Abstract
Objective
To compare pulmonary artery systolic pressure (PASP) between thalassemic patients with pulmonary arterial hypertension (PAH) for whom acetylsalicylic acid (ASA) was and was not prescribed after 1 year.
Methods
A retrospective cohort study was conducted at the hematological outpatient clinic at Chiang Rai Hospital, Chiang Rai, Thailand. All new cases of thalassemia with PAH from January 2007 to January 2012 were studied at the first month and at 12 months. The patients were classified into two groups. In one group, ASA 81 mg daily was prescribed for 1 year, whereas in another group no ASA was prescribed, due to its contraindications, which included bleeding, gastrointestinal side effects, and thrombocytopenia. PASP, estimated by a Doppler echocardiography, was measured by the same cardiologist. Propensity score adjustment was used to control confounding variables by indication and contraindication. Multivariable regression analysis was used to evaluate the effects of ASA.
Results
Of the 63 thalassemia patients with PAH, there were 47 (74.6%) in the ASA group and 16 (25.4%) in the no ASA group. ASA, as compared with no ASA, did not significantly reduce PASP (adjusted difference −0.95; 95% confidence interval −16.99 to 15.10; P=0.906).
Conclusion
Low-dose ASA may not have a beneficial effect on PASP after 1 year of treatment of PAH in thalassemia.
Introduction
Pulmonary arterial hypertension (PAH) is a cardiovascular complication that causes death in thalassemic patients. PAH in thalassemia was reported with a high incidence in several studies.Citation1–Citation4 There was evidence that PAH in thalassemia is associated with platelet activation.Citation5–Citation7 Acetylsalicylic acid (ASA) lowers the thromboxane–prostaglandin I2 (Tx–PGI2) ratio in PAH and inhibits platelet activity. A previous cohort study found that the rise of arterial partial pressure of oxygen (PaO2) in ten out of the 12 β-thalassemic patients after ASA ten grains or persantin administration for 2–4 weeks indicates that the observed hypoxemia is due to reversible platelet aggregation.Citation9 A recent study showed that ASA decreased pulmonary artery pressure, reduced right ventricular hypertrophy, and improved survival in the monocrotaline animal model of PAH.Citation10 The erythrocytes and platelets of thalassemic patients contained higher levels of reactive oxygen and lower levels of intracellular glutathione than normal erythrocytes and plateletsCitation11 that play a role in oxidative stress, thereby leading to the proper therapy.
The standard medication for PAH in thalassemia is not well understood. The mechanism of action of the drugs for PAH is not known. Studies of antiplatelet therapy are required before there are conclusive treatment guidelines for thalassemic patients with PAH. In clinical practice, ASA has been used to prevent and treat PAH in thalassemia in Thailand. There were few studies of ASA or antiplatelet therapy in these cases. The aim of the research was to compare after 1 year of follow-up the pulmonary artery systolic pressure (PASP) of patients with thalassemia and PAH to whom ASA was and was not prescribed.
Materials and methods
A retrospective cohort study was conducted at the hematological outpatient clinic at Chiang Rai Hospital, Chiang Rai, Thailand. All new adult (aged ≥15 years) cases of thalassemia with PAH defined as PASP >35 mmHg by Doppler echocardiography (echo) from January 2007 to January 2012 were evaluated and followed from the first month to 12 months later. The patients were classified into two groups. In one group, ASA 81 mg was prescribed daily for 1 year, and in another group, no ASA was prescribed, due to contraindications for ASA (including bleeding, gastrointestinal side effects, and thrombocytopenia [platelets <100×103/μL]). The physician evaluated drug compliance and side effects. PASP, functional class status, clinical right heart failure, and oxygen saturation were measured at baseline and at the end of 12 months. The functional class status was defined by the New York Heart Association (NYHA) classification.Citation12 Patients with other causes of PAH or who used other antiplatelets and/or anticoagulants were excluded. The study protocol was approved by the Institutional Research Ethics Committee and was carried out in accordance with the Declaration of Helsinki.
Echo procedure
Echo was done by the same cardiologist and the patients’ history was blinded. Complete two-dimensional, M-mode, and Doppler (pulsed wave, continuous wave, and color) echo was performed at rest. In the study patients, a tricuspid regurgitation jet was sought from all available midprecordial and apical positions until a flow signal with the maximum spectral representation of the highest velocities was obtained. Peak velocity was recorded from a holosystolic regurgitant jet. From the maximum velocity (V) of the regurgitant jet, the systolic pressure gradient (∆P) between the right ventricle and the right atrium was calculated by modified Bernoulli equation (∆P = 4VCitation2).Citation13 Right atrial pressure was estimated by the response of the inferior vena cava diameter to inspiration. Right atrial pressure was assumed to be 5 mmHg if the inferior vena cava completely collapsed with inspiration, 10 mmHg if the inferior vena cava dia meter decreased >50% during inspiration, and 15 mmHg if it decreased <50%. If the inferior vena cava diameter was >2.5 cm and reduced by <50% during inspiration, right atrial pressure was assumed to be 20 mmHg.Citation14 Adding the transtricuspid gradient to the mean right atrial pressure provided the right ventricular systolic pressure or peak systolic pulmonary arterial pressure in the absence of right ventricular outflow tract obstruction. PAH was defined as PASP >35 mmHg.Citation15 In cases with an absence of tricuspid regurgitation, at the end of the diastolic pulmonic regurgitant the velocity was calculated using the pressure gradient between the pulmonary artery and right ventricular end diastolic pressure: pulmonary artery pressure =4 (VPR)Citation2 + right atrial pressure.
Statistical analysis
The baseline characteristics were compared using exact probability tests for categorical variables; Student’s t-test or Wilcoxon rank-sum test was used to compare the mean difference of continuous variables. Propensity score adjustment was used to control confounding by ASA indication and contraindication. Propensity scores for prescribing ASA versus no ASA were calculated from a logistic regression model that estimated the likelihood of prescribing ASA based on the observed patient characteristics. Gaussian and an exponential risk regression were carried out. Univariable and multivariable regression analyses were used to evaluate the effects of ASA. Data are presented by frequency, percentage, mean, standard deviation (SD), beta coefficient, 95% confidence interval [CI], and P-value. All statistical analyses were two-tailed. A P-value of <0.05 was considered statistically significant.
Results
A total of 63 thalassemia patients with PAH, 53 with E/β-thal, six with homozygous β-thal, and four with Hb H disease were evaluated. There were 47 (74.6%) in the ASA group and 16 (25.4%) in the no ASA group. Patients in the second group had the following contraindications for ASA: seven (43.7%) bleeding, seven (43.7%) gastrointestinal side effects, and two (12.5%) thrombocytopenia. The mean age was 35.9±16.8 years and 28.3±14.1 years, and the mean PASP was 51.9±13.7 mmHg and 45.6±9.9 mmHg in the ASA group and the no ASA group. The baseline characteristics of the patients did not differ significantly except for red cell transfusion and right ventricular diameter (). The patients in the ASA group received fewer blood transfusions during the follow-up time of 12 months than those without ASA (6.2±4.8 vs 11.0±4.6 units, P=0.002), and the ASA group had wider right ventricular diameter than the no ASA group (29.5±5.8 vs 25.5±4.2 mm, P=0.016).
Table 1 Baseline characteristics of the patientsTable Footnotea
Table 2 Clinical outcomes and echocardiographic findings at 12 monthsTable Footnotea
During the follow-up period of 12 months, PASP increased in 12 of 47 (25.5%) patients in the ASA group and in three of 16 (18.7%) in the no ASA group. Echo findings showed that the patients in the ASA group had a higher mean PASP than the no ASA group, but there was no statistical difference.
After adjusting for propensity score (based on type of thalassemia, splenectomy, O2 saturation, NYHA classification, red cell transfusion, clinical right heart failure, hemoglobin level, platelet count, nucleated red cell, serum ferritin level, baseline PASP, left ventricular ejection fraction, main pulmonary artery diameter, right ventricular diameter, right ventricular systolic function, and diastolic function), there were no statistically significant differences in the functional class status, clinical right heart failure, and oxygen saturation between the two groups (). ASA, as compared with no ASA, did not significantly reduce PASP (adjusted difference −0.95; 95% CI −16.99 to 15.10; P=0.906). None of the patients had deep vein thrombosis, ischemic stroke and pulmonary embolism.
Table 3 Effect of acetylsalicylic acid on clinical outcomes and echocardiographic findings
Discussion
In the present study, ASA did not improve the functional class status, clinical right heart failure, and oxygen saturation and did not have a significant effect on PASP after 12 months. Both the ASA and the no ASA groups had reduced PASP by −4.7±11.0 mmHg and −4.3±7.1 mmHg with no clinical or statistical significance. The results of this study were similar to those of a randomized clinical trial of ASA and simvastatin for PAH, which concluded that the results did not support the routine treatment of patients with PAH with these medications.Citation16 And thalassemia patients who experienced a thromboembolic event and received ASA afterwards had a lower recurrence of thromboembolic event compared with those who were not taking ASA, although these differences were not statistically significant.Citation17 Subgroup analysis of E/β-thal; ASA, as compared with no ASA, did not significantly reduce the PASP (adjusted difference −3.62; 95% CI −11.84 to 4.60; P=0.225). For the transfusion- and nontransfusion-dependent patients, ASA did not significantly change the PASP.
In contrast to the previous study that reported that there was a rise of arterial PaO2 after high-dose ASA administration in thalassemia patients with PAH,Citation9 we found that oxygen saturation rose in the patients who had received low-dose ASA but without statistical significance (adjusted difference 0.31; 95% CI −1.71 to 2.33; P=0.757).
PAH developed in thalassemic patients because of platelet activation and hypercoagulable state.Citation18,Citation19 Therefore, it was reasonable that antiplatelet therapy alone may be less effective for PAH in thalassemia. Its role in the prevention of PAH in thalassemia should be evaluated.
Further studies of PAH management will be required before conclusive recommendations can be made for anti-platelet or anticoagulant therapy or prevention for high risk of PAH in thalassemia (postsplenectomy statusCitation3).
The present study may have some limitations, as it was not a randomized controlled trial, the duration of treatment was only 12 months, and the 6-minute walk test was not used as a clinical outcome due to its retrospective nature. The lack of cardiac catheterization to confirm PASP is a limitation for a therapeutic trial of PAH.Citation20 However, echo is more sensitive and is a commonly used noninvasive tool to screen PAH. More evidence from observational studies or preferably randomized clinical trials may be required before it can be concluded that ASA would offer any beneficial effects to these patients.
The current therapies for PAH in thalassemia include the use of sildenafilCitation21,Citation22 and bosentan.Citation23 However, a large cohort of patients on the topic are needed before definite recommendations can be made.
Conclusion
The present findings suggested that low-dose ASA may not have a beneficial effect on PASP after 1-year treatment of PAH in thalassemia.
Acknowledgments
The authors wish to thank the medical staff members of Chiang Rai Hospital for their assistance and Chiang Mai University for its financial support.
Disclosure
The research was partially supported by a grant from the Graduate School of Chiang Mai University, Thailand. The authors declare no other conflicts of interest in this work.
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