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Platypnea orthodeoxia syndrome in a patient with pulmonary arterial hypertension

T. Sinanis

Department of Cardiology, Heart Center Duisburg, Germany

E-mail : bhuvaneswari.bibleraaj@uhsm.nhs.uk

U. Krüger

Department of Cardiology, Heart Center Duisburg, Germany

W.H. Schöls

Department of Cardiology, Heart Center Duisburg, Germany

DOI: 10.15761/CCRR.1000374

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Abstract

Platypnea orthodeoxia syndrome (POS) is a rare syndrome traditionally defined as dyspnea or hypoxemia observed when changing from a recumbent to an upright or seated position. A patent foramen ovale (PFO) is oft part of the underlying pathophysiology. Here, a 70-year-old woman with known PFO presents with new symptoms of a platypnea orthodeoxia syndrome. A pulmonary arterial hypertension (PAH), treated with Ambrisentan for years, was also known. In order to clarify the etiology of the new hemodynamic state we performed a transesophageal echocardiography (TEE) in an upright position, which excluded a PFO related cause of symptoms. A further investigation shown a COPD (Chronic Obstructive Pulmonary Disease), the treatment of which relieved of symptoms. This is the first described case of Platypnea orthodeoxia syndrome in patient with PAH. Although PFO is a common cause of POS and a PFO closure is often advised, careful differential diagnosis should be kept in mind.

Introduction

Dyspnea is a frequently encountered symptom in medicine. It is one of the main reasons of presentation in the emergency department and one of the most common causes of hospitalization [1]. Dyspnea is also a complaint of nearly 4% of patients seeking treatment in the ambulatory care setting, and population samples have determined the prevalence of dyspnea to be between 17% and 38% [2]. Platypnea orthodeoxia syndrome (POS) is traditionally defined as dyspnea or hypoxemia observed when changing from a recumbent to an upright or seated position [3]. Although there are several potential causes for this phenomenon, POS is classically described as resulting from right-to-left shunting through a patent foramen ovale (PFO) [4,5]. The precise mechanism of shunting through a PFO despite normal intracardiac pressures, however, remains obscure [6].

Case report

A 70-year old woman was referred to our hospital for further investigation of deteriorating shortness of breath. Her symptoms were present for the last 3 months and were felt to have slowly worsened over time.

The patient had been diagnosed with pulmonary arterial hypertension (PAH) in 2010. Right heart catheterization at that time revealed an elevated mean pulmonary artery pressure of 47 mm Hg and a normal wedge pressure (PAWP or PC) of 12 mm Hg. Cardiac index was reduced (1.77 L/min/m²) and pulmonary vascular resistance was significantly elevated (12 Wood units). A rheumatic arthritis with symmetric involvement of multiple joints and positive CCP-antibodies was also known since 2009. For treatment of her arthritis the patient received methotrexat once a week. As no other etiology for PAH was found, the patient´s disease was classified as Dana Point group 1. She was referred to our PAH clinic for specific therapy. Sildenafil was not tolerated and bosentan lead to a drastic elevation of GOT and GPT. Ambrisentan, on the other hand, was well tolerated, improved 6 minute walking distance by 35 meters (from 180 meters to 215 meters) and decreased NT-proBNP plasma levels. Ambrisentan monotherapy was continued through the years 2010 to 2013 as the patient´s general condition stabilized and dyspnea was reduced.

As a result of the PAH, the right ventricle dilated and the right ventricular systolic function declined. With 17 mm, TAPSE was within the normal range. Regarding echocardiographic parameters, left ventricular systolic and diastolic function showed no abnormalities.

At presentation, the patient revealed no alarming clinical signs: RR was 100/60 mm Hg, temperature 36.8° C, blood glucose 106 mg/dl. On blood gas analysis pO2 was found to be 59 mm Hg, pCO2 43 mm Hg, BE +6 mmol/l, pH 7,45, and sO2 90%. Blood chemistry provided the following parameters: troponin 15,6 pg/ml, NT-proBNP 126 pg/ml, hemoglobin 11,3 g/dl, creatinine 0,5 mg/dl, potassium 3,5 mmol/l, sodium 140 mmol/l, CRP < 0,5 mg/dl. The electrocardiogram showed a sinus rhythm (95 beats pro minute) with a known right axis and peaked P waves as a result of the pulmonary hypertension (Figure 1A). The chest X-ray had no signs of pulmoary congestion, pleural effusion or pneumonia (Figure 1B).

Figure 1. 12 lead electrocardiogram (A) and chest X-ray (B) of the patient

The patient described increasing shortness of breath while standing with an improvement when changing to a recumbent position. To substantiate this perception, continuous measurements of heart rate and oxygen saturation in lying, sitting and standing positions were obtained. Results are summarized in Table 1.

Table 1. Changes in oxygen saturation (SO2) and in heart rate (HF) in relation to the position of the patient. bpm = beats per minute.

minutes

lying

sitting

standing

 

SO2 (%)

HF (bpm)

SO2 (%)

HF (bpm)

SO2 (%)

HF (bpm)

0

89

110

89

126

85

132

1'

89

110

87

120

83

133

3'

89

110

86

123

82

135

5'

89

110

85

123

82

134

10'

89

110

84

121

81

137

For further investigation, transesophageal echocardiography (TEE) was performed, combined with continuous registration of heart rate and oxygen saturation. Agitated saline contrast was used to search for intracardiac shunts (Figure 2). As a significant right-to-left shunt would increase left atrial pressure and reduce pulmonary venous flow, the latter was also evaluated by Doppler echocardiography. The goal was to elucidate the potential role of the previously diagnosed persistent foramen ovale (PFO) in the pathophysiology of the clinical symptoms.

Figure 2. Presentation of the PFO without evidence of obstruction to the flow in the pulmonary veins.

In lying position, there was no relevant transition of NaCL bubbles from the right to the left atrium. Accordingly, the flow in the pulmonary veins was not compromised. This was in line with the fact that oxygen saturation reached 89% in lying position, compatible with the patient´s pulmonary hypertension and not suspicious of any right-to-left shunt. When moving the patient to an upright position with the TEE probe in place, the oxygen saturation dropped to 81%. Agitated saline contrast was applied once again, but failed to provide any evidence of intracardiac shunting. Furthermore, pulmonary venous flow was unchanged under these conditions as well. Contrary to our expectations, the PFO did not seem to account for the platypnoe orthodeoxia syndrome. Thus, the diagnostic work-up was extended. Pulmonary function testing revealed chronic obstructive pulmonary disease. Subsequently, inhalative antiinflammatoric/antiobstructive treatment and non-invasive ventilation (NIV) therapy was initiated. Within 2 weeks, the patient´s symptoms resolved.

Discussion

Platypnea-orthodeoxia syndrome (POS) is an uncommon condition characterized by dyspnea and arterial desaturation upon assuming an upright position [7,8]. The syndrome was originally described in patients with pulmonary disease without intracardiac shunts [8].

Current knowledge relates POS to intracardiac shunting, intrapulmonary shunting, ventilation-perfusion mismatch, or a combination of these [9,10].

In the case of anatomical interatrial discontinuities (e.g., patent foramen ovale, atrial septal defects), a functional component modified by positional changes is required as well. Functional components include conditions that increase right atrial pressure, stretch the interatrial septum and/or redirect blood flow through the interatrial communication.

Anatomical as well as functional conditions may lead to intrapulmonary shunting. Arteriovenous anastomoses, pulmonary arteriovenous malformations and grossly distended pulmonary capillaries are potential causes of anatomical shunts. Functional shunts are due to ventilation-perfusion mismatch, that is, hypoventilation of normally perfused segments or hyperperfusion of normally ventilated segments. In either case, insufficiently oxygenated blood mixes with oxygenated blood, thereby resulting in overall desaturation. The mechanisms affecting the degree of intrapulmonary shunting and their relation to positional changes are not fully understood. Clearly, in the upright position, pulmonary perfusion shifts from the apical to the basal parts of the lungs. Right ventricular preload is reduced, and pulmonary artery pressure drops. The effect on pulmonary venous pressure is less predictable, considering the plethora of modifying factors, such as left ventricular function and compliance, left ventricular pre- and afterload, heart rate valvular function. Irrespective of other potential mechanisms, the apico-basal shift of pulmonary perfusion upon standing aggravates the functional significance of any basally located pathology [11]. More pronounced anatomical or functional intrapulmonary shunting in the lower parts combined with a reduced potential for compensation in the upper parts of the lungs will then result in significant deoxygenation. In line with these considerations, our patient also revealed a basal predominance with respect to his COPD (Chronic Obstructive Pulmonary Disease).

The diagnosis of POS is based on the following criteria: 1) platypnea, 2) orthodeoxia (SpO2 <90%), 3) existence of an interatrial or intrapulmonal communication, and 4) right-to-left shunt. Our patient presented with typical symptoms, and the previously diagnosed PFO seemed to provide the pathophysiologic basis. However, contrary to expectations, we were unable to demonstrate a right-to-left shunt across this interatrial discontinuity. As described by Desouza [12], tilt TEE with agitated saline contrast solution is the most effective diagnostic tool for this purpose. In rare cases, a shunt is only seen with Valsalva maneuver, which could not performed in our patient because of his apparent shortness of breath. However, if this shortness of breath would have been related to an interatrial right-to-left shunt, it would have had to be present under just these conditions. In the absence of an intracardiac shunt, contrast-enhanced echocardiography, perfusion scan (scintigraphy) with macroaggregated albumin or pulmonary arteriography might be used to detect intrapulmonary shunting [13]. Based on the favourable clinical course, we refrained from respective diagnostic procedures in our patient.

If POS is definitely related to intracardiac shunting, closure of the interatrial communication represents definitive treatment. In 2001, Rao et al. [14] reported on percutaneous closure of atrial septal defects and PFOs in platypnea-orthodeoxia patients via femoral approach. A jugular approach is feasible as well [15]. Transcatheter closure immediately improves oxygen saturation in upright position. Platypnea resolves completely [16-18]. Symptomatic improvement is seen in >95% of patients. In light of this effective treatment option, it is tempting to proceed with respective interventions once an interatrial communication has been detected. However, this case clearly demonstrates that a PFO might be an “innocent bystander”, where closure would not affect the underlying pathophysiology. Instead, particularly in patients with pulmonary hypertension and right heart failure, an intervention could even be detrimental by preventing preload reduction through right-to-left shunting.

In patients with intrapulmonary shunting, the underlying pulmonary disease must be treated to reduce ventilation-perfusion mismatch. Closure of small airways or microatelectasis have been suggested as potential causes of ventilation-perfusion mismatch in platypnoea-orthodeoxia [19], possibly reversible with CPAP ventilation. Both, mechanical ventilation and application of end-expiratory positive airway pressure (PEEP) tend to increase right-to-left shunting with worsening of hypoxaemia. Our patient experienced a gradual improvement in oxygenation while on mechanical ventilation with PEEP application and also during non-invasive bi-level ventilation.

Conclusion

Awareness and careful clinical evaluation are clues to the diagnosis of POS. Although an interatrial communication is frequently involved in the underlying pathophysiology, it might also coexist without any causal relationship. Thus, a functional analysis of all potential components is required before deciding on a specific therapy.

References

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Editorial Information

Editor-in-Chief

Andy Goren University of Rome G.Marconi

Article Type

Case Report

Publication history

Received date: December 03, 2017
Accepted date: December 21, 2017
Published date: December 23, 2017

Copyright

© 2017 Sinanis T. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Citation

Sinanis T, Krüger U, Schöls WH (2017) Platypnea orthodeoxia syndrome in a patient with pulmonary arterial hypertension. Clin Case Rep Rev 3: DOI: 10.15761/CCRR.1000374

Corresponding author

Theodoros Sinanis

Department of Cardiology, Heart Center Duisburg, Germany.

E-mail : bhuvaneswari.bibleraaj@uhsm.nhs.uk

Figure 1. 12 lead electrocardiogram (A) and chest X-ray (B) of the patient

Figure 2. Presentation of the PFO without evidence of obstruction to the flow in the pulmonary veins.

Table 1. Changes in oxygen saturation (SO2) and in heart rate (HF) in relation to the position of the patient. bpm = beats per minute.

minutes

lying

sitting

standing

 

SO2 (%)

HF (bpm)

SO2 (%)

HF (bpm)

SO2 (%)

HF (bpm)

0

89

110

89

126

85

132

1'

89

110

87

120

83

133

3'

89

110

86

123

82

135

5'

89

110

85

123

82

134

10'

89

110

84

121

81

137