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  • Commentary
  • Open Access

Paper reports overview: Cranberry juice, fluid replacement and bad innovations

Critical Care20015:331

Published: 8 November 2001


  • Fluid Replacement
  • Decubitus Ulcer
  • Paper Report
  • Massive Pulmonary Embolism
  • Cranberry Juice

This commentary reflects on the paper reports published in the Critical Care Forum between 11 September 2001 and 5 November 2001

In the present issue of Critical Care the breadth of ongoing research is reflected in the diversity of the subjects reported on.

More evidence regarding what we should and should not be feeding our patients continues to emerge. A systematic review of immunonutrition trials [1] concludes that this therapy is of no benefit and may indeed be harmful. Outside the critical care arena, however, there is evidence that specific dietary supplements are beneficial, with cranberry juice lowering the incidence of urinary tract infections in a susceptible population [2]. Further trials of dietary supplements in critically ill patients are underway, with ω-3 fatty acids attracting particular interest. The value of enteral nutrition was reinforced by a study that investigated risk factors for the development of decubitus ulcers [3]. That report acts as a timely reminder that, regardless of advances in cutting edge therapies (see below), the quality of basic care must remain a priority. The most striking finding of that study is the marked increase in incidence (from 0.9 to 8.9% over the study period) – a worrying but perhaps unavoidable reflection on the priorities of care. Reducing the incidence of ileus in intensive care unit patients may also be on the horizon with the first successful trial of a new selective gastrointestinal opioid receptor blocker in postoperative patients [4].

The optimal regimen of intravenous fluid replacement remains a topic of considerable interest. Dr Venn discusses a paper by Waters et al. [5], who conducted a randomized trial of normal saline versus Ringer's lactate and found no difference in outcomes despite the propensity of normal saline to provoke an iatrogenic hyperchloraemic acidosis. A new systematic review of the use of albumin as an intravenous fluid therapy [6] concludes that this intervention is not associated with an excess mortality, unlike the previous and controversial systematic review on this topic [7].

Another example of the hazards of technological innervations has emerged from the introduction of automated taps that are employed to reduce cross contamination when hand washing [8]. Alarmingly, a study of the effectiveness of such devices found that, rather than improving control of infection, they actually act as a reservoir for intensive care unit pathogens, in particular Pseudomonas aeruginosa and Legionella spp.

Although not reported on, the following may be of interest. Sepsis research has suffered a further blow with the disappointing results of the high-dose antithrombin III trial [9], in which coadministration of heparin might have been responsible for neutralizing the beneficial effects of this therapy, and most certainly significantly increased the risk for haemorrhage. On a more optimistic note, early experimental work into the efficacy of a naturally occurring group of compounds, the cecropins, that exhibit antiendotoxin activity appears promising [10]. Finally, research into the optimal diagnostic and therapeutic interventions for pulmonary embolus are becoming apparent. The limitations of helical computed tomography are reinforced by the findings of Perrier et al. [11], whereas there appears to be no value of thrombolysis over heparinization in haemodynamically stable patients with massive pulmonary embolism [12].

Authors’ Affiliations

Lecturer in Intensive Care Medicine, Department of Anaesthesia &, University of London,Intensive Care, St George's Hospital Medical School, London, UK


  1. Heyland DK, Novak F, Drover JW, Jain M, Su X, Suchner U: Should immunonutrition become routine in critically ill patients? A systematic review of the evidence. JAMA 2001, 286: 944-953. See paper report 10.1001/jama.286.8.944View ArticlePubMedGoogle Scholar
  2. Kontiokari T, Sundqvist K, Nuutinen M, Pokka T, Koskela M, Uhari M: Randomised trial of cranberry-lingonberry juice and Lactobacillus GG drink for the prevention of urinary tract infections in women. Br Med J 2001, 322: 1571. 10.1136/bmj.322.7302.1571View ArticleGoogle Scholar
  3. Eachempati SR, Hydo LJ, Barie PS: Factors influencing the development of decubitus ulcers in critically ill surgical patients. Crit Care Med 2001, 29: 1678-1682. See paper report ArticlePubMedGoogle Scholar
  4. Taguchi A, Sharma N, Saleem RM, Sessler DI, Carpenter RL, Seyed-sadr M, Kurz A: Selective postoperative inhibition of gastrointestinal opioid receptors. N Engl J Med 2001, 345: 935-940. 10.1056/NEJMoa010564View ArticlePubMedGoogle Scholar
  5. Waters JH, Gottlieb A, Schoenwald P, Popovich MJ, Sprung J, Nelson DR: Normal saline versus lactated Ringer's solution for intraoperative fluid management in patients undergoing abdominal aortic aneurysm repair: an outcome study. Anesth Analg 2001, 93: 817-822. See paper report ArticlePubMedGoogle Scholar
  6. Wilkes MM, Navickis RJ: Patient survival after human albumin administration. A meta-analysis of randomized, controlled trials. Ann Intern Med 2001, 135: 149-164.View ArticlePubMedGoogle Scholar
  7. Cochrane Injuries Group Albumin Reviewers: Human albumin administration in critically ill patients: systematic review of randomised controlled trials. Br Med J 1998, 317: 235-240.View ArticleGoogle Scholar
  8. Halabi M, Wiesholzer-Pittl M, Schoberl J, Mittermayer H: Non-touch fittings in hospitals: a possible source of Pseudomonas aeruginosa and Legionella spp. J Hosp Infect 1998, 49: 117-121. See paper report 10.1053/jhin.2001.1060View ArticleGoogle Scholar
  9. Warren BL, Eid A, Singer P, Pillay SS, Carl P, Novak I, Chalupa P, Atherstone A, Pénzes I, Kübler A, Knaub S, Keinecke H-O, Heinrichs H, Schindel F, Juers M, Bone RC, Opal SM, for the KyberSept ti study group: Caring for the critically ill patient. High-dose antithrombin III in severe sepsis: a randomized controlled trial. JAMA 2001, 286: 1869-1878. 10.1001/jama.286.15.1869View ArticlePubMedGoogle Scholar
  10. Giacometti A, Cirioni O, Ghiselli R, Viticchi C, Mocchegiani F, Riva A, Saba V, Scalise G: Effect of mono-dose intraperitoneal cecropins in experimental septic shock. Crit Care Med 29: 1666-1669.Google Scholar
  11. Perrier A, Howarth N, Didier D, Loubeyre P, Unger PF, de Moerloose P, Slosman D, Junod A, Bounameaux H: Performance of helical computed tomography in unselected outpatients with suspected pulmonary embolism. Ann Intern Med 2001, 135: 88-97.View ArticlePubMedGoogle Scholar
  12. Hamel E, Pacouret G, Vincentelli D, Forissier JF, Peycher P, Pottier JM, Charbonnier B: Thrombolysis or heparin therapy in massive pulmonary embolism with right ventricular dilation: results from a 128-patient monocenter registry. Chest 2001, 120: 120-125. 10.1378/chest.120.1.120View ArticlePubMedGoogle Scholar


© BioMed Central Ltd 2001