Plasma Exchange for Sepsis in



Similar documents
The sensitive marker for glomerular filtration rate (GFR) Estimation of GFR from Serum Cystatin C:

CPT Pediatric Coding Updates The 2009 Current Procedural Terminology (CPT) codes are effective as of January 1, 2009.

the product for which protection was sought as "Centoxin (HA-lA Monoclonal Antibody";

Local Anaesthetic Systemic Toxicity. Dr Thomas Engelhardt, MD, PhD, FRCA Royal Aberdeen Children s Hospital, Scotland

SAVE A LIFE... BY GIVING LIFE!

SARASOTA MEMORIAL HOSPITAL BLOOD COMPONENT CRITERIA AND INDICATIONS SCREENING GUIDELINES

TRANSFUSION MEDICINE

Omega-3 fatty acids improve the diagnosis-related clinical outcome. Critical Care Medicine April 2006;34(4):972-9

Yvette Marie Miller, M.D. Executive Medical Officer American Red Cross October 20, th Annual Great Lakes Cancer Nursing Conference Troy, MI

Medical Direction and Practices Board WHITE PAPER

BLOOD GROUP ANTIGENS AND ANTIBODIES

CENTER FOR DRUG EVALUATION AND RESEARCH

STANDARD BLOOD PRODUCTS AND SERVICES

Blood Physiology. Practical 4. Contents. Practical tasks. Erythrocytes The blood types

Guideline Statement for the Treatment of Disseminated Intravascular Coagulation

Transfusion Medicine

Suggestions for Optimizing Use of Plasma in the Era of TRALI Risk Reduction

INTRAVENOUS FLUIDS. Acknowledgement. Background. Starship Children s Health Clinical Guideline

Heart transplantation

Mother s blood test to check her unborn baby s blood group

Department of Transfusion Medicine and Immunohematology

QUADROX-i Small Adult and Adult Choose maximum safety.

V: Infusion Therapy. College of Licensed Practical Nurses of Alberta, Competency Profile for LPNs, 3rd Ed. 181

Milwaukee School of Engineering Case Study: Factors that Affect Blood Pressure Instructor Version

Paddy McMaster Consultant in Paediatric Intensive Care University Hospital of North Staffordshire Stoke on Trent UK

The Infinite Potential of Stem Cell Japan s Cord Blood Bank and Transplant

BLOOD BANK ANNUAL STATISTICS (HOSPITALS)

Why is prematurity a concern?

Cord Blood Stem Cell Transplantation

Bone Marrow (Stem Cell) Transplant for Sickle Cell Disease

Haemodialysis. Dialysers and Filters Product Range

Section 2 Solving dosage problems

Appendix G - Identification and Selection of Studies

Hemophilia Care. Will there always be new people in the world with hemophilia? Will hemophilia be treated more effectively and safely in the future?

GROWTH AND DEVELOPMENT

V: Infusion Therapy. Alberta Licensed Practical Nurses Competency Profile 217

Evaluation of the Patient with Suspected Platelet Refractory State

Blood & Marrow Transplant Glossary. Pediatric Blood and Marrow Transplant Program Patient Guide

Bone Marrow Transplantation and Peripheral Blood Stem Cell Transplantation: Questions and Answers. Key Points

Sepsis: Identification and Treatment

NICU Level of Care Criteria

Not All Stem Cells are the Same

CHAPTER 10 BLOOD GROUPS: ABO AND Rh

The Sepsis Puzzle: Identification, Monitoring and Early Goal Directed Therapy

Extracorporeal Life Support Organization (ELSO) Guidelines for Neonatal Respiratory Failure

STEM CELLS FROM THE UMBLICAL CORD BLOOD AND UMBLICAL CORD TISSUE

Example 3: Dilantin-125 is available as 125 mg/5 ml. Dilantin-125, 0.3 g PO, is ordered. How much should the nurse administer to the patient?

Multiple Myeloma. This reference summary will help you understand multiple myeloma and its treatment options.

The Initial and 24 h (After the Patient Rehabilitation) Deficit of Arterial Blood Gases as Predictors of Patients Outcome

Thioctacid 600 T Solution for Injection contains 600 mg alpha-lipoic acid

Intraosseous Vascular Access and Lidocaine

DIALYSIS COMPACT. The function, diseases and treatments for the human kidney.

Acknowledgements. PAH in Children: Natural History. The Sildenafil Saga

Questions and Answers for Health Care Providers: Renal Dosing and Administration Recommendations for Peramivir IV

Bachelor s degree in Nursing

SEARCHING FOR A BONE MARROW DONOR

IV solutions may be given either as a bolus dose or infused slowly through a vein into the plasma at a constant or zero-order rate.

Introduction to Blood Management

Intravenous Infusion Lines Enhancing Patient Safety During IV Therapy

Telemedicine Resuscitation & Arrest Trials (TreAT)

POAC CLINICAL GUIDELINE

Public Cord Blood Tissue Bank Committee on Health Care Services and Representative Peaden

8/13/2014. Blood, Sweat (and Tears): Delayed Cord Clamping and Delivery Room Temperature. Delayed Cord Clamping

THE PREPARATION OF SINGLE DONOR CRYOPRECIPITATE

Premature Infant Care

Recommendations: Other Supportive Therapy of Severe Sepsis*

Perfalgan 10 mg/ml, solution for infusion

PACKAGE LEAFLET: INFORMATION FOR THE USER. PARACETAMOL MACOPHARMA 10 mg/ml, solution for infusion. Paracetamol

1. BLOOD GROUP SYSTEMS. Page 1. Haematology LECTURE 10. BLOOD GROUPS AND TRANSFUSIONS OVERVIEW. 1. Blood Group Systems

Early Warning Scores (EWS) Clinical Sessions 2011 By Bhavin Doshi

Clinical Practice Guidelines for Blood Transfusions

BLOOD BANK Department

Application Note. Determination of Nitrite and Nitrate in Fruit Juices by UV Detection. Summary. Introduction. Experimental Sample Preparation

STEM CELL TRANSPLANTS

UMBILICAL CORD BLOOD TRANSPLANTATION: KFSH EXPERIENCE

SOUTHERN WEST MIDLANDS NEWBORN NETWORK

1) Siderophores are bacterial proteins that compete with animal A) Antibodies. B) Red blood cells. C) Transferrin. D) White blood cells. E) Receptors.

Studies on cortisol and prolactin concentrations in umbilical cord blood, amniotic fluid, maternal blood, and breast milk related to perinatal factors

THE BENEFITS OF LIVING DONOR KIDNEY TRANSPLANTATION. feel better knowing

Chapter 21. What Are HIV and AIDS?

Selecting Appropriate Blood Products for Recipients of ABO/Rh Mismatched Stem Cell Transplants. Summary of Significant Changes. Purpose.

The Impact of Maternal, Neonatal and Collections factors on the TNC count of an Umbilical Cord Blood Donation

Red Blood Cell Transfusions for Sickle Cell Disease

Blood-Forming Stem Cell Transplants

Narrator: Transplants using stem cells from the blood, bone marrow or umbilical cord blood

Efficacy and Safety of Insulin Aspart in Patients with Type 1 Diabetes Mellitus

Why and how to have end-of-life discussions with your patients:

Core Measures SEPSIS UPDATES

Preparation of cord blood for infusion: bedside thaw, dilute and wash, or somewhere in between

Ultrafiltration Devices

NHS FORTH VALLEY Neonatal Oxygen Saturation Guideline

The rate of failure to thrive among children aged 2 months - 5 years in Kanaan sub-district / Diyala province

Suffolk County Community College School of Nursing NUR 133 ADULT NURSING I

1. Enzyme Function

I B2.4. Design of the patient information leaflet for VariQuin

Anatomi & Fysiologi The cardiovascular system (chapter 20) The circulation system transports; What the heart can do;

Chapter 16 Reproductive Technology, Gene Therapy, and Stem Cells (modified)

From cells to therapeuticsvivalis. Humalex Fully human antibody discovery platform An integrated therapeutic development offering

Oxygenation and Oxygen Therapy Michael Billow, D.O.

Directed, Autologous and Therapeutic Donations

Transcription:

Tohoku J. Exp. Med., 1989, 159, 249-256 On-Line Neonates Plasma Exchange for Sepsis in and Infants TEIJI TAKAHASHI, YOSHIHIRO ASANUMA, TETSUO KATO, TATSUZO HEBIGUCHI, KENJI KOYAMA and KOUZOU KUDO* The First Department of Surgery and *Department of Microbiology, Akita University School of Medicine, Akita 010 TAKAHASHI, T., ASANUMA, Y., KATO, T., HEBIGUCHI, T., KOYAMA, K. and KUDO, K. On-Line Plasma Exchange for Sepsis in Neonates and Infants. Tohoku J. Exp. Med., 1989, 159 (4), 249-256 - The present study way designed to assess the effectiveness of on-line plasma exchange (on-line P.E.) between septic infants and healthy adults using septic puppies. The plasma separation system consisted of a membrane plasma separator and a plasma treatment system, KM-9027 (Kurarey Co.) equipped with small 2 channel blood and plasma pumps. 5 X 109 CFU/ml/kg of E. coli with endotoxin was injected intravenously into 22 puppies and they were divided into 4 groups, namely untreated group (n = 7), on-line P.E. group (n =5), P.E. group (n =5), sham group (n =5). In the on-line P.E. group, about 80 ml/kg of plasma in septic puppy was replaced during 2 hr with fresh plasma simultaneously obtained from healthy adult dog. As the results, 4 of 5 survived in the on-line P.E. group and 1 of 5 survived in the P.E. group, while all other puppies died within 24 hr. In the P.E. group and on-line P.E. group, mean blood pressure and urinary output were significantly improved (p <0.05) by the treatment. The numbers of E. coli and endotoxin concentration in the blood were reduced significantly (p <0.05) only in the treatment with on-line P.E. opsonic activity recovered significantly (p <0.05) in P.E. group. This system appears to be effective and applicable for sepsis in infants and neonates. on-line plasma exchange ; plasmapheresis ; exchange transfusion ; sepsis ; endotoxin shock Postoperative sepsis in Neonates and infants is associated with high mortality rates, and at present, exchange transfusion is considered the final alternative therapy. Over the past 6 years, we have performed 46 exchange transfusions on 19 neonates and infants with sepsis. The therapy was effective in 15 cases, 12 of which survived. However, exchange transfusion requires massive fresh blood and is associated with such complications as anti-blood cell antibody production, infection, and graft-versus-host disease. In an attempt to simplify the blood supply and to prevent anti-blood cell antibody production, we developed on-line plasma exchange (on-line P.E.) between septic child and healthy adult. The present study was designed to assess the effectiveness of on-line P.E. by perform- Received May 1, 1989; revision accepted for publication November 10, 1989. 249

250 T. Takahashi et al. ing plasma exchanges between adult dogs and septic puppies, separator suitable for use in neonates and infants. using a small plasma MATERIALS AND METHODS Preparation of a sepsis model (Hinshaw et al. 1968) : Escherichia coil strain 5 X 109 CFU/ml/kg was intravenously infused over a 1-hr period to 22 mongrel puppies weighing 1.8-3.2 kg. They were divided into the following four groups : Untreated group (n = 7) : The course of sepsis was observed without treatment. On-line P.E. group (n=5) : The on-line P.E. was performed for 2 hr between puppies and adult dogs weighing approximately 15 kg. P.E. group (n=5) : Plasma exchange was performed for 2 hr using fresh frozen plasma, which was separated by centrifugation from an adult dog one week previously and stored at -40 C. Sham group (n = 5) : Plasma separated from the puppies' own blood was returned to them over a 2-hr period. Methods of on-line P.E. In on-line P.E., blood cells separated from puppies were mixed with plasma separated from adult dogs, and this mixture was returned to the puppies. Plasma separated from puppies was discarded (Fig. 1). The plasma separation system consisted of a membrane plasma separator and a plasma treatment system, KM-9027 (Kurarey Co., Osaka) equipped with a small blood and pump. The membrane plasma separator, custom made by Kurarey Co., was made of a ployvinyl alchohol hollow fiber with an effective surface area of 0.9 m2, mean pore size of 0.4 p m, and volume of 10 ml. The priming volume of the system was 30 ml. The operating conditions were set at a blood flow velocity of 10 ml/min and plasma filtration rate of 1.7 ml/min. The amount of plasma exchanged was equivalent to 50-110 ml/kg. Examination items The following items were measured before injection of E. coli at 3 and 6 hr after the start of E. coli. injection : 1) Survival perides, 2) blood pressure, urinary output, and Fig.1. On-line plasma exchange system between puppy and cells from puppies were mixed with plasma separated from mixture was returned to the puppies. Plasma separated discarded. Arrows show blood and plasma flow. adult dog. Blood adult dogs, and this from puppies was

On-Line Plasma Exchange for Sepsis in Neonates and Infants 251 arterial blood gas analysis, 3) peripheral hematology, 4) the numbers of E. coli in blood (mixed dilution culture method), 5) endotoxin concentrations in blood (measured using the Toxicolor test), and 6) opsonic activity (measured using the chemiluminescence test). Statistical analysis Results are presented as grouped mean and s.d.. Data were analyzed using unpaired Student t-test. Only values of less than p <0.05 compaired with values for sham and untreated groups were considered staistically significant. RESULTS 1) All puppies in the untreated and sham groups died within 24 hr. In the P.E. group, four puppies died within 24 hr and the remaining 1 survived for one more week. In the on-line P.E. group, however, one puppy died within 24 hr, but the remaining 4 survived for more than one week (Table 1). TABLE 1. Number of dogs which survived up and longer than/week to 12 hr, from 12 to 24 hr Fig. 2. Changes in mean blood pressure. o- o, on-line P.E. group (n=5) ; -, P.E. group (n=5) ; o group (n =5); A-., untreated group (n == 7). ~, period of P.E. or on-line P.E. A, sham

252 T. Takahash i et al. Fig. 3. Changes in urine volume., on-line P.E. group ; 0, P.E. group ; mean±s.n. ~ period of P.E. or on-line P.E. sham group ; -, Fig. 4. Changes in base excess. 0 0, on-line P.E. group ;, P.E. group ; o o, sham group ;, period of P.E. or on-line P.E.

On-Line Plasma Exchange for Sepsis in Neonates and Infants 253 2) In the P.E. and on-line P.E. groups, mean blood pressure and urinary output were significantly improved (p <0.05) by the treatment. Mean blood pressure in untreated and sham groups deteriorated up to 3 hr after E. coli injection, the mean blood pressure was kept constant at 40-50 mmhg for up to 6 Fig. 5. Changes in viability of E. coli with time. 0 0, on-line P.E. group ; -, P.E. group ; A -A, sham group ;.., +, period of P.E. or on-line P.E. Fig. 6. Changes in plasma endotoxin concentration. on-line P.E. group ; -, P.E. group ; A -A, sham group ; A -A, ~, period of P.E. or on-line P.E.

254 T. Takahashi et al. Fig. 7. Changes in opsonic index obtained chemiluminescence test. on-line P.E. group ; -, P.E. group ; A -A, sham group ; A., ~, period of P.E. or on-line P.E. hr. Mean blood pressure of the P.E. and on-line P.E. groups started to increase in the middle of the treatment and recovered to 70-80 mmhg at the end of treatment. The mean blood pressure continued increasing thereafter and reached about 100 mmhg (Fig. 2). Urinary output in untreated and sham groups deteriorated after E. coli injection, whereas urinary output in the treatment groups strafed increasing at the end of treatment (Fig. 3). Acid-base equilibrium improved significantly (p <0.05) in only the on-line P.E. at 6 hr after E. coli injection (Fig. 4). 3) The numbers of E. coli and the Endotoxin concentration in the blood were reduced significantly (p <0.05) only in the treatment with on-line P.E. (Figs. 5 and 6). Endotoxin was isolated in separated plasma with a sieving coefficient above 0.95, but E. coli was not detected. 4) Opsonic activity recovered significantly (p <0.05) at the end of the treatment by on-line P.E. However, there were no significant differences between on-line P.E. group and P.E, group (Fig. 7). Opsonic activity of FFP from adult dogs was diminished to 73% that of fresh plasma. DISCUSSION In neonates and infants, the function of the immune system is not sufficient, so postoperative sepsis in neonates and infants is associated with high mortality rates. It is therefore important in pediatric surgery to treat sepsis and accompanied multiple organ failure. In these cases in neonates and infants, the efficacy of exchange blood transfusion is evident when applied in addition to the conventional treatment (Vain et al. 1980). We have treated 19 cases using

On-Line Plasma Exchange for Sepsis in Neonates and Infants 255 exchange blood transfusion a total of 46 times, and 12 patients survived. However, exchange transfusion requires massive fresh blood and is associated with such complications as anti-blood cell antibody production, infection and graftversus-host disease (Operz et al. 1973 ; Parkman et al. 1974). In an effort to increase the effectiveness of exchange transfusion and eliminate its shortcomings, we developed an on-line P.E. system for treating pediatric sepsis which is connected between adult and child. We reported previously that the on-line P.E. between a healthy adult dog and a jaundiced puppy is acceptable with biocompartibility, and seems to be satisfactory from the point of system performance (Asanuma et al. 1987). In the present experiment, the effectiveness of this system was assessed in a septic puppy model. All puppies in the untreated and sham groups died within 24 hr. In the P.E. group, four puppies died within 24 hr and the remaining 1 survived for one more week. In the on-line P.E. group, however, only one puppy died within 24 hr, but the remaining 4 survived for one more week. Blood pressure, urinary output, and acid-base equilibrium were significantly improved by the treatment with on-line P.E. Moreover, the number of E. coli and endotoxin concentration in blood was reduced and opsonic activity recovered significantly by treatment with on-lime P.E. These results suggest that the elimination of toxic substances, primarily endotoxin, and the activation of humoral immunity due to the elevation of opsonic activity were two major mechanisms responsible for the effectiveness of on-line P.E. in treating the septic model. On-line P.E. was more effective for the septic model than P.E. Opsonic activity of FFP from adult dogs on the plasma exchange was diminished to 73% of that of fresh plasma, although there is no statistically significant difference in opsonic activity of puppies between the two groups after treatments. The difference between the two groups seems to be related to the opsonic activity. Our experiments proved the effectiveness of on-line plasma exchange between puppies and adult dogs in septic puppies and elucidated a part of its mechanism. This on-line plasma exchange between adult and child seems an effective new therapeutic method for sepsis in neonates and infants. References 1) Asanuma, Y., Tanaka, J., Takahashi, T., Yoshino, H., Hebiguchi, T., Kato, T. & Koyama, K. (1987) Preclinical evaluation of plasma cross circulation for infants. In: Therapeutic Plasmapheresis, edited by T. Oda, Y. Ishikawa & N. Inoue, Vol. 6, ISAO Press, Cleaveland, pp. 359-364. 2) Hinshaw, L.B., Solomon, L.A., Holmes, D.D. & Greenfield, L.J. (1968) Comparison of canine responses to Eserchia coli organisms and endotoxin. Surg. Gynecol. Obstet., 138, 981-988. 3) Operz, G., Mickey, MR. & Terasaki, P.I. (1973) Blood transfusions and unresponsiveness to HLA. Transplantation, 16, 649-659. 4) Parkman, R., Mosier, D., Umansky, I., Cochran, W., Carpenter, C.B. & Rosen, F.S. (1974) Graft-versus-host disease after intrauterine and exchange transfusions for hemolytic disease of the newborn. N. Engl. J. Med., 290, 359-363.

256 T. Takahashi et al. 5) Vain, N.E., Mazulumian, JR., Swarner, OW. & Cha, C.C. (1980) Role of exchange transfusion in the treatment of severe septicemia. Pediatris, 66, 693-697.