group 4. That came in agreement with ASPIRE registry, in which the 1-year survival rate was 88% for group 1, 90% for group 2, 65% for group 3, 89% for group 4, and 84% for group 5 [9].

In the Giessen registry, the 1-year survival rate was 85.5%, with 1-year survival rate of 88.2% for those with PAH, 86.7% for group 2, 79.5% for patients with group 3, and 89.2% for group 4 [10]. Moreover, in US-NIH and French registry, the 1-year survival rate was 68% and 89.3%, respectively [3, 11]. The lower rate of survival in our study could be explained by the presence of advanced management in the developed countries rather than the developing countries and delayed seeking of medical advice in the developing countries. On the other hand, the higher rate of survival in comparison with US-NIH was attributed to the fact that that registry was in the era before the development of specific therapy.

Regarding the hemodynamics, the mean mPAP was 54.29±14.2 mmHg in PAH and 50.13±11 mmHg in CTEPH. This was similar to other registries [9, 10, 12].

In the present study, there were insignificant roles of age and 6MWT in predicting the survival in each group, which came in contrast with the Giessen registry which stated that the age less than 50 years and 6MWT distance more than 390 m were predictive of survival [10].

Limitations

The present is study is limited by the small number of patients in group 2 (PH due to left heart disease). However, as mentioned before, those patients are usually diagnosed and managed by cardiologists and are not routinely referred to our center.

Conclusions

We concluded that there is a female predominance in patients diagnosed with PH, the mean age was 43.9±13.6 years, PAH was the most common group (57.5%) and group 2 PH was the least common (1.5%). Moreover, the overall 1-year survival rate was 81.8%. Age, 6MWT, and hemodynamic parameters did not have a significant role in predicting survival in our study.

Availability of data and materials

The datasets generated during the current study are not publicly available due to hospital policies and because the data will be used in future research to generate a nationwide registry. However, these datasets are available from the corresponding author on reasonable request.

Abbreviations

6MWT:

6-minute walk test

CI:

Cardiac index

CO:

Cardiac output

CTEPH:

Chronic thrombo-embolic pulmonary hypertension

CTPA:

Computerized tomography pulmonary angiography

HRCT:

High-resolution computerized tomography

LHD:

Left heart disease

mPAP:

Mean pulmonary artery pressure

PAH:

Pulmonary arterial hypertension

PAWP:

Pulmonary artery wedge pressure

PH:

Pulmonary hypertension

PVR:

Pulmonary vascular resistance

PVRI:

Pulmonary vascular resistance index

RHC:

Right heart catheterization

SvO2 :

Mixed venous oxygen saturation

VQ:

Ventilation/perfusion

References

  1. Simonneau G, Galie N, Rubin LJ, Langleben D, Seeger W, Domenighetti G, Gibbs S, Lebrec D, Speich R, Beghetti M, Rich S (2004) Clinical classification of pulmonary hypertension. J Am Coll Cardiol 43(12 Supplement):S5–S12

    Article  Google Scholar 

  2. Moreira EM, Gall H, Leening MJ, Lahousse L, Loth DW, Krijthe BP, Kiefte-de Jong JC, Brusselle GG, Hofman A, Stricker BH, Ghofrani HA, Franco OH, Felix JF (2015) Prevalence of Pulmonary Hypertension in the General Population: The Rotterdam Study. PLoS One 10(6):e0130072

    Article  Google Scholar 

  3. Rich S, Dantzker DR, Ayres SM, Bergofsky EH, Brundage BH, Detre KM, Fishman AP, Goldring RM, Groves BM, Koerner SK, Levy PC (1987) Primary pulmonary hypertension: a national prospective study. Ann Intern Med 107(2):216–223

    CAS  Article  Google Scholar 

  4. Kovacs G, Avian A, Pienn M, Naeije R, Olschewski H (2014) Reading pulmonary vascular pressure tracings. How to handle the problems of zero leveling and respiratory swings. Am J Respir Crit Care Med 190(3):252–257

    PubMed  Google Scholar 

  5. Hoeper MM, Gall H, Seyfarth HJ, Halank M, Ghofrani HA, Winkler J, Golpon H, Olsson KM, Nickel N, Opitz C, Ewert R (2009) Long-term outcome with intravenous iloprost in pulmonary arterial hypertension. Eur Respir J 34(1):132–137

    CAS  Article  Google Scholar 

  6. Mathier MA (2011) The nuts and bolts of interpreting hemodynamics in pulmonary hypertension associated with diastolic heart failure. Advances in Pulm Hypertens 10(1):33–40

    Article  Google Scholar 

  7. Grossman W (2006) Blood flow measurement: cardiac output and vascular resistance. In: Grossman’s Cardiac Catheterization, Angiography, and Intervention. Lippincott Williams & Wilkins, Philadelphia, pp 148–162

    Google Scholar 

  8. Hoeper MM, Bogaard HJ, Condliffe R, Frantz R, Khanna D, Kurzyna M, Langleben D, Manes A, Satoh T, Torres F, Wilkins MR (2013) Definitions and diagnosis of pulmonary hypertension. J Am Coll Cardiol 62(25 Supplement):D42–D50

    Article  Google Scholar 

  9. Hurdman J, Condliffe R, Elliot CA, Davies C, Hill C, Wild JM, Capener D, Sephton P, Hamilton N, Armstrong IJ, Billings C (2012) ASPIRE registry: Assessing the spectrum of pulmonary hypertension identified at a referral centre. Eur Respir J 39(4):945–955

    CAS  Article  Google Scholar 

  10. Gall H, Felix JF, Schneck FK, Milger K, Sommer N, Voswinckel R, Franco OH, Hofman A, Schermuly RT, Weissmann N, Grimminger F (2017) The Giessen Pulmonary Hypertension Registry: Survival in pulmonary hypertension subgroups. J Heart Lung Transplant 36(9):957–967

    Article  Google Scholar 

  11. Thenappan T, Shah SJ, Rich S, Tian L, Archer SL, Gomberg-Maitland M (2010) Survival in pulmonary arterial hypertension: a reappraisal of the NIH risk stratification equation. Eur Respir J 35(5):1079–1087

    CAS  Article  Google Scholar 

  12. McGoon MD, Krichman A, Farber HW, Barst RJ, Raskob GE, Liou TG, Miller DP, Feldkircher K, Giles S (2008) Design of the REVEAL registry for US patients with pulmonary arterial hypertension. Mayo Clin Proc 83(8):923–931

    Article  Google Scholar 

  13. Wysowski DK, Golden L, Burke L (1995) Use of menopausal estrogens and medroxyprogesterone in the United States, 1982–1992. Obstet Gynecol 85(1):6–10

    CAS  Article  Google Scholar 

  14. Idrees MM, Al-Najashi K, Khan A, Al-Dammas S, Al-Awwad H, Batubara E, Al Otai A, Abdulhameed J, Fayed A, Kashour T, Taskforce SR (2014) Pulmonary arterial hypertension in Saudi Arabia: Patients' clinical and physiological characteristics and hemodynamic parameters. A single center experience. Ann Thorac Med 9(4):209

    Article  Google Scholar 

Download references

Acknowledgements

Not applicable.

Funding

This research received no specific grant from any funding agency from commercial or not-for-profit sectors.

Author information

Authors and Affiliations

Authors

Contributions

ME designed the study and supervised the whole work. AIM performed data analysis and submitted the manuscript. AI collected clinical data and coordinated sample collection and statistics. IMS supervised the collection of clinical data and wrote the manuscript. All authors read and approved all of the final manuscript.

Corresponding author

Correspondence to Amira Ismail Mostafa.

Ethics declarations

Ethics approval and consent to participate

The authors assert that this work complies with the ethical standards of the relevant national guides on care and has been approved by the ethics committee of the Faculty of Medicine, Cairo University.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Elshazly, M., Mostafa, A.I., Ibrahim, A. et al. Assessing the spectrum of pulmonary hypertension identified at an Egyptian expert referral center. Egypt J Bronchol 15, 48 (2021). https://doi.org/10.1186/s43168-021-00098-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s43168-021-00098-3

Keywords

  • Pulmonary hypertension
  • Pulmonary arterial hypertension
  • Registry
  • Survival rate