- Case Report
- Open Access
Initial intravenous immunoglobulin doses should be based on adjusted body weight in obese patients with primary immunodeficiency disorders
© The Author(s) 2017
- Received: 12 August 2017
- Accepted: 25 October 2017
- Published: 6 December 2017
Immunoglobulin therapy plays a critical role in the treatment of immunodeficiency disorders as well as autoimmune and inflammatory conditions. In immunodeficient patients, there has been controversy whether initial loading doses of intravenous (IVIG) should be based on actual body weight or a calculated parameter such as adjusted body weight in obese patients.
I describe a patient with Common Variable Immunodeficiency disorder (CVID) who underwent bariatric surgery for morbid obesity. Her weight decreased by 50% to below her calculated ideal body weight (IBW) while her immunoglobulin requirement fell by approximately 20%. Her steady state serum IgG increased from approximately 7 g/l to 11.7 g/l concomitant with weight loss.
I present this observation as support for the recommendation that initial loading doses of SCIG/IVIG in immunodeficiency should be based on adjusted body weight (AjBW) and not actual body weight in obese patients. This has important fiscal implications for treating obese patients with immunodeficiency disorders.
- Bariatric surgery
Immunoglobulin replacement is the standard of care for most patients with symptomatic primary immunodeficiency disorders (PIDs). Immunoglobulin replacement can be undertaken by either subcutaneous (SCIG) or intravenous (IVIG) routes. Current data suggests progressive improvement in health with gradually increasing serum IgG levels . Generally, most patients become less symptomatic when their steady state/trough IgG levels are kept above 7–8 g/l . Many patient factors influence the steady state/trough serum IgG levels following SCIG/IVIG. These include the genotype of the FcRn receptor, the presence of infective or inflammatory conditions such as bronchiectasis. In most cases the maintenance immunoglobulin dose is subsequently adjusted, based on the clinical response [3, 4]. This has been referred to as the biological trough level [5, 6].
In patients with primary immunodeficiency disorders (PIDs) with profoundly low IgG levels, an initial loading dose of IVIG (1 g/kg) is often administered, followed by monthly maintenance doses of 400–800 mg/kg. A loading dose allows a patient to rapidly attain steady state therapeutic IgG levels, which would otherwise take several months, if typical maintenance doses were administered. There has been debate about whether the initial loading dose of IVIG in morbidly obese PID patients should be based on actual body weight or adjusted body weight . Most clinical trials of IVIG therapy have excluded these patients.
Showing actual body weight vs lean body mass, adjusted body weight and ideal body weight in kg
Actual BW (kg)
Lean BW (kg)
Adjusted BW (kg)
Ideal BW (kg)
Serum IgG (g/l)
**Pre serum IgG index (IgG/SCIG/kg)
**Post serum IgG index (IgG/SCIG/kg)
Here I report a patient with common variable immunodeficiency disorder (CVID) who underwent bariatric surgery for morbid obesity. Progressive weight loss was associated with gradual increases in her serum immunoglobulin levels allowing a reduction in dosage. As will be shown here, this observation supports the recommendation that the initial loading dose of IVIG, is most appropriately based on adjusted body weight and not actual body weight in PID patients.
Clinical features and laboratory investigations
Family history of hypogammaglobulinemia
Daughter with CVID
Hb (130–190 g/l)
Neutrophils (1.9–7.5 × E + 9/l)
Platelets (150–400× E + 9/l)
IgG (7–14 g/l)
IgA (0.8–4 g/l)
IgM (0.4–2.5 g/l)
B cells present
Switched memory B cells (CD19+ CD27+ , IgD−: NR 5–21)
Tetanus pre/post (IU/ml)
Diphtheria pre/post (IU/ml)
HIB pre/post µg/ml
Pneumovax® pre/post* (serotypes > 1.3 µg/ml/23)
WES: no causative mutation
T cell responses
Normal lectin responses
Normal responses to tetanus, diphtheria and candida
CVID (Ameratunga et al. criteria)
In spite of morbid obesity, she did not meet the stringent criteria for publically funded bariatric surgery in New Zealand, as she had not developed type 2 diabetes. Following discussion with the bariatric surgical team she was accepted for weight reduction surgery based on likely cost savings from reduced immunoglobulin requirements. She was able to lose 10 kg weight prior to bariatric surgery (Fig. 1). She underwent a roux-en-Y procedure and had an uncomplicated post-operative course.
Following bariatric surgery, she experienced progressive weight loss (Fig. 1) which has stabilised at 63 kg, which is slightly lower than her predicted ideal body weight (Table 1). Concomitant with weight loss, her trough IgG levels began to increase allowing a dosage reduction (Fig. 1). It is likely further reduction in SCIG dosage will be possible in the future. She remains in good health, with a marked improvement in sputum production and has been able to discontinue her prophylactic antibiotics.
My observation offers direct evidence that SCIG requirements will decrease following substantial weight loss (Fig. 1). The patient’s actual weight decreased by 50% but her immunoglobulin requirements have decreased by approximately 20%. Her trough IgG levels were approximately 7 g/l prior to the surgery but increased to 11.7 g/l allowing a reduction in the SCIG dose. As can be seen from Table 1, her apparent SCIG dose/kg almost doubled from 0.44 g/kg/month to 0.81 g/kg/month with her weight loss. The reduced extracellular fluid following loss of adipose tissue is presumably the explanation for the reduced immunoglobulin requirements and increasing serum IgG. There may be other factors contributing to reduced SCIG requirements including amelioration of the inflammatory state associated with obesity and better control of her bronchiectasis .
I have used a calculated IgG index (serum IgG/SCIG dose/per kg ) to determine which derived body weight parameter prior to surgery correlated best with subsequent post weight loss SCIG requirements. This index accounts for changes in steady state serum IgG as well as changes in SCIG/IVIG dose/kg . A version of this IgG index has been used to calculate changes in trough IgG levels when adjusting SCIG/IVIG doses in obese patients . In my patient’s case the SCIG dose was initially kept steady, while her weight decreased.
Following weight loss her actual body weight IgG index (serum IgG/SCIG dose/per kg) was 11.35, which correlated closely with the predicted IgG index from the adjusted body weight (11.2), prior to weight loss (Table 1). The post weight reduction IgG index (11.35) takes into account the increased serum IgG and reduced SCIG dose following weight loss. As noted above, the decreased extracellular fluid compartment following loss of adipose tissue presumably explains the increasing serum IgG levels (Fig. 1). Other derived body weight parameters such as lean body mass and ideal body weight do not effectively model for this increased extracellular fluid compartment in obesity. They did not correlate closely with the post weight loss IgG index (Table 1).
The IgG index calculation in this patient supports basing initial loading doses of IVIG on adjusted body weight rather than actual body weight or ideal body weight (Table 1) in obese PID patients. As noted above subsequent maintenance SCIG/IVIG doses are based on the patient’s clinical response. A lower IVIG loading dose in obese PID patients has many advantages. There is an obvious fiscal benefit. The Hospital stay will shortened for the first visit and there are other advantages including a lower risk of thrombosis and cardiovascular adverse events from the large initial infusion .
Whether this observation indicates a lower IVIG dose can be used in obese patients with autoimmune or inflammatory disorders is less certain. As in other parts of the world, autoimmune and inflammatory disorders now account of the majority of IVIG usage in New Zealand . Immunomodulatory IVIG doses are typically 2 g/kg, given over 2-5 days. The high peak IgG levels may be important for efficacy in autoimmune and inflammatory disorders compared with PIDs, where the steady state during maintenance may be more relevant. Recent studies from Canada provided data that using adjusted body weight can result in major cost savings [8, 17]. However, efficacy data was not provided, which is an important consideration, when adjusting IVIG doses. While there may have been immediate cost savings from a lower dose of IVIG, there is a risk of reduced efficacy, which could result in downstream costs to the health system . Lower IVIG doses based on adjusted body weight in autoimmune and inflammatory disorders will have to be validated in future trials.
Obesity is currently a global public health problem. Bariatric surgery is being increasingly offered to patients with morbid obesity, when other interventions have failed. In these patients, there are many health benefits from weight reduction including reduced risk of diabetes, hypertension, coronary artery disease and osteoarthritis . Generally patients with a BMI > 30 who have co-morbidities are considered suitable candidates for bariatric surgery. Co-morbidities qualifying for bariatric surgery include diabetes, hypertension and joint symptoms. In many countries, there are age limits also. Consensus criteria exclude patients with obesity secondary to endocrine disorders as well as those who have serious psychological disorders.
Bariatric surgical procedures are in evolution . There are several surgical options including Roux-en-Y gastric bypass, sleeve gastrectomy, duodenal switch and adjustable gastric banding. Each of these procedures has its own advantages and disadvantages. Most procedures are carried out laparoscopically, which has many benefits, including reduced surgical morbidity. As seen here PID patients with bronchiectasis appear to tolerate this procedure well.
While there are many advantages of weight reduction, there are significant surgical risks and metabolic complications that must be factored when considering this option. Currently operative mortality is approximately three cases per 1000 . Patients accepted for such surgical procedures undergo intensive counselling and are encouraged to undergo presurgical weight loss under the supervision of the dietician in the Bariatric surgical team. My patient was able to lose almost 10 kg prior to surgery (Fig. 1). Following surgery, she was seen regularly for nutritional advice and monitoring by the bariatric surgical team. Her weight has stabilised at approximately 63 kg and she no longer suffers from hypertension or pre-diabetes.
My observation shows that the absolute SCIG/IVIG requirements will substantially decrease following bariatric surgery in an individual patient. I have calculated a direct cost saving of $10,400 per year based on her reduced SCIG requirements. Over 30 years this saving alone will more than cover the cost of the procedure. She did not meet the strict NZ criteria for publically funded bariatric surgery but the economic argument presented here was an important factor in her qualifying for the procedure. The expected cost savings are materialising. The reduction in immunoglobulin requirements in future PID patients should be factored when a cost–benefit analysis is undertaken.
While this is a single observation, the patient served as her own historical control. This controls for patient related factors including bronchiectasis, genotype of the FcRn receptor etc. Given the increasing prevalence of obesity, there will be other PID patients receiving SCIG/IVIG who undergo weight reduction surgery in the future. It will be important to carefully document their weight loss and to compare it with their SCIG/IVIG requirements. Observations from such patients may be the most convincing evidence that adjusted body weight is the best parameter to base initial loading doses of IVIG in patients with PIDs.
I thank the patient for permission to publish this case for the benefit of others. I thank Dr. Michael Booth for his comments on Bariatric surgery.
The author declares no competing interests.
Consent to publish
The patient has consented to publishing this report. There are no impediments to publish.
There are no additional data.
Ethics approval and consent to participate
This is standard treatment. There are no ethics issues relating to standard clinical practice. This is not an interventional study.
This study was internally funded.
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