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An optimal window of platelet reactivity by LTA assay for patients undergoing percutaneous coronary intervention
Thrombosis Journal volume 19, Article number: 73 (2021)
This study was aimed to determine how platelet reactivity (PR) on dual antiplatelet therapy predicts ischemic and bleeding events in patients underwent percutaneous coronary intervention (PCI).
A total of 2768 patients who had received coronary stent implantation and had taken aspirin 100 mg in combination with clopidogrel 75 mg daily for > 5 days were consecutively screened and 1885 were enrolled. The recruited patients were followed-up for 12 months. The primary end-point was the net adverse clinical events (NACE) of cardiovascular death, nonfatal myocardial infarction (MI), target vessel revascularization (TVR), stent thrombosis (ST) and any bleeding.
1709 patients completed the clinical follow-up. By using the receiver operating characteristic (ROC) curve analysis, the optimal cut-off values were found to be 37.5 and 25.5% respectively in predicting ischemic and bleeding events. Patients were classified into 2 groups according to PR: inside the window group (IW) [adenosine diphosphate (ADP) induced platelet aggregation (PLADP) 25.5–37.4%)] and outside the window group (OW) (PLADP < 25.5% or ≥ 37.5%). The incidence of NACE was 16.8 and 23.1% respectively in the IW and OW group. The hazard ratio of NACE in IW group was significantly lower [0.69 (95% CI, 0.54–0.89, P = 0.004)] than that in the OW group during 12-month follow-up.
An optimal therapeutic window of 25.5–37.4% for PLADP predicts the lowest risk of NACE, which could be referred for tailored antiplatelet treatment while using LTA assay.
Trial registration number: ClinicalTrials.govNCT01968499. Registered 18 October 2013 - Retrospectively registered.
Dual antiplatelet therapy with aspirin and an adenosine diphosphate (ADP)-receptor (P2Y12) inhibitor is a cornerstone of the pharmacological treatment for patients with coronary artery disease undergoing percutaneous coronary intervention (PCI) .
Clopidogrel is one of the most widely used P2Y12 inhibitors, which undergoes a two-step metabolic transformation before binding to the platelet P2Y12 receptor . Studies have shown wide variability of platelet clopidogrel response , indicating that a substantial proportion of patients have inappropriate platelet inhibition at a regular dose of clopidogrel 75 mg once daily. It has been reported that high on-treatment platelet reactivity (HOPR) detected by platelet aggregometry leads to increased risk of thrombotic events [4,5,6,7,8], while low on-treatment platelet reactivity (LOPR) leads to increased risk of bleeding after PCI [9, 10]. Thus, it is important to identify an optimal platelet inhibition or on-treatment platelet reactivity (PR) by platelet aggregometry [11, 12].
This study was to investigate an optimal therapeutic window for PR determined by light transmission aggregometry (LTA) to predict the lowest ischemic and bleeding risks in patients underwent PCI and treated with dual antiplatelet agents.
This is a prospective, single-center, registration study conducted at the First Affiliated Hospital of Nanjing Medical University, Nanjing, China. The study was registered at URL: https://www.clinicaltrials.gov (Unique identifier: NCT01968499) and was approved by the ethics committee of the First Affiliated Hospital of Nanjing Medical University. Written informed consent was obtained from each patient.
A total of 2768 patients were consecutively screened from April 2011 to October 2016 in the First Affiliated Hospital of Nanjing Medical University, among which 883 declined to participate, and the remaining 1885 patients were enrolled in the study (Fig. 1).
The inclusion criteria were patients who had undergone coronary stent implantation and taken aspirin 100 mg in combination with clopidogrel 75 mg daily for > 5 days . Exclusion criteria were patients: 1) intolerant to aspirin or clopidogrel (e.g. history of allergic reactions or gastrointestinal bleeding); 2) taking any other antiplatelet agents in addition to aspirin and clopidogrel (e.g. cilostazol); 3) taking any anticoagulant agents (e.g. vitamin K antagonists, new oral anticoagulants); 4) with myelodysplastic syndrome or abnormal baseline platelet counts of < 80 × 109/L or > 450 × 109/L; 5) with hemoglobin < 90 g/L; 6) with cancer or any other complications that may not suitable to be recruited at the discretion of the investigators.
Six milliliter venous blood was collected into 3.2% citrate vacutainer tubes in the morning 2 h after the patients’ taking clopidogrel (if glycoprotein (GP) IIb/IIIa inhibitors were used, testing would be performed 24 h after drug discontinuation). Blood samples were subjected to platelet function test by LTA within 2 h as previously described . In brief, samples were centrifuged at 200 g for 8 min to obtain platelet-rich plasma (PRP). Platelet-poor plasma (PPP) was prepared by centrifuging the remaining blood at 2465 g for 10 min. Platelet counts were adjusted by the addition of PPP to the PRP to achieve a count of 250 × 109/L. The ADP-induced platelet aggregation (PLADP) was recorded using the maximum platelet aggregation within 8 min after addition of ADP (final concentration 5 μmol/L) by a Chronolog Model 700 aggregometer (Chrono-log Corporation, Havertown, PA, USA) .
The primary end-point was set as the net adverse clinical events (NACE), a composite of ischemic events including cardiovascular death, nonfatal myocardial infarction (MI), target vessel revascularization (TVR), stent thrombosis (ST) and any bleeding defined by the Thrombolysis in Myocardial Infarction (TIMI) criteria . MI was defined in accordance with the Third Universal Definition proposed in 2007 . ST was defined as definite or probable according to the Academic Research Consortium definitions . All the clinical events were independently adjudicated by two investigators blinded to the results of PR tests. Disagreements were resolved by discussion or consultation with a third investigator (Li).
The outcome data were collected by 2 investigators who were blinded to the results of platelet reactivity testing. The patients were followed up in the clinic and less preferably by telephone call if they were unable to attend the clinic. A standard case report form was used to record the outcome.
Statistical analysis was performed using SPSS 22.0 soft-ware (SPSS, Chicago, IL, USA). Continuous variables are expressed as means ± standard deviations (SD) or medians (range [or Inter Quartile Range]). Categorical variables are expressed as frequencies and percentages. Two-sided Mann–Whitney tests were used to compare PLADP between groups. The time to primary endpoint between groups was compared using the Kaplan–Meier method. Survival curves were compared using the log-rank test and hazard ratios were calculated using Cox’s regression models. Sensitivity and specificity of PLADP in predicting thrombotic events were calculated at different thresholds by receiver operating characteristic (ROC) curve analysis. A two-sided P < 0.05 was statistically significant.
Among the enrolled patients, 1709 completed the 12-month clinical follow-up (Fig. 1). There were 45 (2.6%) ischemic events and 328 (19.2%) bleeding events. Ischemic events included 20 deaths, 20 MI, 21 ST and 11 TVR. Bleeding events included 5 major bleeding, 27 minor bleeding and 296 minimal bleeding.
Relationship between PR and 1-year outcome
The average time from PCI to PR test reached 2.50 days. Patients with ischemic events during follow-up had a higher PLADP level compared to those without (36% [IQR: 25–45] vs.29% [IQR: 20–40]; P = 0.054). ROC analysis was performed to evaluate the value of PLADP in predicting ischemic events. As a result, a PLADP cut-off value of 37.5% provided a sensitivity of 48.9%, specificity of 70%, and the largest area under the curve value of 0.58 (Fig. 2a). By comparison, the recommended cut-off value of 46% by LTA provides a sensitivity of 20% and a specificity of 84.3% . While adopting 37.5% as a new cut-off value, 521 patients (30.5%) were defined with HOPR, who experienced a higher rate of ischemic events compared with those without (4.2% vs. 1.9%; P = 0.007, Fig. 3a).
On the other hand, patients who experienced bleeding events had significantly lower PLADP compared with those without bleeding (25% [IQR 18–38] vs.30% [IQR 21–41]; P < 0.001). By ROC analysis, a cut-off value of 25.5% provided a sensitivity of 50.3%, a specificity of 62.6%, and the largest area under the curve of 0.57 in predicting bleeding (Fig. 2b). Using this new cut-off value, 682 (39.9%) patients were defined with LOPR, who experienced a higher rate of bleeding events compared to those without (24.2% vs. 15.9%; P < 0.001, Fig. 3b).
The risk of ischemic events and NACE was non-significantly higher in patients with HOPR compared with those in normal responders (4.2% vs. 2.2%; HR 1.99; P = 0.063 and 19.8% vs. 16.8%; HR 1.19; P = 0.247, for ischemic events and NACE, respectively) (Table 1, Fig. 4), while the risk of total bleeding and NACE was significantly higher in patients with LOPR compared with those in normal responders (24.2% vs. 15.8%; HR 1.61; P = 0.001 and 25.7% vs. 16.8%; HR 1.64; P < 0.001, for bleeding and NACE, respectively) (Table 1, Fig. 4).
Optimal PR or therapeutic window of PR to prevent ischemic and bleeding events
According to the ROC curve analysis, we defined an optimal window of PLADP between 25.5 and 37.5% after dual antiplatelet treatment. As a result, 29.6% of the study population was comprised within this therapeutic window in this study.
We classified the patients into 2 groups according to PR: inside the window group (IW) [PLADP(25.5–37.4%)] and outside the window group (OW) (PLADP < 25.5% or ≥ 37.5%). The baseline demographic characteristics, clinical, angiographic and biological characteristics and medication history were described in Table 2. There were no significant differences in all the baseline characteristics between the 2 groups.
We further analyzed the prognosis according to the newly defined therapeutic window. The NACE rate of the IW group patients was lower than that of the OW group patients (16.8% vs. 23.1%; P = 0.004) (Fig. 3c). Kaplan-Meier analysis showed a significant difference in NACE and bleeding between patients within and outside the window, although no significant difference was found in ischemic events (P = 0.438, 0.024 and 0.004, for ischemic events, bleeding and NACE, respectively)(Fig. 5). The hazard ratio of NACE for OW group was significantly higher during the 12-month follow-up compared with IW group [1.44 (95% CI: 1.12–1.85; P = 0.004)] after adjusting for age, gender, body mass index (BMI), history of smoking, hypertension, diabetes, coronary artery bypass grafting (CABG), PCI, hemoglobin, platelet count, estimated glomerular filtration rate (eGFR), activated partial thromboplastin time (APTT), and international normalized ratio (INR) (Table 3). The total bleeding rate was also significantly higher in OW than IW after adjusting for the confounders [1.33 (95% CI: 1.03–1.72; P = 0.028)], which turned out to be the main contributor to NACE (Table 3).
In this study, we identified an optimal range of platelet reactivity as 25.5–37.4% for PLADP while determined by LTA for patients underwent PCI and on the treatment of regular-dose aspirin and clopidogrel, and approximately one third (29.6%) of the patients meet this therapeutic window. Patients inside the window presented significantly lower risk of NACE than those outside the window during 12-month follow-up.
Several studies have tried to identify a threshold of PR that could stratify patients at risk of ischemic events. Bliden et al.  found that HOPR (defined as PLADP ≥ 50% measured by LTA with ADP concentration of 5 μmol/L) was the only variable being significantly related to ischemic events after adjusting for hypertension, diabetes and use of calcium channel inhibitors. Gurbel et al.  demonstrated that HOPR (defined as PLADP ≥ 46% measured by LTA  with ADP concentration of 5 μmol/L) was an independent risk factor for ischemic events within 2 years of non-emergent PCI (OR = 3.9, P< 0.001).
The cut-off value of PLADP in our study is 37.5%, which is lower than the previous study. However, as demonstrated by the GRAVITAS trial, when HOPR was defined as ≥230 P2Y12 reaction units (PRU) by VerifyNow P2Y12 test, high-dose clopidogrel compared with standard-dose clopidogrel did not reduce the incidence of major adverse cardiovascular events , while the post-hoc analysis found that the achievement of a PRU < 208 was associated with significantly improved clinical outcomes. Consistent with the GRAVITAS trial, our result suggests that a lower cut-off value of PLADP might bring more low responders to the intensified anti-platelet treatment and consequently reduce ischemic events.
In addition to recurrent ischemic events, the prognostic importance of bleeding complications following PCI has also been established. ADAPT-DES trial showed that HOPR (defined by > 208 PRU, by VerifyNow P2Y12 test) was inversely related to TIMI major bleeding (adjusted HR: 0.73, 95% CI: 0.61 to 0.89, P = 0.002) . Studies suggested a possible link between LOPR and bleeding [7,8,9, 18,19,20,21,22,23]. With the LTA method, Tsukahara et al.  found that high-responsiveness was the independent predictor of major bleeding in patients receiving drug-eluting stents and treated with thienopyridine. Parodi et al.  reported that LOPR (PLADP < 40%, 10 μmol/L ADP, LTA assay) were the independent predictor of bleeding events. Consistent with previous studies, we confirmed the predictive value of PR on the occurrence of bleeding events after PCI as measured with the LTA assay, and we suggested a cut-off value of PLADP < 25.5% to predict the bleeding events.
The optimal therapeutic window of PLADP is uncertain, Campo  and Mangiacapra et al.  have reported two therapeutic windows for PR measured with the VerifyNow P2Y12 assay. However, in Campo’s study, they reported all clinical events (ischemic and bleeding) after 1 month and up to 1 year of follow-up. Patients with adverse events during the first month were excluded. In Mangiacapra’s study, only short-term outcome of 1-month clinical events were analyzed. By contrast, using the two thresholds for ischemic and bleeding events, we found an optimal therapeutic window for PLADP by LTA assay, ranging from 25.5 to 37.4%, which was associated with the lowest 1-year incidence of NACE. To the best of our knowledge, our study was the first that use LTA method to demonstrate an optimal therapeutic window for PLADP regarding the 1-year clinical outcome.
Our study has important clinical implications. According to the results, post-PCI evaluation of PR carries important prognostic information, and the antiplatelet treatment should be guided referring to optimal therapeutic window of PR instead of single cut-off value. In particular, for patients with HOPR and higher ischemic risk, more aggressive antiplatelet strategies might be useful. On the other hand, for patients with LOPR and higher bleeding risk, conservative antiplatelet therapies should also be indicated until PR falls within the desired range.
The present study has potential limitations. First, the limited funding support prevented us to perform another cohort to validate the study results. Thus, a prospective study would be needed before using such an assay to try to predict outcomes. Second, the sample size was modest, so we could not analyze the optimal ranges of platelet reactivity for different age groups. Third, platelet reactivity could vary while patients taking clopidogrel treatment for longer term. However, we could not further extend the time of platelet reactivity test due to the limited hospitalization period. Besides, patients would be on high risk of thrombotic events early after PCI, so clopidogrel response in early stage of stent implantation would be more important to overcome or predict the thrombotic events.
An optimal therapeutic window of 25.5–37.4% for PLADP predicts the lowest risk of net adverse cardiovascular events, which could be referred for tailored antiplatelet treatment while using platelet aggregation assay by light transmittance aggregometry.
Availability of data and materials
The datasets used or analyzed during the current study are available from the corresponding author on reasonable request.
Mangiacapra F, Patti G, Barbato E, Peace AJ, Ricottini E, Vizzi V, et al. A therapeutic window for platelet reactivity for patients undergoing elective percutaneous coronary intervention: results of the ARMYDA-PROVE (antiplatelet therapy for reduction of MYocardial damage during angioplasty-platelet reactivity for outcome validation effort) study. JACC Cardiovasc Interv. 2012;5(3):281–9. https://doi.org/10.1016/j.jcin.2012.01.009.
Herbert JM, Savi P. P2Y12, a new platelet ADP receptor, target of clopidogrel. Semin Vasc Med. 2003;3(2):113–22. https://doi.org/10.1055/s-2003-40669.
Stone GW, Witzenbichler B, Weisz G, Rinaldi MJ, Neumann FJ, Metzger DC, et al. Platelet reactivity and clinical outcomes after coronary artery implantation of drug-eluting stents (ADAPT-DES): a prospective multicentre registry study. Lancet. 2013;382(9892):614–23. https://doi.org/10.1016/s0140-6736(13)61170-8.
Gurbel PA, Bliden KP, Saucedo JF, Suarez TA, DiChiara J, Antonino MJ, et al. Bivalirudin and clopidogrel with and without eptifibatide for elective stenting: effects on platelet function, thrombelastographic indexes, and their relation to periprocedural infarction results of the CLEAR PLATELETS-2 (Clopidogrel with Eptifibatide to arrest the reactivity of Platelets) study. J Am Coll Cardiol. 2009;53(8):648–57. https://doi.org/10.1016/j.jacc.2008.10.045.
Gurbel PA, Bliden KP, Samara W, Yoho JA, Hayes K, Fissha MZ, et al. Clopidogrel effect on platelet reactivity in patients with stent thrombosis: results of the CREST study. J Am Coll Cardiol. 2005;46(10):1827–32. https://doi.org/10.1016/j.jacc.2005.07.056.
Gurbel PA, Antonino MJ, Bliden KP, Dichiara J, Suarez TA, Singla A, et al. Platelet reactivity to adenosine diphosphate and long-term ischemic event occurrence following percutaneous coronary intervention: a potential antiplatelet therapeutic target. Platelets. 2008;19(8):595–604. https://doi.org/10.1080/09537100802351065.
Breet NJ, van Werkum JW, Bouman HJ, Kelder JC, Ruven HJ, Bal ET, et al. Comparison of platelet function tests in predicting clinical outcome in patients undergoing coronary stent implantation. JAMA. 2010;303(8):754–62. https://doi.org/10.1001/jama.2010.181.
Cuisset T, Frere C, Quilici J, Gaborit B, Castelli C, Poyet R, et al. Predictive values of post-treatment adenosine diphosphate-induced aggregation and vasodilator-stimulated phosphoprotein index for stent thrombosis after acute coronary syndrome in clopidogrel-treated patients. Am J Cardiol. 2009;104(8):1078–82. https://doi.org/10.1016/j.amjcard.2009.06.007.
Patti G, Pasceri V, Vizzi V, Ricottini E, Di Sciascio G. Usefulness of platelet response to clopidogrel by point-of-care testing to predict bleeding outcomes in patients undergoing percutaneous coronary intervention (from the antiplatelet therapy for reduction of myocardial damage during angioplasty-bleeding study). Am J Cardiol. 2011;107(7):995–1000. https://doi.org/10.1016/j.amjcard.2010.11.025.
Sibbing D, Steinhubl SR, Schulz S, Schömig A, Kastrati A. Platelet aggregation and its association with stent thrombosis and bleeding in clopidogrel-treated patients: initial evidence of a therapeutic window. J Am Coll Cardiol. 2010;56(4):317–8. https://doi.org/10.1016/j.jacc.2010.03.048.
Price MJ. Bedside evaluation of thienopyridine antiplatelet therapy. Circulation. 2009;119(19):2625–32. https://doi.org/10.1161/circulationaha.107.696732.
Bonello L, Tantry US, Marcucci R, Blindt R, Angiolillo DJ, Becker R, et al. Consensus and future directions on the definition of high on-treatment platelet reactivity to adenosine diphosphate. J Am Coll Cardiol. 2010;56(12):919–33. https://doi.org/10.1016/j.jacc.2010.04.047.
Li C, Hirsh J, Xie C, Johnston MA, Eikelboom JW. Reversal of the anti-platelet effects of aspirin and clopidogrel. J Thromb Haemost. 2012;10(4):521–8. https://doi.org/10.1111/j.1538-7836.2012.04641.x.
Rao AK, Pratt C, Berke A, Jaffe A, Ockene I, Schreiber TL, et al. Thrombolysis in myocardial infarction (TIMI) trial--phase I: hemorrhagic manifestations and changes in plasma fibrinogen and the fibrinolytic system in patients treated with recombinant tissue plasminogen activator and streptokinase. J Am Coll Cardiol. 1988;11(1):1–11. https://doi.org/10.1016/0735-1097(88)90158-1.
Thygesen K, Alpert JS, White HD. Universal definition of myocardial infarction. J Am Coll Cardiol. 2007;50(22):2173–95. https://doi.org/10.1016/j.jacc.2007.09.011.
Cannon CP, Battler A, Brindis RG, Cox JL, Ellis SG, Every NR, et al. American College of Cardiology key data elements and definitions for measuring the clinical management and outcomes of patients with acute coronary syndromes. A report of the American College of Cardiology Task Force on clinical data standards (acute coronary syndromes writing committee). J Am Coll Cardiol. 2001;38(7):2114–30. https://doi.org/10.1016/s0735-1097(01)01702-8.
Bliden KP, DiChiara J, Tantry US, Bassi AK, Chaganti SK, Gurbel PA. Increased risk in patients with high platelet aggregation receiving chronic clopidogrel therapy undergoing percutaneous coronary intervention: is the current antiplatelet therapy adequate? J Am Coll Cardiol. 2007;49(6):657–66. https://doi.org/10.1016/j.jacc.2006.10.050.
Price MJ, Berger PB, Teirstein PS, Tanguay JF, Angiolillo DJ, Spriggs D, et al. Standard- vs high-dose clopidogrel based on platelet function testing after percutaneous coronary intervention: the GRAVITAS randomized trial. JAMA. 2011;305(11):1097–105. https://doi.org/10.1001/jama.2011.290.
SIBBING D, SCHULZ S, BRAUN S, MORATH T, STEGHERR J, Mehilli J, et al. Antiplatelet effects of clopidogrel and bleeding in patients undergoing coronary stent placement. 2010;8(2):250–6. https://doi.org/10.1111/j.1538-7836.2009.03709.x.
BONELLO L, MANCINI J, PANSIERI M, MAILLARD L, ROSSI P, COLLET F, et al. Relationship between post-treatment platelet reactivity and ischemic and bleeding events at 1-year follow-up in patients receiving prasugrel. 2012;10(10):1999–2005. https://doi.org/10.1111/j.1538-7836.2012.04875.x.
Collet J-P, Cuisset T, Rangé G, Cayla G, Elhadad S, Pouillot C, et al. Bedside Monitoring to Adjust Antiplatelet Therapy for Coronary Stenting. 2012;367(22):2100–9. https://doi.org/10.1056/NEJMoa1209979.
Gurbel PA, Bliden KP, Navickas IA, Mahla E, Dichiara J, Suarez TA, et al. Adenosine diphosphate–induced platelet-fibrin clot strength: A new thrombelastographic indicator of long-term poststenting ischemic events. Am Heart J. 2010;160(2):346–54. https://doi.org/10.1016/j.ahj.2010.05.034.
Mokhtar OA, Lemesle G, Armero S, Mancini J, Bonello C, Tahirou I, et al. Relationship between platelet reactivity inhibition and non-CABG related major bleeding in patients undergoing percutaneous coronary intervention. Thromb Res. 2010;126(2):e147–e9. https://doi.org/10.1016/j.thromres.2010.01.013.
Tsukahara K, Kimura K, Morita S, Ebina T, Kosuge M, Hibi K, et al. Impact of high-responsiveness to dual antiplatelet therapy on bleeding complications in patients receiving drug-eluting stents. Circ J. 2010;74(4):679–85. https://doi.org/10.1253/circj.cj-09-0601.
Parodi G, Bellandi B, Venditti F, Carrabba N, Valenti R, Migliorini A, et al. Residual platelet reactivity, bleedings, and adherence to treatment in patients having coronary stent implantation treated with prasugrel. Am J Cardiol. 2012;109(2):214–8. https://doi.org/10.1016/j.amjcard.2011.08.034.
Campo G, Parrinello G, Ferraresi P, Lunghi B, Tebaldi M, Miccoli M, et al. Prospective evaluation of on-clopidogrel platelet reactivity over time in patients treated with percutaneous coronary intervention relationship with gene polymorphisms and clinical outcome. J Am Coll Cardiol. 2011;57(25):2474–83. https://doi.org/10.1016/j.jacc.2010.12.047.
This work was supported by a grant from the National Natural Science Funding of China (81170181), a grant from the Jiangsu Province’s Key Provincial Talents Program (ZDRCA2016013), the Second Level of 333 High Level Talent Training Project in Jiangsu Province (BRA2019099), the Special Fund for Key R & D Plans (Social Development) of Jiangsu Province (BE2019754), and a Project Funded by the Priority Academic Program Development of Jiangsu Higher Education Institutes (PAPD).
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This study was approved by the ethics committee of the First Affiliated Hospital of Nanjing Medical University based on the Declaration of Helsinki. Written informed consent was obtained from each patient.
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Wang, J., Wang, J., Dong, Z. et al. An optimal window of platelet reactivity by LTA assay for patients undergoing percutaneous coronary intervention. Thrombosis J 19, 73 (2021). https://doi.org/10.1186/s12959-021-00323-5
- Light transmittance aggregometry
- Platelet reactivity
- Percutaneous coronary intervention
- Therapeutic window