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JUSTIN D.
SHANKS
09/29/2014
PREDNISOLONE & M.
INDICUS PRANII IN
TUBERCULOUS
PERICARDITIS
(IMPI TRIAL):
TX A&M SSHP JOURNAL CLUB REVIEW
IMPI TRIAL
Published on September 2, 2014 at NEJM.org
PERICARDIUM
¡  What is pericarditis?
§  Pericarditis is an inflammation of the pericardium that surrounds the
heart.
¡  How does it present acutely?
§  Pain that typically presents with precordial chest pain with radiation
which may be relieved by sitting up and bending forward and is often
worsened by lying or inspiration.
§  The pain resembles angina or a heart attack acutely.
§  Colchicine 0.5 mg BID added to NSAID or as mono-therapy appears to
be effective for for the initial attack and prevention.
§  Systemic corticosteroid therapy is reserved for connective tissue diseases,
auto-reactive or uremic pericarditis.
PERICARDITIS BACKGROUND
¡  How is Tuberculous Pericarditis different?
§  Primarily seen in AIDS patients with a mortality rate of untreated
acute effusive TB pericarditis that approaches 85%.
§  Clinical presentation:
§  Variable
§  Acute pericarditis w/ or w/out effusions
§  Cardiac tamponade
§  Acute constriction pericarditis or chronic pericarditis
§  Pericardial constriction occurs in 30-50% of the patients.
§  Chronic inflammation of the pericardium leading to impaired filling of
ventricles and reduced ventricular function.
§  Pericardium has effusions and sometimes calcification of the fibers that
constrict upon the heart.
§  Pericardiectomy is the only treatment for permanent constriction.
TUBERCULOUS PERICARDITIS
BACKGROUND
¡  Tuberculous Pericarditis
§  Diagnosis:
§  Identification of Mycobacterium tuberculosis in the pericardial fluid or
tissue; ELISPOT tests for M. tuberculosis antigen as well are useful.
§  Tuberculin tests may be positive or negative
§  Peri/epicardial biopsy with caseous granuloma
§  Granulocytes and macrophages > 40 U/mL
§  Treatment:
§  Pericarditomy and pericardiectomy rarely needed, use only if constriction
develops after antituberculous drugs + prednisone
§  Various antituberculous drug combinations of different lengths
§  Prednisone at 1-2mg/kg per day for 5-7 days may be associated with
fewer deaths; controversial with limited data
§  High doses of prednisone (1-2 mg/kg per day) should be used since rifampin induces its
metabolism
TUBERCULOUS PERICARDITIS
EUROPEAN SOCIETY OF CARDIOLOGY GUIDELINES
¡  Current therapy to treat TB pericarditis consists of medical
treatment for 6 months with:
§  rifampicin (rifampin)
§  isoniazid
§  pyrazinamide
§  ethambutol
¡  Treatment also includes:
§  Pericardial drainage for cardiac tamponade
§  Pericardiectomy for pericardial constriction
TUBERCULOUS PERICARDITIS
IMPI TRIAL
Published on September 2, 2014 at NEJM.org
¡  Despite antituberculosis therapy, pericardial drainage, or
pericardiectomy morbidity and mortality remain high in
patients with tuberculous pericarditis.
§  26% mortality within 6 months
§  40% mortality in AIDS patients
¡  “Glucocorticoid therapy in patients with TB pericarditis to
attenuate the inflammation may improve outcomes and
decrease risk of death by reducing cardiac tamponade and
pericardial constriction.”
§  “A meta-analysis of all trials of adjunctive glucocorticoid therapy for
all forms of tuberculosis also suggested reduced mortality.”
¡  IMPI hypothesis: Adjunctive prednisolone would benefit
tuberculous pericarditis patients overall.
IMPI TRIAL
¡  Furthermore, preliminary evidence suggests that repeated
doses of intradermal heat-killed Mycobacterium indicus pranii
may reduce inflammation and increase the CD4+ and T-cell
count in HIV patients
§  Mycobacterium indicus pranii is a nonpathogenic, saprophytic, rapid
growing atypical mycobacterium species.
§  Shown clinical benefit with pulmonary tuberculosis patients and HIV in
leprosy patients.
¡  IMPI hypothesis: Intradermal M. indicus pranii could be
effective in suppressing inflammation in patients with
tuberculous pericarditis.
IMPI TRIAL
¡  What was IMPI?
§  IMPI was a randomized, double-blind, placebo controlled, intention to
treat, multi-center/national, 2-2 factorial trial.
¡  Who were the patients in IMPI?
§  1,400 adult patients in Africa with definite or probable tuberculous
pericarditis were enrolled in the study.
§  Approximately 66% of the patients had co-morbid HIV infections
§  All patients received treatment for TB and HIV according to WHO
guidelines.
IMPI TRIAL
IMPI TRIAL
¡  Study design primary objective: To assess the effectiveness
and safety of prednisolone and M. indicus pranii
§  Published in the American Heart Journal in February 2013
¡  Primary outcome in published IMPI trial: Efficacy outcome was
a composite of death or first occurrence of cardiac tamponade
requiring pericariocentesis or constrictive pericarditis
§  Secondary efficacy outcomes were individual components of primary
outcome with the addition of hospitalization.
¡  Safety outcome: Occurrence of opportunistic infections and
cancer, as well as the effect of interventions on the CD4+ T-
cell count and the incidence of immune reconstitution
inflammatory syndrome.
IMPI TRIAL
IMPI TRIAL
¡  How did they conduct IMPI?
§  Prednisolone or placebo was administered for 6 weeks
§  Week 1 dose: 120 mg daily
§  Week 2 dose: 90 mg daily
§  Week 3 dose: 60 mg daily
§  Week 4 dose: 30 mg daily
§  Week 5 dose: 15 mg daily
§  Week 6 dose: 5 mg daily
§  Prednisolone median follow up time: 636.5 days (1.7 years)
§  This 6 week duration came from an effective adjunctive
dexamethasone regimen withTuberculous Meningitis (31% RRR).
§  M. indicus pranii injections were given ID at time of enrollment, then
again at 2 weeks, 4 weeks, 6 weeks, and then at 3 months.
§  M indicus pranii median follow up time: 720.5 days (1.9 years)
IMPI TRIAL
¡  How did they conduct IMPI?
§  Needed to recruit 1,400 patients for the study to have 90% power to
detect a 22.9% reduction in the hazard ratio.
§  Met power analysis
§  Two sided type I error rate of 5%, alpha = 0.05
§  Conducted seven interim analyses without adjustment of alpha
§  Increases the likelihood that any difference found may be due to chance alone and may not
be true.
§  Trial was conducted from January 2009 to February 2014,
approximately 5 years.
IMPI TRIAL
IMPI RESULTS
PRIMARY EFFICACY OUTCOME
¡  No statistically significant difference with either prednisolone
or M. indicus pranii for the primary endpoint.
IMPI RESULTS
SECONDARY EFFICACY OUTCOME
¡  Constrictive pericarditis: Placebo vs. prednisolone; 7.8% vs. 4.4%, 44% relative risk
reduction, p=0.009
§  Absolute risk reduction: 3.4%; NNT: 30
¡  Hospitalization: Placebo vs. prednisolone; 25.2% vs. 20.7%, 21% relative risk reduction,
p=0.04
§  Absolute risk reduction: 4.5%; NNT: 23
IMPI RESULTS
SAFETY OUTCOMES
¡  Cancer: Placebo vs. prednisolone; 0.6% vs. 1.8%, 227% relative risk increase,
p=0.03
§  Absolute risk increase: 1.2%; NNH: 84
§  Similar data with M. indicus pranii
¡  HIV-related cancer: Placebo vs. prednisolone; 0.1% vs. 1.3%, 804% relative risk
increase, p=0.04
§  Absolute risk increase: 1.2%; NNH: 84
§  Similar data with M indicus pranii
¡  Reduction in the incidence of hospitalization could be attributed
to the reduction in constrictive pericarditis.
§  Pericardiectomy is the definitive treatment for chronic pericardial
constriction, but it itself is associated with high perioperative morbidity
and mortality
§  However, cardiac surgery isn’t widely available in Africa making the finding of
a reduction in constrictive pericarditis more relevant.
¡  The increase in HIV-related cancer with prednisolone is
consistent with two other studies of HIV-associated tuberculosis
§  Possible that glucocorticoids and M. indicus pranii act synergistically to
increase the risk of cancer in immunosuppressed patients.
¡  IMPI investigators point out that a definite diagnosis of
tuberculosis in the pericardium or elsewhere in the body was
made in only 25% of the patients.
§  Interventions may have not been effective because few patients actually
had tuberculous pericarditis.
§  However, the results were consistent between patients with definite and
probable diagnoses as well.
IMPI TRIAL
DISCUSSION
¡  Mayosi B.M., eta al. Prednisolone and Mycobacterium indicus pranii in
Tuberculous Pericarditis. New England Journal of Medicine. 2014 Sep
18;371(12):1121-30.
¡  Mayosi B.M., PhilD, et al. Rationale and design of the Investigation of the
Management of Pericarditis (IMPI) trial: A 2X2 factorial randomized double-
blind multicenter trial of adjunctive prednisolone and Mycobacterium w
immunotherapy in tuberculous pericarditis. American Heart Journal. 2013
Feb;165:109-115.
¡  Maisch B, et al. Guidelines on the Diagnosis and Management of
Pericardial Diseases: The Task Force on the Diagnosis and Management of
Pericardial Diseases of the European Society of Cardiology. European Heart
Journal. 2004;25:587-610.
¡  Mayosi BM, Burgess LJ, et al. Tuberculous pericarditis. Circulation.
2005;112:3608-16.
¡  Trautner BW and Darouiche RO. Tuberculous Pericarditis: Optimal Diagnosis
and Management. Clinical Infectious Diseases. 2001;33:954-61.
¡  Thwaites GE, Nguyen DB, eta al. Dexamethasone for the treatment of
tuberculous meningitis in adolescents and adults. New England Journal of
Medicine. 2004;35:1741-51.
IMPI TRIAL
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IMPI_journal_club

  • 1. JUSTIN D. SHANKS 09/29/2014 PREDNISOLONE & M. INDICUS PRANII IN TUBERCULOUS PERICARDITIS (IMPI TRIAL): TX A&M SSHP JOURNAL CLUB REVIEW
  • 2. IMPI TRIAL Published on September 2, 2014 at NEJM.org
  • 4. ¡  What is pericarditis? §  Pericarditis is an inflammation of the pericardium that surrounds the heart. ¡  How does it present acutely? §  Pain that typically presents with precordial chest pain with radiation which may be relieved by sitting up and bending forward and is often worsened by lying or inspiration. §  The pain resembles angina or a heart attack acutely. §  Colchicine 0.5 mg BID added to NSAID or as mono-therapy appears to be effective for for the initial attack and prevention. §  Systemic corticosteroid therapy is reserved for connective tissue diseases, auto-reactive or uremic pericarditis. PERICARDITIS BACKGROUND
  • 5. ¡  How is Tuberculous Pericarditis different? §  Primarily seen in AIDS patients with a mortality rate of untreated acute effusive TB pericarditis that approaches 85%. §  Clinical presentation: §  Variable §  Acute pericarditis w/ or w/out effusions §  Cardiac tamponade §  Acute constriction pericarditis or chronic pericarditis §  Pericardial constriction occurs in 30-50% of the patients. §  Chronic inflammation of the pericardium leading to impaired filling of ventricles and reduced ventricular function. §  Pericardium has effusions and sometimes calcification of the fibers that constrict upon the heart. §  Pericardiectomy is the only treatment for permanent constriction. TUBERCULOUS PERICARDITIS BACKGROUND
  • 6. ¡  Tuberculous Pericarditis §  Diagnosis: §  Identification of Mycobacterium tuberculosis in the pericardial fluid or tissue; ELISPOT tests for M. tuberculosis antigen as well are useful. §  Tuberculin tests may be positive or negative §  Peri/epicardial biopsy with caseous granuloma §  Granulocytes and macrophages > 40 U/mL §  Treatment: §  Pericarditomy and pericardiectomy rarely needed, use only if constriction develops after antituberculous drugs + prednisone §  Various antituberculous drug combinations of different lengths §  Prednisone at 1-2mg/kg per day for 5-7 days may be associated with fewer deaths; controversial with limited data §  High doses of prednisone (1-2 mg/kg per day) should be used since rifampin induces its metabolism TUBERCULOUS PERICARDITIS EUROPEAN SOCIETY OF CARDIOLOGY GUIDELINES
  • 7. ¡  Current therapy to treat TB pericarditis consists of medical treatment for 6 months with: §  rifampicin (rifampin) §  isoniazid §  pyrazinamide §  ethambutol ¡  Treatment also includes: §  Pericardial drainage for cardiac tamponade §  Pericardiectomy for pericardial constriction TUBERCULOUS PERICARDITIS
  • 8. IMPI TRIAL Published on September 2, 2014 at NEJM.org
  • 9. ¡  Despite antituberculosis therapy, pericardial drainage, or pericardiectomy morbidity and mortality remain high in patients with tuberculous pericarditis. §  26% mortality within 6 months §  40% mortality in AIDS patients ¡  “Glucocorticoid therapy in patients with TB pericarditis to attenuate the inflammation may improve outcomes and decrease risk of death by reducing cardiac tamponade and pericardial constriction.” §  “A meta-analysis of all trials of adjunctive glucocorticoid therapy for all forms of tuberculosis also suggested reduced mortality.” ¡  IMPI hypothesis: Adjunctive prednisolone would benefit tuberculous pericarditis patients overall. IMPI TRIAL
  • 10. ¡  Furthermore, preliminary evidence suggests that repeated doses of intradermal heat-killed Mycobacterium indicus pranii may reduce inflammation and increase the CD4+ and T-cell count in HIV patients §  Mycobacterium indicus pranii is a nonpathogenic, saprophytic, rapid growing atypical mycobacterium species. §  Shown clinical benefit with pulmonary tuberculosis patients and HIV in leprosy patients. ¡  IMPI hypothesis: Intradermal M. indicus pranii could be effective in suppressing inflammation in patients with tuberculous pericarditis. IMPI TRIAL
  • 11. ¡  What was IMPI? §  IMPI was a randomized, double-blind, placebo controlled, intention to treat, multi-center/national, 2-2 factorial trial. ¡  Who were the patients in IMPI? §  1,400 adult patients in Africa with definite or probable tuberculous pericarditis were enrolled in the study. §  Approximately 66% of the patients had co-morbid HIV infections §  All patients received treatment for TB and HIV according to WHO guidelines. IMPI TRIAL
  • 13. ¡  Study design primary objective: To assess the effectiveness and safety of prednisolone and M. indicus pranii §  Published in the American Heart Journal in February 2013 ¡  Primary outcome in published IMPI trial: Efficacy outcome was a composite of death or first occurrence of cardiac tamponade requiring pericariocentesis or constrictive pericarditis §  Secondary efficacy outcomes were individual components of primary outcome with the addition of hospitalization. ¡  Safety outcome: Occurrence of opportunistic infections and cancer, as well as the effect of interventions on the CD4+ T- cell count and the incidence of immune reconstitution inflammatory syndrome. IMPI TRIAL
  • 15. ¡  How did they conduct IMPI? §  Prednisolone or placebo was administered for 6 weeks §  Week 1 dose: 120 mg daily §  Week 2 dose: 90 mg daily §  Week 3 dose: 60 mg daily §  Week 4 dose: 30 mg daily §  Week 5 dose: 15 mg daily §  Week 6 dose: 5 mg daily §  Prednisolone median follow up time: 636.5 days (1.7 years) §  This 6 week duration came from an effective adjunctive dexamethasone regimen withTuberculous Meningitis (31% RRR). §  M. indicus pranii injections were given ID at time of enrollment, then again at 2 weeks, 4 weeks, 6 weeks, and then at 3 months. §  M indicus pranii median follow up time: 720.5 days (1.9 years) IMPI TRIAL
  • 16. ¡  How did they conduct IMPI? §  Needed to recruit 1,400 patients for the study to have 90% power to detect a 22.9% reduction in the hazard ratio. §  Met power analysis §  Two sided type I error rate of 5%, alpha = 0.05 §  Conducted seven interim analyses without adjustment of alpha §  Increases the likelihood that any difference found may be due to chance alone and may not be true. §  Trial was conducted from January 2009 to February 2014, approximately 5 years. IMPI TRIAL
  • 17. IMPI RESULTS PRIMARY EFFICACY OUTCOME ¡  No statistically significant difference with either prednisolone or M. indicus pranii for the primary endpoint.
  • 18. IMPI RESULTS SECONDARY EFFICACY OUTCOME ¡  Constrictive pericarditis: Placebo vs. prednisolone; 7.8% vs. 4.4%, 44% relative risk reduction, p=0.009 §  Absolute risk reduction: 3.4%; NNT: 30 ¡  Hospitalization: Placebo vs. prednisolone; 25.2% vs. 20.7%, 21% relative risk reduction, p=0.04 §  Absolute risk reduction: 4.5%; NNT: 23
  • 19. IMPI RESULTS SAFETY OUTCOMES ¡  Cancer: Placebo vs. prednisolone; 0.6% vs. 1.8%, 227% relative risk increase, p=0.03 §  Absolute risk increase: 1.2%; NNH: 84 §  Similar data with M. indicus pranii ¡  HIV-related cancer: Placebo vs. prednisolone; 0.1% vs. 1.3%, 804% relative risk increase, p=0.04 §  Absolute risk increase: 1.2%; NNH: 84 §  Similar data with M indicus pranii
  • 20. ¡  Reduction in the incidence of hospitalization could be attributed to the reduction in constrictive pericarditis. §  Pericardiectomy is the definitive treatment for chronic pericardial constriction, but it itself is associated with high perioperative morbidity and mortality §  However, cardiac surgery isn’t widely available in Africa making the finding of a reduction in constrictive pericarditis more relevant. ¡  The increase in HIV-related cancer with prednisolone is consistent with two other studies of HIV-associated tuberculosis §  Possible that glucocorticoids and M. indicus pranii act synergistically to increase the risk of cancer in immunosuppressed patients. ¡  IMPI investigators point out that a definite diagnosis of tuberculosis in the pericardium or elsewhere in the body was made in only 25% of the patients. §  Interventions may have not been effective because few patients actually had tuberculous pericarditis. §  However, the results were consistent between patients with definite and probable diagnoses as well. IMPI TRIAL DISCUSSION
  • 21. ¡  Mayosi B.M., eta al. Prednisolone and Mycobacterium indicus pranii in Tuberculous Pericarditis. New England Journal of Medicine. 2014 Sep 18;371(12):1121-30. ¡  Mayosi B.M., PhilD, et al. Rationale and design of the Investigation of the Management of Pericarditis (IMPI) trial: A 2X2 factorial randomized double- blind multicenter trial of adjunctive prednisolone and Mycobacterium w immunotherapy in tuberculous pericarditis. American Heart Journal. 2013 Feb;165:109-115. ¡  Maisch B, et al. Guidelines on the Diagnosis and Management of Pericardial Diseases: The Task Force on the Diagnosis and Management of Pericardial Diseases of the European Society of Cardiology. European Heart Journal. 2004;25:587-610. ¡  Mayosi BM, Burgess LJ, et al. Tuberculous pericarditis. Circulation. 2005;112:3608-16. ¡  Trautner BW and Darouiche RO. Tuberculous Pericarditis: Optimal Diagnosis and Management. Clinical Infectious Diseases. 2001;33:954-61. ¡  Thwaites GE, Nguyen DB, eta al. Dexamethasone for the treatment of tuberculous meningitis in adolescents and adults. New England Journal of Medicine. 2004;35:1741-51. IMPI TRIAL REFERENCES