Pulmonary Hypertension and Cardiac Surgery: Perioperative Management in a Resource Limited Setting
Mahamadoun Coulibaly1,2orcid, Mamady Doumbia1, Binta Diallo1, Salia Ismaila Traore1, Aminata Dabo1, Siriman Abdoulaye Koita1,2, Abdoulhamidou Almeimoune2,3orcid, Moustapha Issa Mangane2,3, Thierno Madane Diop2,3, Seydina Alioune Beye2,4orcid, Baba Ibrahima Diarra5, Modibo Doumbia5, Sanoussy Daffé6, Mamadou Touré2,6, Souleymane Samate1, Brehima Bolimpe Coulibaly1, Ousmane Nientao7, Mamadou Karim Toure2,8, Youssouf Coulibaly2,9
1Department of Anesthesia, Intensive Care, and Emergency Medicine, “LE LUXEMBOURG” Mother and Child University Hospital, Bamako, Mali.
2Faculty of Medicine and Odontostomatology of Bamako (FMOS/USTTB), Bamako, Mali.
3Department of Anesthesia, Intensive Care, and Emergency Medicine, Gabriel Touré University Hospital, Bamako, Mali.
4Anesthesia and Intensive Care Unit, Mohamed VI Perinatal Clinic, Bamako, Mali.
5Cardiac Surgery Unit, André Festoc Mother and Child University Hospital “LE LUXEMBOURG”, Bamako, Mali.
6Cardiology Department, “LE LUXEMBOURG” Mother and Child University Hospital, Bamako, Mali.
7Anesthesia and Intensive Care Department, CNOS University Hospital, Bamako, Mali.
8Anesthesia and Intensive Care Department, Dermatology Hospital University Hospital, Bamako, Mali.
9Anesthesia and Intensive Care Department, Point G University Hospital, Bamako, Mali.
DOI: 10.4236/wjcs.2025.1511023   PDF    HTML   XML   8 Downloads   76 Views  

Abstract

Introduction: Pulmonary hypertension (PH) is a hemodynamic and pathophysiological condition characterized by abnormally elevated pressures in the pulmonary vasculature. It is defined by a mean pulmonary arterial pressure ≥ 25 mmHg at rest by right heart catheterization. He is frequently associated with cardiovascular surgery and is a common complication that has been observed after surgery utilizing cardiopulmonary bypass (CPB). Preoperative PH has been significantly linked to morbidity and is a risk factor for poor outcome post-surgery. Some specific features in sub-Saharan Africa: given the lack of access to cardiac surgery, PAH occurs very frequently in cases of advanced heart disease in patients with congenital heart disease or rheumatic valve disease that has been treated late. Objective: The purpose of this study was to evaluate a protocol for managing PH during cardiac surgery under cardiopulmonary bypass in resource limited settings. Patients and Methods: This is a descriptive and analytical retrospective study that included all patients who underwent cardiopulmonary bypass surgery at the “Le Luxembourg” Mother and Child University Hospital between January 1, 2023, and June 30, 2024, and who had a preoperative systolic pulmonary artery pressure (SPAP) ≥ 35 mmHg. Preoperatively, all patients included were given Furosemide: 1 mg/kg and Sildenafil 5 or 10 mg/8 hours in children and 20 mg/8 hours in adults. In the operating room, a nasogastric tube was inserted to administer sildenafil at the end of surgery, and weaning from CPB was performed using Milrinone at a syringe pump rate of 5 μg/kg/min, combined with Norepinephrine as needed depending on hemodynamic status. We analyzed the mean changes in PAPS from the preoperative assessment to discharge from intensive care. Results: During the period, 292 patients underwent surgery, 142 of whom had PH, representing a prevalence of 48.63%. Our patients had an average age of 11.57 ± 11. There was a female predominance of 51.4%. The average length of preoperative hospitalization was 5 days [3 - 8]. The time between diagnosis and surgical treatment was between 1 and 5 years in 62.8% of cases. It was ≤1 year in 29.6% of cases. The clinical signs were dominated by dyspnea in 43.7% of cases. Pulmonary artery systolic pressure was between 51 - 100 mmHg in 29.58% and >100 mmHg in 19.72% of cases, with a mean preoperative sPAP of 59 mmHg [35 - 110]. Congenital heart disease accounted for 52.11% of surgical indications, and valvular heart disease for 47.89%. Surgical indications for mitral valve disease accounted for 35.92% of cases and those for congenital heart disease for 52.11%. The mean duration of CPB was 110 min ± 50. There were no intraoperative episodes of pulmonary hypertension. At the end of surgery, the average time to postoperative extubation in intensive care was 3.53 hours ± 2.2. There was a significant decrease in sPAP between the preoperative and postoperative periods. A comparison of pre- and post-operative sPAP averages using a t-test was significant with a P-value < 0.001 (t: 27.978). The main postoperative complications are: Overall cardiac failure: 4.2%; respiratory failure: 2.1%; hematological complications: 0.7%. We recorded a perioperative mortality rate of 5.6%. Conclusion: PH complicates rheumatic valve disease and certain congenital heart diseases. It is common in our resource-limited setting, where access to cardiac surgery is insufficient. It is associated with high perioperative morbidity and mortality. Management is well codified, but the therapeutic classes are sometimes unavailable in our countries. The postoperative protocol of furosemide + sildenafil and milrinone appears to give good results.

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Coulibaly, M., Doumbia, M., Diallo, B., Traore, S.I., Dabo, A., Koita, S.A., Al-meimoune, A., Mangane, M.I., Diop, T.M., Beye, S.A., Diarra, B.I., Doumbia, M., Daffé, S., Touré, M., Samate, S., Coulibaly, B.B., Nientao, O., Toure, M.K. and Coulibaly, Y. (2025) Pulmonary Hypertension and Cardiac Surgery: Perioperative Management in a Resource Limited Setting. World Journal of Cardiovascular Surgery, 15, 233-242. doi: 10.4236/wjcs.2025.1511023.

1. Introduction

Pulmonary hypertension (PH) is a hemodynamic and pathophysiological condition characterized by abnormally elevated pressures in the pulmonary vasculature. It is defined by a mean pulmonary arterial pressure ≥ 25 mmHg at rest by right heart catheterization [1]. PH can be caused by an increase in pulmonary blood flow, pulmonary vascular resistance, pulmonary venous pressure or a combination of these factors. Pulmonary hypertension is frequently associated with cardiovascular surgery and is a common complication that has been observed after surgery utilizing cardiopulmonary bypass (CPB). Preoperative PH has been significantly linked to morbidity and is a risk factor for poor outcome post-surgery [2]. Accurate preoperative assessment and diligent anesthetic management are crucial for the best outcome [3]. The anesthetic management of such patients requires a thorough understanding of the etiology, pathophysiology, type, and severity of PH along with the nature of the surgical procedure [4]. Some specific features in sub-Saharan Africa: given the lack of access to cardiac surgery, PAH occurs very frequently in cases of advanced heart disease in patients with congenital heart disease or rheumatic valve disease that has been treated late.

2. Objective

The purpose of this study was to evaluate a protocol for managing PH during cardiac surgery under cardiopulmonary bypass in resource limited settings.

3. Patients and Methods

This is a descriptive and analytical retrospective study that included all patients who underwent cardiopulmonary bypass surgery at the “Le Luxembourg” Mother and Child University Hospital between January 1, 2023, and June 30, 2024, and who had a preoperative systolic pulmonary artery pressure (SPAP) ≥ 35 mmHg. Preoperatively, all patients included were given Furosemide: 1 mg/kg and Sildenafil 5 or 10 mg/8 hours in children and 20 mg/8 hours in adults. In the operating room, a nasogastric tube was inserted to administer sildenafil at the end of surgery, and weaning from CPB was performed using Milrinone at a syringe pump rate of 5 μg/kg/min, combined with Norepinephrine as needed depending on hemodynamic status. We analyzed the mean changes in PAPS from the preoperative assessment to discharge from intensive care using a T-test to compare averages.

4. Results

During the period, 292 patients underwent surgery, 142 of whom had PH, representing a prevalence of 48.63%. Our patients had an average age of 11.57 ± 11. There was a female predominance of 51.4%. The average length of preoperative hospitalization was 5 days [3 - 8]. The time between diagnosis and surgical treatment was between 1 and 5 years in 62.8% of cases. It was ≤1 year in 29.6% of cases. The clinical signs were dominated by dyspnea in 43.7% of cases. SPO2 was <80% in 6.3% of patients and between 80% - 94% in 15.5% of cases. Pulmonary artery systolic pressure was between 51 - 100 mmHg in 29.58% and >100 mmHg in 19.72% of cases, with a mean preoperative sPAP of 59 mmHg [35 - 110]. Table 1 shows the preoperative epidemiological and clinical characteristics of our patients.

Congenital heart disease accounted for 52.11% of surgical indications, and valvular heart disease for 47.89%. Surgical indications for mitral valve disease accounted for 35.92% of cases and those for congenital heart disease for 52.11%.

Table 1. Epidemio-clinical characteristics.

Diagnosis delay

Frequence

Percentage

0 - 12 months

42

29.6

1 - 5 years

89

62.8

6 - 10 years

9

6.3

11 - 15 years

2

1.3

Total

142

100

Clinical signs

Frequence

Percentage

Dyspnea

62

43.7

Cough

16

11.3

Palpitations

9

6.3

Digital hippocratism

8

5.6

Hepatomegaly

2

1.4

Jaundice

2

1.4

Preoperative pulse oximetry (SPO2)

Frequence

Percentage

<80%

9

6.3

80% - 94%

22

15.5

>94%

111

78.2

Total

142

100

Preoperative systolic pulmonary artery pressure (sPAP)

Frequence

Percentage

36 - 50 mmHg

72

50.70

51 - 100 mmHg

42

29.58

sup a 100 mmHg

28

19.72

Total

142

100

Indication: Mitral valve disease

Frequence

Percentage

Mitral insufficiency

31

21.83

Mitral stenosis

20

14.08

Total

51

35.92

Indication: Aortic valve disease

Frequence

Percentage

Aortic insufficiency

13

9.15

Aortic stenosis

4

2.82

Total

17

11.97

Indication: Congenital heart disease

Frequence

Percentage

Ventricular septal defect

48

33.80

Atrial septal defect

23

16.20

Ventricular septal defect + Atrial septal defect

3

2.11

Total

74

52.11

The mean duration of CPB was 110 min ± 50. There were no intraoperative episodes of pulmonary hypertension. At the end of surgery, the average time to postoperative extubation in intensive care was 3.53 hours ± 2.2. Table 2 and Figure 1 show the different variations in sPAP on postoperative days 1, 2, and 3 compared to the preoperative period. A comparison of pre- and post-operative sPAP averages using a t-test was significant with a P-value < 0.001 (t: 27.978). The main postoperative complications are reported in Table 3: Overall cardiac failure: 4.2%; respiratory failure: 2.1%; hematological complications: 0.7%. We recorded a perioperative mortality rate of 5.6%.

Table 2. Perioperative variations in pulmonary artery systolic pressure (sPAP).

sPAP interval

Percentage Preoperative

Percentage J1 Postoperative

Percentage J2 Postoperative

Percentage J3 Postoperative

20 - 35 mmHg

18

42

56

36 - 50 mmHg

50.70

32

30

25

51 - 100 mmHg

29.58

11

12

7

SUP A 100 mmHg

19.72

2

0

0

Total

100.00

63

84

88

Figure 1. Perioperative variations in pulmonary artery systolic pressure (sPAP).

Table 3. Main complications.

Complications

Frequence

Percentage

Global heart failure

6

4.2

Respiratory complications

3

2.1

Hemorrhagic complications

1

0.7

Death

8

5.6

5. Discussion

Pulmonary hypertension (PH) is frequently associated with cardiovascular surgery and is a common complication that has been observed after surgery utilizing cardiopulmonary bypass (CPB) Preoperative PH has been significantly linked to morbidity and is a risk factor for poor outcome post surgery [2]. This effect is mediated via two pathways deleterious right ventricular remodeling, and exacerbation of perioperative stress placed on the Right Ventricle (RV) both of which predispose these patients to postoperative RV failure [5]. The prevalence of PH may vary widely across specific populations: from 7.4% in patients with systemic sclerosis to 68.7% in patients with cardiac surgery [1]. PH is common in low-income countries, unlike in other parts of the world. The REMEDY study found a prevalence of 29.9% and 19% in low-income countries and upper-middle-income countries, respectively [6]. In a Malian series for rheumatic valve disease surgery, we found that: 19.1% had PASP between 35 and 50 mmHg and 25% had PASP > 50 mmHg [7]. Lindberg et al. [8] were found a 2% incidence of severe PH and a 0.7% incidence of PH crisis after cardiac surgical procedures.

This high prevalence could be explained, among other things, by delays in treatment and limited access to surgery in these regions of the world. In our series, 62.8% of patients waited between 1 and 5 years to receive surgical treatment. Kingué et al. reported that patients were seen late in the course of the disease, with 40% presenting with heart failure and in New York Heart Association class III or IV [9].

PH is an independent predictor of increased morbidity and mortality (4% - 24%) following surgery, and these patients are high‑risk candidates depending on severity of disease and surgical procedure [10].

The assessment of perioperative risk depends on the type of surgery, the severity of PH, and the functional status of the patient. The outcomes of major surgeries showed mortality and short-term morbidity rates of 7% and 42%, respectively [4].

Perioperative risk factors for PH after cardiac surgery and CPB include preoperative PH, fluid overload, acidosis, hypoxia, positive pressure ventilation, elevated sympathetic tone, ischemia-reperfusion injury, pulmonary reperfusion syndrome, left ventricular diastolic or systolic failure, acute respiratory distress syndrome, embolism such as air embolism, thromboembolism, amniotic fluid embolism, and CO2 embolism, systemic inflammatory response, the necessity of blood transfusions, mechanical failure, loss of vasculature such as pneumonectomy, duration of CPB, and pharmacological agents [11]. In addition, hypoxia, hypercarbia, and pulmonary embolism which can appear before, during, or after CPB are contributors to PH development. When hypoxia is present, pulmonary vessels tend to constrict due to a direct effect on the microcirculation [2]. Inflammation has also been identified to play a role in PH after cardiac surgery and CPB [2]. There are several mechanisms that cause inflammation during cardiac surgery with CPB. Mechanisms that cause inflammation during cardiac surgery include blood exposure to synthetic surfaces during CPB, lung damage due to ischemia-reperfusion, splanchnic hypoperfusion-induced endotoxemia, blood recirculation during cardiotomy suction, utilization of protamine, and injury to the surgical tissue.

Although PAP may decrease after valvular surgery, the period immediately after separation from CPB may be complicated by a higher PAP, particularly among patients with pre-existing PH. PVR may increase after CPB because of atelectasis, ischemia-reperfusion injury, endothelial damage, and the release of inflammatory mediators that increase capillary permeability. Ventricular dysfunction, which is common in the immediate post by pass period [2].

Different therapeutic classes are used to treat these PHs depending on their pathophysiological classes, clinical status, and, of course, the availability of therapies. [4]. These are:

Group 1: Anticoagulation, diuretics, oxygen therapy, and digoxin. Therapeutic approach is guided by functional status and objective testing as follows: Low risk, functional Class I - III patients may be treated with oral Phosphodiesterase-5 (PDE‑5) inhibitors, oral endothelin receptor antagonists (ERAs), or inhaled prostacyclins.

High risk, functional Class III - IV patients should be treated with intravenous (IV) or subcutaneous prostacyclins.

Group 2: They are managed with therapies for left heart failure. A small trial suggested potential benefit of PDE‑5 inhibitors in patients with heart failure and a preserved ejection fraction. ERAs and prostacyclins should not be used.

Group 3: Management is directed at the underlying lung disease. Pulmonary vasodilators do not have a role and worsens ventilation perfusion (VQ) matching in these patients.

Group 4: PH is potentially curable with pulmonary thromboendarterectomy. There may be a role for pulmonary vasodilators in those who are not surgical candidates.

Group 5: Management is directed at the underlying disease.

Studies have demonstrated the success of Inhaled NO (iNO)in treating postoperative PH as a selective pulmonary vasodilator for patients undergoing cardiac surgery and CPB. In a study, it was concluded that iNO greatly decreases mPAP in patients with postoperative PH, helps with vasodilation, and does not cause hemodynamic complications [2].

Several studies have shown sildenafil to be successful in treating postoperative PH. Sildenafil, a PDE5 inhibitor, has been shown to be promising in treating PH due to mitral valve surgery. In a double-blind, placebo-controlled randomized trial, it was found that giving sildenafil postoperatively is safe and that it lowers pulmonary vascular pressure and mean pulmonary pressure without causing ventilation–perfusion mismatch or systemic hypotension [12]. A meta-analysis studying the role of sildenafil in pulmonary hypertension [13] retrouvait: Sildenafil treatment resulted in a significant improvement in the Six-Minute Walk Distance (6 MWD). Quality of Life (QOL) assessment, using the Chronic Heart Failure Questionaire, revealed improvements in breathlessness, fatigue, emotional function, and overall score with sildenafil. New York Heart Association (NYHA) Classification improved with sildenafil in one study while another study found no reclassification.

Milrinone has been demonstrated to be effective in treating postoperative PH for patients undergoing mitral valve surgery. A study found that IV milrinone is superior to oral sildenafil in managing PH after pediatric cardiac surgery and ending pulmonary hypertensive crisis [14].

In our context, therapies such as ERAs, inhaled prostacyclins, subcutaneous prostacyclins, or inhaled nitric oxide (NO) are not available. Hence the implementation of this protocol (sildenafil + furosemide preoperatively and weaning from CPB under milrinone). Our protocol appears to be yielding good results, with a significant decrease in sPAP values. Furthermore, no hypertensive crises were observed during the perioperative period.

6. Limitations of the Study

This study is an ambitious undertaking, but it does have a number of practical limitations that we feel are important to highlight here. It is a retrospective study that was conducted in a single center (monocentric, the only cardiac surgery center in the country). The fact that pulmonary pressure measurements were taken by echocardiography rather than right heart catheterization may have an impact on the assessments, but has the advantage of being practical, since echocardiography is the method available to us and the one we use on a daily basis.

7. Conclusion

PH complicates rheumatic valve disease and certain congenital heart diseases. It is common in our resource-limited setting, where access to cardiac surgery is insufficient. It is associated with high perioperative morbidity and mortality. Management is well codified, but the therapeutic classes are sometimes unavailable in our countries. The postoperative protocol of furosemide + sildenafil and milrinone appears to give good results.

Ethical Considerations

Patient confidentiality was respected throughout the conduct of this work. Patients or their legal representatives authorized the use of their data in this work. Authorization from the local ethics committee of the “LE LUXEMBOURG” Mother and Child University Hospital, Bamako was obtained prior to the conduct of this work.

Conflicts of Interest

The authors report no conflicts of interest in relation to this work.

References

[1] Bigna, J.J., Noubiap, J.J., Nansseu, J.R. and Aminde, L.N. (2017) Prevalence and Etiologies of Pulmonary Hypertension in Africa: A Systematic Review and Meta-Analysis. BMC Pulmonary Medicine, 17, Article No. 183.[CrossRef] [PubMed]
[2] Fayad, F.H., Sellke, F.W. and Feng, J. (2022) Pulmonary Hypertension Associated with Cardiopulmonary Bypass and Cardiac Surgery. Journal of Cardiac Surgery, 37, 5269-5287.[CrossRef] [PubMed]
[3] Thunberg, C.A., Gaitan, B.D., Grewal, A., Ramakrishna, H., Stansbury, L.G. and Grigore, A.M. (2013) Pulmonary Hypertension in Patients Undergoing Cardiac Surgery: Pathophysiology, Perioperative Management, and Outcomes. Journal of Cardiothoracic and Vascular Anesthesia, 27, 551-572.[CrossRef] [PubMed]
[4] Sarkar, M.S. and Desai, P.M. (2018) Pulmonary Hypertension and Cardiac Anesthesia: Anesthesiologist’s Perspective. Annals of Cardiac Anaesthesia, 21, 116-122.[CrossRef] [PubMed]
[5] Hawkins, R.B., Strobel, R.J., Mehaffey, J.H., Quader, M.A., Joseph, M., Speir, A.M., et al. (2023) Pulmonary Hypertension and Operative Risk in Mitral Valve and Coronary Surgery. Journal of Surgical Research, 286, 49-56.[CrossRef] [PubMed]
[6] Zühlke, L., Engel, M.E., Karthikeyan, G., Rangarajan, S., Mackie, P., Cupido, B., et al. (2015) Characteristics, Complications, and Gaps in Evidence-Based Interventions in Rheumatic Heart Disease: The Global Rheumatic Heart Disease Registry (the REMEDY Study). European Heart Journal, 36, 1115-1122.
[7] Coulibaly, M., Koita, S.A., Doumbia, M., Diallo, B., Traore, S.I., Diarra, B.I., et al. (2022) First Malian Series of Surgery for Rheumatic Valve Disease: Opening of the Centre, Clinical Features and Peri-Operative Realities. Cardiovascular Journal of Africa, 33, 41-45.[CrossRef] [PubMed]
[8] Lindberg, L., Olsson, A.K., Jögi, P. and Jonmarker, C. (2002) How Common Is Severe Pulmonary Hypertension after Pediatric Cardiac Surgery? The Journal of Thoracic and Cardiovascular Surgery, 123, 1155-1163.[CrossRef] [PubMed]
[9] Kingué, S., Ba, S.A., Balde, D., Diarra, M.B., Anzouan-Kacou, J., Anisubia, B., et al. (2016) The VALVAFRIC Study: A Registry of Rheumatic Heart Disease in Western and Central Africa. Archives of Cardiovascular Diseases, 109, 321-329.[CrossRef] [PubMed]
[10] Blaise, G., Langleben, D. and Hubert, B. (2003) Pulmonary Arterial Hypertension: Pathophysiology and Anesthetic Approach. Anesthesiology, 99, 1415-1432.[CrossRef] [PubMed]
[11] Minai, O.A., Yared, J., Kaw, R., Subramaniam, K. and Hill, N.S. (2013) Perioperative Risk and Management in Patients with Pulmonary Hypertension. Chest, 144, 329-340.[CrossRef] [PubMed]
[12] Ram, E., Sternik, L., Klempfner, R., Eldar, M., Goldenberg, I., Peled, Y., et al. (2019) Sildenafil for Pulmonary Hypertension in the Early Postoperative Period after Mitral Valve Surgery. Journal of Cardiothoracic and Vascular Anesthesia, 33, 1648-1656.[CrossRef] [PubMed]
[13] Feghali, E.J. and Yammine, Y. (2024) The Role of Sildenafil in Pulmonary Hypertension from Left Heart Disease and Elevated Pulmonary Vascular Resistance: A Systematic Review and Meta-Analysis. CHEST, 166, A6519.[CrossRef
[14] Peiravian, F., Amirghofran, A.A., Ghamsari, H. and Emaminia, A. (2013) Additive Effect of Phosphodiesterase Inhibitors in Control of Pulmonary Hypertension after Congenital Cardiac Surgery in Children. Iranian Journal of Pediatrics, 23, 19-26.

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