Literature DB >> 34853877

Efficacy of Short-Term Oral Prednisolone Treatment in the Management of Pericardial Effusion Following Pediatric Cardiac Surgery.

Masahiro Mizumoto1, Naoki Masaki2, Sadahiro Sai2.   

Abstract

A standard treatment for pericardial effusion without cardiac tamponade after pediatric cardiac surgery has not been established. We evaluated the efficacy of short-term oral prednisolone administration, which is the initial treatment for postoperative pericardial effusion without cardiac tamponade at our institution. Between October 2008 and March 2020, 1429 pediatric cardiac surgeries were performed at our institution. 91 patients required postoperative treatment for pericardial effusion. 81 were treated with short-term oral prednisolone. Pericardial effusion was evaluated using serial echocardiography during diastole. Pericardial drainage was performed for patients with circumferential pericardial effusion with a maximum diameter of ≥ 10 mm or signs of cardiac tamponade. Short-term oral prednisolone treatment was administered to patients with circumferential pericardial effusion with a maximum diameter of < 10 mm or localized pericardial effusion with a maximum diameter of ≥ 5 mm. Patients with localized pericardial effusion with a maximum diameter of < 5 mm were observed. Prednisolone (2 mg/kg/day) was administered orally for 3 days, added as needed. Short-term oral prednisolone treatment was effective in 71 cases and 90% of patients were regarded as responders. The remaining patients were deemed non-responders who required pericardial drainage. Overall, 55 responders were deemed early responders whose pericardial effusion disappeared within 3 days. There were no cases of deaths, infections, or recurrence of pericardial effusion. The amount of drainage fluid on the day of surgery was higher in the non-responders. In conclusion, short-term oral prednisolone treatment is effective and safe for treating pericardial effusion without cardiac tamponade after pediatric cardiac surgery.
© 2021. The Author(s).

Entities:  

Keywords:  Pediatric cardiac surgery; Pericardial effusion; Postpericardiotomy syndrome; Prednisolone; Steroid

Mesh:

Substances:

Year:  2021        PMID: 34853877      PMCID: PMC9005424          DOI: 10.1007/s00246-021-02783-y

Source DB:  PubMed          Journal:  Pediatr Cardiol        ISSN: 0172-0643            Impact factor:   1.655


Introduction

The incidence of pericardial effusion (PE) after pediatric cardiac surgery has decreased due to advances in perioperative medical care techniques; however, it is still not uncommon. The postoperative PE should be taken care, because it carries the risk of progressing to cardiac tamponade. In the event of accompanying cardiac tamponade, it is generally accepted that pericardial drainage should be indicated [1]. However, in the absence of cardiac tamponade, there is no standard treatment established for postoperative PE, as the preferred treatment differs between various institutions. Generally, several studies have indicated that oral aspirin is often selected as the initial treatment for postpericardiotomy syndrome, whereas additional steroids and colchicine are administered in refractory cases [2-4]. However, there is no consensus regarding the doses to be administered, administration methods, or durations. Furthermore, it takes time for the therapeutic effects to appear. At our institution, short-term oral prednisolone administration is the initial treatment for postoperative PE without cardiac tamponade. In this study, we retrospectively evaluated the effectiveness of this treatment.

Patients and Methods

Between October 2008 and March 2020, 1429 pediatric cardiac surgeries were performed at our institution and postoperative PE requiring therapeutic intervention was observed in 91 patients (6.4%). Among these patients, 81 received short-term oral prednisolone treatment as the first choice. This study was approved by Miyagi children’s hospital ethics committee and all patients provided informed consent. The study subjects, comprising 45 boys and 36 girls, had a median age of 27.0 (11.0–67.5) months and a weight of 10.1 (7.0–16.3) kg. Repeat median sternotomy was performed in 14 of the patients. For all patients, PE was evaluated in the circumferential or localized regions (anterior, lateral, posterior, and inferior) using serial echocardiography, per the short axis, long axis, and four-chamber views in the diastolic phase. The maximum diameter (mm) between the epicardium and pericardium was measured. Figure 1 shows our postoperative PE treatment protocol. Pericardial drainage was indicated in patients with signs of cardiac tamponade or those with circumferential PE with a maximum diameter of ≥ 10 mm. Short-term oral prednisolone treatment was indicated for patients with circumferential PE with a maximum diameter of < 10 mm or localized PE with a maximum diameter of ≥ 5 mm in the absence of signs of cardiac tamponade. In our regimen, prednisolone was administered orally at 2 mg/kg/day, in two divided doses, for 3 days, added as needed. There was no concomitant use with anti-inflammatory drugs (NSAID) such as aspirin or colchicine for postoperative PE. Patients with localized PE with a maximum diameter of < 5 mm were observed. Table 1 shows the main heart diseases and the types of surgery. Ventricular septal defect, tetralogy of Fallot, and atrial septal defect (ASD) accounted for most of the cases. Furthermore, pulmonary artery banding was commonly performed in the palliative surgery. For patients who underwent palliative surgery or for those in whom it was anticipated that subsequent repeat surgery was necessary, a Gore-Tex® sheet (W. L. Gore & Associates, Inc., USA) was placed as a pericardial substitute, while direct closure of the pericardium was performed in the other cases.
Fig. 1

Treatment protocol for PE. PE pericardial effusion, PSL prednisolone

Table 1

Cardiac diagnosis and type of surgery

Cardiac disease (n = 81)Type of surgery (n = 81)
VSD24VSD closure24
TOF17TOF repair17
ASD10ASD closure10
Valvular disease8PAB8
AVSD6Valvular operation8
PA/VSD3Fontan3
SV3mBTS2
Others10Others9

ASD atrial septal defect, AVSD atrioventricular septal defect, mBTS modified Blalock–Taussig shunt, PA pulmonary atresia, PAB pulmonary artery banding, SV single ventricle, TOF tetralogy of Fallot, VSD ventricular septal defect

Treatment protocol for PE. PE pericardial effusion, PSL prednisolone Cardiac diagnosis and type of surgery ASD atrial septal defect, AVSD atrioventricular septal defect, mBTS modified Blalock–Taussig shunt, PA pulmonary atresia, PAB pulmonary artery banding, SV single ventricle, TOF tetralogy of Fallot, VSD ventricular septal defect Patients were divided into a responder group, comprising patients whose PE disappeared or significantly decreased with short-term oral prednisolone treatment alone, and a non-responder group, comprising patients who required pericardial drainage after prednisolone treatment. Responders were defined as the disappearance or decrease of localized PE to < 5 mm in all echocardiography, per the short axis, long axis, and four-chamber views. Non-responders were defined as the increase of circumferential PE to > 10 mm in any view of echocardiography or accompanying cardiac tamponade. We analyzed the pre-, intra-, and postoperative risk factors for the non-responders of short-term oral prednisolone treatment. The postoperative blood testing, chest radiography, and echocardiography were performed at 1 week after the surgery.

Statistical Analyses

JMP 15 (SAS Institute Japan, Tokyo) was used to perform chi-square and Fisher’s exact tests for the statistical analyses. The data are shown as the median ± interquartile range, and a p value of < 0.05 was considered significant.

Results

There were no deaths, side effects of prednisolone, such as infection, or recurrence of PE. The prednisolone treatment was commenced on postoperative day 8 (8.0–10.0) and the drainage tube after the initial surgery was removed on postoperative day 2.0 (2.0–3.0) in all 81 cases who were administered oral prednisolone. Figure 2 shows the outcomes of the short-term oral prednisolone treatments. In 71 cases, the treatments were effective and approximately 90% of the patients were regarded as responders. Pericardial drainage was required for 10 non-responders. In the non-responder group, the median period of oral prednisolone treatment was 3.0 (1.0–3.0) days, and pericardial drainage was performed immediately after confirmation of increased PE during short-term oral prednisolone treatment. There were no complications from cardiac tamponade and delayed drainage. The property of drained fluid was bloody in eight cases and chylous in two cases. In the responder group, the median period of oral prednisolone treatment and until disappearance of or marked decrease in PE were 3.0 (3.0–3.0) and 3.0 (1.0–3.0) days, respectively. Of these, 55 of the responders were considered as early responders, with a response observed within 3 days from the commencement of the oral prednisolone administration (Fig. 3). Although the remaining 16 responders received additional oral prednisolone, PE was disappeared or significantly decreased without complications or side effects of prednisolone.
Fig. 2

Results of short-term oral PSL treatment. PE pericardial effusion, PSL prednisolone

Fig. 3

Day of effect on PE decrease in PSL responders. PE pericardial effusion, PSL prednisolone

Results of short-term oral PSL treatment. PE pericardial effusion, PSL prednisolone Day of effect on PE decrease in PSL responders. PE pericardial effusion, PSL prednisolone Tables 2 and 3 show the analysis of the risk factors of prednisolone non-responders. Among the preoperative factors, the hemoglobin level was higher in non-responders, but there was no significant difference in the frequency of cyanotic heart disease, which can be a cause of polycythemia. Although there were no significant differences between the intra- and postoperative factors, the postoperative cardiothoracic ratio and amount of drainage fluid on the day of surgery tended to be higher in the non-responders than in responders and the inflammatory reaction level tended to be higher in the responders than in non-responders.
Table 2

Risk analysis of PSL non-responder characteristics and preoperative factors

VariablesResponderNon-responderp
(n = 71)(n = 10)
Age (month)29.0 (11.0–66.0)19.5 (9.8–192.8)0.807
Male/female37/348/20.172
Body weight (kg)10.5 (7.1–16.1)9.8 (5.4–32.4)0.858
Previous surgery1220.681
CTR (%)54.5 (51.0–59.1)56.5 (51.0–61.4)0.486
LVEF (%)65.4 (56.3–68.4)69.2 (58.9–73.7)0.273
Hb (g/dL)13.5 (12.5–14.3)15.2 (13.5–16.8)0.019
BNP (pg/mL)23.6 (13.2–51.5)24.3 (19.7–92.9)0.457
Cardiac disease0.512
 VSD231
 TOF143
 ASD91
 Valvular disease62
 Others193

ASD atrial septal defect, BNP brain natriuretic peptide, CTR cardiothoracic ratio, LVEF left ventricular ejection fraction, PSL prednisolone, TOF tetralogy of Fallot, VSD ventricular septal defect

Table 3

Risk analysis of PSL non-responder operative and postoperative factors

VariablesResponderNon-responderp
(n = 71)(n = 10)
 < Operative factors > 
 Emergent or urgent220.073
 Operation time (min)275 (182–412)304 (166–401)0.88
 CPB use6280.619
 CPB time (min)144 (92–232)175 (149–233)0.427
 Aorta clamp time (min)67 (46–125)108 (88–122)0.3
 Blood transfusion5160.528
 < Postoperative factors > 
 CTR (%)57.0 (53.0–61.0)61.0 (57.5–66.0)0.019
 Hb (g/dL)12.9 (11.8–14.4)13.9 (12.9–15.1)0.151
 CRP (mg/dL)2.56 (0.77–3.10)1.87 (0.20–3.23)0.113
 BNP (pg/mL)117 (85–224)192 (102–372)0.35
Drainage output (mL/kg/h)
 (First 4 h)1.20 (0.61–2.15)1.80 (0.98–3.89)0.087

BNP brain natriuretic peptide, CPB cardiopulmonary bypass, CTR cardiothoracic ratio, PSL prednisolone

Risk analysis of PSL non-responder characteristics and preoperative factors ASD atrial septal defect, BNP brain natriuretic peptide, CTR cardiothoracic ratio, LVEF left ventricular ejection fraction, PSL prednisolone, TOF tetralogy of Fallot, VSD ventricular septal defect Risk analysis of PSL non-responder operative and postoperative factors BNP brain natriuretic peptide, CPB cardiopulmonary bypass, CTR cardiothoracic ratio, PSL prednisolone

Discussion

In this study, we followed our institution’s treatment protocol for PE after cardiac surgery and demonstrated that the administration of oral prednisolone at a dose of 2 mg/kg/day for 3 days results in good outcomes, as indicated by the 90% response rate with no deaths or complications. In addition, its effect was observed in the short term, as the median period until the disappearance of or marked decrease in PE after the prednisolone treatments began was 3.0 days. The incidence of PE after congenital heart disease surgery has declined due to advances in perioperative medical care. In the 1980s, the PE rate was 53–65% [5-7], but it declined to 13.6–23.0% in the 1990s [8-10] and to 10% in recent years [11, 12]. Despite the consistent decline of the PE rate, postoperative PE remains a serious complication that can cause cardiac tamponade. In this study, the incidence of PE requiring treatment after pediatric cardiac surgery was 6.4%. Pericardial drainage is indicated for patients with signs of cardiac tamponade. However, the standard treatment for PE in patients who have no symptoms of cardiac tamponade after cardiac surgery differs between institutions. In general, postpericardiotomy syndrome is considered a potential cause of PE; therefore, oral aspirin or NSAID are often selected as the initial treatment. However, the use of aspirin has some shortcomings as its therapeutic effect is variable and it takes time for PE to decrease [10, 11]. Additionally, oral aspirin treatment has been reported to have no prophylactic effect on postoperative PE [7]. In refractory cases, additional administration of steroids or colchicine can be considered [2-4]. Only a few reports have examined any details of steroid treatment for PE after pediatric cardiac surgery, such as the type of drug to use or the method and duration of administration [11, 12]. Reports on the use of colchicine for postoperative PE often describe its prophylactic use and treatment of recurrence in adults [3, 13–18]. However, its safety and efficacy in children are unclear [12]. Furthermore, colchicine therapy is often administered over several months and in conjunction with oral NSAID (aspirin and ibuprofen) and prednisolone. Therefore, its clinical use in children is considered arduous. Dalili et al. [11] reported that oral aspirin treatments of 50–70 mg/kg/day (divided into four doses) resulted in a response rate of 77%, with a mean time to PE disappearance of 13 ± 8 days, whereas oral prednisolone treatments of 1 mg/kg/day (divided into four doses) resulted in a response rate of 90%, with a mean time to PE disappearance of 7 ± 3 days. The response rate in the current study was equivalent to these results; however, it is likely that our treatment protocol was more useful because patients in the current study only received two doses of oral prednisolone per day and its therapeutic effects were observed in the shorter term. For proper drug compliance in children, it is important for clinicians to consider a shorter term of treatment and smaller number of doses per day. Shorter-term treatments may also lead to reduced hospital stays. Alternatively, it should be noted that there were 10 non-responders who required pericardial drainage. Various risk factors for PE after pediatric cardiac surgery have been reported, such as advanced age, large physique, female sex, trisomy 21, ASD surgery, the Fontan procedure, cardiopulmonary bypass, postoperative warfarin administration, large amounts of postoperative fluid drainage, and previous cardiac surgery [10–12, 19]. Considering these variables, we conducted a prednisolone unresponsiveness risk factor analysis using patient background and pre-, intra-, and postoperative factors. Although the patient background and pre- and intraoperative factors were not significant indicators of the ineffectiveness of prednisolone, among the postoperative factors, the cardiothoracic ratio was significantly higher and the amount of drainage fluid on the day of surgery tended to be higher in non-responders. The fluid drained was bloody in eight of the 10 non-responders; therefore, a large amount of bloody drainage fluid on the day of surgery might be a predictor of postoperative PE and non-responsiveness to short-term prednisolone treatment. This study has some limitations. First, the sample size was small. Based on our encouraging results, further studies with a larger number of subjects are needed. Second, our protocol did not specify in detail when to commence short-term oral prednisolone treatments. Furthermore, routine postoperative echocardiography was performed 1 week after surgery; therefore, short-term oral prednisolone treatment was started on postoperative day 8 in most cases. In previous studies [10, 11], the mean timing of the PE diagnosis was reported to be on postoperative day 11 and most cases were diagnosed within 2 weeks after cardiac surgery. Thus, the commencement of short-term oral prednisolone treatment on postoperative day 8 in this study might have contributed to the high-treatment response rate. Although earlier postoperative treatments could have been more effective, the appropriate timing of the treatments should be carefully examined. Prophylactic steroid use for postpericardiotomy syndrome was ineffective in a previous study [20]. In addition, attention should be paid to adverse reactions to steroid use in the early postoperative phase.

Conclusion

In this study, short-term oral prednisolone administration for the treatment of PE with no signs of cardiac tamponade after pediatric cardiac surgery showed a notable response rate of 90% with an earlier therapeutic effect, indicating that it is a safe and effective novel treatment.
  20 in total

1.  Colchicine for Post-Operative Pericardial Effusion: Preliminary Results of the POPE-2 Study.

Authors:  Philippe Meurin; Sophie Lelay-Kubas; Bernard Pierre; Helena Pereira; Bruno Pavy; Marie Christine Iliou; Jean Louis Bussiere; Helene Weber; Jean Pierre Beugin; Titi Farrokhi; Anne Bellemain-Appaix; Laura Briota; Jean-Yves Tabet
Journal:  J Am Coll Cardiol       Date:  2015-09-08       Impact factor: 24.094

2.  Decreased incidence of postoperative pericardial effusions after cardiac surgery for congenital heart disease.

Authors:  A S Prabhu; R D Ross; M R Heinert; H L Walters; M Hakimi
Journal:  Am J Cardiol       Date:  1996-04-01       Impact factor: 2.778

Review 3.  Colchicine for the primary prevention of the postpericardiotomy syndrome.

Authors:  Diana R Mack; William D Cahoon; Denise K Lowe
Journal:  Ann Pharmacother       Date:  2011-06-07       Impact factor: 3.154

Review 4.  Management of Acute and Recurrent Pericarditis: JACC State-of-the-Art Review.

Authors:  Juan Guido Chiabrando; Aldo Bonaventura; Alessandra Vecchié; George F Wohlford; Adolfo G Mauro; Jennifer H Jordan; John D Grizzard; Fabrizio Montecucco; Daniel Horacio Berrocal; Antonio Brucato; Massimo Imazio; Antonio Abbate
Journal:  J Am Coll Cardiol       Date:  2020-01-07       Impact factor: 24.094

5.  Determinants of pericardial drainage for cardiac tamponade following cardiac surgery.

Authors:  Giulio Pompilio; Sara Filippini; Marco Agrifoglio; Elisa Merati; Gianfranco Lauri; Stefano Salis; Francesco Alamanni; Alessandro Parolari
Journal:  Eur J Cardiothorac Surg       Date:  2011-02-03       Impact factor: 4.191

6.  COlchicine for the Prevention of the Post-pericardiotomy Syndrome (COPPS): a multicentre, randomized, double-blind, placebo-controlled trial.

Authors:  Massimo Imazio; Rita Trinchero; Antonio Brucato; Maria Elena Rovere; Anna Gandino; Roberto Cemin; Stefania Ferrua; Silvia Maestroni; Edoardo Zingarelli; Alberto Barosi; Caterina Simon; Fabrizio Sansone; Davide Patrini; Ettore Vitali; Paolo Ferrazzi; David H Spodick; Yehuda Adler
Journal:  Eur Heart J       Date:  2010-08-30       Impact factor: 29.983

7.  The effect of short-term prophylactic methylprednisolone on the incidence and severity of postpericardiotomy syndrome in children undergoing cardiac surgery with cardiopulmonary bypass.

Authors:  A R Mott; C D Fraser; A V Kusnoor; N M Giesecke; G J Reul; K L Drescher; C H Watrin; E O Smith; T F Feltes
Journal:  J Am Coll Cardiol       Date:  2001-05       Impact factor: 24.094

8.  Postoperative pericardial effusion and its relation to postpericardiotomy syndrome.

Authors:  S K Clapp; A Garson; H P Gutgesell; D A Cooley; D G McNamara
Journal:  Pediatrics       Date:  1980-10       Impact factor: 7.124

9.  Pericardial effusion after open heart surgery for congenital heart disease.

Authors:  E W Y Cheung; S A Ho; K K Y Tang; A K T Chau; C S W Chiu; Y F Cheung
Journal:  Heart       Date:  2003-07       Impact factor: 5.994

Review 10.  Recurrent pericardial effusion after cardiac surgery: the use of colchicine after recalcitrant conventional therapy.

Authors:  Luca Dainese; Antioco Cappai; Paolo Biglioli
Journal:  J Cardiothorac Surg       Date:  2011-08-10       Impact factor: 1.637

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