Skip to main content

Severe methanol poisoning treated with a novel hemodialysis system: a case report, analysis, and review


In May and June 2020, an outbreak of methanol poisoning arose in the southwest United States linked to ingestion of contaminated hand sanitizer imported during the coronavirus disease 2019 pandemic, ultimately resulting in over a dozen hospitalizations and at least four deaths in New Mexico and Arizona. In this report, we describe one of these cases in which profound methanol intoxication was successfully treated with the Tablo® Hemodialysis System, the first reported case of toxic alcohol poisoning treated with this novel device. We carry out a formal regression analysis of the serial methanol levels obtained in this case to conservatively estimate that intermittent hemodialysis with Tablo achieved a clearance of methanol of 239 mL/min (95% confidence interval, 173–305 mL/min), a clearance that is well within the previously published standard of care. We conclude by reviewing both the treatment of toxic alcohol poisoning and the determinants of small molecule clearance with hemodialysis, emphasizing the importance of optimizing the dialytic treatment of intoxications with extended treatment times and the use of high-efficiency dialyzers.


Toxic alcohol poisoning continues, even in the twenty-first century, to account for dozens of deaths annually in the United States (US) [1, 2]. Worldwide, it has been estimated that hundreds of people have died in 2020 alone related to misuse of methanol during the coronavirus disease 2019 (COVID-19) pandemic [3]. Early diagnosis and treatment of toxic alcohol poisoning remain essential to preventing morbidity and mortality. In this report, we present and analyze a case of severe methanol intoxication that was successfully treated with intermittent hemodialysis (IHD) using the Tablo® Hemodialysis System (Outset Medical, San Jose, CA, USA), the first reported case of toxic alcohol poisoning treated with this novel device.

Case presentation

A 36-year-old man with alcohol dependence was brought by emergency medical services (EMS) to a local emergency department (ED) after being found down by his family with depressed mental status and slurred speech. He was initially diaphoretic and hypotensive with pupils fixed bilaterally at 5 mm. EMS administered a 2-L saline bolus with normalization of his blood pressure. However, due to his mental status (with a reported Glasgow Coma Scale of 6–7), endotracheal intubation was performed for airway protection soon after arrival to the ED. Initial labs were reportedly notable for an undetectable blood ethanol level and an anion gap of > 40 mmol/L. He was given fomepizole and transferred to our facility.

Upon arrival later that afternoon to our medical intensive care unit, his exam was notable for stable vital signs but persistently depressed mental status with fixed symmetric pupils. He weighed 100 kg. Admission labs (see Table 1) were notable for a persistent anion gap metabolic acidosis and an extremely elevated osmolar gap of > 200 mOsm/kg. Toxicology and nephrology were consulted. A toxic alcohol panel was drawn and additional IV fomepizole was administered with IV folate, thiamine, and pyridoxine. Vascular access for hemodialysis (HD) was placed in the right internal jugular vein (15-cm 12-French Power-Trialysis catheter, Bard Access Systems, Salt Lake City, UT). Computed tomography (CT) of the head revealed “symmetric hypoattenuation in the bilateral basal ganglia involving portion of the putamen and external capsule… suspicious for hypoxic-ischemic injury or potentially toxic-metabolic injury in the correct clinical setting.” The alcohol panel results obtained just prior to the initiation of HD revealed a methanol level above the upper limit of detection (> 156 mmol/L or > 500 mg/dL). The patient received three total HD sessions. His first treatment was interrupted due to poor function of his vascular access, which persisted despite the use of in-line heparin, ultimately requiring a second dialysis access to be placed (30-cm right femoral Power-Trialysis). The first two treatments were performed with the Tablo Hemodialysis System. The third treatment was performed with a conventional IHD machine (Gambro Phoenix, Baxter International, Deerfield, IL, USA) and was also interrupted due to circuit clotting. All dialysis treatments utilized a Revaclear™ dialyzer [Baxter International, polyarylethersulfone, membrane surface area 1.4 m2, KOA for urea 1170 mL/min at blood flow rate (Qb) of 300 mL/min and dialysate flow rate (Qd) of 500 mL/min, KUF 50 mL/h/mmHg]. See Table 2 and Fig. 1 for treatment sequence and serial methanol levels.

Table 1 Labs upon admission to the medical ICU
Table 2 Treatment events including hemodialysis prescription
Fig. 1
figure 1

Methanol levels (measured and estimated) and treatment events. Included are measured methanol levels as well as estimated levels at the start and end of hemodialysis treatments #2 and #3. The drop in methanol levels during the Tablo treatment (HD#2) is highlighted in orange. The estimated methanol levels at the start and end of HD#2 and HD#3 were calculated assuming an endogenous methanol half-life (in the presence of ADH inhibition) of 52 h. ADH, alcohol dehydrogenase; ED, emergency department; HD, hemodialysis; UD, undetectable. To convert methanol levels from mmol/L to mg/dL, multiply by 3.2. *This level of 7.2 mmol/L (23 mg/dL) was drawn off of the dialysis catheter during treatment and is felt to be spurious. Note that there was an 85-min interruption in HD#3 which is not graphically depicted

Following the three sessions of HD, his anion gap, osmolar gap, and blood gas normalized. His methanol levels decreased and became undetectable on hospital day 4. He was extubated on hospital day 3 but had significant agitation and alcohol withdrawal leading to reintubation the next day. On hospital day 6, repeat head CT showed “further progression of vasogenic edema within the region of the basal ganglia bilaterally when compared to prior CT… consistent with known diagnosis of [methanol] ingestion.” By hospital day 8, his mental status improved sufficiently to allow for extubation. However, despite overall clinical improvement, the patient had significant visual impairment. He was examined by ophthalmology and had severe limitation of his visual acuity (e.g., finger-counting limited to 8–12 inches). The patient reported that the ingestion was not meant as self-harm but was rather an attempt to treat alcohol withdrawal with hand sanitizer. He was discharged on hospital day 14. When contacted by phone 2 months later, he reported his vision was unchanged.


The second dialysis treatment (HD#2), which was preceded by a measurable methanol level, allows for an estimation of the efficiency of the Tablo system in treating methanol poisoning. Such assessment requires the use of previously published data, including the data compiled in the 2015 recommendations published by the EXtracorporeal TReatments In Poisoning (EXTRIP) workgroup [4].

First, in the setting of alcohol dehydrogenase (ADH) inhibition (in this case by fomepizole), the endogenous clearance of methanol is quite low relative to HD, with a half-life that averages 52–54 h [5, 6], but is typically even higher in the presence of very high methanol levels such as in this case [5]. This range of half-lives corresponds to reported ranges of renal clearance of 5–6 mL/min and non-renal (presumed pulmonary) clearance of 7–13 mL/min [4]. Methanol has a volume of distribution of 0.6–0.8 L/kg [4, 7] and, given its unicompartmental kinetics, there is no rebound of methanol after HD [8, 9]. In contrast to methanol, the renal clearance of formate, though variable and pH-dependent, is much higher, consistently reported at > 170 mL/min, and the additional clearance of formate by IHD appears small (and of unclear clinical relevance) relative to endogenous clearance [4, 5, 8,9,10,11].

In this case, if we conservatively assume an endogenous methanol half-life of 52 h, the serum level of methanol of 64.9 mmol/L (208 mg/dL) at approximately 8 am on day 2 would have decayed to approximately 62.4 mmol/L (200 mg/dL) by the start of dialysis 3 h later. Notably, since methanol does not exhibit rebound after dialysis, the level of 7.2 mmol/L (23 mg/dL) obtained before the end of HD#2 is presumed spurious, likely because it was obtained off the dialysis catheter during treatment, and it is excluded from our analysis.

Calculation of clearances

We undertook a regression analysis of the methanol levels in logarithmic space, incorporating the previously existing data for the non-dialytic clearance and volume of distribution of methanol into a formal statistical analysis that enabled us to estimate dialytic clearance using the measurements available to us. The unicompartmental kinetics of methanol and the lack of rebound imply a continuous decline of the levels of the toxin over time. Therefore, a measurement obtained at time t, C(t), can be related to the level, C(0), obtained at an arbitrary initial time (t = 0) according to the logarithmic formula:

$$ \log C(t)=\log C(0)-\frac{K_{\mathrm{ND}}\bullet t}{V}-\frac{K_{\mathrm{Tablo}}\bullet \Delta {t}_{\mathrm{Tablo}}}{V}-\frac{K_{\mathrm{HD}}\bullet \Delta {t}_{\mathrm{HD}}}{V} $$

where KND is the non-dialytic (renal + non-renal) clearance set at 16 mL/min (median of data range reported by EXTRIP [4]), V is the volume of distribution of methanol (conservatively set to 60 kg for this estimate), ∆tTablo is the total treatment duration with Tablo to time t, and ∆tHD is the total treatment duration with conventional IHD to time t. We set time zero to the time the 64.9 mmol/L (208 mg/dL) level was obtained. Using this formal approach, the estimates for the two clearances were 341 mL/min [95% confidence interval (CI) 252–429 mL/min] for conventional IHD (KHD) and 239 mL/min (95% CI 173–305 mL/min) for Tablo (KTablo). Both of these clearances are well within the range of clearances achieved with IHD previously reported in the literature of 77–400 mL/min (mean 208 mL/min) [4].

Another way to assess the efficacy of methanol clearance in this case is to compare the duration of dialysis required in this case to two previously published methods [8, 12] for estimating the duration of IHD needed to treat methanol poisoning. The total observed treatment time for our patient was 9.42 h, including 305 min (ΔtTablo) with Tablo during HD#2 and 260 min (ΔtHD) during HD#3 with conventional IHD (accounting for the interruption in HD#3).

The first method, published by Hirsch et al. in 2001 [8], estimates the duration (t, in hours) to achieve a methanol level of 5 mmol/L (16 mg/dL) to be:

$$ t=-V\bullet \ln \left(\frac{5}{A}\right)/\left(0.06\bullet k\right) $$

where V is the estimate of total body water, A is the initial methanol concentration (in mmol/L), and k is 80% of the manufacturer-specified dialyzer urea clearance (in mL/min) at the given Qd. However, in this specific case, rather than estimating k from the dialyzer characteristics, we can use the estimates generated from our in vivo data for methanol clearance specific to both Tablo and conventional IHD (KTablo and KHD, respectively). Using these two estimated values for methanol clearance as k in the Hirsch equation gives an estimated duration of 10.6 and 7.4 h, for Tablo and conventional IHD, respectively, to bring the methanol level down from 62.4 mmol/L (200 mg/dL, the estimated level at the beginning of HD#2) to 5 mmol/L (16 mg/dL), assuming we had used only Tablo or only conventional IHD for both treatments. Since we used Tablo followed by conventional IHD, the total clearance can be estimated as the time-weighted average of the clearances of the two methods:

$$ {K}_{\mathrm{ave}}=\frac{\Delta {t}_{\mathrm{Tablo}}}{\Delta {t}_{\mathrm{Tablo}}+\Delta {t}_{\mathrm{HD}}}\bullet {K}_{\mathrm{Tablo}}+\frac{\Delta {t}_{\mathrm{HD}}}{\Delta {t}_{\mathrm{Tablo}}+\Delta {t}_{\mathrm{HD}}}\bullet {K}_{\mathrm{HD}} $$

which yields a Kave of 286 mL/min. Using this Kave for k in the Hirsch equation yields an estimated treatment time of 8.81 h, which is similar to the observed 9.42 h it took in this case.

Lachance et al. in 2015 published gender-specific equations for predicting treatment duration for high-efficiency HD [12]. Specifically, they proposed the equations of:

$$ t=3.390\bullet \left(\ln \left(\frac{MCi}{4}\right)\right) $$

for women, and:

$$ t=3.534\bullet \left(\ln \left(\frac{MCi}{4}\right)\right) $$

for men, where MCi is the initial methanol concentration (in mmol/L) and t is the time (in hours) needed to achieve a methanol level of 6 mmol/L (19.2 mg/dL). For our man with an initial methanol level of 64.9 mmol/L (208 mg/dL), one would predict a treatment time of 9.7 h, which closely matches our observed treatment time of 9.42 h using the combination of Tablo and conventional IHD.


Several brands of imported hand sanitizer distributed in the southwest US during the COVID-19 pandemic were found by the US Food and Drug Administration (FDA) in June of 2020 to be contaminated with methanol. This ultimately led to an outbreak of methanol poisoning which resulted in 15 known hospitalizations and at least four deaths in New Mexico and Arizona in May and June of 2020 [2, 13]. Of these 15 patients, nine, including our subject treated with the Tablo device, ultimately required renal replacement therapy (RRT) [2].

As the primary mediator of toxicity is not methanol but formate, the outcome of methanol poisoning depends on more than the presenting methanol level. However, levels greater than 15.6–31.2 mmol/L (50–100 mg/dL) have been associated with an increased risk of death or permanent disability [4, 14]. We did not have access to formate levels in this case, but the initial methanol level of > 156 mmol/L (> 500 mg/dL) is on the same order of magnitude as some of the highest levels recorded in survivors of methanol poisoning [15] and was the highest initial level documented in this particular outbreak tracked by the US Centers for Disease Control [2]. The significant visual impairment noted in this case, though unfortunate, is consistent with previously reported cases of methanol intoxication at levels well below 156 mmol/L (500 mg/dL) that resulted in permanent visual impairment [2, 9, 16, 17].


Features of the Tablo Hemodialysis System

Tablo is a next-generation, self-contained hemodialysis system capable of adaptive kidney replacement therapy from hospital to home. Tablo was approved by the FDA for use in hospitals and dialysis centers in 2016 and for in-home use in 2020. Tablo contains three primary components: (1) the Tablo Console, a compact, easily transportable console with integrated water purification, on-demand dialysate production, and touchscreen interface; (2) the Tablo Cartridge, a disposable, single-use organizer with pre-strung bloodlines compatible with any commercially available dialyzer that easily clicks into place; and (3) the TabloHub, a web-based portal enabling Tablo to stay connected with two-way wireless communication, cloud-based system monitoring, treatment analytics, and clinical recordkeeping that can be integrated with electronic medical records. See Table 3 for further device and operating specifications.

Table 3 Device and operating specifications for Tablo Hemodialysis System

The integrated water purification system includes sediment filter, carbon filter, reverse osmosis system, and ultrafilter, allowing the use of any source of drinking water (as defined by US Environmental Protection Agency standards) to generate dialysate that meets the standards of the Association for the Advancement of Medical Instrumentation. The logistical advantage of being able to use any potable water source and the small device footprint result in increased portability, ease of use, and simplified sterilization, which led to our institutional adoption of Tablo as our default portable IHD device during our initial COVID-19 surge.

In addition, through sensor and software-based innovation, Tablo has been designed with the flexibility to perform dialysis for up to 24 h, allowing it to serve as a single device replacement for both traditional IHD and continuous renal replacement therapy (CRRT) devices or as a cost-effective solution for prolonged intermittent renal replacement therapy (PIRRT, also known as sustained low-efficiency dialysis or SLED) [18]. PIRRT is a hybrid therapy that utilizes low Qb, similar to CRRT, with Qd and ultrafiltration rates that are intermediate to traditional CRRT and traditional IHD with a typical duration of therapy between 6 and 12 h. PIRRT can be used as either a replacement for CRRT or as a bridge between CRRT and IHD therapies. PIRRT has been shown to have clinically equivalent results to CRRT in the ICU [19, 20]. The use of Tablo, specifically, as a PIRRT device has been shown to be substantially less expensive than similar duration therapy with traditional IHD and CRRT devices [18]. This flexibility has led some hospitals in the US to adopt Tablo as their only RRT device, using it to deliver IHD to hemodynamically stable patients and extended therapies to unstable patients in the ICU. This case report is particularly informative to these institutions as our analysis suggests that the standard of care for the dialytic treatment of toxic alcohol poisoning can be readily achieved with IHD using Tablo.

The treatment of methanol poisoning

With severe methanol intoxication, early initiation of therapy is critical. Empiric treatment with fomepizole at the outside ED likely had a significant benefit in this case and highlights the importance of initiating treatment prior to the availability of toxic alcohol levels when clinical suspicion is high. This is especially true in most facilities, such as ours, in which toxic alcohol panels take several hours or longer to result. In addition to immediate treatment with an ADH inhibitor such as fomepizole or ethanol, cofactor support (with IV folate or folinic acid for methanol poisoning and/or IV pyridoxine and thiamine for ethylene glycol poisoning) is also recommended in the setting of suspected toxic alcohol poisoning to help shift the metabolism of the parent alcohols away from the toxic acids (e.g., formic acid and oxalic acid) towards less toxic metabolites [4, 14].

Though experts and guidelines recommend somewhat differing thresholds for RRT initiation, prompt RRT is the cornerstone of therapy for severe toxic alcohol poisoning [4, 14, 21, 22]. EXTRIP, for example, recommends RRT for methanol poisoning in all cases with neurologic impairment (seizures, coma, or visual deficit); for metabolic acidosis that is severe (pH ≤ 7.15 or anion gap > 24 mmol/L) or persistent despite supportive care; if methanol levels are greater than 15.6 to 21.8 mmol/L (50–70 mg/dL), depending on the concomitant use of fomepizole or ethanol; or in the context of impaired kidney function [4]. In cases in which the need for RRT is unclear or borderline, consultation with toxicology is vital. Whenever IHD is employed, strong consideration should be given to the use of a higher KOA dialyzer and/or a longer duration of treatment than that of a traditional IHD session in order to maximize methanol clearance. While the Hirsch [8] and Lachance [12] equations can be used to predict the duration of IHD required based on initial methanol levels, the initial treatment duration, as is in this case, is often selected empirically, though some have recommended a longer initial empiric duration of 8 h of IHD [4, 9]. Regardless, serial methanol levels should be monitored if available, and RRT should be continued until both the pH and anion gap have normalized and the methanol level is less than 6.2 mmol/L (20 mg/dL) [4]. Importantly, fomepizole is dialyzable and therefore requires dose adjustment if being used in the context of RRT. Nephrologists should also be aware that (though in-line heparin was used in this case) the most recent EXTRIP guideline recommends avoiding systemic anticoagulation with RRT due to reports of intracranial hemorrhage occurring in a substantial minority of patients with methanol poisoning [4, 23].

The average reported clearances of methanol with IHD, CRRT, and peritoneal dialysis are 208, 37, and 37 mL/min, respectively, underlying the superiority of IHD, whenever feasible, for treating methanol poisoning [4]. In this case, the achieved clearance well above the reported mean for IHD with both Tablo, at a Qd of 300 mL/min, and a traditional IHD machine, at a greater than two times higher Qd, underscores the modest impact of Qd on methanol clearance.

Impact of dialysate flow rate on small molecule clearance

As described in the original Michaels’ equation [24], clearance (K) of urea (and that of other small dialyzable solutes) in countercurrent HD is a function of Qd, Qb, and the product of the mass transfer coefficient and membrane surface area (KOA) of a given dialyzer:

$$ K= Qb\bullet \left(\frac{\exp \left(\frac{KoA\left(1-\frac{Qb}{Qd}\right)}{Qb}\right)-1}{\exp \left(\frac{KoA\left(1-\frac{Qb}{Qd}\right)}{Qb}\right)-\frac{Qb}{Qd}}\right) $$

Within the ranges of Qb, Qd, and KOA that are typically used for IHD, the mathematical impact of Qd is the least of these three variables. While IHD is often prescribed with a Qd set to 1.5 to 2 times Qb, multiple recent studies, including both empiric human data [25,26,27,28,29] and analysis of modeled data, suggest the effect on Kt/V of decreasing Qd to 300–400 mL/min is modest. Of note, this has been specifically demonstrated with the Revaclear dialyzer, which, like other modern dialyzers, has been designed with enhanced dialysate flow distribution which minimizes the effect of Qd on KOA [28, 29].

The maximum Qd accommodated by Tablo is 300 mL/min. A recent kinetic modeling analysis of the effect of decreasing Qd from 500 to 300 mL/min at Qb rates of 300–400 mL/min concluded that the resulting drop in equilibrated Kt/Vurea would be relatively small at 0.12–0.22, a difference that could be nearly fully counteracted by using a dialyzer with a higher KOA (1480 versus 1170 mL/min) and extending treatment time by 15 min [30]. A recent in vivo study of six patients on maintenance dialysis sequentially treated with Tablo with a Qd of 300 mL/min and a conventional IHD machine (Gambro Phoenix) with Qd of 500 mL/min yielded clearance curves for urea, potassium, phosphate, and β2-microglobuin which were remarkably similar, with no statistically significant difference in the levels of any of the four solutes by the end of 4 h of treatment despite the differing Qd rates [27].


This is the first reported case of the use of the Tablo Hemodialysis System for the treatment of toxic alcohol poisoning. Our analysis of this case illustrates that IHD with Tablo can achieve a clearance of methanol that is well within the previously published standard of care. This clearance could likely be enhanced further with a high KOA dialyzer. Hemodialysis, with any device, remains an effective way to treat toxic alcohol poisoning, especially when combined with pharmacologic ADH antagonism and when optimized with extended treatment times and use of a higher KOA dialyzer.

Availability of data and materials

All data are either included or available upon request.



Alcohol dehydrogenase


Confidence interval


Continuous renal replacement therapy


Computed tomography


Coronavirus disease 2019


Emergency department


Emergency medical services


EXtracorporeal TReatments In Poisoning workgroup


United States Food and Drug Administration




Intermittent hemodialysis

K :


K O A :

Product of the mass transfer coefficient and membrane surface area of a dialyzer


Prolonged intermittent renal replacement therapy

Qb :

Blood flow rate

Qd :

Dialysate flow rate


Sustained low-efficiency dialysis


United States


  1. Ghannoum M, Hoffman RS, Mowry JB, Lavergne V. Trends in toxic alcohol exposures in the United States from 2000 to 2013: a focus on the use of antidotes and extracorporeal treatments. Semin Dial. 2014;27(4):395–401.

    Article  PubMed  Google Scholar 

  2. Yip L, Bixler D, Brooks DE, Clarke KR, Datta SD, Dudley S Jr, et al. Serious adverse health events, including death, associated with ingesting alcohol-based hand sanitizers containing methanol - Arizona and New Mexico, May-June 2020. MMWR Morb Mortal Wkly Rep. 2020;69(32):1070–3.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. Islam MS, Sarkar T, Khan SH, Mostofa Kamal AH, Hasan SMM, Kabir A, et al. COVID-19-related infodemic and its impact on public health: a global social media analysis. Am J Trop Med Hyg. 2020;103(4):1621–9.

    Article  PubMed  PubMed Central  Google Scholar 

  4. Roberts DM, Yates C, Megarbane B, Winchester JF, Maclaren R, Gosselin S, et al. Recommendations for the role of extracorporeal treatments in the management of acute methanol poisoning: a systematic review and consensus statement. Crit Care Med. 2015;43(2):461–72.

    Article  CAS  PubMed  Google Scholar 

  5. Hovda KE, Andersson KS, Urdal P, Jacobsen D. Methanol and formate kinetics during treatment with fomepizole. Clin Toxicol (Phila). 2005;43(4):221–7.

    Article  CAS  Google Scholar 

  6. Brent J, McMartin K, Phillips S, Aaron C, Kulig K. Methylpyrazole for Toxic Alcohols Study G. Fomepizole for the treatment of methanol poisoning. N Engl J Med. 2001;344(6):424–9.

    Article  CAS  PubMed  Google Scholar 

  7. Graw M, Haffner HT, Althaus L, Besserer K, Voges S. Invasion and distribution of methanol. Arch Toxicol. 2000;74(6):313–21.

    Article  CAS  PubMed  Google Scholar 

  8. Hirsch DJ, Jindal KK, Wong P, Fraser AD. A simple method to estimate the required dialysis time for cases of alcohol poisoning. Kidney Int. 2001;60(5):2021–4.

    Article  CAS  PubMed  Google Scholar 

  9. Zakharov S, Pelclova D, Navratil T, Belacek J, Kurcova I, Komzak O, et al. Intermittent hemodialysis is superior to continuous veno-venous hemodialysis/hemodiafiltration to eliminate methanol and formate during treatment for methanol poisoning. Kidney Int. 2014;86(1):199–207.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Kerns W 2nd, Tomaszewski C, McMartin K, Ford M, Brent J. Alcohols MSGMfT. Formate kinetics in methanol poisoning. J Toxicol Clin Toxicol. 2002;40(2):137–43.

    Article  CAS  PubMed  Google Scholar 

  11. Hantson P, Haufroid V, Wallemacq P. Formate kinetics in methanol poisoning. Hum Exp Toxicol. 2005;24(2):55–9.

    Article  CAS  PubMed  Google Scholar 

  12. Lachance P, Mac-Way F, Desmeules S, De Serres SA, Julien AS, Douville P, et al. Prediction and validation of hemodialysis duration in acute methanol poisoning. Kidney Int. 2015;88(5):1170–7.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Fazio M. 3 die in New Mexico after drinking hand sanitizer, officials say. New York Times June. 2020;26.

  14. Kraut JA, Kurtz I. Toxic alcohol ingestions: clinical features, diagnosis, and management. Clin J Am Soc Nephrol. 2008;3(1):208–25.

    Article  CAS  PubMed  Google Scholar 

  15. Martens J, Westhovens R, Verberckmoes R, Delooz H, Daenens P. Recovery without sequelae from severe methanol intoxication. Postgrad Med J. 1982;58(681):454–6.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Desai T, Sudhalkar A, Vyas U, Khamar B. Methanol poisoning: predictors of visual outcomes. JAMA Ophthalmol. 2013;131(3):358–64.

    Article  CAS  PubMed  Google Scholar 

  17. Liu JJ, Daya MR, Carrasquillo O, Kales SN. Prognostic factors in patients with methanol poisoning. J Toxicol Clin Toxicol. 1998;36(3):175–81.

    Article  CAS  PubMed  Google Scholar 

  18. Demirjian S, Layne M, Chertow G, Alvarez L. A novel hemodialysis system, deployed for PIRRT, provides volume management at lower cost than CRRT. AKI & CRRT 2019: 24th International Conference on Advances in Critical Care Nephrology. San Diego, California2019.

  19. Kovacs B, Sullivan KJ, Hiremath S, Patel RV. Effect of sustained low efficient dialysis versus continuous renal replacement therapy on renal recovery after acute kidney injury in the intensive care unit: a systematic review and meta-analysis. Nephrology (Carlton). 2017;22(5):343–53.

    Article  Google Scholar 

  20. Zhang L, Yang J, Eastwood GM, Zhu G, Tanaka A, Bellomo R. Extended daily dialysis versus continuous renal replacement therapy for acute kidney injury: a meta-analysis. Am J Kidney Dis. 2015;66(2):322–30.

    Article  PubMed  Google Scholar 

  21. Kraut JA, Mullins ME. Toxic alcohols. N Engl J Med. 2018;378(3):270–80.

    Article  CAS  PubMed  Google Scholar 

  22. Ng PCY, Long BJ, Davis WT, Sessions DJ, Koyfman A. Toxic alcohol diagnosis and management: an emergency medicine review. Intern Emerg Med. 2018;13(3):375–83.

    Article  PubMed  Google Scholar 

  23. Phang PT, Passerini L, Mielke B, Berendt R, King EG. Brain hemorrhage associated with methanol poisoning. Crit Care Med. 1988;16(2):137–40.

    Article  CAS  PubMed  Google Scholar 

  24. Michaels AS. Operating parameters and performance criteria for hemodialyzers and other membrane-separation devices. Trans Am Soc Artif Intern Organs. 1966;12:387–92.

    CAS  PubMed  Google Scholar 

  25. Kashiwagi T, Sato K, Kawakami S, Kiyomoto M, Enomoto M, Suzuki T, et al. Effects of reduced dialysis fluid flow in hemodialysis. J Nippon Med Sch. 2013;80(2):119–30.

    Article  PubMed  Google Scholar 

  26. Albalate M, Perez-Garcia R, de Sequera P, Corchete E, Alcazar R, Ortega M, et al. Is it useful to increase dialysate flow rate to improve the delivered Kt? BMC Nephrol. 2015;16(1):20.

    Article  PubMed  PubMed Central  Google Scholar 

  27. Augustin DA, Spry LA, Prichard SS, Chertow GM, Alvarez L. In-vivo dialysis kinetics of 300 mL/min and 500 mL/min dialysate flows (abstract). J Am Soc Nephrol. 2018;29:S620.

    Article  Google Scholar 

  28. Bhimani JP, Ouseph R, Ward RA. Effect of increasing dialysate flow rate on diffusive mass transfer of urea, phosphate and beta2-microglobulin during clinical haemodialysis. Nephrol Dial Transplant. 2010;25(12):3990–5.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  29. Ward RA, Idoux JW, Hamdan H, Ouseph R, Depner TA, Golper TA. Dialysate flow rate and delivered Kt/Vurea for dialyzers with enhanced dialysate flow distribution. Clin J Am Soc Nephrol. 2011;6(9):2235–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Leypoldt JK, Prichard S, Chertow GM, Alvarez L. Differential molecular modeling predictions of mid and conventional dialysate flows. Blood Purif. 2019;47(4):369–76.

    Article  CAS  PubMed  Google Scholar 

Download references





Author information

Authors and Affiliations



CPA and MAA conceptualized the report. ACI and JPT wrote the original draft and created the tables and figure. JPT and CPA carried out the data analyses. All authors contributed to the manuscript content, reviewed and edited the manuscript, and approved the final draft.

Corresponding author

Correspondence to J. Pedro Teixeira.

Ethics declarations

Ethics approval and consent to participate

Not applicable (Per University of New Mexico IRB Policy, retrospective case reports do not require IRB approval.)

Consent for publication

Consent for publication of this case report was obtained from the patient.

Competing interests

Dr. Aragon is the Chief Medical Officer of Outset Medical. The remaining authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This 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 The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Illescas, A.C., Argyropoulos, C.P., Combs, S.A. et al. Severe methanol poisoning treated with a novel hemodialysis system: a case report, analysis, and review. Ren Replace Ther 7, 43 (2021).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: