| Literature DB >> 35160247 |
Umberto Anceschi1, Marilda Mormando2, Cristian Fiori3, Orazio Zappalà4, Bernardino De Concilio5, Aldo Brassetti1, Alessandro Carrara6, Maria Consiglia Ferriero1, Gabriele Tuderti1, Leonardo Misuraca1, Alfredo Maria Bove1, Riccardo Mastroianni1, Alfonsina Chiefari2, Marialuisa Appetecchia2, Giuseppe Tirone4, Francesco Porpiglia3, Antonio Celia5, Michele Gallucci1, Giuseppe Simone1.
Abstract
BACKGROUND: To propose a trifecta that summarizes endpoints and predicts their maintenance after adrenalectomy (n = 90) for unilateral primary aldosteronism (UPA).Entities:
Keywords: Conn’s syndrome; PASO; adrenalectomy; primary aldosteronism; trifecta
Year: 2022 PMID: 35160247 PMCID: PMC8836466 DOI: 10.3390/jcm11030794
Source DB: PubMed Journal: J Clin Med ISSN: 2077-0383 Impact factor: 4.241
List of preoperative drugs used in the cohort for the TIS score assessment.
| Type of Drug | Minimum Dosage | Maximum Dosage |
|---|---|---|
| Zofenopril | 7.5 | 60 |
| Nebivolol | 5 | 10 |
| Ramipril | 2.5 | 10 |
| Nifedipine | 30 | 60 |
| Enalapril | 5 | 40 |
| Manidipine | 10 | 20 |
| Doxazosine | 2 | 16 |
| Furosemide | 25 | 1000 |
| Indapamide | 1 | 5 |
| Delapril | 15 | 60 |
| Irbesartan | 150 | 300 |
| Losartan | 12.5 | 150 |
| Hydrochlorothiazide | 12.5 | 200 |
| Clonidine | 75 | 900 |
| Carvedilol | 6.25 | 50 |
| Atenolol | 25 | 100 |
| Amlodipine | 5 | 10 |
| Valsartan | 40 | 320 |
| Olmesartan | 5 | 40 |
| Lercanidipine | 10 | 30 |
| Aldactone | 25 | 400 |
| Canrenone | 50 | 800 |
| Barnidipine | 5 | 20 |
| Pentoxyfilline | 400 | 1200 |
| Bisoprolol | 2.5 | 10 |
Baseline and preoperative data.
| Variable | Overall | Total | Partial |
|
|---|---|---|---|---|
| Age at surgery (median, IQR) | 54 (44–65) | 54 (44.5–63) | 57 (43.5–67.5) | 0.408 |
| Follow-up (months, median, range) | 42 (27–54) | 41 (24–50) | 46 (32.7–57.5) | 0.223 |
| Gender ( | ||||
| Male | 36 (40%) | 23 (37.7%) | 13 (44.8%) | |
| Female | 54 (60%) | 38 (62.3%) | 16 (55.2%) | 0.519 |
| ASA score ( | ||||
| 1–2 | 73 (81.1%) | 50 (82%) | 23 (79.3%) | |
| 3–4 | 17 (18.9%) | 11 (18%) | 6 (20.7%) | 0.763 |
| Adrenal mass size (cm, | 3 (2–5) | 4.2 (2.35–6) | 2.7 (1.8–2.85) | 0.001 |
| Side ( | ||||
| Left | 45 (50%) | 23 (37.7%) | 22 (75.9%) | |
| Rigth | 45 (50%) | 38 (62.3%) | 7 (24.1%) | 0.001 |
| Preoperative Hypertension ( | ||||
| Yes | 80 (88.8%) | 53 (86.8%) | 27 (93.1%) | |
| No | 10 (11.2%) | 8 (13.2%) | 2 (6.9%) | 0.456 |
| Preoperative Hypokalemia ( | ||||
| Yes | 27 (30%) | 21 (65.6%) | 6 (20.7%) | |
| No | 63 (70%) | 40 (34.4%) | 23 (79.3%) | 0.184 |
| Number of drugs ( | ||||
| No drugs | 9 (10%) | 7 (11.4%) | 2 (6.8%) | |
| One class medication | 50 (55.5%) | 32 (52.4%) | 18 (62%) | |
| Combined class medication (≥2) | 31 (34.5%) | 22 (36%) | 9 (31.2%) | 0.676 |
| Preoperative TIS score (median, IQR) | 0.5 (0.25–1) | 0.5 (0.25–1.09) | 0.5 (0.25–1) | 0.989 |
Perioperative and pathologic outcomes.
| Variable | Overall | Total | Partial |
|
|---|---|---|---|---|
| Preoperative Hb (g/dL, median, IQR) | 13.8 (12.8–14.6) | 13.4 (12.5–14.3) | 14.3 (13.4–14.9) | 0.058 |
| Postoperative Hb (g/dL, median, IQR) | 12.6 (11.7–13.5) | 12.3 (11.6–13.4) | 13.3 (11.7–13.5) | 0.271 |
| ΔHb (g/dL, median, IQR) | 1.1 (0.3–2.1) | 1.1 (0.1–1.8) | 1.1 (0.4–2.35) | 0.337 |
| LOS (days, median, IQR) | 4 (3–5) | 4 (3–5) | 3 (2.5–4) | 0.038 |
| Overall complications ( | 10 (11.1%) | 7 (11.5%) | 3 (10.3%) | 0.873 |
| Perioperative transfusions rate ( | 3 (3.4%) | 2 (3.2%) | 1 (3.4%) | 0.967 |
| Clavien Grade ( | ||||
| I | 6 | 6 | 2 | 0.940 |
| II | 3 | 2 | 1 | |
| III | - | - | - | |
| IV | 1 | 1 | - | |
| V | - | - | - | 0.488 |
| Follow-up (months, median range) | 42 (27–54) | 41 (24–50) | 46 (32.7–57.5) | 0.223 |
| Histology ( | ||||
| Adenoma | 70 (77.8%) | 48 (78.7%) | 22 (75.8%) | |
| Hyperplasia | 20 (22.2%) | 13 (21.3%) | 7 (24.1%) | 0.209 |
Early and long-term functional outcomes after MIPA or MITA.
| Variable | Overall | Total | Partial |
|
|---|---|---|---|---|
| Trifecta | 19 (21.1%) | 10 (16.3%) | 9 (31%) | 0.312 |
| - 3-month ∆TIS ≥ 50% | 25 (27.8%) | 13 (21.3%) | 12 (41.3%) | 0.067 |
| - No CKD ≥ 2 | 80 (88.9%) | 53 (86.8%) | 27 (93.1%) | 0.813 |
| - No hypokalemia (3 months) | 76 (84.4%) | 51 (83.6%) | 25 (86.2%) | 0.837 |
| Follow-up (months, median, IQR) | 42 (27–54) | 41 (24–50) | 46 (32.7–57.5) | 0.223 |
| Hypokalemia at last follow-up ( | 12 (13.3%) | 9 (14.8%) | 3 (10.3%) | 0.565 |
| Cortisol replacement at last follow-up ( | 4 (6.5%) | 4 (6.5%) | - | - |
| Complete clinical success ( | 54 (60%) | 33 (54%) | 21 (72.4%) | 0.097 |
| Partial clinical success ( | 16 (17.7%) | 14 (23%) | 2 (6.8%) | 0.136 |
| Absent clinical success ( | 20 (22.3%) | 14 (23%) | 6 (20.7%) | 0.136 |
| Complete biochemical success ( | 75 (83.3%) | 50 (81.9%) | 25 (86.2%) | 0.918 |
| Partial biochemical success ( | 11 (12.3%) | 7 (11.4%) | 4 (13.7%) | 0.918 |
| Absent biochemical success ( | 4 (4.4%) | 3 (4.91%) | 1 (3.4%) | 0.918 |
Early and long-term functional outcomes according to PASO criteria.
| Variable | Overall | Total | Partial |
|
|---|---|---|---|---|
| Complete clinical success | ||||
| - No medication/Controlled BP | 54 (60%) | 33 (54%) | 21 (72.4%) | 0.097 |
| Partial clinical success | 16 (17.7%) | 14 (23%) | 2 (6.8%) | |
| - Drug escalation (Controlled BP) | 8 (8.9%) | 7 (11.5%) | 1 (3.4%) | |
| - Switch to a lower class of medication (Controlled BP) | 2 (2.2%) | 2 (3.3%) | - | |
| - No drugs (Moderate BP reduction) | 4 (4.4%) | 4 (6.6%) | - | 0.136 |
| - Switch to comparable medication (Moderate BP reduction) | 2 (2.2%) | 1 (1.6%) | 1 (3.4%) | |
| Absent clinical success | 20 (22.3%) | 14 (23%) | 6 (20.7%) | |
| - Unchanged dosage medication | 14 (15.6%) | 9 (14.8%) | 5 (17.2%) | |
| - Increased dosage | 3 (3.3%) | 3 (4.9%) | - | 0.136 |
| - Switch to a stronger class of medication | 3 (3.3%) | 2 (3.3%) | 1 (3.4%) |
Univariable and multivariable logistic regression analysis to identify predictors of trifecta achievement.
| Variable | Univariable Analysis | Multivariable Analysis | ||||||
|---|---|---|---|---|---|---|---|---|
| OR | 95.0% CI | OR | 95.0% CI | |||||
| Lower | Higher | Lower | Higher | |||||
| Age | 3.44 | 1.04 | 11.4 | 0.04 | 3.07 | 0.88 | 10.6 | 0.07 |
| Gender | 1.32 | 0.46 | 3.77 | 0.594 | - | - | - | - |
| ASA score | ||||||||
| 1–2 | 0.76 | 0.19 | 2.98 | 0.698 | - | - | - | - |
| 3–4 | ||||||||
| Adenoma size (cm) | 1.18 | 1.02 | 1.39 | 0.04 | 1.14 | 0.95 | 1.36 | 0.152 |
| Surgical approach | 1.31 | 0.37 | 4.64 | 0.675 | - | - | - | - |
| TIS score (0.5≤ vs. ≥0.5) | 3.53 | 1.21 | 10.3 | 0.02 | 3.28 | 1.07 | 10.9 | 0.03 |
Figure 1Probability of complete clinical success according to PASO criteria.
Figure 2Probability of complete biochemical success according to PASO criteria.
Figure 3Probability of simultaneous complete clinical and biochemical success according to PASO criteria.
Univariable and multivariable logistic regression analysis to identify predictors of complete clinical success according to PASO criteria.
| Variable | Univariable Analysis | Multivariable Analysis | ||||||
|---|---|---|---|---|---|---|---|---|
| HR | 95.0% CI | HR | 95.0% CI | |||||
| Lower | Higher | Lower | Higher | |||||
| Age (≤50 year vs. ≥50 year) | 0.81 | 0.44 | 1.47 | 0.501 | - | - | - | - |
| Gender | 1.18 | 0.62 | 2.26 | 0.596 | - | - | - | - |
| ASA score | ||||||||
| 1–2 | 0.65 | 0.30 | 1.38 | 0.262 | - | - | - | - |
| 3–4 | ||||||||
| Adenoma size (≤6 cm vs. ≥6 cm) | 1.12 | 1.01 | 1.24 | 0.03 | 1.16 | 0.99 | 1.24 | 0.05 |
| MIPA vs. MITA | 1.63 | 0.67 | 3.95 | 0.276 | - | - | - | - |
| Perioperative complications (CD II–V) | 0.18 | 0.02 | 1.34 | 0.09 | ||||
| ΔTIS reduction ≥ 50 | 2.47 | 1.3 | 4.69 | 0.006 | ||||
| No Hypokalemia (3 months) | 0.70 | 0.33 | 1.47 | 0.350 | ||||
| Trifecta | 2.96 | 1.56 | 5.82 | 0.002 | 2.84 | 1.45 | 5.58 | 0.002 |
Univariable and multivariable logistic regression analysis to identify predictors of complete biochemical success according to PASO criteria.
| Variable | Univariable Analysis | Multivariable Analysis | ||||||
|---|---|---|---|---|---|---|---|---|
| HR | 95.0% CI | HR | 95.0% CI | |||||
| Lower | Higher | Lower | Higher | |||||
| Age (≤50 y vs. ≥50 y) | 1 | 0.98 | 1.02 | 0.738 | - | - | - | - |
| Gender | 1.30 | 0.75 | 2.26 | 0.336 | - | - | - | - |
| ASA score | ||||||||
| 1–2 | 0.68 | 0.36 | 1.28 | 0.237 | - | - | - | - |
| 3–4 | ||||||||
| Adenoma size (≤6 cm vs. ≥ 6 cm) | 2.72 | 1.46 | 5.06 | 0.001 | 2.87 | 1.53 | 5.36 | 0.001 |
| MIPA vs. MITA | 1.27 | 0.74 | 2.18 | 0.370 | - | - | - | - |
| Perioperative complications (CD II–V) | 1 | 0.45 | 2.23 | 0.984 | ||||
| ΔTIS reduction ≥ 50% | 1.20 | 0.66 | 2.19 | 0.546 | ||||
| No Hypokalemia (3 months) | 0.25 | 0.10 | 0.64 | 0.004 | ||||
| Trifecta | 1.97 | 1.07 | 3.65 | 0.03 | 2.10 | 1.13 | 3.90 | 0.018 |
Univariable and multivariable logistic regression analysis to identify predictors of simultaneous complete clinical and biochemical success according to PASO criteria.
| Variable | Univariable Analysis | Multivariable Analysis | ||||||
|---|---|---|---|---|---|---|---|---|
| HR | 95.0% CI | HR | 95.0% CI | |||||
| Lower | Higher | Lower | Higher | |||||
| Age (≤50 y vs. ≥50 y) | 0.95 | 0.49 | 1.85 | 0.890 | - | - | - | - |
| Gender | 1.44 | 0.69 | 3.01 | 0.326 | - | - | - | - |
| ASA score | ||||||||
| 1–2 | 0.48 | 0.19 | 1.19 | 0.114 | - | - | - | - |
| 3–4 | ||||||||
| Adenoma size (≤6 cm vs. ≥ 6 cm) | 2.50 | 1.08 | 5.79 | 0.032 | 3.81 | 1.68 | 8.65 | 0.001 |
| MIPA vs. MITA | 1.97 | 0.79 | 4.86 | 0.141 | - | - | - | - |
| Perioperative complications (CD II–V) | 0.22 | 0.03 | 1.62 | 0.137 | ||||
| ΔTIS reduction ≥ 50% | 2.2 | 1.07 | 4.49 | 0.031 | ||||
| No Hypokalemia (3 months) | 0.34 | 0.12 | 0.97 | 0.045 | ||||
| Trifecta | 4.10 | 2.01 | 8.43 | <0.001 | 4.29 | 2.08 | 8.86 | <0.001 |