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      Hypotension caused by oral administration of 5-aminolevulinic acid persists after surgery in patients undergoing transurethral resection of bladder tumor under spinal anesthesia

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      JA Clinical Reports
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          Abstract

          To the Editor, 5-Aminolevulinic acid (ALA) is utilized for photodynamic diagnosis to detect superficial bladder cancer and its adverse effect is hypotension [1–5]. Compared to general anesthesia, spinal anesthesia is not indicated as an increased risk factor for 5-ALA-induced hypotension from anesthesia induction to the start of surgery in patients undergoing transurethral resection of bladder tumor (TUR-BT) with 5-ALA [2, 3]. However, no studies exist that have investigated the precise perioperative hypotensive effects by 5-ALA under spinal anesthesia. This retrospective study assessed the hypotensive effect of 5-ALA on hemodynamic change of spinal anesthesia in patients undergoing TUR-BT not only during surgery but also after the ward admission. The medical records of 129 patients who underwent TUR-BT under spinal anesthesia using 0.5% hyperbaric bupivacaine in Kyoto City Hospital between January 2018 and March 2019 were divided into two groups, based on whether 5-ALA was used (ALA group, n = 66) or not used (control group, n = 63). The ALA group received 5-ALA (20 mg/kg) orally 3 h before the start of surgery. The change in noninvasive blood pressure (BP) on the day of surgery and the dosage of vasopressors used during spinal anesthesia were analyzed. No significant difference existed between the two groups in the patients’ preoperative characteristics. Intravenous fluid volume during anesthesia was significantly higher in the ALA group than in the control group (Table 1). Systolic and diastolic BP were significantly lower in the ALA group than in the control group from spinal anesthesia until 2 h after the ward admission. In the ALA group, systolic and diastolic BP significantly remained decreased from spinal anesthesia until 2 h after the ward admission (Fig. 1). The total dosage of ephedrine and phenylephrine were higher in the ALA group than in the control group (Table 1). Table 1 The patients’ preoperative characteristics, anesthesia profiles and the drugs administered during anesthesia Control group (n = 63) ALA group (n = 66) P value Age (years) 71 ± 11 74 ± 10 0.27 Height (cm) 162 ± 15 161 ± 14 0.58 Weight (kg) 65 ± 17 65 ± 18 0.97 Sex (male/female) 59 (94%)/4 (6%) 55 (83%)/11 (17%) 0.07 Regular use of antihypertensive drug 24 (38%) 23 (35%) 0.70 Regular use of renin-angiotensin system inhibitor 14 (22%) 11 (17%) 0.42 Duration of surgery (minutes) 43 ± 25 44 ± 20 0.84 Duration of anesthesia (minutes) 75 ± 28 80 ± 22 0.25 Dose of 0.5% hyperbaric bupivacaine of spinal anesthesia (mL) 3.1 ± 0.3 3.0 ± 0.3 0.20 Sensory block level just before surgerya T8 (T2–T11) T6 (T2–L1) 0.26 Sensory block level at the end of surgerya T6 (T2–T12) T5 (T2–T12) 0.49 Intravenous fluid volume during anesthesia (mL) 570 ± 191 758 ± 284 < 0.001 Use of vasopressorsb 10 (16%) 47 (71%) < 0.001 Use of ephedrine 8 (13%) 37 (56%) < 0.001 Total dose of ephedrine (mg) 1.0 ± 3.0 6.9 ± 9.0 < 0.001 Use of phenylephrine 6 (10%) 30 (45%) < 0.001 Total dose of phenylephrine (mg) 0.013 ± 0.042 0.21 ± 0.34 < 0.001 Values are presented as mean ± standard deviation or number (%) aMedian (maximum-minimum) bEphedrine or phenylephrine or both were used ALA aminolevulinic acid Fig. 1 Time courses of systolic blood pressure and diastolic blood pressure. Values are presented as mean ± standard deviation. *P < 0.05, post-operating room admission versus before 5-ALA p.o./morning. # P < 0.05, the ALA group versus the control group. ALA aminolevulinic acid, BP blood pressure, p.o. per os Additive hypotensive effect induced by spinal anesthesia and 5-ALA was prominent after spinal anesthesia induction not only during surgery but also for 2 h after the ward admission, as shown by the BP changes in our ALA group. Since the duration of the hypotensive effect by 5-ALA is longer than that of hyperbaric bupivacaine of spinal anesthesia, the systolic BP in the ALA group did not return to the baseline level even 2 h after the ward admission, unlike in the control group. We cannot easily state that spinal anesthesia using hyperbaric bupivacaine is a safe technique from our result, when considering the postoperative period. Our reflection point is that hypotension may be encouraged by hypovolemia in the ALA group, because all patients did not have intravenous fluids after 5-ALA administration before spinal anesthesia. Other risk factors that increase the incidence of 5-ALA-induced hypotension have been reported to be the regular use of antihypertensive drugs, particularly renin-angiotensin system inhibitor drugs [2, 4] and a history of ALA-induced hypotension [5]. In conclusion, orally administered 5-ALA before TUR-BT under spinal anesthesia induced significant hypotension after spinal anesthesia induction until 2 h after surgery and an increased need for vasopressors and intravenous volume. Anesthesiologists should have a strategy for safe anesthetic management against long-lasting hypotension by 5-ALA.

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          Risk factors for developing oral 5-aminolevulinic acid-induced side effects in patients undergoing fluorescence guided resection.

          Oral 5 aminolevulinic acid (5-ALA) is used to assist surgical resection of malignant tumours in the brain and other locations. Hypotension and alteration of liver functions have been reported as potential adverse effects. This study was designed to assess the incidence and contributing factors that cause 5-ALA induced side effects in a cohort of 90 patients. Hypotension occurred in 11% of patients irrespective of 5-ALA dose. The only contributing factor was the presence of cardiovascular disease and antihypertensive drug therapy with an odd ratio of 17.7. Liver function were disturbed in 2% in patients who received 20mg or less/kg body weight compared to 4% in those who received a dose of >20mg/kg 5-ALA. The liver dysfunction was minor and was not clinically significant. We concluded that 5-ALA induced side effects were minimal and hypotension more likely to occur in patients receiving antihypertensive drug therapy.
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            Hemodynamic effects of 5-aminolevulinic acid in humans.

            Endogenous protoporphyrin IX (PpIX), which results from the oral administration of 5-aminolevulinic acid (ALA), is being investigated for its efficacy as a photosensitizing agent for photodynamic therapy (PDT). Clinical use of ALA has been associated with only mild gastrointestinal side effects. The hemodynamic effects of orally administered ALA in doses used for PDT are unknown. Six patients with a significant history of cardiac disease underwent Swan-Ganz catheterization prior to ALA administration and abdominal operation for PDT. Hemodynamic data collection began at least 1 h prior to ALA, and continued for at least 4 h subsequently, during which time no other medications were administered. When compared to measurements made prior to ALA administration, all patients displayed a significant decrease in systolic and diastolic blood pressures, pulmonary artery systolic and diastolic pressures as well as pulmonary vascular resistance. Five of the six patients also developed a decrease in systemic vascular resistance. No significant changes in pulmonary capillary wedge pressure, cardiac output or cardiac index was observed, but the mean pulse rate rose significantly. These findings cannot be explained on the basis of other cardiovascular depressants or to poor central volume status. Although no adverse sequela were appreciated as a result of the observed hemodynamic changes, this potential should be recognized in patients undergoing PDT using ALA.
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              Intraoperative hypotension caused by oral administration of 5-aminolevulinic acid for photodynamic diagnosis in patients with bladder cancer.

              To analyze perioperative blood pressure in patients undergoing transurethral resection of bladder tumor with photodynamic diagnosis.
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                Author and article information

                Contributors
                masami@kb3.so-net.ne.jp
                sppc21hv06@yahoo.co.jp
                higasono@gmail.com
                arai@kuhp.kyoto-u.ac.jp
                Journal
                JA Clin Rep
                JA Clin Rep
                JA Clinical Reports
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                2363-9024
                21 November 2020
                21 November 2020
                December 2020
                : 6
                : 93
                Affiliations
                GRID grid.415597.b, ISNI 0000 0004 0377 2487, Department of Anesthesia, , Kyoto City Hospital, ; 1-2 Mibuhigashitakada-cho, Nakagyo-ku, Kyoto, 604-8845 Japan
                Article
                399
                10.1186/s40981-020-00399-4
                7680493
                33219885
                2a1c9541-6e2f-4f39-97ec-4e010508f3c0
                © The Author(s) 2020

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 5 October 2020
                : 2 November 2020
                : 10 November 2020
                Categories
                Letter to the Editor
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                © The Author(s) 2020

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