Abstract
Background
Pectus excavatum is the most common chest wall deformity. There is still controversy about cardiopulmonary limitations of this disease and benefits of surgical repair. This study evaluates the impact of pectus excavatum on the cardiopulmonary function of adult patients before and after a modified minimally invasive repair.
Methods and Results
In this retrospective cohort study, an electronic database was used to identify consecutive adult (aged ≥18 years) patients who underwent cardiopulmonary exercise testing before and after primary pectus excavatum repair at Mayo Clinic Arizona from 2011 to 2020. In total, 392 patients underwent preoperative cardiopulmonary exercise testing; abnormal oxygen consumption results were present in 68% of patients. Among them, 130 patients (68% men, mean age, 32.4±10.0 years) had post‐repair evaluations. Post‐repair tests were performed immediately before bar removal with a mean time between repair and post‐repair testing of 3.4±0.7 years (range, 2.5–7.0). A significant improvement in cardiopulmonary outcomes (P<0.001 for all the comparisons) was seen in the post‐repair evaluations, including an increase in maximum, and predicted rate of oxygen consumption, oxygen pulse, oxygen consumption at anaerobic threshold, and maximal ventilation. In a subanalysis of 39 patients who also underwent intraoperative transesophageal echocardiography at repair and at bar removal, a significant increase in right ventricle stroke volume was found (P<0.001).
Conclusions
Consistent improvements in cardiopulmonary function were seen for pectus excavatum adult patients undergoing surgery. These results strongly support the existence of adverse cardiopulmonary consequences from this disease as well as the benefits of surgical repair.
Keywords: cardiothoracic surgery, echocardiography, exercise testing, pectus excavatum
Subject Categories: Exercise Testing, Computerized Tomography (CT), Echocardiography, Treatment
Nonstandard Abbreviations and Acronyms
- CPET
cardiopulmonary exercise testing
- HI
Haller index
- MIRPE
minimally invasive repair of pectus excavatum
- PE
pectus excavatum
- TEE
transesophageal echocardiography
- VO2 max
maximum rate of oxygen consumption
Clinical Perspective
What Is New?
This study demonstrates that external cardiac compression from the pectus excavatum deformity can cause negative cardiopulmonary consequences.
More than two thirds of adult patients studied showed abnormal cardiopulmonary function before undergoing surgical repair.
A consistent improvement in cardiopulmonary outcomes was demonstrated after the minimally invasive repair of pectus excavatum.
What Are the Clinical Implications?
Pectus excavatum is not merely a cosmetic disorder and symptomatic patients should be thoroughly evaluated to assess cardiopulmonary deficits associated with the cardiac compression.
When cardiopulmonary implications are suspected or detected, surgical correction should be considered to provide functional benefits.
Pectus excavatum (PE) is the most common congenital chest wall deformity with symptoms affecting patients at different ages. 1 In many cases, symptoms including dyspnea, tachycardia, dizziness, and chest pain manifest during exertion and exercise. 2 Some evidence suggests that symptoms may progress as the patient ages. 3 Adverse cardiopulmonary effects of PE may be underestimated by many physicians, in part because of the contradictory findings of previously published data. 2 , 4 , 5
Patients frequently report subjective symptom resolution and improvement in exercise tolerance following surgical repair. 6 , 7 However, there are few objective and consistent publications documenting improvement in cardiopulmonary function following surgical repair, especially on the ability to exercise. 2 , 4 , 5 The existing literature is inconclusive, hampered by small, statistically underpowered patient cohorts, short‐ versus long‐term results, rest versus exercise studies, and inconsistent testing measures. 2 , 4
Cardiopulmonary exercise testing (CPET) is an established clinical tool for evaluating exercise capacity and provides assessment of the integrative exercise responses involving the pulmonary, cardiovascular, and skeletal muscle systems. 8 Data documenting improvement in CPET outcomes in the pediatric PE population after surgery are compelling 9 , 10 ; however, it is unclear if adult patients would equally benefit from surgery. 11 , 12
Our previous studies using intraoperative transesophageal echocardiogram (TEE) showed significant and immediate improvements in anatomic and functional cardiac parameters following pectus repair (including right and left ventricular dimensions, stroke volume, and speckle tracking strain). 13 , 14 This study was performed as a next step to evaluate the effects of PE on cardiopulmonary function and exercise in adult patients, and to assess whether a minimally invasive “Nuss” surgical repair (MIRPE) offers significant benefit.
METHODS
Study Design, Data Sources, and Population
A retrospective cohort study was designed including patients identified in an electronic database at a single institution (Mayo Clinic, Phoenix, AZ). Consecutive adult patients (aged ≥18 years) with PE who underwent MIRPE between January 1, 2011 and December 31, 2020 and who underwent pre‐ and postoperative CPET performed at our institution were included. Patients with only preoperative CPET were used to identify the prevalence and severity of PE‐related cardiopulmonary compromise. Exclusion criteria included patients undergoing revision surgery rather than primary repair; patients with additional conditions other than PE (pulmonary, cardiovascular, and musculoskeletal diseases) that could affect CPET results; patients with CPET evaluations performed with non‐standardized protocols or at other institutions; or patients who experienced postoperative complications that could affect cardiopulmonary function.
Electronic medical records were used to collect baseline demographic characteristics, pre‐, intra‐, and postoperative testing, surgical information, and postoperative complications. Pre‐ and postoperative CPET outcomes were compared. Prespecified subgroup analysis of changes in the percentage of predicted maximum rate of oxygen consumption (VO2 max) was stratified according to demographic characteristics, anatomical PE indices as assessed by cross sectional imaging, and cardiopulmonary basal parameters. Institutional review board approved retrospective review of patients’ medical charts and studies as well as the waiver of informed consent. The data that support the findings of this study are available from the corresponding author upon reasonable request.
Surgical Procedure
Surgical correction of PE was performed using a modified minimally invasive “Nuss” procedure as previously described. 15 The indications for surgical repair included Haller index (HI) ≥3.25; Correction index ≥20%; significant or progressing cardiopulmonary symptoms, and/or evidence for right heart compression. 15 , 16 , 17 Intrathoracic pectus bars were recommended for removal 3 to 3.5 years following surgery. 15
Cardiopulmonary Exercise Testing
The predicted values for CPET parameters were based on age, sex, height, and weight. Both CPET and surgery were performed at a single institution/surgeon (D.E.J.). Cardiopulmonary tests were performed with the same equipment and identical protocols during the entire study period.
Incremental exercise tests were performed using a calibrated electromagnetically upright cycle (Corival, Lode, Groningen, The Netherlands) with a non‐invasive, photo‐acoustic gas‐rebreathing analyzer (Ultima Series, MGC Diagnostics Corporation, Saint Paul, MN). Surface electrocardiography, blood pressure measurements, pulse oximetric signals, and end‐tidal CO2 tracing were monitored during the entire study. A standardized 1‐minute step protocol at 25 W/min was used. The participants were asked to pedal at a steady pace of 60 rpm. Maximal incremental exercise was performed until exhaustion. Peak exercise was defined as the highest work level reached during the incremental exercise test. CPET results were defined as abnormal (VO2 max <80% of predicted) or normal (VO2 max ≥80% of predicted).
Before and After Correction TEE Image Analysis
When available, intraoperative TEE image analysis was performed. Digital images stored on the institutional server were retrieved and displayed in an image viewer (FUJIFILM, Indianapolis, IN). Measurements were made using electronic calipers. For 2‐dimensional images and for Doppler, an average of 2 measurements was used. All patients were in sinus rhythm and all measurements were performed by a single experienced observer (J.M.F.). Right ventricular stroke volume was assessed by pulsed‐wave Doppler of the right ventricle outflow tract in the deep transgastric view with as parallel alignment to right ventricle outflow tract as possible. Velocity time integral and right ventricle outflow tract diameter were used to measure right ventricle stroke volume at the time of MIRPE (before sternal elevation) and at the time of bar removal.
Statistical Analysis
Statistical comparison between preoperative and postoperative results was performed using Student paired t‐test for continuous variables and McNemar test for categorical variables comparison. Statistical comparison between baseline results of patients with and without postoperative tests was done using independent sample t‐test for continuous variables and χ2 for categorical variables. To determine or evaluate the association between independent variables (baseline computed tomography and magnetic resonance imaging findings) and the dependent variable (improvement in VO2 max outcomes, with a binary variable created to indicate whether or not there was an improvement in the percentage of predicted VO2 max) binary logistic regression was performed.
Statistical analyses were conducted using IBM SPSS Statistics, version 25.0 (IBM Corporation, Armonk, NY). Data were presented as mean±SD for continuous variables and frequencies and percentages for categorical variables; P values of <0.05 were considered statistically significant for all analyses.
RESULTS
Study Participants
A total of 392 patients underwent preoperative CPET at our institution; baseline characteristics and preoperative CPET results are depicted in Table 1. A high proportion of patients (68%) had abnormal preoperative VO2 max results.
Table 1.
Baseline Characteristics and Cardiopulmonary Exercise Testing Results of 392 Patients Undergoing Preoperative Cardiopulmonary Evaluation
n=392 | |
---|---|
Sex, n (%) | |
Men | 267 (68.1%) |
Women | 125 (31.9%) |
Age, y | 31.0±9.8 |
Height, cm | 178.4±8.9 |
Weight, kg | 72.5±26.1 |
Body mass index, kg/m2 | 22.7±8.5 |
Anatomical parameters | |
Haller index | 4.6±2.2 |
Correction index (%) | 35.4±14.1 |
Preoperative CPET | |
Estimated METS | 9.2±1.8 |
Actual METS | 7.6±1.8 |
Work, W | 167.9±45.8 |
Work (W per kg body weight) | 2.3±0.6 |
RER | 1.2±0.1 |
DBP at rest, mm Hg | 80.4±10.3 |
DBP at peak exercise, mm Hg | 83.5±12.0 |
SBP at rest, mm Hg | 121.5±14.5 |
SBP at peak exercise, mm Hg | 163.6±25.9 |
Heart rate at rest, bpm | 90.4±15.2 |
Maximum heart rate, bpm | 161.6±16.1 |
VE/VCO2 slope | 27.6±4.9 |
VO2 max | |
Relative VO2 max, mL/kg per min | 26.5±6.2 |
Relative VO2 max/predicted, % | 73.6±15.8 |
% of patients with abnormal VO2 max results | 67.9% |
O2 pulse | |
O2 pulse, mL/beat | 11.7±3.5 |
O2 pulse/predicted, % | 86.0±17.3 |
% of patients with O2 pulse values <80% of predicted | 34.4% |
Anaerobic threshold | |
VO2 at anaerobic threshold, mL/kg per min | 15.8±5.0 |
Peak ventilation | |
VE BTPS, L/min | 67.2±19.5 |
VE BTPS/predicted, % | 43.4±14.0 |
CPET indicates cardiopulmonary exercise testing; DBP, diastolic blood pressure; RER, respiratory exchange ratio; SBP, systolic blood pressure; VE BTPS, ventilation at body temperature ambient pressure, saturated; VE/VCO2 slope, slope of the relationship between ventilation and carbon dioxide output from start of exercise until the respiratory compensation point if reached; VO2 max, maximum rate of oxygen consumption; and W, Watts.
Among patients with a preoperative CPET, 130 (68% men, mean HI 4.7±2.5, mean Correction index 36.7±13.8%) underwent postoperative CPET and were included in the cohort. Postoperative tests were performed at evaluations immediately before bar removal procedure. In this cohort group, preoperative symptoms included dyspnea (96%), difficulty keeping up with peers (84%), palpitations (72%), and syncopal episodes (4%). A large proportion of patients (91%) noted progression of symptoms as they aged. Mean time between MIRPE and post‐repair CPET was 3.4±0.7 years (range, 2.5–7.0). Two bars were placed in 69% of patients and 3 bars in 31%.
Among cases not completing a postoperative test, 184 patients (184/262, 70.2%) did not undergo the bar removal procedure by the end of the study period and 78 patients (78/262, 29.8%) underwent a bar removal procedure during the study period but declined to undergo a postoperative CPET evaluation because of personal reasons that included costs, timing constraints, scheduling conflicts, and insurance issues. Comparison of preoperative CPETs results between patients who underwent a postoperative CPET and those who did not can be found in Table S1.
Comparison Between CPET Outcomes Before and After Surgical Repair
A significant postoperative improvement in all CPET parameters was noted (Table 2), including an increase (P<0.001 for all the comparisons) in the relative VO2 max, absolute VO2 max, O2 pulse, VO2 at anaerobic threshold, and maximal ventilation. Forty patients (31%) had normal VO2 max values preoperatively, whereas 76 postoperative patients (58%) showed normal VO2 max values (P<0.001 for the comparison). Both in preoperative and postoperative tests mean respiratory exchange ratio was >1.15 (Table 2). A significant improvement in the percentage of predicted VO2 max value was found across all prespecified subgroups, including patients with pre‐operative normal VO2 max values and HI ≤3.25 (Table 3).
Table 2.
Cardiopulmonary Exercise Testing Results Comparison Before and After Pectus Excavatum Repair (n=130)
Variable | Preoperative CPET | Postoperative CPET | P value (95% CI for the difference) |
---|---|---|---|
Demographics | |||
Age, y | 32.4±10.0 | 35.5±14.2 | |
Weight, kg | 72.8±15.4 | 75.3±15.4 | <0.001 (1.3 to 3.5) |
Body mass index, kg/m2 | 22.5±3.6 | 23.0±3.5 | 0.002 (0.2 to 0.9) |
Maximum workload | |||
Estimated METS | 9.4±1.5 | 9.7±1.7 | 0.032 (0.02 to 0.50) |
Actual METS | 7.4±1.7 | 8.1±2.0 | <0.001 (0.5 to 1.0) |
Work, W | 174.5±44.8 | 185.2±44.1 | <0.001 (5.9 to 15.5) |
Work (W per kg body weight) | 2.4±0.5 | 2.5±0.5 | 0.040 (0.0 to 0.1) |
Heart rate at rest, bpm | 90.8±13.9 | 83.4±15.3 | <0.001 (4.8 to 10.0) |
Maximum heart rate, bpm | 161.6±15.4 | 164.7±14.3 | 0.013 (0.6 to 5.4) |
RER | 1.22±0.1 | 1.24±0.1 | 0.029 (0.0 to 0.1) |
DBP at rest, mm Hg | 82.1±10.7 | 78.9±8.8 | 0.003 (1.1 to 5.4) |
DBP at peak exercise, mm Hg | 84.4±11.9 | 83.8±11.7 | 0.600 (−2.8 to 1.7) |
SBP at rest, mm Hg | 124.9±14.7 | 123.6±13.6 | 0.376 (−4.4 to 1.6) |
SBP at peak exercise, mm Hg | 164.5±26.2 | 180.6±26.7 | <0.001 (11.7 to 20.3) |
VE/CO2 slope | 27.0±5.2 | 26.1±3.5 | 0.075 (−1.9 to 0.1) |
VO2 max | |||
Relative VO2 max, mL/kg per min | 25.9±6.0 | 28.5±7.0 | <0.001 (1.6 to 3.5) |
Relative VO2 max/predicted (%) | 72.8±15.4 | 84.2±20.6 | <0.001 (8.6 to 14.1) |
Absolute VO2 max, L/min | 1.9±0.6 | 2.1±0.6 | <0.001 (0.2 to 0.3) |
Normal VO2 max values (n) | 30.8% (40) | 58.5% (76) | <0.001 |
O2 pulse | |||
O2 pulse, mL/beat | 11.7±3.6 | 12.9±3.7 | <0.001 (0.8 to 1.6) |
O2 pulse/predicted, % | 84.5±16.9 | 94.3±21.4 | <0.001 (6.9 to 12.6) |
Anaerobic threshold | |||
VO2 at anaerobic threshold, mL/kg per min | 14.6±4.3 | 16.9±6.4 | <0.001 (1.2 to 3.3) |
Maximal ventilation | |||
VE BTPS, L/min | 67.5±18.8 | 73.3±17.7 | <0.001 (3.1 to 8.4) |
VE BTPS/predicted, % | 39.2±9.8 | 48.7±12.4 | <0.001 (7.6 to 11.5) |
DBP indicates diastolic blood pressure; METS, metabolic equivalents; RER, respiratory exchange ratio; SBP, systolic blood pressure; VE BTPS, ventilation at body temperature ambient pressure, saturated; VE/VCO2 slope, slope of the relationship between ventilation and carbon dioxide output from start of exercise until the respiratory compensation point if reached; and VO2 max, maximum rate of oxygen consumption.
Table 3.
Changes in Percentage of Predicted Relative VO2 Max According to Prespecified Subgroup Analysis
Subgroup | Preoperative % of predicted VO2 max | Postoperative % of predicted VO2 max | P value (95% CI for the difference) |
---|---|---|---|
Sex | |||
Women | 75.4±15.3 | 90.4±17.0 | <0.001 (10.7–19.2) |
Men | 71.6±15.5 | 81.4±21.6 | <0.001 (6.2–13.2) |
Age, y | |||
≤32 | 68.5±13.7 | 79.3±19.8 | <0.001 (6.4–15.0) |
>32 | 77.0±16.0 | 89.0±20.4 | <0.001 (8.5–15.6) |
Inspiratory Haller index | |||
>3.25 | 72.1±15.1 | 83.3±20.2 | <0.001 (8.3–14.2) |
≤3.25 | 76.8±17.1 | 88.9±22.5 | 0.005 (4.0–20.3) |
Basal % of predicted VO2 max | |||
Abnormal (<80%) | 64.8±9.3 | 77.4±17.0 | <0.001 (9.2–15.8) |
Normal (≥80%) | 90.8±10.7 | 99.6±19.9 | 0.001 (3.8–13.8) |
VO2 max indicates maximum rate of oxygen consumption.
TEE Evaluation Before and After Correction in a Subgroup of Patients
Thirty‐nine patients had intraoperative TEE imaging available for both MIRPE and bar removal and were included in a subanalysis of CPET results and TEE findings (Figure). Mean time between intraoperative TEE performed at the time of MIRPE and during bar removal was 3.4±0.6 years (range, 2.8–5.5). In this subanalysis the significant improvement in postoperative CPET outcomes was supported by a significant increase in right ventricle velocity time integral and stroke volume at the time of bar removal when compared with presurgical assessment (Table 4).
Figure 1. Forty‐two‐year‐old male patient with severe pectus excavatum presenting dyspnea and chest pain.
A, Front photo of the patient before repair. Note the sternal depression and the distorted anatomy of the chest wall. B, Axial chest computed tomography through the site of maximal posterior sternal displacement shows focal compression of the base of the right ventricle and the tricuspid annulus with leftward displacement of the heart (inspiratory Haller index 4.4). C, Intraoperative transesophageal echocardiography images show compression at the tricuspid annulus and at basal level of the right ventricle before sternal elevation. D, Complete release and improvement of tricuspid annulus and right ventricle diameters after Nuss repair, which correlated with an improvement in VO2 max at postoperative cardiopulmonary exercise testing (from 23.80 to 27.40 mL/kg per minute).
Table 4.
Transesophageal Echocardiography and Cardiopulmonary Exercise Testing Outcomes in the Subanalysis of 39 Patients Who Underwent Intraoperative Transesophageal Echocardiography at Primary Surgery (Before Sternal Elevation) and at Bars Removal
Variable | Preoperative | Postoperative | P value (95% CI for the difference) |
---|---|---|---|
VO2 max | |||
VO2 max, mL/kg per min | 26.1±6.8 | 29.1±8.5 | <0.001 (0.9–5.0) |
VO2 max/predicted (%) | 70.8±17.0 | 82.5±22.0 | <0.001 (6.6–16.9) |
Absolute VO2 max, L/min | 1.9±0.5 | 2.2±0.6 | <0.001 (0.1–0.4) |
O2 pulse | |||
O2 pulse, mL/beat | 11.8±3.4 | 13.1±3.8 | 0.009 (0.3–2.3) |
O2 pulse/predicted, % | 83.0±17.4 | 92.2±24.2 | 0.008 (2.6–15.8) |
Anaerobic threshold | |||
VO2 at anaerobic threshold, mL/kg per min | 14.4±4.4 | 17.5±7.5 | 0.006 (0.9–5.3) |
TEE | |||
RVOT VTI, cm | 14.2±3.3 | 16.3±3.4 | 0.005 (0.7–3.5) |
Right ventricle SV, mL | 41.1±13.2 | 54.6±15.6 | <0.001 (7.3–17.6) |
RVOT indicates right ventricle outflow tract; SV, stroke volume; TEE, transesophageal echocardiography; VO2 max, maximum rate of oxygen consumption; and VTI, velocity time integral.
Association Between Baseline Characteristics and CPET Results
The association between cardiopulmonary outcomes and baseline anatomical indices as assessed by cross‐sectional imaging was investigated. Inspiratory imaging was performed in all the patients, with end‐expiratory imaging available in 85 (65%) of the 130 patients in the cohort. No significant association (P>0.05 for all associations) was found in a univariate analysis between the improvement in VO2 max and anatomical variables (HI, Correction index, sternal tilt, or cardiac compression index) (Table 5).
Table 5.
Association Between Baseline Anatomical Characteristics and Cardiopulmonary Improvement
Variable | P for association | Odds ratio | 95% CI for odds ratio |
---|---|---|---|
Inspiratory measurements | |||
Haller index | 0.12 | 1.27 | 0.94–1.71 |
Correction index | 0.12 | 1.03 | 0.99–1.06 |
Sternal tilt | 0.57 | 1.01 | 0.97–1.05 |
Cardiac compression index | 0.20 | 1.37 | 0.84–2.24 |
Expiratory measurements | |||
Haller index | 0.56 | 1.06 | 0.88–1.27 |
Correction index | 0.48 | 1.01 | 0.98–1.04 |
Sternal tilt | 0.86 | 1.01 | 0.95–1.06 |
Cardiac compression index | 0.94 | 1.02 | 0.64–1.63 |
DISCUSSION
Opinions differ on whether patients with PE suffer cardiopulmonary limitations. 2 , 4 , 5 This controversy affects referral of patients for evaluation to centers experienced with this disease and impacts the ability to obtain insurance coverage for surgical correction. The National Health Service, the publicly funded healthcare system of the United Kingdom, has recently made the decision that treatment for PE will no longer be funded, 18 adversely impacting the quality of life for patients suffering cardiopulmonary limitations. 6 , 19 , 20 , 21
The debate about whether surgical PE repair provides cardiopulmonary improvement remains unsettled owing to the limitations of previous work in this area, including small underpowered studies showing contradictory results and the use of heterogeneous diagnostic methods and outcomes to determine the presence of cardiopulmonary deficits. 2 , 4 Our previous studies examining >160 patients who underwent intraoperative TEE showed significant and immediate improvements in anatomic and functional cardiac parameters following repair. 13 , 14 The TEE improvement in adults aged >30 years was also striking with a >65% increase in right ventricular output seen following surgical PE correction. 3 Others have reported similar positive outcomes by TEE, and improvement in cardiac magnetic resonance imaging functional parameters has also been reported 1 year after PE repair. 22 , 23 Nevertheless, validation of anatomical and functional imaging parameters using direct physiological assessment, such as CPET, is important. This study was performed to take the next step in documenting gains in exercise function following surgical PE correction.
CPET is an established diagnostic test capable of determining exercise capacity and providing information about pulmonary and cardiovascular systems function. Therefore, it is an appropriate method to assess the physiologic impact of PE and the potential improvement in deficits following surgical correction. 8 , 24 Although some studies have showed no changes or only mild improvements in CPET results following surgical repair, 25 , 26 most studies have shown postsurgical improvement in cardiopulmonary parameters in pediatric patients. 9 , 10
Compared with pediatric patients, the cardiopulmonary impact of PE surgical repair in adult patients is less well studied. In our study, 68% of the 392 adult patients with preoperative evaluations had measurable cardiopulmonary deficits. In the 130 patients with post‐repair CPETs, a significant improvement was seen in all cardiopulmonary parameters. To the best of our knowledge, only 2 related publications have addressed the physiologic impact of PE surgical repair in adult population. 11 , 12 An underpowered prospective study showed a non‐significant trend towards improvement in VO2 max in 15 patients following MIRPE. 11 A second prospective study including 70 patients documented significant improvements in CPET parameters following surgical repair using an open modified Ravitch procedure. 12 In at least 1 study, the Nuss procedure has been associated with greater pulmonary function improvements following bar removal compared with the Ravitch procedure. 27 Because there is a greater loss of chest wall pliability associated with the Ravitch procedure as compared with the Nuss procedure, the Nuss procedure has been proposed as the superior method of surgical PE correction. 27 , 28 In addition, this improved chest wall pliability may contribute to the significant improvements detected by CPET despite the presence of the intrathoracic bars in our study.
Our post‐repair CPETs were performed before bar removal. The presence of 2 (69%) and 3 (31%) intrathoracic bars may have significantly limited the physiological improvements detected in our patients, and further improvements may be possible with CPET evaluations performed at 6 months to 1 year after bar removal. In this investigation, the percentage of patients who reached normal VO2 max values increased significantly after surgical correction (31% before surgery versus 58% after surgery, P<0.001). Nevertheless, nearly half of patients did not reach normalization while their bars were still in place. Our study found consistent CPET improvements in both younger adults (aged ≤32 years) and older adults (aged >32 years) suggesting that PE correction may be equally beneficial to older patients. Although it is possible that some level of incomplete recovery occurs because of structural damage resulted from long periods of cardiac compression and/or displacement caused by the PE defect, the improvements seen in all age groups argued against this. Whether or not further improvements in CPET parameters may be realized at longer term evaluation following bar removal remains a subject for future investigation.
Another important finding in the subgroup analyses was the significant improvement in the percentage of predicted VO2 max even in patients with apparently normal preoperative cardiopulmonary function (95% were symptomatic). Therefore, even patients with preoperative normal CPET parameters should be considered for repair if symptoms or other factors support surgery.
In a subset of patients undergoing CPET before and after surgical repair and with intraoperative TEE imaging available both at the time of MIRPE and at bar removal, there was a significant increase in TEE cardiac functional parameters at the time of bar removal. These improvements parallel the physiologic benefits assessed by CPET, further support the implications of our findings, and support the observations of previously published TEE studies in this population. 13 , 14 , 22
The relationship between anatomic parameters assessed by cross‐sectional imaging and cardiopulmonary impact is controversial. Some investigators found that anatomical variables, such as HI, Correction index, sternal tilt, or the site of maximum compression may predict the adverse physiologic impact of PE on cardiopulmonary function. 29 , 30 , 31 , 32 In contrast, other reports found no association between cross‐sectional indices and cardiac function. 13 , 33 In our study, an association between the preoperative cross‐sectional imaging anatomic parameters and the improvement in VO2 max was not detected, probably as a result of the wide heterogeneity of PE malformations (including differences in the depth of the depression, location of the site of maximum depression, and severity of heart displacement) 34 which may contribute to the inability of standard imaging indices to consistently capture the severity of the adverse physiological impact of PE. Based on our data, we suggest that the approach to assessment of PE severity should not be based on a single diagnostic test or parameter, which clearly carries implications given that specific anatomical parameters, such as HI, are used as criteria for surgical intervention insurance coverage. 35 Indeed, our study shows that the surgical eligibility HI threshold of >3.25 did not segregate patients who experienced physiologic improvement as assessed by the percentage of predicted VO2 max following surgery, from those who did not.
The strengths of this study include the use of physiologic, as opposed to anatomic, assessment of cardiopulmonary function using CPET parameters as well as a larger cohort of patients than previous published literature. Nevertheless, our conclusions may be limited by the retrospective nature of the study and the lack of formal estimation of patients’ physical activity before and after surgical repair. Additionally, there was a statistically significant increase in patients’ weight and body mass index between the pre‐ and postsurgical assessment; to minimize the impact of this limitation we also compared the absolute VO2 max values. Furthermore, the greater patient weight in postoperative testing would theoretically limit our ability to detect physiological improvement.
Our study carries implications on the needs for future investigations. First, CPET assessment of the long‐term durability of the positive physiologic impact as well as the time required to peak realization of physiologic improvement following PE repair requires study. Such a study may provide insight as to whether cardiopulmonary improvement requires additional time following bar removal for patients who failed to reach normal VO2 max values at pre‐bar removal CPET evaluation. An additional research focus should include identification of the combination of anatomical and functional parameters most capable of predicting the greatest improvement in cardiopulmonary function following surgical repair. Identification of such parameters would be highly useful for identifying patients in whom corrective surgery will have the most substantial impact and for calculating the risk‐benefit ratios for operative repair in an aging population. 3
CONCLUSIONS
To our knowledge, this investigation is the first to demonstrate a consistent improvement in cardiopulmonary function as assessed by CPET for adult patients with PE undergoing MIRPE. Results strongly support the existence of adverse cardiopulmonary consequences of PE as well as the benefits of surgical repair, even for patients with apparently normal baseline cardiopulmonary function and without severe anatomical defects.
There is an urgent need for a more holistic approach to PE that emphasizes physiologic disability and is not focused solely on the cosmetic consequences. Further investigations into the long‐term physiological effects of PE repair as well as the predictors of improvement of adverse physiology will be important for optimizing patient selection for correction.
Sources of Funding
None.
Disclosures
Jaroszewski is a consultant and has IP/royalty rights under Mayo Clinic Ventures with Zimmer Biomet, Inc. The remaining authors have no disclosures to report.
Supporting information
Table S1
Supplemental Material is available at https://www.ahajournals.org/doi/suppl/10.1161/JAHA.121.022149
For Sources of Funding and Disclosures, see page 8.
See Editorial by XXXX
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Supplementary Materials
Table S1