Volume 13, Issue 2 pp. 210-216
ORIGINAL ARTICLE

Age is not a good predictor of irreversibility of pulmonary hypertension in congenital cardiac malformations with left-to-right shunt

Amir-Reza Hosseinpour MD FRCS(C-Th)

Amir-Reza Hosseinpour MD FRCS(C-Th)

Department of Cardiac Surgery, University Hospital of Vaud, Lausanne, Switzerland

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Marie-Hélène Perez MD

Marie-Hélène Perez MD

Pediatric Intensive Care, University Hospital of Vaud, Lausanne, Switzerland

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David Longchamp MD

David Longchamp MD

Pediatric Intensive Care, University Hospital of Vaud, Lausanne, Switzerland

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Jacques Cotting MD

Jacques Cotting MD

Pediatric Intensive Care, University Hospital of Vaud, Lausanne, Switzerland

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Nicole Sekarski MD

Nicole Sekarski MD

Department of Pediatric Cardiology, University Hospital of Vaud, Lausanne, Switzerland

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Michel Hurni MD

Michel Hurni MD

Department of Cardiac Surgery, University Hospital of Vaud, Lausanne, Switzerland

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René Prêtre MD

René Prêtre MD

Department of Cardiac Surgery, University Hospital of Vaud, Lausanne, Switzerland

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Stefano Di Bernardo MD

Corresponding Author

Stefano Di Bernardo MD

Department of Pediatric Cardiology, University Hospital of Vaud, Lausanne, Switzerland

Correspondence Stefano Di Bernardo, Department of pediatric cardiology, University Hospital of Vaud, 46 Bugnon Street, Lausanne 1011, Switzerland. Email: [email protected]Search for more papers by this author
First published: 25 October 2017
Citations: 4

Funding information: The Marisa Sophie Foundation

Abstract

Objective

Congenital cardiac malformations with high pulmonary blood flow and pressure due to left-to-right shunts are usually repaired in early infancy for both the benefits of early relief of heart failure and the fear that the concomitant pulmonary hypertension may become irreversible unless these defects are corrected at an early age. Age, however, has been a poor predictor of irreversibility of pulmonary hypertension in our experience, which is presented here.

Design

A retrospective observational study. We defined “late” as age ≥2 years. We examined clinical, echocardiographic, and hemodynamic data from all patients aged ≥2 years with such malformations referred to us from 2004 untill 2015.

Setting

Department of Pediatric Cardiology and Cardiac Surgery, University Hospital of Vaud, Lausanne, Switzerland.

Patients

There were 39 patients, aged 2–35 years (median: 5 years), without chromosomal abnormalities. All had malformations amenable to biventricular repair, and all had high systolic right ventricular pressures by echocardiography prior to referral.

Interventions

All patients underwent catheterization for assessment of pulmonary hypertension. If this was reversible, surgical correction was offered.

Outcome measures

(1) Operability based on reversibility of pulmonary hypertension. (2) When surgery was offered, mortality and evidence of persisting postoperative pulmonary hypertension were examined.

Results

Eighteen patients had no pulmonary hypertension, 5 of variable ages were inoperable due to irreversible pulmonary hypertension, and 16 had reversible pulmonary hypertension. Therefore, 34 patients underwent corrective surgery, with no immediate or late mortality. Pulmonary arterial and right ventricular pressures decreased noticeably in all operated patients. This is sustained to date; they are all asymptomatic with no echocardiographic evidence of pulmonary hypertension at a median follow-up of 7 years (range 2–13 years).

Conclusions

Pulmonary hypertension may still be reversible in many surprisingly old patients with left-to-right shunt lesions, who may therefore still be operable.

CONFLICT OF INTEREST

None

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