Objective: To compare surgical and device closure of isolated secundum atrial septal defect (ASD) in terms of hospital costs, clinical outcome, and impact on the patient and family.
Design: Prospective, observational study.
Setting: Paediatric tertiary referral centre.
Patients: Consecutive local children with a secundum ASD, admitted between 1 May 1999 and 1 May 2001.
Methods: Parents completed a standardised questionnaire at recruitment (on admission), at discharge, and one month after the procedure. Clinical and hospital generated cost data were collated at discharge.
Results: 62 children were included in the analysis: 19 who underwent surgical repair and 43 who underwent device closure with the Amplatzer septal occluder. Median procedure times and hospital stay were significantly longer for surgical patients (170 (147 to 180) v 92 (70 to 115) minutes and 88 (78 to 112) v 29 (28 to 30) hours, respectively; p < 0.01). There was no difference in the complication rate. No device patients required intensive care or blood products. The median values for postoperative pain score, analgesia use, and convalescence time were greater for surgical patients. The median cost of each procedure was similar, but higher nursing and laboratory costs contributed to a slightly greater total cost for surgical repair (Aus$12 969 ($11 569 to $14 215) v Aus$11 845 ($10 669 to $12 555), p = 0.03).
Conclusions: Device closure of ASD involves a shorter hospital stay, causes less discomfort and familial disturbance, and carries less cost than surgical closure. However, there should be guarded acceptance of this technique until long term data are available.
- atrial septal defect
- Amplatzer septal occluder
- cost analysis
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Improved clinical outcome is a necessary but insufficient justification for the replacement of conventional treatment with a new health intervention. Total costs, functional health status, and patient satisfaction also need to be considered, and are prominent in the current debate over the procedure of choice for closure of isolated secundum atrial septal defects (ASD).
In many paediatric cardiac institutions surgical closure is reserved for the patients whose families choose surgical repair or whose lesions remain unsuitable for device closure.1–3 Surgical closure of secundum ASD has a high success rate, with low morbidity and a favourable long term outcome.4,5 In comparison, ASD occlusion devices vary in their success, but the closure rate with the Amplatzer septal occluder6 (AGA Medical, Golden Valley, Minnesota, USA) is close to 95% and the morbidity is low.7–11 Advantages claimed for device closure include better cosmesis, avoidance of cardiopulmonary bypass, and shorter hospital stay.1,12,13 However, there is no long term information about the outcome and safety of the intracardiac prostheses.
We gathered data prospectively from contemporary groups of children who were suitable for either surgical or device closure of secundum ASD. We assessed the impact of each procedure on the patient and their family, and the total cost of device closure relative to surgical closure in a single institution within the Australian health system.
The study was a prospective observational survey using structured questionnaires.
We recruited consecutive patients from Victoria who were admitted to the Royal Children's Hospital between 1 May 1999 and 1 May 2001 for closure of an isolated secundum ASD. During this time there was no institutional policy for selecting either surgical or device closure for moderate sized central defects of the oval fossa. The treating cardiologist and parents made the decision regarding closure during the outpatient assessment.
Surgical ASD closure
Surgical ASD closure was undertaken through a limited midline sternotomy (n = 7), lower half sternotomy (n = 7), or lateral thoracotomy (n = 5), using cardiopulmonary bypass. Closure of the defect was accomplished either directly (n = 10) or with a pericardial patch (n = 9).
Patients recovered in the intensive care unit and were transferred to the cardiology ward after extubation. According to unit protocol, all received intravenous morphine postoperatively for the first 24 hours. Oral codeine and paracetamol were then given as required.
Transcatheter ASD closure
All transcatheter ASD closures were performed by one of two paediatric cardiac interventionalists, using only the Amplatzer septal occluder. The procedure was carried out under general anaesthesia using previously described methods.14 Aspirin was given for three months after device insertion at antiplatelet dosage.
Clinical data collection
Patients were recruited at the time of clerking into the hospital. The parents of each patient completed a standardised questionnaire on admission, at discharge, and at the first outpatient follow up appointment. Clinical information was collated at the time of discharge from hospital.
The total cost to the hospital of each patient's admission was calculated using the Royal Children's Hospital's computerised clinical costing system, “Transition II” (Eclipsys, The Outcomes Company, Boca Raton, Florida, USA). This system gives a value to each episode of patient care. The method of costing relies on each service area of the hospital weighting the product or services they provide. Costs from the general ledger are then allocated to these products, based on the weighting. Indirect costs are also allocated to each product, but capital and depreciation costs are not included.
As a result, the system produces an itemised cost report for each patient which includes the costs of the operating theatre and anaesthesia, the cost of the ASD device, surgical and medical fees, nursing care, laboratory investigations, radiology, pharmaceutical costs, and physiotherapy. All values are expressed in Australian dollars.
Results were analysed according to the final successful method of closure for each patient. Non-parametric statistical methods were used. Continuous data were compared using the Mann–Whitney U test and categorical data using Fisher's exact test. The results are expressed as median (interquartile range). A probability value of p < 0.05 was considered significant.
The results represent 62 children: 19 (10 male, 9 female) who underwent closure by surgery and 43 (22 male, 21 female) who underwent closure by device. There was one failed attempt at device closure, with subsequent successful surgery. This child's data were included with those of the surgical patients. Five additional patients were admitted for device closure but found unsuitable during transoesophageal echocardiography in the catheter laboratory. They were excluded from the analysis.
These children were aged from 0.9–17 years, and they weighed from 6.6–78 kg. The largest diameter of the atrial defect on preoperative transthoracic echocardiography ranged from 6–30 mm. Table 1 gives the clinical characteristics of each group. The children undergoing surgical closure were significantly younger and smaller than those undergoing device closure, though the diameter of the defects in each group was similar.
A comparison of the procedural aspects of all patients studied is shown in table 2. Children undergoing device closure experienced a shorter duration of anaesthesia, a shorter inpatient stay, required analgesia for a shorter period, and had a lower postoperative pain score than surgical patients. Six children in the surgical group (< 12 kg) required packed blood cells for the cardiopulmonary bypass prime. Blood products were not required by any patient in the device group. Complications occurring in the two groups are listed in table 3.
By the first post-procedural day, 1/19 surgical patients and 14/43 device patients had resumed preadmission physical activity levels (p < 0.01), and by one week these proportions were 4/19 and 36/43, respectively (p < 0.01).
At the time of discharge more parents of children in the surgical group than in the device group were concerned about the tenderness or vulnerability of their child's wound (10/19 v 4/43, respectively; p < 0.01).
Echocardiographic evaluation three months after the procedure showed a small residual shunt in four patients in the device group (complete closure rate 91%). No patient had a residual shunt in the surgical group (p = 0.3).
Approximately one third of both groups of parents were concerned about the long term outcome of the procedure. Parents of children in the surgical group were worried about the invasiveness of the procedure, the effects of cardiopulmonary bypass, and the residual scar. Parents of children in the device group expressed concerns about dislodgement of the device and the long term safety of the device.
Fathers of children undergoing surgical closure took a median of four days off work, versus one day taken by fathers of those undergoing device closure. There was no significant difference in the amount of leave taken by mothers.
Figure 1 is a simplified account of the median hospital cost of surgical and device closure for the individuals in the study. Procedural costs (theatre + anaesthetic + device as applicable) were less for surgical closure than for device closure. However, the requirement for intensive care and the longer hospital stay caused greater nursing, laboratory, and pharmacy costs to contribute to a slightly greater total cost for surgical repair (Aus$12 969 ($11 569 to $14 215) v Aus$11 845 ($10 669 to $12 555)).
Though transcatheter device closure may be appropriate treatment for secundum ASD, there has never been a truly randomised comparison of device and conventional surgical repair.
This is a prospective assessment of children with isolated, moderate sized, central defects of the oval fossa, who were potential candidates for either surgical or device repair. We examined contemporary study groups and completed the study four years after device repair was initiated in our institution,14 minimising any learning curve effects.
While the above factors should diminish bias in the comparison, there were fewer patients in the group undergoing surgery, and they were significantly younger and smaller than the group undergoing device repair. This dissimilarity between the groups is unlikely to affect the cost of repair, but the median size of the atrial defects in each group was similar, possibly indicating proportionally larger lesions in the surgical group.
The age and weight differences between our study groups indicate a bias towards surgical treatment for younger and smaller children. This is supported by cautionary evidence in published reports,15 and by the fact that a major complication occurred in the smallest and youngest child in the device group of our study. A current priority should be the improvement of our ability to select patients appropriately for device closure.
We have contributed to contemporary data by assessing a broad range of short term outcomes, but importantly this is the first prospective analysis of the cost of device versus surgical closure of ASD in the Australian health care system. The major area of cost savings to the hospital is in elimination of the requirement for intensive care, and the greatly reduced length of hospital admission. However, the significant cost of the device itself may alter the balance of costs in different health care systems, particularly in less industrialised nations. Recently published abstracts show that transcatheter closure of an ASD carries a substantial cost advantage in Switzerland,16 but surgical closure appears to carry a cost advantage in the UK and Thailand.17,18
In a paediatric population, device closure of an isolated secundum ASD carries many short term advantages for the patient, family, and the treating hospital. However, final judgement in comparison with conventional surgical treatment will not be possible until long term outcome data are available.
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